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Page 1
Novel mutations in a Thai patient with methylmalonic acidemia.
Champattanachai V, Ketudat Cairns JR, Shotelersuk V, Keeratichamroen S, Sawangareetrakul P, Srisomsap C, Kaewpaluek V, Svasti J. Champattanachai V, et al. Among authors: keeratichamroen s. Mol Genet Metab. 2003 Aug;79(4):300-2. doi: 10.1016/s1096-7192(03)00106-9. Mol Genet Metab. 2003. PMID: 12948746
Proteomic analysis of cholangiocarcinoma cell line.
Srisomsap C, Sawangareetrakul P, Subhasitanont P, Panichakul T, Keeratichamroen S, Lirdprapamongkol K, Chokchaichamnankit D, Sirisinha S, Svasti J. Srisomsap C, et al. Among authors: keeratichamroen s. Proteomics. 2004 Apr;4(4):1135-44. doi: 10.1002/pmic.200300651. Proteomics. 2004. PMID: 15048994
The molecular basis of mucopolysaccharidosis type I in two Thai patients.
Ketudat Cairns JR, Keeratichamroen S, Sukcharoen S, Champattanachai V, Ngiwsara L, Lirdprapamongkol K, Liammongkolkul S, Srisomsap C, Surarit R, Wasant P, Svasti J. Ketudat Cairns JR, et al. Among authors: keeratichamroen s. Southeast Asian J Trop Med Public Health. 2005 Sep;36(5):1308-12. Southeast Asian J Trop Med Public Health. 2005. PMID: 16438163
Clinical and molecular characterization of an extended family with Fabry disease.
Wattanasirichaigoon D, Svasti J, Cairns JR, Tangnararatchakit K, Visudtibhan A, Keeratichamroen S, Ngiwsara L, Khowsathit P, Onkoksoong T, Lekskul A, Mongkolsiri D, Jariengprasert C, Thawil C, Ruencharoen S. Wattanasirichaigoon D, et al. Among authors: keeratichamroen s. J Med Assoc Thai. 2006 Sep;89(9):1528-35. J Med Assoc Thai. 2006. PMID: 17100396
Molecular characterization of type 3 (neuronopathic) Gaucher disease in Thai patients.
Suwannarat P, Keeratichamroen S, Wattanasirichaigoon D, Ngiwsara L, Cairns JR, Svasti J, Visudtibhan A, Pangkanon S. Suwannarat P, et al. Among authors: keeratichamroen s. Blood Cells Mol Dis. 2007 Nov-Dec;39(3):348-52. doi: 10.1016/j.bcmd.2007.06.015. Epub 2007 Aug 8. Blood Cells Mol Dis. 2007. PMID: 17689991
Molecular analysis of the iduronate-2-sulfatase gene in Thai patients with Hunter syndrome.
Keeratichamroen S, Cairns JR, Wattanasirichaigoon D, Wasant P, Ngiwsara L, Suwannarat P, Pangkanon S, Kuptanon J, Tanpaiboon P, Rujirawat T, Liammongkolkul S, Svasti J. Keeratichamroen S, et al. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S303-11. doi: 10.1007/s10545-008-0876-z. Epub 2008 May 20. J Inherit Metab Dis. 2008. PMID: 18500569
Clinical and molecular findings in Thai patients with isolated methylmalonic acidemia.
Vatanavicharn N, Champattanachai V, Liammongkolkul S, Sawangareetrakul P, Keeratichamroen S, Ketudat Cairns JR, Srisomsap C, Sathienkijkanchai A, Shotelersuk V, Kamolsilp M, Wattanasirichaigoon D, Svasti J, Wasant P. Vatanavicharn N, et al. Among authors: keeratichamroen s. Mol Genet Metab. 2012 Aug;106(4):424-9. doi: 10.1016/j.ymgme.2012.05.012. Epub 2012 May 29. Mol Genet Metab. 2012. PMID: 22695176
Decreasing activity and altered protein processing of human iduronate-2-sulfatase mutations demonstrated by expression in COS7 cells.
Charoenwattanasatien R, Cairns JR, Keeratichamroen S, Sawangareetrakul P, Tanpaiboon P, Wattanasirichaigoon D, Pangkanon S, Svasti J, Champattanachai V. Charoenwattanasatien R, et al. Among authors: keeratichamroen s. Biochem Genet. 2012 Dec;50(11-12):990-7. doi: 10.1007/s10528-012-9538-9. Epub 2012 Sep 19. Biochem Genet. 2012. PMID: 22990955 No abstract available.
24 results