Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Jiuxiang Lin"'
Publikováno v:
Head & Face Medicine, Vol 19, Iss 1, Pp 1-9 (2023)
Abstract Objective The aim of this study was to systematically explore the inclination of the lower central incisor and symphysis in alveolar bone in severe skeletal class III patients. Materials and methods A total of 198 severe skeletal class III p
Externí odkaz:
https://doaj.org/article/47e7d1a8c8704150896d0a234ff2b620
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
Publikováno v:
ACS Omega, Vol 5, Iss 30, Pp 18685-18692 (2020)
Externí odkaz:
https://doaj.org/article/6f61e6cb4a16474daace715c088907ce
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:
Shi-Jian Zhang, Peiqi Meng, Jieni Zhang, Peizeng Jia, Jiuxiang Lin, Xiangfeng Wang, Feng Chen, Xiaoxing Wei
Publikováno v:
Genomics, Proteomics & Bioinformatics, Vol 16, Iss 5, Pp 354-364 (2018)
The isolated type of orofacial cleft, termed non-syndromic cleft lip with or without cleft palate (NSCL/P), is the second most common birth defect in China, with Asians having the highest incidence in the world. NSCL/P involves multiple genes and com
Externí odkaz:
https://doaj.org/article/ff198f69774c498abcbef3bcca16e6fb
Publikováno v:
Protein & Cell, Vol 8, Iss 9, Pp 686-695 (2017)
ABSTRACT Inflammatory bowel disease (IBD) is an intestinal immune-dysfunctional disease worldwide whose prevalence increasing in Asia including China. It is a chronic disease of the gastrointestinal tract with unknown cause. Exosomes are small vesicl
Externí odkaz:
https://doaj.org/article/b7c727efb9e24b36845c03f776f62f82
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
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155683 (2016)
In this study, we sought to investigate the oral microbiota structure of children with cleft lip and palate (CLP) and explore the pre-operative oral bacterial composition related to the prognosis of alveolar bone grafting. In total, 28 patients (19 b
Externí odkaz:
https://doaj.org/article/55802a0eefd64c228efcc6a2f71f50fa
Autor:
Huaxiang Zhao, Jieni Zhang, Mengqi Zhang, Feng Deng, Leilei Zheng, Hui Zheng, Feng Chen, Jiuxiang Lin
Publikováno v:
F1000Research, Vol 4 (2016)
Aims: To investigate the association between the methylenetetrahydrofolate dehydrogenase 1 (MTHFD1) polymorphism rs 2236225 (c.1958G>A) and susceptibility to non-syndromic cleft of the lip and/or palate (NSCL/P). Methods: An extensive literature revi
Externí odkaz:
https://doaj.org/article/a66caa63e6964dab866b4b180e5579ec