Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kuo-Ting Philip Chen"'
Autor:
Yi-Chieh Lu, Kuo-Ting Philip Chen, Hsien-Fang Chang, Yah-Huei Wu-Chou, Yin-Ting Lin, Lun-Jou Lo
Publikováno v:
The Cleft Palate-Craniofacial Journal. 57:671-677
Objective: Nonsyndromic oral clefts are common birth defect with complex etiology. In the present study, we attempt to further validate the possible role for ABCA4 and ARHGAP29 in the susceptibility to nonsyndromic oral clefts. Design: We performed a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f9449f14d3875586646a7c67dfcc27
https://doi.org/10.1177/1055665619899764
https://doi.org/10.1177/1055665619899764
Autor:
Yah-Huei Wu-Chou, Kuo-Ting Philip Chen, Yi-Chieh Lu, Yin-Ting Lin, Hsien-Fang Chang, Lun-Jou Lo
SUPPLEMENTARY_INFORMATION for The SNP rs560426 Within ABCA4-ARHGAP29 Locus and the Risk of Nonsyndromic Oral Clefts by Yah-Huei Wu-Chou, Kuo-Ting Philip Chen, Yi-Chieh Lu, Yin-Ting Lin, Hsien-Fang Chang and Lun-Jou Lo in The Cleft Palate-Craniofacial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6175a5c95f597c6e79b967492643c6a1
Autor:
Kuo-Ting Philip Chen, Yin-Ting Lin, Yah-Huei Wu-Chou, Hsien-Fang Chang, Yi-Chieh Lu, Lun-Jou Lo
Publikováno v:
The Cleft Palate-Craniofacial Journal. 56:778-785
Objective:To evaluate genetic variants within the regulatory regions of interferon regulatory factor 6 (IRF6) and TP63 for the etiology of nonsyndromic oral clefts risk factors.Design:We performed ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5693aa2fdc912ed1b82e19a8dfd1c2ca
https://doi.org/10.1177/1055665618809244
https://doi.org/10.1177/1055665618809244
Autor:
Yah-Huei, Wu-Chou, Yi-Chieh, Lu, Kuo-Ting Philip, Chen, Hsien-Fang, Chang, Yin-Ting, Lin, Lun-Jou, Lo
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 56(6)
To evaluate genetic variants within the regulatory regions of interferon regulatory factor 6 (We performed allelic transmission disequilibrium test analysis on 5 eligible single-nucleotide polymorphisms (SNPs) and SNP haplotypes using the Family-Base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::701197443ceab60069513b1766b404e6
https://pubmed.ncbi.nlm.nih.gov/30419764
https://pubmed.ncbi.nlm.nih.gov/30419764
Publikováno v:
The Laryngoscope. 122(1)
Objectives/Hypothesis: To evaluate the incidence of concomitant otitis media with effusion (OME) in children with cleft palate in Taiwan and the reliability of preoperative tympanometry. Study Design: Individual prospective cohort study. Methods: We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08a3dbf0c10098ac7f312b1d337e5a15
https://pubmed.ncbi.nlm.nih.gov/22183637
https://pubmed.ncbi.nlm.nih.gov/22183637
Publikováno v:
BMC Medical Genetics
Background Interferon Regulatory Factor 6 (IRF6) is a member of the IRF family of transcription factors. It has been suggested to be an important contributor to orofacial development since mutations of the IRF6 gene has been found in Van der Woude (V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d05cad4a21c7220499bea60282c1922