Browsing by Author Vorasuk Shotelersuk

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Issue DateTitleAuthor(s)
2001Association between MTHFR polymorphisms and frontoethmoidal encephalomeningocele and cleft lip with or without cleft palateChupong Ittiwut
2004Association between polymorphisms in maternal genes of folate metabolism and down syndromeThivaratana Sinthuwiwat
2003Association between polymorphisms in TGF(Beta)-3, IRF6, SKI and MTHFD1 and frontoethmoidal encephalomeningocele and oral cleftChalurmpon Srichomthong
2005Biochemical and molecular analysis of Thai patients with gaucher diseaseKampon Phipatthanananti, 1982-
2005Biochemical and molecular analysis of Thai patients with multiple carboxylase deficiencySuphawee Janklat
2008Functional and genetic analyses of cholesteryl ester transfer protein and hepatic lipase in Thai subjects with hyperalphalipoproteinemiaWanee Plengpanich
2017Generation and characterization of HLA-Universal, iPSC-derived plateletsPhatchara Norbnop
2014GENOME AND EXOME SEQUENCES OF MONOZYGOTIC TWINS WITH TRISOMY 21, DISCORDANT FOR A CONGENITAL HEART DEFECTPongsathorn Chaiyasap
2018-12-14Human asparagine synthetase associates with the mitotic spindleChalongrat Noree; Monfort, Elena; Vorasuk Shotelersuk
2008Identification and molecular characterization of mutations in the Alpha-L-Iduronidase gene responsible for mucopolysaccharidosis type 1Korrakot Prommajan
2009Identification of a gene responsible for bilateral amastia with ectodermal dysplasiaSurasawadee Ausavarat
2016In vitro study of efficacy of pramlintide in osteosarcomaApiruk Sangsin
2018-07-16The most 5′ truncating homozygous mutation of WNT1 in siblings with osteogenesis imperfecta with a variable degree of brain anomalies: a case reportChulaluck Kuptanon; Chalurmpon Srichomthong; Apiruk Sangsin; Dool Kovitvanitcha; Kanya Suphapeetiporn; Vorasuk Shotelersuk
2012Mutation analysis of Filaggrin, SLC25A46, and TMEM232 in Thai patients with atopic dermatitisPiyamai Changate
2011Mutation and functional studies of DcR3 in patients with SLEChayanin Chokdeemeeboon
22/12/2017PATHOMECHANISM OF X-LINKED OSTEOGENESIS IMPERFECTA-
2009Pratical techniques of mutation detections for particular genetic diseases in Thai patientsPramuk Amarinthnukrowh
2014TARGET EDITING OF THE WISKOTT-ALDRICH SYNDROME (WAS) GENE USING ZINC FINGER NUCLEASESPramuk Amarinthnukrowh
2008Use of Antisense Morpholino Oligonuckeotides in correction of a novel splicing defect the BTK gene causing Bruton agammaglobulinemiaNatthakorn Rattanachartnarong
2015Using whole exome sequencing to identify mutations of four different human diseasesWipa Panmontha