Browsing by Author Kanya Suphapeetiporn

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Showing results 1 to 14 of 14
Issue DateTitleAuthor(s)
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
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
2009Mutation and functional analysis of SUMO1, PDGFRa and miR-140 gens in non-syndromic oral cleftsSawitree Rattanasopha
2011Mutation and functional studies of DcR3 in patients with SLEChayanin Chokdeemeeboon
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
2016The 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 MutationSusama Chokesuwattanaskul
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