Limwongse C - Search Results

1

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

2

STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.

Chiraphapphaiboon W, Thongnoppakhun W, Limjindaporn T, Sawasdichai S, Roothumnong E, Prangphan K, Pamornpol B, Limwongse C, Pithukpakorn M. Chiraphapphaiboon W, et al. Among authors: limwongse c. Cureus. 2023 Feb 1;15(2):e34495. doi: 10.7759/cureus.34495. eCollection 2023 Feb. Cureus. 2023. PMID: 36874343 Free PMC article.

3

Identification of Genomic Alterations in Thai Patients With Colorectal Cancer Using Next-Generation Sequencing-Based Multigene Cancer Panel.

Jinda W, Moungthard H, Limwongse C, Pithukpakorn M, Saelee P, Pokkasup N, Khunpukdee S, Sukthaworn S, Jumpasri J. Jinda W, et al. Among authors: limwongse c. Cureus. 2023 May 16;15(5):e39067. doi: 10.7759/cureus.39067. eCollection 2023 May. Cureus. 2023. PMID: 37323311 Free PMC article.

4

Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia.

Hantaweepant C, Suktitipat B, Pithukpakorn M, Chinthammitr Y, Limwongse C, Tansiri N, Sawatnatee S, Takpradit C, Rotchanapanya W, Pongudom S, Charoenprasert K, Paiboonsukwong K, Thamprasert W, Nolwachai N, Rattanasawat W, Sae-Aeng B, Khorwanichakij N, Saetow P, Saengboon S, Kamjornpreecha K, Pholmoo W, Dujjawan B, Siritanaratkul N. Hantaweepant C, et al. Among authors: limwongse c. Hematology. 2023 Dec;28(1):2187155. doi: 10.1080/16078454.2023.2187155. Hematology. 2023. PMID: 36939018

5

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.

6

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: limwongse c. Clin Genet. 2004 Nov;66(5):452-60. doi: 10.1111/j.1399-0004.2004.00325.x. Clin Genet. 2004. PMID: 15479191

7

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: limwongse c. Int J Hematol. 2004 Aug;80(2):136-9. doi: 10.1532/ijh97.a20402. Int J Hematol. 2004. PMID: 15481441

8

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: limwongse c. 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.

9

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: limwongse c. Cancer Genet Cytogenet. 2005 Oct 15;162(2):127-34. doi: 10.1016/j.cancergencyto.2005.03.011. Cancer Genet Cytogenet. 2005. PMID: 16213360

10

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: limwongse c. Ophthalmic Genet. 2006 Mar;27(1):21-7. doi: 10.1080/13816810500481667. Ophthalmic Genet. 2006. PMID: 16543198

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