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CUIR at Chulalongkorn University
Browsing by Author Vorasuk Shotelersuk
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Showing results 1 to 20 of 27
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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