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Browsing by Author Vorasuk Shotelersuk

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Showing results 1 to 20 of 27 next >

Issue Date	Title	Author(s)
2001	Association between MTHFR polymorphisms and frontoethmoidal encephalomeningocele and cleft lip with or without cleft palate	Chupong Ittiwut
2004	Association between polymorphisms in maternal genes of folate metabolism and down syndrome	Thivaratana Sinthuwiwat
2003	Association between polymorphisms in TGF(Beta)-3, IRF6, SKI and MTHFD1 and frontoethmoidal encephalomeningocele and oral cleft	Chalurmpon Srichomthong
2005	Biochemical and molecular analysis of Thai patients with gaucher disease	Kampon Phipatthanananti, 1982-
2005	Biochemical and molecular analysis of Thai patients with multiple carboxylase deficiency	Suphawee Janklat
2005	Determination of the mechanism causing mesomelic dysplasia, Kantaputra type	Thanyapat Wanitchanon
2018	Establishment of an in vitro system to screen for substances to improve osteogenesis imperfecta osteoblasts’ functions	Wandee Udomchaiprasertkul
2008	Functional and genetic analyses of cholesteryl ester transfer protein and hepatic lipase in Thai subjects with hyperalphalipoproteinemia	Wanee Plengpanich
2023	Functional studies of p.N258K and p.G279D variants in the KCNQ2 gene	Suphalak Chokvithaya
2017	Generation and characterization of HLA-Universal, iPSC-derived platelets	Phatchara Norbnop
2014	GENOME AND EXOME SEQUENCES OF MONOZYGOTIC TWINS WITH TRISOMY 21, DISCORDANT FOR A CONGENITAL HEART DEFECT	Pongsathorn Chaiyasap
2018-12-14	Human asparagine synthetase associates with the mitotic spindle	Chalongrat Noree; Monfort, Elena; Vorasuk Shotelersuk
2008	Identification and molecular characterization of mutations in the Alpha-L-Iduronidase gene responsible for mucopolysaccharidosis type 1	Korrakot Prommajan
2009	Identification of a gene responsible for bilateral amastia with ectodermal dysplasia	Surasawadee Ausavarat
2020	Identification of a new disease gene for a familial autoimmune disease	Thivaratana Sinthuwiwat
2016	In vitro study of efficacy of pramlintide in osteosarcoma	Apiruk Sangsin
2018-07-16	The most 5′ truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case report	Chulaluck Kuptanon; Chalurmpon Srichomthong; Apiruk Sangsin; Dool Kovitvanitcha; Kanya Suphapeetiporn; Vorasuk Shotelersuk
2012	Mutation analysis of Filaggrin, SLC25A46, and TMEM232 in Thai patients with atopic dermatitis	Piyamai Changate
2008	Mutation and functional analysis of the thyroid hormone receptor β gene in thai families with resistance to thyroid hormone	Sarai Pongjantarasatian
2011	Mutation and functional studies of DcR3 in patients with SLE	Chayanin Chokdeemeeboon

Showing results 1 to 20 of 27 next >