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CUIR at Chulalongkorn University
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