Limwongse C - Search Results

1

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. Phasukkijwatana N, et al. Among authors: limwongse c. Hum Genet. 2010 Jul;128(1):39-49. doi: 10.1007/s00439-010-0821-8. Epub 2010 Apr 21. Hum Genet. 2010. PMID: 20407791

2

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. Chuenkongkaew WL, et al. Among authors: limwongse c. Eur J Neurol. 2005 May;12(5):388-91. doi: 10.1111/j.1468-1331.2004.01060.x. Eur J Neurol. 2005. PMID: 15804271

3

Thailand mutation and variation database (ThaiMUT).

Ruangrit U, Srikummool M, Assawamakin A, Ngamphiw C, Chuechote S, Thaiprasarnsup V, Agavatpanitch G, Pasomsab E, Yenchitsomanus PT, Mahasirimongkol S, Chantratita W, Palittapongarnpim P, Uyyanonvara B, Limwongse C, Tongsima S. Ruangrit U, et al. Among authors: limwongse c. Hum Mutat. 2008 Aug;29(8):E68-75. doi: 10.1002/humu.20787. Hum Mutat. 2008. PMID: 18484585

4

Polyglutamined expanded androgen receptor interacts with chaperonin CCT.

Pongtepaditep S, Limjindaporn T, Lertrit P, Srisawat C, Limwongse C. Pongtepaditep S, et al. Among authors: limwongse c. Eur J Med Genet. 2012 Nov;55(11):599-604. doi: 10.1016/j.ejmg.2012.06.013. Epub 2012 Jul 14. Eur J Med Genet. 2012. PMID: 22796525

5

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. Jinda W, et al. Among authors: limwongse c. Invest Ophthalmol Vis Sci. 2014 Apr 7;55(4):2259-68. doi: 10.1167/iovs.13-13567. Invest Ophthalmol Vis Sci. 2014. PMID: 24618324

6

Genetics and genomics in Thailand: challenges and opportunities.

Shotelersuk V, Limwongse C, Mahasirimongkol S. Shotelersuk V, et al. Among authors: limwongse c. Mol Genet Genomic Med. 2014 May;2(3):210-6. doi: 10.1002/mgg3.83. Epub 2014 May 14. Mol Genet Genomic Med. 2014. PMID: 24936510 Free PMC article. No abstract available.

7

Genetic variant screening of MC3R and MC4R genes in early-onset obese children and their relatives among a Thai population: family-based study.

Wannaiampikul S, Phonrat B, Tungtrongchitr A, Limwongse C, Chongviriyaphan N, Santiprabhob J, Tungtrongchitr R. Wannaiampikul S, et al. Among authors: limwongse c. Genet Mol Res. 2015 Dec 22;14(4):18090-102. doi: 10.4238/2015.December.22.35. Genet Mol Res. 2015. PMID: 26782456 Free article.

8

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. Jinda W, et al. Among authors: limwongse c. Mol Vis. 2016 Apr 21;22:342-51. eCollection 2016. Mol Vis. 2016. PMID: 27122965 Free PMC article.

9

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. Jinda W, et al. Among authors: limwongse c. Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2413-2420. doi: 10.1167/iovs.16-21322. Invest Ophthalmol Vis Sci. 2017. PMID: 28453600

10

Novel and de novo PKD1 mutations identified by multiple restriction fragment-single strand conformation polymorphism (MRF-SSCP).

Thongnoppakhun W, Limwongse C, Vareesangthip K, Sirinavin C, Bunditworapoom D, Rungroj N, Yenchitsomanus PT. Thongnoppakhun W, et al. Among authors: limwongse c. BMC Med Genet. 2004 Feb 3;5:2. doi: 10.1186/1471-2350-5-2. BMC Med Genet. 2004. PMID: 15018634 Free PMC article.

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