Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Yong-Qing Sun"'
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:
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:
Shang Li, Hua‐ying Hu, Jun‐Jun Xu, Zhan‐ke Feng, Yong‐qing Sun, Xu Chen, Kai Yang, Ya‐zhou Li, Dong‐liang Zhang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background Congenital insensitivity to pain (CIP) conditions are a group of Mendelian disorders with clinical and genetic heterogeneity. CIP with anhidrosis (CIPA) is a distinct subtype caused by biallelic variants in the NTRK1 gene. Methods
Externí odkaz:
https://doaj.org/article/eb40b0c9466548898d9f64b02237c430
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:
Xiao-hui Wang, Zhen-bao Liu, Jian-xiong Liang, Zhi-yong Yang, Yong-qing Sun, Chang-jun Wang, Yue Qi
Publikováno v:
Materials Research Express, Vol 8, Iss 5, p 056504 (2021)
The static recrystallization (SRX) behavior of an ultrahigh-strength stainless steel (UHSSS) was investigated via double-hit isothermal compression tests. The results revealed that the kinetics of static recrystallization and the corresponding micros
Externí odkaz:
https://doaj.org/article/e3fc88b9e58542b38d447731fabf64c7
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:
Xu Chen, Zhan-Ke Feng, Huaying Hu, Jun‐Jun Xu, Ya‐zhou Li, Yong-qing Sun, Kai Yang, Dong‐liang Zhang, Shang Li
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Congenital insensitivity to pain (CIP) conditions are a group of Mendelian disorders with clinical and genetic heterogeneity. CIP with anhidrosis (CIPA) is a distinct subtype caused by biallelic variants in the NTRK1 gene. Methods In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bba077390e55fdd036bfa4ab7022d27
https://doi.org/10.1002/mgg3.1839
https://doi.org/10.1002/mgg3.1839
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