Zobrazeno 1 - 10
of 18
pro vyhledávání: '"You-Sheng Yan"'
Autor:
Kai Yang, Ying-yi Luan, Shan Wang, You-sheng Yan, Yi-peng Wang, Jue Wu, Yong-qing Sun, Jing Zhang, Wen-qi Chen, Yu-lan Xiang, Ze-lu Li, Dong-liang Zhang, Cheng-hong Yin
Publikováno v:
iScience, Vol 27, Iss 4, Pp 109358- (2024)
Summary: Mesenchymal stem cell (MSC)-mediated coupling of osteogenesis and angiogenesis is a critical phenomenon in bone formation. Herein, we investigated the role and mechanism of SGMS1 in the osteogenic differentiation of MSCs and, in combination
Externí odkaz:
https://doaj.org/article/c956789ee343452f8d9453b8da94352a
Autor:
Kai Yang, Jue Wu, Shang Li, Shan Wang, Jing Zhang, Yi-peng Wang, You-sheng Yan, Hua-ying Hu, Ming-fang Xiong, Chao-bo Bai, Yong-qing Sun, Wen-qi Chen, Yang Zeng, Jun-liang Yuan, Cheng-hong Yin
Publikováno v:
Cell Death Discovery, Vol 9, Iss 1, Pp 1-15 (2023)
Abstract Hippocampal neuronal damage may induce cognitive impairment. Neurotrophic tyrosine kinase receptor 1 (NTRK1) reportedly regulates neuronal damage, although the underlying mechanism remains unclear. The present study aimed to investigate the
Externí odkaz:
https://doaj.org/article/59839e9a0a1342d5a4955354421fbdd3
Autor:
Qing‐bing He, Cai‐hong Wu, Dong‐lan Sun, Jia‐yu Yuan, Hua‐ying Hu, Kai Yang, Wen‐qi Chen, You‐sheng Yan, Guang‐yue Yin, Jing Zhang, Ya‐zhou Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 3, Pp n/a-n/a (2024)
Abstract Background The MYH3‐associated myosinopathies comprise a spectrum of rare neuromuscular disorders mainly characterized by distal arthrogryposis with or without other features like pterygia and vertebrae fusion. CPSKF1B (contractures, ptery
Externí odkaz:
https://doaj.org/article/cd96c595951949e38729fc14258a8b2d
Autor:
Kai Yang, Li‐Man Fu, Xiao‐Yang Chu, Jing Zhang, Wen‐Qi Chen, You‐Sheng Yan, Yi‐Peng Wang, Dong‐Liang Zhang, Cheng‐Hong Yin, Qing Guo
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 7, Pp n/a-n/a (2023)
Abstract Background Miller syndrome is a rare type of postaxial acrofacial dysostosis caused by biallelic mutations in the DHODH gene, which is characterized mainly by craniofacial malformations of micrognathia, orofacial clefts, cup‐shaped ears, a
Externí odkaz:
https://doaj.org/article/febe9e52bd1948dcb157e822212bc045
Autor:
Kai Yang, Yi-Cheng Xu, Hua-Ying Hu, Ya-Zhou Li, Qian Li, Ying-Yi Luan, Yan Liu, Yong-Qing Sun, Zhan-Ke Feng, You-Sheng Yan, Cheng-Hong Yin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Congenital insensitivity to pain with anhidrosis (CIPA), a rare autosomal recessive sensory neuropathy, was caused mainly by biallelic mutations in the NTRK1 gene. The pathogenesis of CIPA still needs further elucidation.Methods: Here, we
Externí odkaz:
https://doaj.org/article/779403bfacf44645aa83d692ab1e6e19
Autor:
Yan-xia Huang, Chun-yan Gao, Chun-yan Zheng, Xu Chen, You-sheng Yan, Yong-qing Sun, Xing-yue Dong, Kai Yang, Dong-liang Zhang
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
BackgroundThe low-density lipoprotein receptor-related protein 6 (LRP6) gene is a recently defined gene that is associated with the autosomal-dominant inherited tooth agenesis (TA). In the present study, a family of four generations having TA was rec
Externí odkaz:
https://doaj.org/article/6706a3004e4045cf9e2f5fe58f6a28e3
Autor:
Kai, Yang, Yan, Liu, Jue, Wu, Jing, Zhang, Hua-Ying, Hu, You-Sheng, Yan, Wen-Qi, Chen, Shu-Fa, Yang, Li-Juan, Sun, Yong-Qing, Sun, Qing-Qing, Wu, Cheng-Hong, Yin
Publikováno v:
Genes. 13(9)
Osteogenesis imperfecta (OI) is a rare mendelian skeletal dysplasia with autosomal dominant or recessive inheritance pattern, and almost the most common primary osteoporosis in prenatal settings. The diversity of clinical presentation and genetic eti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::834b867202c13f86fca12c63a23a21bd
https://pubmed.ncbi.nlm.nih.gov/36140746
https://pubmed.ncbi.nlm.nih.gov/36140746
Autor:
Jue Wu, Jian‑Jiang Zhu, Li Lin, You‑Sheng Yan, Ya Tan, Dong‑Liang Zhang, Kai Yang, Xing‑Yue Dong
Publikováno v:
Molecular Medicine Reports
Previous studies have suggested that pathogenic variants in interferon regulatoryse factor 6 (IRF6) can account for almost 70% of familial Van der Woude Syndrome (VWS) cases. However, gene modifiers that account for the phenotypic variability of IRF6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78a012a9a2c971a1ffc7ca6a0e2cf979
http://europepmc.org/articles/PMC7457716
http://europepmc.org/articles/PMC7457716
Autor:
Xu Chen, Kai Yang, Chun-yan Zheng, Xing-yue Dong, Yan-xia Huang, Chun-yan Gao, Yong-qing Sun, You-sheng Yan, Dong‐liang Zhang
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in Genetics
BackgroundThe low-density lipoprotein receptor-related protein 6 (LRP6) gene is a recently defined gene that is associated with the autosomal-dominant inherited tooth agenesis (TA). In the present study, a family of four generations having TA was rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9581df9dc5d4f62687fccf3c6f2557f7
https://www.frontiersin.org/articles/10.3389/fgene.2021.688241/full
https://www.frontiersin.org/articles/10.3389/fgene.2021.688241/full
Autor:
Kai, Yang, Hua-Ying, Hu, Jing, Zhang, You-Sheng, Yan, Wen-Qi, Chen, Yan, Liu, Yong-Qing, Sun, Qing, Guo, Cheng-Hong, Yin
Publikováno v:
Am J Transl Res
Charcot-Marie-Tooth (CMT) 2A disease, a genetic axonal nervous lesion, results from MFN2 pathogenic variation, and this gene plays a pivotal role in mitochondrial dynamics and calcium signaling. However, the underlying mechanism linking MFN2 defect t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f453c9646f6d11c383c00a718c96f7e
https://pubmed.ncbi.nlm.nih.gov/34786076
https://pubmed.ncbi.nlm.nih.gov/34786076