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Items: 43

1.

The prehistoric peopling of Southeast Asia.

McColl H, Racimo F, Vinner L, Demeter F, Gakuhari T, Moreno-Mayar JV, van Driem G, Gram Wilken U, Seguin-Orlando A, de la Fuente Castro C, Wasef S, Shoocongdej R, Souksavatdy V, Sayavongkhamdy T, Saidin MM, Allentoft ME, Sato T, Malaspinas AS, Aghakhanian FA, Korneliussen T, Prohaska A, Margaryan A, de Barros Damgaard P, Kaewsutthi S, Lertrit P, Nguyen TMH, Hung HC, Minh Tran T, Nghia Truong H, Nguyen GH, Shahidan S, Wiradnyana K, Matsumae H, Shigehara N, Yoneda M, Ishida H, Masuyama T, Yamada Y, Tajima A, Shibata H, Toyoda A, Hanihara T, Nakagome S, Deviese T, Bacon AM, Duringer P, Ponche JL, Shackelford L, Patole-Edoumba E, Nguyen AT, Bellina-Pryce B, Galipaud JC, Kinaston R, Buckley H, Pottier C, Rasmussen S, Higham T, Foley RA, Lahr MM, Orlando L, Sikora M, Phipps ME, Oota H, Higham C, Lambert DM, Willerslev E.

Science. 2018 Jul 6;361(6397):88-92. doi: 10.1126/science.aat3628.

PMID:
29976827
2.

Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 Genes.

Jinda W, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Trinavarat A, Atchaneeyasakul LO.

Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2413-2420. doi: 10.1167/iovs.16-21322.

PMID:
28453600
3.

Exome sequencing in Thai patients with familial obesity.

Kaewsutthi S, Santiprabhob J, Phonrat B, Tungtrongchitr A, Lertrit P, Tungtrongchitr R.

Genet Mol Res. 2016 Jul 14;15(2). doi: 10.4238/gmr.15028311.

4.

A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.

Jinda W, Poungvarin N, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Suriyaphol P, Atchaneeyasakul LO.

Mol Vis. 2016 Apr 21;22:342-51. eCollection 2016.

5.

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.

Tun AW, Chaiyarit S, Kaewsutthi S, Katanyoo W, Chuenkongkaew W, Kuwano M, Tomonaga T, Peerapittayamongkol C, Thongboonkerd V, Lertrit P.

PLoS One. 2014 Sep 12;9(9):e106779. doi: 10.1371/journal.pone.0106779. eCollection 2014.

6.

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.

Boonyarit H, Mahasirimongkol S, Chavalvechakul N, Aoki M, Amitani H, Hosono N, Kamatani N, Kubo M, Lertrit P.

Forensic Sci Int Genet. 2014 Jul;11:166-73. doi: 10.1016/j.fsigen.2014.03.010. Epub 2014 Mar 27.

PMID:
24747184
7.

Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genes.

Jinda W, Taylor TD, Suzuki Y, Thongnoppakhun W, Limwongse C, Lertrit P, Suriyaphol P, Trinavarat A, Atchaneeyasakul LO.

Invest Ophthalmol Vis Sci. 2014 Apr 7;55(4):2259-68. doi: 10.1167/iovs.13-13567.

PMID:
24618324
8.

Mitochondrial DNA history of Sri Lankan ethnic people: their relations within the island and with the Indian subcontinental populations.

Ranaweera L, Kaewsutthi S, Win Tun A, Boonyarit H, Poolsuwan S, Lertrit P.

J Hum Genet. 2014 Jan;59(1):28-36. doi: 10.1038/jhg.2013.112. Epub 2013 Nov 7.

PMID:
24196378
9.

Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in Thailand.

Istikharah R, Tun AW, Kaewsutthi S, Aryal P, Kunhapan B, Katanyoo W, Chuenkongkaew W, Lertrit P.

Exp Eye Res. 2013 Nov;116:55-7. doi: 10.1016/j.exer.2013.08.007. Epub 2013 Aug 22. Review.

PMID:
23973714
10.

Polyglutamined expanded androgen receptor interacts with chaperonin CCT.

Pongtepaditep S, Limjindaporn T, Lertrit P, Srisawat C, Limwongse C.

Eur J Med Genet. 2012 Nov;55(11):599-604. doi: 10.1016/j.ejmg.2012.06.013. Epub 2012 Jul 14.

PMID:
22796525
11.

Stability of epitheliotrophic factors in autologous serum eye drops from chronic Stevens-Johnson syndrome dry eye compared to non-autoimmune dry eye.

Phasukkijwatana N, Lertrit P, Liammongkolkul S, Prabhasawat P.

Curr Eye Res. 2011 Sep;36(9):775-81. doi: 10.3109/02713683.2011.587935.

PMID:
21851164
12.

Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.

Kaewsutthi S, Phasukkijwatana N, Joyjinda Y, Chuenkongkaew W, Kunhapan B, Tun AW, Suktitipat B, Lertrit P.

Invest Ophthalmol Vis Sci. 2011 Jul 1;52(7):4742-8. doi: 10.1167/iovs.10-5816.

PMID:
21398275
13.

Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.

Phasukkijwatana N, Kunhapan B, Stankovich J, Chuenkongkaew WL, Thomson R, Thornton T, Bahlo M, Mushiroda T, Nakamura Y, Mahasirimongkol S, Tun AW, Srisawat C, Limwongse C, Peerapittayamongkol C, Sura T, Suthammarak W, Lertrit P.

Hum Genet. 2010 Jul;128(1):39-49. doi: 10.1007/s00439-010-0821-8. Epub 2010 Apr 21.

PMID:
20407791
14.

Characterization of 2-deoxy-D-glucose uptake in fibroblast cultures derived from patients with A3243G mitochondrial DNA mutation.

Luangtrakool K, Tate FY, Shepherd R, Campbell S, Sue CM, Lertrit P.

Southeast Asian J Trop Med Public Health. 2008 Jul;39(4):745-52.

PMID:
19058615
15.

Genetic history of Southeast Asian populations as revealed by ancient and modern human mitochondrial DNA analysis.

Lertrit P, Poolsuwan S, Thosarat R, Sanpachudayan T, Boonyarit H, Chinpaisal C, Suktitipat B.

Am J Phys Anthropol. 2008 Dec;137(4):425-40. doi: 10.1002/ajpa.20884.

PMID:
18615504
16.

Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.

Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.

J Neuroophthalmol. 2006 Dec;26(4):264-7.

PMID:
17204919
17.

Transmission of heteroplasmic G11778A in extensive pedigrees of Thai Leber hereditary optic neuropathy.

Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Luangtrakool K, Kunhapan B, Lertrit P.

J Hum Genet. 2006;51(12):1110-7. Epub 2006 Oct 28.

PMID:
17072496
18.

The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.

Phasukkijwatana N, Chuenkongkaew WL, Suphavilai R, Suktitipat B, Pingsuthiwong S, Ruangvaravate N, Atchaneeyasakul LO, Warrasak S, Poonyathalang A, Sura T, Lertrit P.

J Hum Genet. 2006;51(4):298-304. Epub 2006 Feb 14.

PMID:
16477364
19.

Proportion of 11778 mutant mitochondrial DNA and clinical expression in a thai population with leber hereditary optic neuropathy.

Chuenkongkaew WL, Suphavilai R, Vaeusorn L, Phasukkijwatana N, Lertrit P, Suktitipat B.

J Neuroophthalmol. 2005 Sep;25(3):173-5.

PMID:
16148621
20.

Oculopharyngodistal myopathy in a Thai family.

Witoonpanich R, Phankhian S, Sura T, Lertrit P, Phudhichareonrat S.

J Med Assoc Thai. 2004 Dec;87(12):1518-21.

PMID:
15822551
21.

An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy.

Chuenkongkaew WL, Lertrit P, Limwongse C, Nilanont Y, Boonyapisit K, Sangruchi T, Chirapapaisan N, Suphavilai R.

Eur J Neurol. 2005 May;12(5):388-91.

PMID:
15804271
22.

Case report: A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation.

Chuenkongkaew W, Lertrit P, Suphavilai R.

Southeast Asian J Trop Med Public Health. 2004 Mar;35(1):167-8.

PMID:
15272763
23.

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.

Ueyama H, Li YH, Fu GL, Lertrit P, Atchaneeyasakul LO, Oda S, Tanabe S, Nishida Y, Yamade S, Ohkubo I.

Proc Natl Acad Sci U S A. 2003 Mar 18;100(6):3357-62. Epub 2003 Mar 7.

24.

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.

Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.

J Hum Genet. 2002;47(11):594-604.

PMID:
12436196
25.

Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case report.

Sitburana O, Witoonpanich R, Phudhichareonrat S, Lertrit P, Supavilai R.

J Med Assoc Thai. 2001 Jul;84(7):1051-5.

PMID:
11759966
26.

Leber's hereditary optic neuropathy in Thailand.

Chuenkongkaew WL, Lertrit P, Poonyathalang A, Sura T, Ruangvaravate N, Atchaneeyasakul L, Suphavilai R.

Jpn J Ophthalmol. 2001 Nov-Dec;45(6):665-8.

PMID:
11754915
27.

Experience of ApoE study in Thai elderly.

Senanarong V, Harnphadungkit K, Lertrit P, Mitrpant C, Udompunthurak S, Limwong C, Prayoonwiwat N, Poungvarin N.

J Med Assoc Thai. 2001 Feb;84(2):182-7.

PMID:
11336076
28.

A unique 3.5-kb deletion of the mitochondrial genome in Thai patients with Kearns-Sayre syndrome.

Lertrit P, Imsumran A, Karnkirawattana P, Devahasdin V, Sangruchi T, Atchaneeyasakul L, Mungkornkarn C, Neungton N.

Hum Genet. 1999 Jul-Aug;105(1-2):127-31.

PMID:
10480366
29.

Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.

Lertrit P, Ruangvaravate N, Trongpanich Y, Imsumran A, Mungkornkarn C, Neungton N.

J Med Assoc Thai. 1999 Jan;82(1):59-64.

PMID:
10087740
30.

Mitochondrial DNA polymorphism in substantia nigra.

Kapsa RM, Jean-Francois MJ, Lertrit P, Weng S, Siregar N, Ojaimi J, Donnan G, Masters C, Byrne E.

J Neurol Sci. 1996 Dec;144(1-2):204-11.

PMID:
8994125
31.

Molecular examination of GH gene deletion in familial growth hormone deficiency.

Lekhakula S, Lertrit P, Tuchinda C, Angsusingha K, Kangsadalampai S, Wacharasindhu S, Futrakul A, Sritawil K.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:207-11.

PMID:
8629108
32.

Mitochondrial genome analysis in Kearns-Sayre syndrome.

Lertrit P, Atchaneeyasakul L, Devahastin V, Saechan V, Sangruchi T, Neungton N, Lekhakula S.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:162-5.

PMID:
8629098
33.

Update in molecular genetics: mitochondrial energy transduction disorders.

Marzuki S, Sudoyo H, Lertrit P.

Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:155-61. Review. No abstract available.

PMID:
8629096
34.

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction.

Lertrit P, Kapsa RM, Jean-Francois MJ, Thyagarajan D, Noer AS, Marzuki S, Byrne E.

Hum Mol Genet. 1994 Nov;3(11):1973-81.

PMID:
7874114
35.

Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.

Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.

Aust N Z J Med. 1994 Apr;24(2):188-93.

PMID:
8042948
36.

Rapid and noninvasive screening of patients with mitochondrial myopathy.

Kotsimbos N, Jean-Francois MJ, Huizing M, Kapsa RM, Lertrit P, Siregar NC, Marzuki S, Sue C, Byrne E.

Hum Mutat. 1994;4(2):132-5.

PMID:
7981717
37.

mtDNA in congenital myotonic dystrophy.

Thyagarajan D, Byrne E, Noer AS, Lertrit P, Kapsa R, Marzuki S.

Am J Hum Genet. 1993 Jan;52(1):207-10. No abstract available.

38.

Significance of mitochondrial DNA deletions in myotonic dystrophy.

Thyagarajan D, Byrne E, Noer S, Lertrit P, Utthanophol P, Kapsa R, Marzuki S.

Acta Neurol Scand. 1993 Jan;87(1):32-6.

PMID:
8093820
39.
40.

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.

Lertrit P, Noer AS, Jean-Francois MJ, Kapsa R, Dennett X, Thyagarajan D, Lethlean K, Byrne E, Marzuki S.

Am J Hum Genet. 1992 Sep;51(3):457-68.

41.

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base.

Marzuki S, Noer AS, Lertrit P, Thyagarajan D, Kapsa R, Utthanaphol P, Byrne E.

Hum Genet. 1991 Dec;88(2):139-45.

PMID:
1757091
42.

Mitochondrial DNA sequence analysis in congenital myotonic dystrophy.

Thyagarajan D, Byrne E, Noer S, Lertrit P, Utthanophol P, Kapsa R, Marzuki S.

Ann Neurol. 1991 Nov;30(5):724-7.

PMID:
1763896
43.

A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.

Noer AS, Sudoyo H, Lertrit P, Thyagarajan D, Utthanaphol P, Kapsa R, Byrne E, Marzuki S.

Am J Hum Genet. 1991 Oct;49(4):715-22.

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