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DENG, Yanfei, HUANG, Guiting, ZOU, Lingxiu, NONG, Tianying, YANG, Xiaoling, CUI, Jiayu, WEI, Yingming, YANG, Sufang, SHI, Deshun
Published in Journal of Veterinary Medical Science (2018)
Published in Journal of Veterinary Medical Science (2018)
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The mucolipidosis III-causing mutation in GNPTAB, c.1760G>C, disrupts the development of somites in rats
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Published in Genes & diseases (01.11.2024)
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Novel de novo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation
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Published in Genes & diseases (01.05.2024)
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A novel mutation in ext2 caused hereditary multiple exostoses through reducing the synthesis of heparan sulfate
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Published in Genetics and molecular biology (01.01.2021)
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A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report
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Published in Heliyon (15.04.2024)
Published in Heliyon (15.04.2024)
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Identification of a novel TBX5 mutation in a Chinese family with rare symptoms of Holt–Oram syndrome
Li, Xia, Shi, Weizhe, Ding, Xuejiao, Li, Jingchun, Li, Yiqiang, Wu, Jianping, Yuan, Zhe, Nong, Tianying, Xu, Hongwen, Zhu, Mingwei
Published in Heliyon (01.11.2022)
Published in Heliyon (01.11.2022)
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A TNNI2 variant c.525G>T causes distal arthrogryposis in a Chinese family
Li, Yue, Nong, Tianying, Li, Yiqiang, Li, Xia, Li, Zhaohui, Lv, Hui, Xu, Hongwen, Li, Jingchun, Zhu, Mingwei
Published in Molecular genetics & genomic medicine (01.12.2022)
Published in Molecular genetics & genomic medicine (01.12.2022)
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Hypoxia enhances buffalo adipose‐derived mesenchymal stem cells proliferation, stemness, and reprogramming into induced pluripotent stem cells
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Published in Journal of cellular physiology (01.10.2019)
Published in Journal of cellular physiology (01.10.2019)
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Novel denovo TRPV4 mutation identified in a Chinese family with metatropic dysplasia inhibits chondrogenic differentiation
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Published in Genes & diseases (01.05.2024)
Published in Genes & diseases (01.05.2024)
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Analysis of a case of Multiple pterygium syndrome due to a novel variant of CHRNG gene
Chen, Yiru, Nong, Tianying, Shi, Weizhe, Li, Jiangui, Ding, Xuejiao, Li, Yue, Zhu, Mingwei, Xu, Hongwen
Published in Zhonghua yi xue yi chuan xue za zhi (10.06.2023)
Published in Zhonghua yi xue yi chuan xue za zhi (10.06.2023)
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Journal Article
A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report
Shang, Liyuan, Shi, Weizhe, Xu, Yibo, Nong, Tianying, Li, Xia, Li, Zhaohui, Liu, Yanhan, Li, Jingchun, Tang, Ya-Ping, Zhu, Mingwei, Xu, Hongwen
Published in Heliyon (15.04.2024)
Published in Heliyon (15.04.2024)
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Establishment and application of FKBP10 gene conditional knockout mouse model in limb bud mesenchymal stem cells
XU HONGWEN, TANG YAPING, LI JINGCHUN, SHANG LIYUAN, ZHU MINGWEI, LI CHAOHUI, XU YIBO, NONG TIANYING, LI XIA
Year of Publication 04.06.2024
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Year of Publication 04.06.2024
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Construction method and application of WNT1 mutant gene knock-in rat osteogenesis imperfect animal model
XU HONGWEN, WANG XIUMIN, TANG YAPING, SHANG LIYUAN, ZHU MINGWEI, LI XIN, SHI WEIZHE, XU YIBO, NONG TIANYING, LI XIA, XIAN CAIXIA
Year of Publication 21.06.2024
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Year of Publication 21.06.2024
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