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Page 1
High Frequency of KRAS Codon 146 and FBXW7 Mutations in Thai Patients with Stage II-III Colon Cancer.
Korphaisarn K, Pongpaibul A, Roothumnong E, Pongsuktavorn K, Thamlikitkul L, Anekpuritanang T, Poungvarin N, Thongnoppakhun W, Pithukpakorn M. Korphaisarn K, et al. Among authors: thongnoppakhun w. Asian Pac J Cancer Prev. 2019 Aug 1;20(8):2319-2326. doi: 10.31557/APJCP.2019.20.8.2319. Asian Pac J Cancer Prev. 2019. PMID: 31450901 Free PMC article. Clinical Trial.
Association between ADAM33 polymorphisms and asthma in a Thai population.
Thongngarm T, Jameekornrak A, Limwongse C, Sangasapaviliya A, Jirapongsananuruk O, Assawamakin A, Chaiyaratana N, Luangwedchakarn V, Thongnoppakhun W. Thongngarm T, et al. Among authors: thongnoppakhun w. Asian Pac J Allergy Immunol. 2008 Dec;26(4):205-11. Asian Pac J Allergy Immunol. 2008. PMID: 19317339 Free article.
Six novel ATP7B mutations in Thai patients with Wilson disease.
Panichareon B, Taweechue K, Thongnoppakhun W, Aksornworanart M, Pithukpakorn M, Yenchitsomanus PT, Limwongse C, Limjindaporn T. Panichareon B, et al. Among authors: thongnoppakhun w. Eur J Med Genet. 2011 Mar-Apr;54(2):103-7. doi: 10.1016/j.ejmg.2010.10.008. Epub 2010 Oct 27. Eur J Med Genet. 2011. PMID: 21034864
Mycophenolic acid AUC in Thai kidney transplant recipients receiving low dose mycophenolate and its association with UGT2B7 polymorphisms.
Pithukpakorn M, Tiwawanwong T, Lalerd Y, Assawamakin A, Premasathian N, Tasanarong A, Thongnoppakhun W, Vongwiwatana A. Pithukpakorn M, et al. Among authors: thongnoppakhun w. Pharmgenomics Pers Med. 2014 Dec 5;7:379-85. doi: 10.2147/PGPM.S72760. eCollection 2014. Pharmgenomics Pers Med. 2014. PMID: 25540593 Free PMC article.
HLA-DRB1 and HLA-DQB1 Are Associated with Adult-Onset Immunodeficiency with Acquired Anti-Interferon-Gamma Autoantibodies.
Pithukpakorn M, Roothumnong E, Angkasekwinai N, Suktitipat B, Assawamakin A, Luangwedchakarn V, Umrod P, Thongnoppakhun W, Foongladda S, Suputtamongkol Y. Pithukpakorn M, et al. Among authors: thongnoppakhun w. PLoS One. 2015 May 26;10(5):e0128481. doi: 10.1371/journal.pone.0128481. eCollection 2015. PLoS One. 2015. PMID: 26011559 Free PMC article.
Novel Mutation of the TINF2 Gene in a Patient with Dyskeratosis Congenita.
Panichareon B, Seedapan T, Thongnoppakhun W, Limwongse C, Pithukpakorn M, Limjindaporn T. Panichareon B, et al. Among authors: thongnoppakhun w. Case Rep Dermatol. 2015 Aug 12;7(2):212-9. doi: 10.1159/000439042. eCollection 2015 May-Aug. Case Rep Dermatol. 2015. PMID: 26351433 Free PMC article.
Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.
Suktitipat B, Sathirareuangchai S, Roothumnong E, Thongnoppakhun W, Wangkiratikant P, Vorasan N, Krittayaphong R, Pithukpakorn M, Boonyapisit W. Suktitipat B, et al. Among authors: thongnoppakhun w. PLoS One. 2017 Jul 13;12(7):e0180056. doi: 10.1371/journal.pone.0180056. eCollection 2017. PLoS One. 2017. PMID: 28704380 Free PMC article.
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.
54 results