{"id":2212,"date":"2023-10-15T02:18:49","date_gmt":"2023-10-14T19:18:49","guid":{"rendered":"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/patcharee\/"},"modified":"2024-03-04T15:01:15","modified_gmt":"2024-03-04T08:01:15","slug":"patcharee","status":"publish","type":"page","link":"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/en\/patcharee\/","title":{"rendered":"patcharee-en"},"content":{"rendered":"\n  <div class=\"banner has-hover\" id=\"banner-261593875\">\n          <div class=\"banner-inner fill\">\n        <div class=\"banner-bg fill\" >\n                                                \n                    <\/div>\n\t\t\n\t<div class=\"ux-shape-divider ux-shape-divider--bottom ux-shape-divider--style-arrow-2\">\n\t\t<svg viewBox=\"0 0 1000 100\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" preserveAspectRatio=\"none\">\n\t<path class=\"ux-shape-fill\" d=\"M1000 100H0L0 96H480.929C482.255 96 483.527 95.4732 484.464 94.5355L497.879 81.1213C499.05 79.9497 500.95 79.9497 502.121 81.1213L515.536 94.5355C516.473 95.4732 517.745 96 519.071 96H1000V100Z\"\/>\n<\/svg>\n\t<\/div>\n        <div class=\"banner-layers container\">\n            <div class=\"fill banner-link\"><\/div>            \n   <div id=\"text-box-892653933\" class=\"text-box banner-layer x5 md-x5 lg-x0 y10 md-y10 lg-y10 res-text\">\n                     <div data-animate=\"fadeInUp\">           <div class=\"text-box-content text dark\">\n              \n              <div class=\"text-inner text-center\">\n                  \n\t<div id=\"text-157155857\" class=\"text\">\n\t\t\n<p style=\"font-size: 50%;\"><a href=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/en\/staff-of-teachers\/\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-448\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/left-arrow_545680-400x400.png\" alt=\"\" width=\"25\" height=\"25\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/left-arrow_545680-400x400.png 400w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/left-arrow_545680-280x280.png 280w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/left-arrow_545680.png 512w\" sizes=\"auto, (max-width: 25px) 100vw, 25px\" \/>\u00a0 <u>Faculty members<\/u><\/a><\/p>\n\t\t\n<style>\n#text-157155857 {\n  font-size: 1.8rem;\n  text-align: left;\n}\n@media (min-width:550px) {\n  #text-157155857 {\n    font-size: 2.5rem;\n  }\n}\n@media (min-width:850px) {\n  #text-157155857 {\n    font-size: 3rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n              <\/div>\n           <\/div>\n       <\/div>                     \n<style>\n#text-box-892653933 {\n  width: 60%;\n}\n#text-box-892653933 .text-box-content {\n  font-size: 100%;\n}\n<\/style>\n    <\/div>\n \n        <\/div>\n      <\/div>\n\n            \n<style>\n#banner-261593875 {\n  padding-top: 80px;\n  background-color: #1d59bb;\n}\n#banner-261593875 .ux-shape-divider--bottom svg {\n  height: 150px;\n  --divider-width: 100%;\n}\n@media (min-width:550px) {\n  #banner-261593875 {\n    padding-top: 100px;\n  }\n}\n@media (min-width:850px) {\n  #banner-261593875 {\n    padding-top: 120px;\n  }\n}\n<\/style>\n  <\/div>\n\n\n\n\t<section class=\"section\" id=\"section_919052151\">\n\t\t<div class=\"section-bg fill\" >\n\t\t\t\t\t\t\t\t\t\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n\t<div id=\"gap-1084445384\" class=\"gap-element clearfix\" style=\"display:block; height:auto;\">\n\t\t\n<style>\n#gap-1084445384 {\n  padding-top: 30px;\n}\n<\/style>\n\t<\/div>\n\t\n<div class=\"row align-center\"  id=\"row-120187283\">\n\n\t<div id=\"col-1704010081\" class=\"col small-12 large-12\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div id=\"text-3350743405\" class=\"text\">\n\t\t\n<h2>Professor Patcharee Lertrit Wichyanuwat<\/h2>\n\t\t\n<style>\n#text-3350743405 {\n  font-size: 0.8rem;\n  text-align: center;\n}\n@media (min-width:550px) {\n  #text-3350743405 {\n    font-size: 0.9rem;\n  }\n}\n@media (min-width:850px) {\n  #text-3350743405 {\n    font-size: 0.9rem;\n    text-align: left;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-1704010081 > .col-inner {\n  margin: 0px 0px -20px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n\n\t<div id=\"col-550853243\" class=\"col medium-8 small-12 large-5\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div class=\"img has-hover x md-x lg-x y md-y lg-y\" id=\"image_310988282\">\n\t\t\t\t\t\t\t\t<div class=\"img-inner dark\" >\n\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"752\" height=\"489\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/04.png\" class=\"attachment-large size-large\" alt=\"\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/04.png 752w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/04-615x400.png 615w\" sizes=\"auto, (max-width: 752px) 100vw, 752px\" \/>\t\t\t\t\t\t\n\t\t\t\t\t<\/div>\n\t\t\t\t\t\t\t\t\n<style>\n#image_310988282 {\n  width: 100%;\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-550853243 > .col-inner {\n  margin: 0px 0px -20px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n\n\t<div id=\"col-781696391\" class=\"col medium-10 small-12 large-7\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<div class=\"row\"  id=\"row-491774954\">\n\n\t<div id=\"col-1675556611\" class=\"col small-12 large-12\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div id=\"text-3956926737\" class=\"text\">\n\t\t\n<ul>\n<li>M.D., Faculty of Medicine Siriraj Hospital, Mahidol University, Thailand<\/li>\n<li>Ph.D. (Biochemistry), Monash University, Melbourne, Australia<\/li>\n<li>Certificated Thai Board of Family Medicine , Faculty of Medicine Siriraj Hospital<\/li>\n<\/ul>\n\t\t\n<style>\n#text-3956926737 {\n  font-size: 1rem;\n  line-height: 1.5;\n}\n@media (min-width:550px) {\n  #text-3956926737 {\n    line-height: 1.3;\n  }\n}\n@media (min-width:850px) {\n  #text-3956926737 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\n\t\t<div class=\"icon-box featured-box icon-box-left text-left\"  >\n\t\t\t\t\t<div class=\"icon-box-img\" style=\"width: 21px\">\n\t\t\t\t<div class=\"icon\">\n\t\t\t\t\t<div class=\"icon-inner\" >\n\t\t\t\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"400\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/suitcase_1243560-400x400.png\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/suitcase_1243560-400x400.png 400w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/suitcase_1243560-280x280.png 280w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/suitcase_1243560.png 512w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/>\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t<div class=\"icon-box-text last-reset\">\n\t\t\t\t\t\t\t\t\t\n\t<div id=\"text-2977269396\" class=\"text\">\n\t\t\n<p>Office : 1018 Srisavarindira Bldg. 10th Fl. Department of Biochemistry. Faculty of Medicine Siriraj Hospital, Bangkoknoi, Bangkok 10700<\/p>\n\t\t\n<style>\n#text-2977269396 {\n  font-size: 1rem;\n}\n@media (min-width:850px) {\n  #text-2977269396 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t\n\n\t\t<div class=\"icon-box featured-box icon-box-left text-left\"  >\n\t\t\t\t\t<div class=\"icon-box-img\" style=\"width: 21px\">\n\t\t\t\t<div class=\"icon\">\n\t\t\t\t\t<div class=\"icon-inner\" >\n\t\t\t\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"400\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/flask_2729603-400x400.png\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/flask_2729603-400x400.png 400w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/flask_2729603-280x280.png 280w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/flask_2729603.png 512w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/>\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t<div class=\"icon-box-text last-reset\">\n\t\t\t\t\t\t\t\t\t\n\t<div id=\"text-1189188030\" class=\"text\">\n\t\t\n<p>Laboratory : Metabolic and mitochondrial laboratory, 926 Srisavarindira Bldg. 9rd Fl.<\/p>\n\t\t\n<style>\n#text-1189188030 {\n  font-size: 1rem;\n}\n@media (min-width:850px) {\n  #text-1189188030 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t\n\n\t\t<div class=\"icon-box featured-box icon-box-left text-left\"  >\n\t\t\t\t\t<div class=\"icon-box-img\" style=\"width: 21px\">\n\t\t\t\t<div class=\"icon\">\n\t\t\t\t\t<div class=\"icon-inner\" >\n\t\t\t\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"400\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/telephone_3891977-400x400.png\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/telephone_3891977-400x400.png 400w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/telephone_3891977-280x280.png 280w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/telephone_3891977.png 512w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/>\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t<div class=\"icon-box-text last-reset\">\n\t\t\t\t\t\t\t\t\t\n\t<div id=\"text-1114362752\" class=\"text\">\n\t\t\n<p>Phone : 02)-419-8735 (office), (02)-419-5361 (lab)<br \/>\nFax: (02)-276-8548, (02)-419-9141<\/p>\n\t\t\n<style>\n#text-1114362752 {\n  font-size: 1rem;\n}\n@media (min-width:850px) {\n  #text-1114362752 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t\n\n\t\t<div class=\"icon-box featured-box icon-box-left text-left\"  >\n\t\t\t\t\t<div class=\"icon-box-img\" style=\"width: 21px\">\n\t\t\t\t<div class=\"icon\">\n\t\t\t\t\t<div class=\"icon-inner\" >\n\t\t\t\t\t\t<img loading=\"lazy\" decoding=\"async\" width=\"400\" height=\"400\" src=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/mail_1324171-2-400x400.png\" class=\"attachment-medium size-medium\" alt=\"\" srcset=\"https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/mail_1324171-2-400x400.png 400w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/mail_1324171-2-280x280.png 280w, https:\/\/www2.si.mahidol.ac.th\/department\/biochemistry\/wp-content\/uploads\/2023\/10\/mail_1324171-2.png 512w\" sizes=\"auto, (max-width: 400px) 100vw, 400px\" \/>\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t\t\t<div class=\"icon-box-text last-reset\">\n\t\t\t\t\t\t\t\t\t\n\t<div id=\"text-15716066\" class=\"text\">\n\t\t\n<p>E-Mail : <a href=\"mailto:patcharee.ler@mahidol.ac.th\">patcharee.ler@mahidol.ac.th<\/a>, <a href=\"mailto:lertrito@yahoo.com\">lertrito@yahoo.com<\/a><\/p>\n\t\t\n<style>\n#text-15716066 {\n  font-size: 1rem;\n}\n@media (min-width:850px) {\n  #text-15716066 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-1675556611 > .col-inner {\n  margin: 0px 0px -20px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-781696391 > .col-inner {\n  margin: 0px 0px -20px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n<\/div>\n\t\t<\/div>\n\n\t\t\n<style>\n#section_919052151 {\n  padding-top: 0px;\n  padding-bottom: 0px;\n}\n<\/style>\n\t<\/section>\n\t\n\n\t<section class=\"section\" id=\"section_736659066\">\n\t\t<div class=\"section-bg fill\" >\n\t\t\t\t\t\t\t\t\t\n\t\t\t\n\n\t\t<\/div>\n\n\t\t\n\n\t\t<div class=\"section-content relative\">\n\t\t\t\n<div class=\"row\"  id=\"row-71444182\">\n\n\t<div id=\"col-1192096336\" class=\"col small-12 large-12\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n<div class=\"accordion\">\n\t<div id=\"accordion-1669466551\" class=\"accordion-item\">\n\t\t<a id=\"accordion-1669466551-label\" class=\"accordion-title plain active\" href=\"#accordion-item-research-profile\" aria-expanded=\"true\" aria-controls=\"accordion-1669466551-content\">\n\t\t\t<button class=\"toggle\" aria-label=\"Toggle\"><i class=\"icon-angle-down\" aria-hidden=\"true\"><\/i><\/button>\n\t\t\t<span>Research Profile<\/span>\n\t\t<\/a>\n\t\t<div id=\"accordion-1669466551-content\" class=\"accordion-inner\" style=\"display: block;\" aria-labelledby=\"accordion-1669466551-label\">\n\t\t\t\n\t<div id=\"text-3404967393\" class=\"text\">\n\t\t\n<h5>Glucose uptake assay in the cells derived from Diabetes Mellitus type 2 patients containing mitochondrial DNA mutation.<br \/>\n<span style=\"color: #000;\"><u>Background and scope<\/u><\/span><\/h5>\n<p>This project aims to investigate the ability of the cell (either fibroblast or transformed lymphocyte) derived from DM type II patients who carry mitochondrial mutation suspected to be the caused of this disease. The project will included either the culture of skin fibroblast or transformation of lymphocyte from the patients investigated from previous project to carry the mitochondrial mutation. Glucose uptake assay will be performed in the cell of the patients as well as normal control. The data will be analysed.<\/p>\n<h5>Mitochondrial DNA mutation in sensori-neural hearing loss in Thailand.<br \/>\n<span style=\"color: #000;\"><u>Background and scope<\/u><\/span><\/h5>\n<p>This project attempts to identify the mitochondrial DNA mutation in Thai population who has hearing problem. The patients who have hearing loss, sensori neural type, and positive family history will be from Department of Oto-Rhino-Laryngology, Siriraj Hospital. Total cell DNA will be extracted from whole blood samples. DNA sequencing will be performed in the rRNA coding region of mitochondrial genome. The data will be analysed compare to normal health controls.<\/p>\n<h5>Genetic relationship among populations speaking Tai Kadai language.<br \/>\n<span style=\"color: #000;\"><u>Background and scope<\/u><\/span><\/h5>\n<p>This project will emphasize in the population genetics of people living in Southern China and Southeast Asia. The hair follicle will be collected from various populations who speak Tai-Kadai language family in these areas and the mitochondrial genome (HVS-1 region) will be studied. The nucleotide diversity, phylogenetic tree and population tree will be constructed from their mitochondrial HVS-1 sequences. The genetic distance of inter and intra population of these people will be analysed and interpreted.<\/p>\n<h5>Ancient DNA analysis in 2 prehistoric populations of Thailand.<br \/>\n<span style=\"color: #000;\"><u>Background and scope<\/u><\/span><\/h5>\n<p>The purpose of this project is to investigate the genetic relationship between 2 ancient populations from Ban Non Wat, Pimai, Nakorn Ratchasima in the northeastern and from Kok Phanomdi, Chonburi, and the present population now living in Thailand. The molar tooth from the skeletal remains excavated from those sites will be used for the DNA extraction. The mitochondrial genome (HVS-1 region) will be sequenced from each sample. The nucleotide diversity, phylogenetic tree and population tree will be constructed from their mitochondrial HVS-1 sequences. The genetic distance of inter and intra population of these people together with the present populations around these areas will be performed.<\/p>\n\t\t\n<style>\n#text-3404967393 {\n  font-size: 1rem;\n  line-height: 2;\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t<div id=\"accordion-3287736411\" class=\"accordion-item\">\n\t\t<a id=\"accordion-3287736411-label\" class=\"accordion-title plain\" href=\"#accordion-item-publications\" aria-expanded=\"false\" aria-controls=\"accordion-3287736411-content\">\n\t\t\t<button class=\"toggle\" aria-label=\"Toggle\"><i class=\"icon-angle-down\" aria-hidden=\"true\"><\/i><\/button>\n\t\t\t<span>Publications<\/span>\n\t\t<\/a>\n\t\t<div id=\"accordion-3287736411-content\" class=\"accordion-inner\" aria-labelledby=\"accordion-3287736411-label\">\n\t\t\t\n\t<div id=\"text-3334284457\" class=\"text\">\n\t\t\n\n<div class=\"wpdt-c row wpDataTableContainerSimpleTable wpDataTables wpDataTablesWrapper\n\"\n    >\n        <table id=\"wpdtSimpleTable-14\"\n           style=\"border-collapse:collapse;\n                   border-spacing:0px;\"\n           class=\"wpdtSimpleTable wpDataTable\"\n           data-column=\"2\"\n           data-rows=\"52\"\n           data-wpID=\"14\"\n           data-responsive=\"0\"\n           data-has-header=\"0\">\n\n                    <tbody>        <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A1\"\n                    data-col-index=\"0\"\n                    data-row-index=\"0\"\n                    style=\" width:10.186092066601%;                    padding:10px;\n                    \"\n                    >\n                                        1.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B1\"\n                    data-col-index=\"1\"\n                    data-row-index=\"0\"\n                    style=\" width:89.813907933399%;                    padding:10px;\n                    \"\n                    >\n                                        Thyagarajan, D., Byrne, E., Noer, S., <b><u>Lertrit, P.,<\/u><\/b> Utthanophol, P., Kapsa, R., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/1763896\/\"><u>(1991). Mitochondrial DNA sequence analysis in congenital myotonic dystrophy.<\/u><\/a> Annals of neurology, 30(5), 724\u2013727. https:\/\/doi.org\/10.1002\/ana.410300514                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A2\"\n                    data-col-index=\"0\"\n                    data-row-index=\"1\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        2.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B2\"\n                    data-col-index=\"1\"\n                    data-row-index=\"1\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Noer, A. S., Sudoyo, H., <b><u>Lertrit, P.,<\/u><\/b> Thyagarajan, D., Utthanaphol, P., Kapsa, R., Byrne, E., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/1910259\/\"><u>(1991). A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome. <\/u><\/a>American journal of human genetics, 49(4), 715\u2013722.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A3\"\n                    data-col-index=\"0\"\n                    data-row-index=\"2\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        3.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-fs-000016 wpdt-align-left\"\n                                            data-cell-id=\"B3\"\n                    data-col-index=\"1\"\n                    data-row-index=\"2\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Marzuki, S., Noer, A. S.,<b><u>Lertrit, P.,<\/u><\/b> Thyagarajan, D., Kapsa, R., & Byrne, E. (1992). Molecular pathology of mitochondrial respiratory disorders: Normal nucleotide variants of human mitochondrial genome and mtDNA lesion in MERRF encephalomyopathy. In T. Sato (Ed.), Mitochondrial encephalomyopathies (Progress in Neuropathology, Vol. 9, pp. 131\u2013150). New York: Raven Press.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A4\"\n                    data-col-index=\"0\"\n                    data-row-index=\"3\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        4.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B4\"\n                    data-col-index=\"1\"\n                    data-row-index=\"3\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Marzuki, S., Noer, A. S., <b><u>Lertrit, P.,<\/u><\/b>Thyagarajan, D., Kapsa, R., Utthanaphol, P., & Byrne, E. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/1757091\/\"><u>(1991). Normal variants of human mitochondrial DNA and translation products: the building of a reference data base.<\/u><\/a>  Human genetics, 88(2), 139\u2013145. https:\/\/doi.org\/10.1007\/BF00206061                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A5\"\n                    data-col-index=\"0\"\n                    data-row-index=\"4\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        5.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B5\"\n                    data-col-index=\"1\"\n                    data-row-index=\"4\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Marzuki, S.,<b><u>Lertrit, P.,<\/u><\/b> Noer, A. S., Kapsa, R. M. I., Sudoyo, H., Byrne, E., & Thyagarajan, D. <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC1682561\/\"><u>(1992). Reply to Howell et al.: The need for a joint effort in the construction of a reference data base for normal sequence variants of human mtDNA. <\/u><\/a> American Journal of Human Genetics, 50(6), 1337\u20131340.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A6\"\n                    data-col-index=\"0\"\n                    data-row-index=\"5\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        6.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B6\"\n                    data-col-index=\"1\"\n                    data-row-index=\"5\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b>  Noer, A. S., Jean-Francois, M. J., Kapsa, R., Dennett, X., Thyagarajan, D., Lethlean, K., Byrne, E., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/1323207\/\"><u>(1992). A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I. <\/u><\/a>American journal of human genetics, 51(3), 457\u2013468.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A7\"\n                    data-col-index=\"0\"\n                    data-row-index=\"6\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        7.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B7\"\n                    data-col-index=\"1\"\n                    data-row-index=\"6\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Noer, A. S., Byrne, E., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/1487239\/\"><u>(1992). Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathy.<\/u><\/a>  Human genetics, 90(3), 251\u2013254. https:\/\/doi.org\/10.1007\/BF00220072                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A8\"\n                    data-col-index=\"0\"\n                    data-row-index=\"7\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        8.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B8\"\n                    data-col-index=\"1\"\n                    data-row-index=\"7\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Howell, N., McCullough, D. A., Kubacka, I., Halvorson, S., Mackey, D., Marzuki, S., <b><u>Lertrit, P.,<\/u><\/b> Noer, A. S., Kapsa, R. M. I., Sudoyo, H., Byrne, E., & Thyagarajan, D. <a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC1682555\/\"><u>(1992). The sequence of human mtDNA: The question of errors versus polymorphisms.<\/u><\/a> American Journal of Human Genetics, 50(6), 1333\u20131340.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A9\"\n                    data-col-index=\"0\"\n                    data-row-index=\"8\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        9.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B9\"\n                    data-col-index=\"1\"\n                    data-row-index=\"8\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Thyagarajan, D., Byrne, E., Noer, S., <b><u>Lertrit, P.,<\/u><\/b> Utthanophol, P., Kapsa, R., & Marzuki, S.  <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8093820\/\"><u>(1993). Significance of mitochondrial DNA deletions in myotonic dystrophy.<\/u><\/a> Acta neurologica Scandinavica, 87(1), 32\u201336. https:\/\/doi.org\/10.1111\/j.1600-0404.1993.tb04071.x                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A10\"\n                    data-col-index=\"0\"\n                    data-row-index=\"9\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        10.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B10\"\n                    data-col-index=\"1\"\n                    data-row-index=\"9\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Thyagarajan, D., Byrne, E., Noer, A. S., <b><u>Lertrit, P.,<\/u><\/b> Kapsa, R., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8192709\/\"><u>(1993). mtDNA in congenital myotonic dystrophy.<\/u><\/a> American journal of human genetics, 52(1), 207\u2013210.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A11\"\n                    data-col-index=\"0\"\n                    data-row-index=\"10\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        11.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B11\"\n                    data-col-index=\"1\"\n                    data-row-index=\"10\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Kapsa, R. M., Jean-Francois, M. J., Thyagarajan, D., Noer, A. S., Marzuki, S., & Byrne, E. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/7874114\/\"><u>(1994). Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction. <\/u><\/a>Human molecular genetics, 3(11), 1973\u20131981. https:\/\/doi.org\/10.1093\/hmg\/3.11.1973                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A12\"\n                    data-col-index=\"0\"\n                    data-row-index=\"11\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        12.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B12\"\n                    data-col-index=\"1\"\n                    data-row-index=\"11\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Kotsimbos, N., Jean-Francois, M. J., Huizing, M., Kapsa, R. M., <b><u>Lertrit, P.,<\/u><\/b> Siregar, N. C., Marzuki, S., Sue, C., & Byrne, E. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/7981717\/\"><u>(1994). Rapid and noninvasive screening of patients with mitochondrial myopathy.<\/u><\/a> Human mutation, 4(2), 132\u2013135. https:\/\/doi.org\/10.1002\/humu.1380040207                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A13\"\n                    data-col-index=\"0\"\n                    data-row-index=\"12\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        13.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B13\"\n                    data-col-index=\"1\"\n                    data-row-index=\"12\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Jean-Francois, M. J.,<b><u>Lertrit, P.,<\/u><\/b> Berkovic, S. F., Crimmins, D., Morris, J., Marzuki, S., & Byrne, E.<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8042948\/\"><u> (1994). Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.  <\/u><\/a>Australian and New Zealand journal of medicine, 24(2), 188\u2013193. https:\/\/doi.org\/10.1111\/j.1445-5994.1994.tb00556.x                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A14\"\n                    data-col-index=\"0\"\n                    data-row-index=\"13\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        14.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B14\"\n                    data-col-index=\"1\"\n                    data-row-index=\"13\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Atchaneeyasakul, L., <b><u>Lertrit, P.,<\/u><\/b> Devahastin, V., & Sangruchi, T. (1994). Case report: Kearns\u2013Sayre syndrome. Thai Journal of Ophthalmology, 8, 145\u2013153.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A15\"\n                    data-col-index=\"0\"\n                    data-row-index=\"14\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        15.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B15\"\n                    data-col-index=\"1\"\n                    data-row-index=\"14\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Marzuki, S., Sudoyo, H., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8629096\/\"><u>(1995). Update in molecular genetics: mitochondrial energy transduction disorders. <\/u><\/a>The Southeast Asian journal of tropical medicine and public health, 26 Suppl 1, 155\u2013161.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A16\"\n                    data-col-index=\"0\"\n                    data-row-index=\"15\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        16.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B16\"\n                    data-col-index=\"1\"\n                    data-row-index=\"15\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Atchaneeyasakul, L., Devahastin, V., Saechan, V., Sangruchi, T., Neungton, N., & Lekhakula, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8629098\/\"><u>(1995). Mitochondrial genome analysis in Kearns-Sayre syndrome. <\/u><\/a>The Southeast Asian journal of tropical medicine and public health, 26 Suppl 1, 162\u2013165.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A17\"\n                    data-col-index=\"0\"\n                    data-row-index=\"16\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        17.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B17\"\n                    data-col-index=\"1\"\n                    data-row-index=\"16\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Lekhakula, S., <b><u>Lertrit, P.,<\/u><\/b> Tuchinda, C., Angsusingha, K., Kangsadalampai, S., Wacharasindhu, S., Futrakul, A., & Sritawil, K.  <a href=\"https:\/\/europepmc.org\/article\/med\/8629108\"><u>(1995). Molecular examination of GH gene deletion in familial growth hormone deficiency. <\/u><\/a>The Southeast Asian journal of tropical medicine and public health, 26 Suppl 1, 207\u2013211.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A18\"\n                    data-col-index=\"0\"\n                    data-row-index=\"17\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        18.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B18\"\n                    data-col-index=\"1\"\n                    data-row-index=\"17\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Kapsa, R. M., Jean-Francois, M. J., <b><u>Lertrit, P.,<\/u><\/b> Weng, S., Siregar, N., Ojaimi, J., Donnan, G., Masters, C., & Byrne, E. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/8994125\/\"><u>(1996). Mitochondrial DNA polymorphism in substantia nigra.<\/u><\/a>Journal of the neurological sciences, 144(1-2), 204\u2013211. https:\/\/doi.org\/10.1016\/s0022-510x(96)00247-x                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A19\"\n                    data-col-index=\"0\"\n                    data-row-index=\"18\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        19.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B19\"\n                    data-col-index=\"1\"\n                    data-row-index=\"18\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Siripurkpong, P., Harnyuttanakorn, P., Chindaduangratana, C., Kotchabhakdi, N.,<b><u>Wichyanuwat, P.,<\/u><\/b> & Casalotti, S. O. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/9274984\/\"><u>(1997). Dexamethasone, but not stress, induce measurable changes of mitochondrial benzodiazepine receptor mRNA levels in rats.<\/u><\/a> European journal of pharmacology, 331(2-3), 227\u2013235. https:\/\/doi.org\/10.1016\/s0014-2999(97)01039-x                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A20\"\n                    data-col-index=\"0\"\n                    data-row-index=\"19\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        20.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B20\"\n                    data-col-index=\"1\"\n                    data-row-index=\"19\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Imsumran, A., Trongpanich, Y., Karnkirawattana, P., Devahasdin, V., Atchaneeyasakul, L., & others. <a href=\"https:\/\/pesquisa.bvsalud.org\/portal\/resource\/pt\/sea-137597\"><u>(1998). Mitochondrial genetics of mitochondrial diseases in Thailand. <\/u><\/a>Siriraj Hospital Gazette, 50, 53\u201364.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A21\"\n                    data-col-index=\"0\"\n                    data-row-index=\"20\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        21.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B21\"\n                    data-col-index=\"1\"\n                    data-row-index=\"20\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Dumrongdej, P., <b><u>Lertrit, P.,<\/u><\/b> Wongmanee, U., Panichkul, N., & Neungton, N. (1998). Serum ceruloplasmin in Wilson's disease. Siriraj Hospital Gazette, 50, 576\u2013581.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A22\"\n                    data-col-index=\"0\"\n                    data-row-index=\"21\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        22.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B22\"\n                    data-col-index=\"1\"\n                    data-row-index=\"21\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Ruangvaravate, N., Trongpanich, Y., Imsumran, A., Mungkornkarn, C., & Neungton, N. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/10087740\/\"><u>(1999). Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.  <\/u><\/a>Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 82(1), 59\u201364.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A23\"\n                    data-col-index=\"0\"\n                    data-row-index=\"22\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        23.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B23\"\n                    data-col-index=\"1\"\n                    data-row-index=\"22\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Imsumran, A., Karnkirawattana, P., Devahasdin, V., Sangruchi, T., Atchaneeyasakul, L., Mungkornkarn, C., & Neungton, N. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/10480366\/\"><u>(1999). A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndrome. <\/u><\/a>Human genetics, 105(1-2), 127\u2013131. https:\/\/doi.org\/10.1007\/s004399900062                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A24\"\n                    data-col-index=\"0\"\n                    data-row-index=\"23\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        24.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B24\"\n                    data-col-index=\"1\"\n                    data-row-index=\"23\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.,<\/u><\/b> Choopayak, C., Udomsangpetch, R., Chansiri, K., & Mungkornkarn, C. <a href=\"https:\/\/mahidol.elsevierpure.com\/en\/publications\/the-mitochondrial-cytochrome-oxidase-subunit-iii-gene-and-protein?utm_source=chatgpt.com\"><u>(1999). The mitochondrial cytochrome oxidase subunit III gene and protein sequence analysis in chloroquine-resistant Plasmodium falciparum.<\/u><\/a> Journal of Biochemistry, Molecular Biology and Biophysics, 3(3-4), 161-170.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A25\"\n                    data-col-index=\"0\"\n                    data-row-index=\"24\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        25.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B25\"\n                    data-col-index=\"1\"\n                    data-row-index=\"24\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Sitburana, O., Witoonpanich, R., Phudhichareonrat, S., <b><u>Lertrit, P.,<\/u><\/b>  & Supavilai, R. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/11759966\/\"><u>(2001). Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report. <\/u><\/a>Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 84(7), 1051\u20131055.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A26\"\n                    data-col-index=\"0\"\n                    data-row-index=\"25\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        26.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B26\"\n                    data-col-index=\"1\"\n                    data-row-index=\"25\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Senanarong, V., Harnphadungkit, K., <b><u>Lertrit, P.,<\/u><\/b>  Mitrpant, C., Udompunthurak, S., Limwong, C., Prayoonwiwat, N., & Poungvarin, N. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/11336076\/\"><u>(2001). Experience of ApoE study in Thai elderly. <\/u><\/a>Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 84(2), 182\u2013187.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A27\"\n                    data-col-index=\"0\"\n                    data-row-index=\"26\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        27.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B27\"\n                    data-col-index=\"1\"\n                    data-row-index=\"26\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Chuenkongkaew, W. L., <b><u>Lertrit, P.,<\/u><\/b> Poonyathalang, A., Sura, T., Ruangvaravate, N., Atchaneeyasakul, L., & Suphavilai, R. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/11754915\/\"><u>(2001). Leber's hereditary optic neuropathy in Thailand.<\/u><\/a> Japanese journal of ophthalmology, 45(6), 665\u2013668. https:\/\/doi.org\/10.1016\/s0021-5155(01)00423-3                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A28\"\n                    data-col-index=\"0\"\n                    data-row-index=\"27\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        28.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B28\"\n                    data-col-index=\"1\"\n                    data-row-index=\"27\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Sudoyo, H., Suryadi, H., <b><u>Lertrit, P.,<\/u><\/b> Pramoonjago, P., Lyrawati, D., & Marzuki, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/12436196\/\"><u>(2002). Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. <\/u><\/a>Journal of human genetics, 47(11), 594\u2013604. https:\/\/doi.org\/10.1007\/s100380200091                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A29\"\n                    data-col-index=\"0\"\n                    data-row-index=\"28\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        29.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B29\"\n                    data-col-index=\"1\"\n                    data-row-index=\"28\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Ueyama, H., Li, Y. H., Fu, G. L., <b><u>Lertrit, P.,<\/u><\/b> Atchaneeyasakul, L. O., Oda, S., Tanabe, S., Nishida, Y., Yamade, S., & Ohkubo, I. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/12626747\/\"><u>(2003). An A-71C substitution in a green gene at the second position in the red\/green visual-pigment gene array is associated with deutan color-vision deficiency.<\/u><\/a>Proceedings of the National Academy of Sciences of the United States of America, 100(6), 3357\u20133362. https:\/\/doi.org\/10.1073\/pnas.0637437100                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A30\"\n                    data-col-index=\"0\"\n                    data-row-index=\"29\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        30.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B30\"\n                    data-col-index=\"1\"\n                    data-row-index=\"29\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Witoonpanich, R., Phankhian, S., Sura, T.,<b><u>Lertrit, P.,<\/u><\/b> & Phudhichareonrat, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/15822551\/\"><u>(2004). Oculopharyngodistal myopathy in a Thai family.<\/u><\/a> Journal of the Medical Association of Thailand = Chotmaihet thangphaet, 87(12), 1518\u20131521.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A31\"\n                    data-col-index=\"0\"\n                    data-row-index=\"30\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        31.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B31\"\n                    data-col-index=\"1\"\n                    data-row-index=\"30\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Chuenkongkaew, W., <b><u>Lertrit, P.,<\/u><\/b> & Suphavilai, R.<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/15272763\/\"><u> (2004). Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation. <\/u><\/a>The Southeast Asian journal of tropical medicine and public health, 35(1), 167\u2013168.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A32\"\n                    data-col-index=\"0\"\n                    data-row-index=\"31\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        32.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B32\"\n                    data-col-index=\"1\"\n                    data-row-index=\"31\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Chuenkongkaew, W. L., Suphavilai, R., Vaeusorn, L., Phasukkijwatana, N., <b><u>Lertrit, P.,<\/u><\/b> & Suktitipat, B. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/16148621\/\"><u>(2005). Proportion of 11778 mutant mitochondrial DNA and clinical expression in a thai population with leber hereditary optic neuropathy. <\/u><\/a>Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society, 25(3), 173\u2013175. https:\/\/doi.org\/10.1097\/01.wno.0000176631.87234.49                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A33\"\n                    data-col-index=\"0\"\n                    data-row-index=\"32\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        33.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B33\"\n                    data-col-index=\"1\"\n                    data-row-index=\"32\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Chuenkongkaew, W. L., Samsen, P.,<b><u>Lertrit, P.<\/u><\/b>,& Thanasombatsakul, N. <a href=\"https:\/\/www.scopus.com\/pages\/publications\/27744491300\"><u>(2005). An unusual electrophysiologic finding in acute stage of Leber\u2019s hereditary optic neuropathy. <\/u><\/a>Neuro-Ophthalmology Japan, 22(3), 454\u2013458.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A34\"\n                    data-col-index=\"0\"\n                    data-row-index=\"33\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        34.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B34\"\n                    data-col-index=\"1\"\n                    data-row-index=\"33\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Chuenkongkaew, W. L., <b><u>Lertrit, P.<\/u><\/b>, Limwongse, C., Nilanont, Y., Boonyapisit, K., Sangruchi, T., & et al. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/15804271\/\"><u>(2005). An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy. <\/u><\/a> European Journal of Neurology, 12(5), 388\u2013391. https:\/\/doi.org\/10.1111\/j.1468-1331.2005.01003.x                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A35\"\n                    data-col-index=\"0\"\n                    data-row-index=\"34\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        35.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B35\"\n                    data-col-index=\"1\"\n                    data-row-index=\"34\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Tharaphan, P., Chuenkongkaew, W. L., Luangtrakool, K., Sanpachudayan, T., Suktitipat, B., Suphavilai, R., Srisawat, C., Sura, T., & <b><u>Lertrit, P.<\/u><\/b><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/17204919\/\"><u> (2006). Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy. <\/u><\/a> Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society, 26(4), 264\u2013267. https:\/\/doi.org\/10.1097\/01.wno.0000249318.88991.c4                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A36\"\n                    data-col-index=\"0\"\n                    data-row-index=\"35\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        36.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B36\"\n                    data-col-index=\"1\"\n                    data-row-index=\"35\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Phasukkijwatana, N., Chuenkongkaew, W. L., Suphavilai, R., Suktitipat, B., Pingsuthiwong, S., Ruangvaravate, N., Atchaneeyasakul, L. O., Warrasak, S., Poonyathalang, A., Sura, T., & <b><u>Lertrit, P.<\/u><\/b><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/18615504\/\"><u>(2006). The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees. <\/u><\/a>Journal of human genetics, 51(4), 298\u2013304. https:\/\/doi.org\/10.1007\/s10038-006-0361-1                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A37\"\n                    data-col-index=\"0\"\n                    data-row-index=\"36\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        37.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B37\"\n                    data-col-index=\"1\"\n                    data-row-index=\"36\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Phasukkijwatana, N., Chuenkongkaew, W. L., Suphavilai, R., Luangtrakool, K., Kunhapan, B., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/17072496\/\"><u>(2006). Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy. <\/u><\/a>Journal of human genetics, 51(12), 1110\u20131117. https:\/\/doi.org\/10.1007\/s10038-006-0073-6                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A38\"\n                    data-col-index=\"0\"\n                    data-row-index=\"37\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        38.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B38\"\n                    data-col-index=\"1\"\n                    data-row-index=\"37\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Luangtrakool, K., Tate, F. Y., Shepherd, R., Campbell, S., Sue, C. M., &<b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/19058615\/\"><u>(2008). Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation. <\/u><\/a>The Southeast Asian journal of tropical medicine and public health, 39(4), 745\u2013752.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A39\"\n                    data-col-index=\"0\"\n                    data-row-index=\"38\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        39.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B39\"\n                    data-col-index=\"1\"\n                    data-row-index=\"38\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        <b><u>Lertrit, P.<\/u><\/b>, Poolsuwan, S., Thosarat, R., Sanpachudayan, T., Boonyarit, H., Chinpaisal, C., & Suktitipat, B.<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/18615504\/\"><u>(2008). Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis.<\/u><\/a>American journal of physical anthropology, 137(4), 425\u2013440. https:\/\/doi.org\/10.1002\/ajpa.20884                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A40\"\n                    data-col-index=\"0\"\n                    data-row-index=\"39\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        40.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B40\"\n                    data-col-index=\"1\"\n                    data-row-index=\"39\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Phasukkijwatana, N., Kunhapan, B., Stankovich, J., Chuenkongkaew, W. L., Thomson, R., Thornton, T., Bahlo, M., Mushiroda, T., Nakamura, Y., Mahasirimongkol, S., Tun, A. W., Srisawat, C., Limwongse, C., Peerapittayamongkol, C., Sura, T., Suthammarak, W., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/20407791\/\"><u>(2010). Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.<\/u><\/a> Human genetics, 128(1), 39\u201349. https:\/\/doi.org\/10.1007\/s00439-010-0821-8                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A41\"\n                    data-col-index=\"0\"\n                    data-row-index=\"40\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        41.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B41\"\n                    data-col-index=\"1\"\n                    data-row-index=\"40\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Phasukkijwatana, N., <b><u>Lertrit, P.<\/u><\/b>, Liammongkolkul, S., & Prabhasawat, P. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/21851164\/\"><u>(2011). Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye. <\/u><\/a> Current eye research, 36(9), 775\u2013781. https:\/\/doi.org\/10.3109\/02713683.2011.587935                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A42\"\n                    data-col-index=\"0\"\n                    data-row-index=\"41\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        42.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B42\"\n                    data-col-index=\"1\"\n                    data-row-index=\"41\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Kaewsutthi, S., Phasukkijwatana, N., Joyjinda, Y., Chuenkongkaew, W., Kunhapan, B., Tun, A. W., Suktitipat, B., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/21398275\/\"><u>(2011). Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.<\/u><\/a> Investigative ophthalmology & visual science, 52(7), 4742\u20134748. https:\/\/doi.org\/10.1167\/iovs.10-5816                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A43\"\n                    data-col-index=\"0\"\n                    data-row-index=\"42\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        43.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B43\"\n                    data-col-index=\"1\"\n                    data-row-index=\"42\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Pongtepaditep, S., Limjindaporn, T., <b><u>Lertrit, P.<\/u><\/b>, Srisawat, C., & Limwongse, C. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/22796525\/\"><u>(2012). Polyglutamined expanded androgen receptor interacts with chaperonin CCT. <\/u><\/a>European journal of medical genetics, 55(11), 599\u2013604. https:\/\/doi.org\/10.1016\/j.ejmg.2012.06.013                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A44\"\n                    data-col-index=\"0\"\n                    data-row-index=\"43\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        44.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B44\"\n                    data-col-index=\"1\"\n                    data-row-index=\"43\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Istikharah, R., Tun, A. W., Kaewsutthi, S., Aryal, P., Kunhapan, B., Katanyoo, W., Chuenkongkaew, W., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/23973714\/\"><u> (2013). Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand. <\/u><\/a>Experimental eye research, 116, 55\u201357. https:\/\/doi.org\/10.1016\/j.exer.2013.08.007                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A45\"\n                    data-col-index=\"0\"\n                    data-row-index=\"44\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        45.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B45\"\n                    data-col-index=\"1\"\n                    data-row-index=\"44\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Tun, A. W., Chaiyarit, S., Kaewsutthi, S., Katanyoo, W., Chuenkongkaew, W., Kuwano, M., Tomonaga, T., Peerapittayamongkol, C., Thongboonkerd, V., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/25215595\/\"><u>(2014). Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation. <\/u><\/a>PloS one, 9(9), e106779. https:\/\/doi.org\/10.1371\/journal.pone.0106779                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell \"\n                                            data-cell-id=\"A46\"\n                    data-col-index=\"0\"\n                    data-row-index=\"45\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        46.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-fs-000016 wpdt-align-left\"\n                                            data-cell-id=\"B46\"\n                    data-col-index=\"1\"\n                    data-row-index=\"45\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Ranaweera, L., Kaewsutthi, S., Tun, A. W., Boonyarit, H., Poolsuwan, S., & <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/www.nature.com\/articles\/jhg2013112\"><u>(2014). Mitochondrial DNA history of Sri Lankan ethnic people: Their relations within the island and with the Indian subcontinental populations.<\/u><\/a> Journal of Human Genetics, 59(1), 28\u201336. https:\/\/doi.org\/10.1038\/jhg.2013.112                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A47\"\n                    data-col-index=\"0\"\n                    data-row-index=\"46\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        47.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B47\"\n                    data-col-index=\"1\"\n                    data-row-index=\"46\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Boonyarit, H., Mahasirimongkol, S., Chavalvechakul, N., Aoki, M., Amitani, H., Hosono, N., Kamatani, N., Kubo, M., &  <b><u>Lertrit, P.<\/u><\/b> <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/24747184\/\"><u>(2014). Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai population.<\/u><\/a> Forensic science international. Genetics, 11, 166\u2013173. https:\/\/doi.org\/10.1016\/j.fsigen.2014.03.010                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A48\"\n                    data-col-index=\"0\"\n                    data-row-index=\"47\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        48.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B48\"\n                    data-col-index=\"1\"\n                    data-row-index=\"47\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Kaewsutthi, S., Santiprabhob, J., Phonrat, B., Tungtrongchitr, A., <b><u>Lertrit, P.,<\/u><\/b> & Tungtrongchitr, R.<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/27421018\/\"><u> (2016). Exome sequencing in Thai patients with familial obesity.<\/u><\/a>Genetics and molecular research : GMR, 15(2), 10.4238\/gmr.15028311. https:\/\/doi.org\/10.4238\/gmr.15028311                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A49\"\n                    data-col-index=\"0\"\n                    data-row-index=\"48\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        49.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B49\"\n                    data-col-index=\"1\"\n                    data-row-index=\"48\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Jinda, W., Poungvarin, N., Taylor, T. D., Suzuki, Y., Thongnoppakhun, W., Limwongse, C., <b><u>Lertrit, P.,<\/u><\/b> Suriyaphol, P., & Atchaneeyasakul, L. O. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/27122965\/\"><u>(2016). A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa. <\/u><\/a>Molecular vision, 22, 342\u2013351.                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A50\"\n                    data-col-index=\"0\"\n                    data-row-index=\"49\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        50.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B50\"\n                    data-col-index=\"1\"\n                    data-row-index=\"49\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Jinda, W., Taylor, T. D., Suzuki, Y., Thongnoppakhun, W., Limwongse, C., <b><u>Lertrit, P.,<\/u><\/b> Trinavarat, A., & Atchaneeyasakul, L. O. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/28453600\/\"><u>(2017). Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes. <\/u><\/a>Investigative ophthalmology & visual science, 58(4), 2413\u20132420. https:\/\/doi.org\/10.1167\/iovs.16-21322                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A51\"\n                    data-col-index=\"0\"\n                    data-row-index=\"50\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        51.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B51\"\n                    data-col-index=\"1\"\n                    data-row-index=\"50\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        McColl, H., Racimo, F., Vinner, L., Demeter, F., Gakuhari, T., Moreno-Mayar, J. V., van Driem, G., Gram Wilken, U., Seguin-Orlando, A., de la Fuente Castro, C., Wasef, S., Shoocongdej, R., Souksavatdy, V., Sayavongkhamdy, T., Saidin, M. M., Allentoft, M. E., Sato, T., Malaspinas, A. S., Aghakhanian, F. A., Korneliussen, T., \u2026 Willerslev, E. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/29976827\/\"><u>(2018). The prehistoric peopling of Southeast Asia. <\/u><\/a>Science (New York, N.Y.), 361(6397), 88\u201392. https:\/\/doi.org\/10.1126\/science.aat3628                    <\/td>\n                                        <\/tr>\n                            <tr class=\"wpdt-cell-row \" >\n                                <td class=\"wpdt-cell wpdt-fs-000016\"\n                                            data-cell-id=\"A52\"\n                    data-col-index=\"0\"\n                    data-row-index=\"51\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        52.                    <\/td>\n                                                <td class=\"wpdt-cell wpdt-align-left wpdt-valign-top wpdt-fs-000016 wpdt-tc-000000\"\n                                            data-cell-id=\"B52\"\n                    data-col-index=\"1\"\n                    data-row-index=\"51\"\n                    style=\"                    padding:10px;\n                    \"\n                    >\n                                        Veenin, K., Wattanasirichaigoon, D., Suktitipat, B., Noojarern, S., <b><u>Lertrit, P.,<\/u><\/b> Tim-Aroon, T., Kaewsutthi, S., & Treepongkaruna, S. <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/35685918\/\"><u>(2022). Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome. <\/u><\/a>Frontiers in pediatrics, 10, 876436. https:\/\/doi.org\/10.3389\/fped.2022.876436                    <\/td>\n                                        <\/tr>\n                    <\/table>\n<\/div><style id='wpdt-custom-style-14'>\ntable#wpdtSimpleTable-14{ table-layout: fixed !important; }\ntable#wpdtSimpleTable-14 td, table.wpdtSimpleTable14 th { white-space: normal !important; }\n.wpdt-fs-000016 { font-size: 16px !important;}\n.wpdt-tc-000000 { color: #000000 !important;}\n<\/style>\n<style>\n        \/* table font color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable thead th,\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable tbody td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tbody td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tfoot td {\n        color: #000000 !important;\n    }\n            \/* th background color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable.bt[data-has-header='1'] td.wpdt-header-classes,\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable thead th,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th.sorting {\n        background-color: #1D59BB !important;\n        background-image: none !important;\n    }\n                \/* th font color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable.bt[data-has-header='1'] td.wpdt-header-classes,\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable thead th,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th {\n        color: #FFFFFF !important;\n    }\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th.sorting:after,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th.sorting_asc:after {\n        border-bottom-color: #FFFFFF !important;\n    }\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable thead th.sorting_desc:after {\n        border-top-color: #FFFFFF !important;\n    }\n        \n                \/* odd rows background color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable tr.odd td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.odd td {\n        background-color: #F7F7F7 !important;\n    }\n            \/* even rows background color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable tr.even td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.even td,\n    .wpdt-c .wpDataTablesWrapper table.has-columns-hidden tr.row-detail > td {\n        background-color: #FFFFFF !important;\n    }\n                    \/* rows hover background color *\/\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable tr.odd:hover > td,\n    .wpdt-c.wpDataTablesWrapper table.wpdtSimpleTable tr.even:hover > td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.odd:hover > td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.odd:hover > td.sorting_1,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.even:hover > td,\n    .wpdt-c .wpDataTablesWrapper table.wpDataTable tr.even:hover > td.sorting_1 {\n        background-color: #E9E9E9 !important;\n    }\n                        \n                <\/style>\n\n\t\t\n<style>\n#text-3334284457 {\n  font-size: 1rem;\n}\n@media (min-width:550px) {\n  #text-3334284457 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t<\/div>\n\t\n\t<div id=\"accordion-2414678065\" class=\"accordion-item\">\n\t\t<a id=\"accordion-2414678065-label\" class=\"accordion-title plain\" href=\"#accordion-item-abstract\/presentation\" aria-expanded=\"false\" aria-controls=\"accordion-2414678065-content\">\n\t\t\t<button class=\"toggle\" aria-label=\"Toggle\"><i class=\"icon-angle-down\" aria-hidden=\"true\"><\/i><\/button>\n\t\t\t<span>Abstract\/presentation<\/span>\n\t\t<\/a>\n\t\t<div id=\"accordion-2414678065-content\" class=\"accordion-inner\" aria-labelledby=\"accordion-2414678065-label\">\n\t\t\t\n<div class=\"row\"  id=\"row-1383336154\">\n\n\t<div id=\"col-855369205\" class=\"col medium-1 small-1 large-1\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div id=\"text-3255425561\" class=\"text\">\n\t\t\n<p>1.<br \/>\n\t\t\n<style>\n#text-3255425561 {\n  font-size: 1rem;\n  text-align: center;\n}\n@media (min-width:550px) {\n  #text-3255425561 {\n    font-size: 1rem;\n  }\n}\n<\/style>\n\t<\/div>\n\t\n\t\t<\/div>\n\t\t\t\t\n<style>\n#col-855369205 > .col-inner {\n  margin: 0px 0px -30px 0px;\n}\n<\/style>\n\t<\/div>\n\n\t\n\n\t<div id=\"col-962439324\" class=\"col medium-11 small-10 large-11\"  >\n\t\t\t\t<div class=\"col-inner\"  >\n\t\t\t\n\t\t\t\n\t<div id=\"text-858076298\" class=\"text\">\n\t\t\n<p>Witoonpanich R, Jindahra P, <strong><u>Lertrit P<\/u><\/strong>, et al. Autosomal dominant progressive external ophthalmoplegia: Report of a Thai family. 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