Thongnoppakhun W - Search Results

1

Tumor mutational profile of triple negative breast cancer patients in Thailand revealed distinctive genetic alteration in chromatin remodeling gene.

Niyomnaitham S, Parinyanitikul N, Roothumnong E, Jinda W, Samarnthai N, Atikankul T, Suktitipat B, Thongnoppakhun W, Limwongse C, Pithukpakorn M. Niyomnaitham S, et al. Among authors: thongnoppakhun w. PeerJ. 2019 Feb 25;7:e6501. doi: 10.7717/peerj.6501. eCollection 2019. PeerJ. 2019. PMID: 30828495 Free PMC article.

2

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. BMC Med Genet. 2004 Feb 3;5:2. doi: 10.1186/1471-2350-5-2. BMC Med Genet. 2004. PMID: 15018634 Free PMC article.

3

High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.

Wattanasirichaigoon D, Limwongse C, Jariengprasert C, Yenchitsomanus PT, Tocharoenthanaphol C, Thongnoppakhun W, Thawil C, Charoenpipop D, Pho-iam T, Thongpradit S, Duggal P. Wattanasirichaigoon D, et al. Among authors: thongnoppakhun w. Clin Genet. 2004 Nov;66(5):452-60. doi: 10.1111/j.1399-0004.2004.00325.x. Clin Genet. 2004. PMID: 15479191

4

Hemoglobin Pakse: presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism.

Turbpaiboon C, Siritantikorn A, Thongnoppakhun W, Bunditworapoom D, Limwongse C, Yenchitsomanus PT, Siritanaratkul N, Wilairat P. Turbpaiboon C, et al. Among authors: thongnoppakhun w. Int J Hematol. 2004 Aug;80(2):136-9. doi: 10.1532/ijh97.a20402. Int J Hematol. 2004. PMID: 15481441

5

A Thai family with hereditary pancreatitis and increased cancer risk due to a mutation in PRSS1 gene.

Pho-Iam T, Thongnoppakhun W, Yenchitsomanus PT, Limwongse C. Pho-Iam T, et al. Among authors: thongnoppakhun w. World J Gastroenterol. 2005 Mar 21;11(11):1634-8. doi: 10.3748/wjg.v11.i11.1634. World J Gastroenterol. 2005. PMID: 15786540 Free PMC article.

6

Mutations of the FLT3 gene in adult acute myeloid leukemia: determination of incidence and identification of a novel mutation in a Thai population.

Auewarakul CU, Sritana N, Limwongse C, Thongnoppakhun W, Yenchitsomanus PT. Auewarakul CU, et al. Among authors: thongnoppakhun w. Cancer Genet Cytogenet. 2005 Oct 15;162(2):127-34. doi: 10.1016/j.cancergencyto.2005.03.011. Cancer Genet Cytogenet. 2005. PMID: 16213360

7

Novel and de-novo truncating PAX6 mutations and ocular phenotypes in Thai aniridia patients.

Atchaneeyasakul LO, Trinavarat A, Dulayajinda D, Kumpornsin K, Thongnoppakhun W, Yenchitsomanus PT, Limwongse C. Atchaneeyasakul LO, et al. Among authors: thongnoppakhun w. Ophthalmic Genet. 2006 Mar;27(1):21-7. doi: 10.1080/13816810500481667. Ophthalmic Genet. 2006. PMID: 16543198

8

Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian population.

Auewarakul CU, Leecharendkeat A, Thongnoppakhun W, Limwongse C, Tocharoentanaphol C. Auewarakul CU, et al. Among authors: thongnoppakhun w. Haematologica. 2006 May;91(5):675-8. Epub 2006 Apr 19. Haematologica. 2006. PMID: 16627249

9

Mutation analysis of the GNE gene in distal myopathy with rimmed vacuoles (DMRV) patients in Thailand.

Liewluck T, Pho-Iam T, Limwongse C, Thongnoppakhun W, Boonyapisit K, Raksadawan N, Murayama K, Hayashi YK, Nishino I, Sangruchi T. Liewluck T, et al. Among authors: thongnoppakhun w. Muscle Nerve. 2006 Dec;34(6):775-8. doi: 10.1002/mus.20583. Muscle Nerve. 2006. PMID: 16810679

10

Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.

Atchaneeyasakul LO, Jinda W, Sakolsatayadorn N, Trinavarat A, Ruangvoravate N, Thanasombatskul N, Thongnoppakhun W, Limwongse C. Atchaneeyasakul LO, et al. Among authors: thongnoppakhun w. Ophthalmic Genet. 2008 Sep;29(3):139-44. doi: 10.1080/13816810802087394. Ophthalmic Genet. 2008. PMID: 18766995

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