Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Huaxiang, Zhao"'
Treatment and genetic analysis of multiple supernumerary and impacted teeth in an adolescent patient
Publikováno v:
BMC Oral Health, Vol 24, Iss 1, Pp 1-9 (2024)
Abstract Background Multiple supernumerary teeth, combined with numerous impacted teeth, can lead to various malocclusions, posing significant treatment challenges. While certain genes associated with syndromic cases of multiple supernumerary and imp
Externí odkaz:
https://doaj.org/article/b26a3156e5ef47f8b3876ade834aa164
Autor:
Shujie Hou, Xuqin Liang, Yuhua Jiao, Boxi Yan, Kangying Liu, Hongmei Lin, Yi Ding, Huimei Huang, Jieni Zhang, Huaxiang Zhao
Publikováno v:
Journal of Clinical Pediatric Dentistry; Nov2024, Vol. 48 Issue 6, p1-11, 11p
Autor:
Wenjie Zhong, Huaxiang Zhao, Wenbin Huang, Mengqi Zhang, Qian Zhang, Yue Zhang, Chong Chen, Zulihumaer Nueraihemaiti, Dilifeire Tuerhong, Huizhe Huang, Gulibaha Maimaitili, Feng Chen, Jiuxiang Lin
Publikováno v:
Genes and Diseases, Vol 8, Iss 5, Pp 689-697 (2021)
The Patched 1 (PTCH1) gene encodes a membrane receptor involved in the Hedgehog (Hh) signaling pathway, an abnormal state of which may result in congenital defects or human tumors. In this study, we conducted whole-exome sequencing on a three-generat
Externí odkaz:
https://doaj.org/article/0483e18d8154472bbab1376c06be6507
Autor:
Jieni Zhang, Huaxiang Zhao, Wenbin Huang, Fengqi Song, Wenjie Zhong, Mengqi Zhang, Yunfan Zhang, Zhibo Zhou, Jiuxiang Lin, Feng Chen
Publikováno v:
Genes and Diseases, Vol 7, Iss 3, Pp 440-447 (2020)
Cleft lip and/or palate (CL/P) is a most common craniofacial birth defect which has multifactorial etiology. In our study, we aimed to discover the underlying etiological gene variation in a Chinese family diagnosed as non-syndromic CL/P (NSCL/P). Th
Externí odkaz:
https://doaj.org/article/5cc1e3a0597b4ad590c31d6a0e84ac70
Functional Characterization of a Novel IRF6 Frameshift Mutation From a Van Der Woude Syndrome Family
Autor:
Mengqi Zhang, Jieni Zhang, Huaxiang Zhao, Vitaly Ievlev, Wenjie Zhong, Wenbin Huang, Robert A. Cornell, Jiuxiang Lin, Feng Chen
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundLoss-of-function mutations in interferon regulatory factor-6 (IRF6) are responsible for about 70% of cases of Van Der Woude Syndrome (VWS), an autosomal dominant developmental disorder characterized by pits and/or sinuses of the lower lip a
Externí odkaz:
https://doaj.org/article/a463e08eefd5442ea72365460133eb0c
Autor:
Peiqi Meng, Huaxiang Zhao, Wenbin Huang, Yunfan Zhang, Wenjie Zhong, Mengqi Zhang, Peizeng Jia, Zhibo Zhou, Gulibaha Maimaitili, Feng Chen, Jieni Zhang, Jiuxiang Lin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 9, Pp n/a-n/a (2019)
Abstract Background Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial birth defect. Its etiology is complex and it has a lifelong influence on affected individuals. Despite many studies, the pathogenic gene
Externí odkaz:
https://doaj.org/article/612708aa6d044c5ab7d1fa1c66d12478
Autor:
Wenbin Huang, Shiying Zhang, Jiuxiang Lin, Yi Ding, Nan Jiang, Jieni Zhang, Huaxiang Zhao, Feng Chen
Publikováno v:
Journal of Genetics and Genomics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d168968f57d6bba94e1ab871104ee106
https://doi.org/10.1016/j.jgg.2023.03.012
https://doi.org/10.1016/j.jgg.2023.03.012
Autor:
Le Chang, Qianqian Huang, Zhanping Ren, Yanhao Wang, Yuhua Jiao, Yongwei Tao, Huaxiang Zhao, Yuxia Hou
Publikováno v:
Journal of Clinical Pediatric Dentistry; Nov2023, Vol. 47 Issue 6, p155-162, 8p
Autor:
Gulibaha Maimaitili, Jiuxiang Lin, Huizhe Huang, Chong Chen, Huaxiang Zhao, Zulihumaer Nueraihemaiti, Wenbin Huang, Wenjie Zhong, Dilifeire Tuerhong, Yue Zhang, Feng Chen, Qian Zhang, Mengqi Zhang
Publikováno v:
Genes and Diseases, Vol 8, Iss 5, Pp 689-697 (2021)
The Patched 1 (PTCH1) gene encodes a membrane receptor involved in the Hedgehog (Hh) signaling pathway, an abnormal state of which may result in congenital defects or human tumors. In this study, we conducted whole-exome sequencing on a three-generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f843c7df087a2505bc2d15909ca2b9a5
https://doi.org/10.1016/j.gendis.2019.12.010
https://doi.org/10.1016/j.gendis.2019.12.010
