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Browsing by Author Kanya Suphapeetiporn

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Showing results 1 to 19 of 19

Issue Date	Title	Author(s)
2018	Establishment of an in vitro system to screen for substances to improve osteogenesis imperfecta osteoblasts’ functions	Wandee Udomchaiprasertkul
2017	Generation and characterization of HLA-Universal, iPSC-derived platelets	Phatchara Norbnop
2022	Genetic analysis of focal segmental glomerulosclerosis in Thailand	Suramath Isaranuwatchai
2014	GENOME AND EXOME SEQUENCES OF MONOZYGOTIC TWINS WITH TRISOMY 21, DISCORDANT FOR A CONGENITAL HEART DEFECT	Pongsathorn Chaiyasap
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
2009	Mutation and functional analysis of SUMO1, PDGFRa and miR-140 gens in non-syndromic oral clefts	Sawitree Rattanasopha
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
2017	Pathomechanism of x-linked osteogenesis imperfecta	Siraprapa Tongkobpetch
2009	Pratical techniques of mutation detections for particular genetic diseases in Thai patients	Pramuk Amarinthnukrowh
2014	TARGET EDITING OF THE WISKOTT-ALDRICH SYNDROME (WAS) GENE USING ZINC FINGER NUCLEASES	Pramuk Amarinthnukrowh
2016	The Use Of Induced Pluripotent Stem Sells (iPSCs) And Mesenchymal Stem Cells (MSCs) To Study The Genetic Basis Of Human DiseasesI. The Use Of Mesenchymal Stem Cells (MSCs) For Treatment Of Diabetic Wound In Nude Mice.II. The Use Of Induced Pluripotent Stem Cells (iPSCs) In Modeling Neutrophil Defects Resulting From A Single-Gene Mutation	Susama Chokesuwattanaskul
2008	Use of Antisense Morpholino Oligonuckeotides in correction of a novel splicing defect the BTK gene causing Bruton agammaglobulinemia	Natthakorn Rattanachartnarong
2015	Using whole exome sequencing to identify mutations of four different human diseases	Wipa Panmontha

Showing results 1 to 19 of 19