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Patcharee Lertrit

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Suttikarn Pongtepaditep; Chatchawan Srisawat; Patcharee Lertrit; Thawornchai Limjindaporn; Chanin Limwongse
Polyglutamined expanded androgen receptor interacts with chaperonin CCT.
Nopasak Phasukkijwatana; Patcharee Lertrit; Sompong Liammongkolkul; Pinnita Prabhasawat
Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye.
Supannee Kaewsutthi; Bussaraporn Kunhapan; Wanicha L Chuenkongkaew; Yutthana Joyjinda; Nopasak Phasukkijwatana; Bhoom Suktitipat; Aung Win Tun; Patcharee Lertrit
Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.

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All Publications

2012: Suttikarn Pongtepaditep; Chatchawan Srisawat; Patcharee Lertrit; Thawornchai Limjindaporn; Chanin Limwongse
Polyglutamined expanded androgen receptor interacts with chaperonin CCT.
European journal of medical genetics 2012;55(11):599-604.
2011: Nopasak Phasukkijwatana; Patcharee Lertrit; Sompong Liammongkolkul; Pinnita Prabhasawat
Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye.
Current eye research 2011;36(9):775-81.
2011: Supannee Kaewsutthi; Bussaraporn Kunhapan; Wanicha L Chuenkongkaew; Yutthana Joyjinda; Nopasak Phasukkijwatana; Bhoom Suktitipat; Aung Win Tun; Patcharee Lertrit
Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
Investigative ophthalmology & visual science 2011;52(7):4742-8.
2010: Nopasak Phasukkijwatana; Bussaraporn Kunhapan; Jim Stankovich; Wanicha L Chuenkongkaew; Russell Thomson; Timothy Thornton; Melanie Bahlo; Taisei Mushiroda; Yusuke Nakamura; surakameth mahasirimongkol; Aung Win Tun; Chatchawan Srisawat; Chanin Limwongse; Chayanon Peerapittayamongkol; Thanyachai Sura; Wichit Suthammarak; Patcharee Lertrit
Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.
Human genetics 2010;128(1):39-49.
2008: Patcharee Lertrit; Samerchai Poolsuwan; Rachanie Thosarat; Thitima Sanpachudayan; Hathaichanoke Boonyarit; Chatchai Chinpaisal; Bhoom Suktitipat
Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis.
American journal of physical anthropology 2008;137(4):425-40.
2008: Komon Luangtrakool; Farrah-Yasmin Tate; Rachael Shepherd; Sarah Campbell; Carolyn M Sue; Patcharee Lertrit
Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation.
The Southeast Asian journal of tropical medicine and public health 2008;39(4):745-52.
2006: Pattamon Tharaphan; Wanicha L Chuenkongkaew; Komon Luangtrakool; Thitima Sanpachudayan; Bhoom Suktitipat; Rungnapa Suphavilai; Chatchawan Srisawat; Thanyachai Sura; Patcharee Lertrit
Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2006;26(4):264-7.
2006: Nopasak Phasukkijwatana; Wanicha L Chuenkongkaew; Rungnapa Suphavilai; Komon Luangtrakool; Bussaraporn Kunhapan; Patcharee Lertrit
Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.
Journal of human genetics 2006;51(12):1110-7.
2006: Nopasak Phasukkijwatana; Wanicha L Chuenkongkaew; Rungnapa Suphavilai; Bhoom Suktitipat; Sarinee Pingsuthiwong; Ngamkae Ruangvaravate; La-ongsri Atchaneeyasakul; Sukhuma Warrasak; Anuchit Poonyathalang; Thanyachai Sura; Patcharee Lertrit
The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.
Journal of human genetics 2006;51(4):298-304.
2005: Wanicha L Chuenkongkaew; Rungnapa Suphavilai; Lookjan Vaeusorn; Nopasak Phasukkijwatana; Patcharee Lertrit; Bhoom Suktitipat
Proportion of 11778 mutant mitochondrial DNA and clinical expression in a thai population with leber hereditary optic neuropathy.
Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society 2005;25(3):173-5.
2005: Wanicha L Chuenkongkaew; Patcharee Lertrit; Chanin Limwongse; Y Nilanont; Kanokwan Boonyapisit; Tumtip Sangruchi; Niphon Chirapapaisan; Rungnapa Suphavilai
An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2005;12(5):388-91.
2004: Rawiphan Witoonpanich; Sriphan Phankhian; Thanyachai Sura; Patcharee Lertrit; Suchart Phudhichareonrat
Oculopharyngodistal myopathy in a Thai family.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2004;87(12):1518-21.
2004: Wanicha L Chuenkongkaew; Patcharee Lertrit; Rungnapa Suphavilai
Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.
The Southeast Asian journal of tropical medicine and public health 2004;35(1):167-8.
2003: Hisao Ueyama; Yao-Hua Li; Gui-Lian Fu; Patcharee Lertrit; La-ongsri Atchaneeyasakul; Sanae Oda; Shoko Tanabe; Yasuhiro Nishida; Shinichi Yamade; Iwao Ohkubo
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.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(6):3357-62.
2002: Herawati Sudoyo; Helena Suryadi; Patcharee Lertrit; Patcharin Pramoonjago; Diana Lyrawati; Sangkot Marzuki
Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Journal of human genetics 2002;47(11):594-604.
2001: Wanicha L Chuenkongkaew; Patcharee Lertrit; Anuchit Poonyathalang; Thanyachai Sura; Ngamkae Ruangvaravate; La-ongsri Atchaneeyasakul; Rungnapa Suphavilai
Leber's hereditary optic neuropathy in Thailand.
Japanese journal of ophthalmology 2001;45(6):665-8.
2001: O Sitburana; Rawiphan Witoonpanich; Suchart Phudhichareonrat; Patcharee Lertrit; R Supavilai
Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2001;84(7):1051-5.
2001: Vorapun Senanarong; Kamolthip Harnphadungkit; Patcharee Lertrit; C Mitrpant; Suthipol Udompunthurak; C Limwong; Naraporn Prayoonwiwat; Niphon Poungvarin
Experience of ApoE study in Thai elderly.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2001;84(2):182-7.
1999: Patcharee Lertrit; arisa imsumran; P Karnkirawattana; V Devahasdin; Tumtip Sangruchi; La-ongsri Atchaneeyasakul; C Mungkornkarn; Neelobol Neungton
A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndrome.
Human genetics 1999;105(1-2):127-31.
1999: Patcharee Lertrit; Ngamkae Ruangvaravate; Y Trongpanich; arisa imsumran; C Mungkornkarn; Neelobol Neungton
Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 1999;82(1):59-64.
1995: S Lekhakula; Patcharee Lertrit; Chanisada Tuchinda; Kitti Angsusingha; S Kangsadalampai; Suttipong Wacharasindhu; A Futrakul; K Sritawil
Molecular examination of GH gene deletion in familial growth hormone deficiency.
The Southeast Asian journal of tropical medicine and public health 1995;26 Suppl 1():207-11.
1995: Patcharee Lertrit; L Atchaneeyasakul; V Devahastin; Vannarat Saechan; Tumtip Sangruchi; Neelobol Neungton; S Lekhakula
Mitochondrial genome analysis in Kearns-Sayre syndrome.
The Southeast Asian journal of tropical medicine and public health 1995;26 Suppl 1():162-5.