Analysis of marketed orphan drugs in China
Zhi, Wei, Liu, Meilin, Yang, Dan, Zhang, Shanshan, Lu, Yanqin, Han, Jinxiang
Published in Intractable & Rare Diseases Research (31.08.2023)
Published in Intractable & Rare Diseases Research (31.08.2023)
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Journal Article
The novel role of IFITM1–3 in myogenic differentiation of C2C12 cells
Zhang, Yongtao, Lu, Yanqin, Li, Xianxian, Zhang, Shanshan, Liu, Pengchao, Hao, Xiaoyang, Han, Jinxiang
Published in Intractable & Rare Diseases Research (31.08.2023)
Published in Intractable & Rare Diseases Research (31.08.2023)
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Journal Article
Pan-cancer analysis of osteogenesis imperfecta causing gene SERPINF1
Zhang, Chao, Yang, Wei, Zhang, Shanshan, Zhang, Yongtao, Liu, Pengchao, Li, Xianxian, Zhi, Wei, Yang, Dan, Li, Mian, Lu, Yanqin
Published in Intractable & Rare Diseases Research (01.02.2022)
Published in Intractable & Rare Diseases Research (01.02.2022)
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Journal Article
Integrative overview of IFITMs family based on Bioinformatics analysis
Liu, Pengchao, Zhang, Yongtao, Zhang, Shanshan, Peng, Chuanming, Yang, Wei, Li, Xianxian, Zhang, Chao, Li, Mian, Han, Jinxiang, Lu, Yanqin
Published in Intractable & Rare Diseases Research (31.08.2021)
Published in Intractable & Rare Diseases Research (31.08.2021)
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Journal Article
Comprehensive bioinformatics analysis of susceptibility genes for developmental dysplasia of the hip
Yang, Wei, Jin, Guiyang, Qian, Keying, Zhang, Chao, Zhi, Wei, Yang, Dan, Lu, Yanqin, Han, Jinxiang
Published in Intractable & Rare Diseases Research (31.05.2022)
Published in Intractable & Rare Diseases Research (31.05.2022)
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Journal Article
Circ_KIAA0922 regulates Saos-2 cell proliferation and osteogenic differentiation by regulating the miR-148a-3p/SMAD5 axis and activating the TGF-β signaling pathway
Zhang, Shanshan, Zhang, Yongtao, Yang, Dan, Zhi, Wei, Li, Junfeng, Liu, Meilin, Lu, Yanqin, Han, Jinxiang
Published in Intractable & Rare Diseases Research (30.11.2023)
Published in Intractable & Rare Diseases Research (30.11.2023)
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Journal Article
Myoblast differentiation of C2C12 cell may related with oxidative stress
Li, Xianxian, Zhang, Shanshan, Zhang, Yongtao, Liu, Pengchao, Li, Mian, Lu, Yanqin, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.08.2021)
Published in Intractable & Rare Diseases Research (01.08.2021)
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Journal Article
Influence of different intensities of vibration on proliferation and differentiation of human periodontal ligament stem cells
Zhang, Chunxiang, Lu, Yanqin, Zhang, Linkun, Liu, Yang, Zhou, Yi, Chen, Yangxi, Yu, Haiyang
Published in Archives of medical science (19.06.2015)
Published in Archives of medical science (19.06.2015)
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Journal Article
Circular RNAs and hereditary bone diseases
Zhai, Naixiang, Lu, Yanqin, Wang, Yanzhou, Ren, Xiuzhi, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2018)
Published in Intractable & Rare Diseases Research (01.02.2018)
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Journal Article
Comprehensive bioinformatic analysis of Wnt1 and Wnt1-associated diseases
Peng, Chuanming, Lu, Yanqin, Ren, Xiuzhi, Wang, Yanzhou, Zhang, Shie, Chen, Mei, Liu, Junlong, Fang, Fengling, Li, Tianyou, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2020)
Published in Intractable & Rare Diseases Research (01.02.2020)
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Journal Article
The expression profile of IFITM family gene in rats
Lu, Yanqin, Zuo, Qingli, Zhang, Yao, Wang, Yanzhou, Li, Tianyou, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.11.2017)
Published in Intractable & Rare Diseases Research (01.11.2017)
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Journal Article
Health assessment of patients with achondroplasia, pseudoachondroplasia,and rickets based on 3D non-linear diagnostics
Zhang, Jian, Lu, Yanqin, Wang, Yanzhou, Li, Tianyou, Peng, Chuanming, Zhang, Shie, Gao, Qingxia, Li, Wei, Liu, Chunshang, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2020)
Published in Intractable & Rare Diseases Research (01.02.2020)
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Journal Article
Complex heterozygous WNT1 mutation in severe recessive osteogenesis imperfecta of a Chinese patient
Lu, Yanqin, Dai, Yunzhang, Wang, Yanzhou, Zhai, Naixiang, Zhang, Jian, Liu, Junlong, Yin, Xiaoli, Li, Tianyou, Ren, Xiuzhi, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2018)
Published in Intractable & Rare Diseases Research (01.02.2018)
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Journal Article
Osteogenesis imperfecta type III/Ehlers-Danlos overlap syndrome in a Chinese man
Lu, Yanqin, Wang, Yanzhou, Rauch, Frank, Li, Hu, Zhang, Yao, Zhai, Naixiang, Zhang, Jian, Ren, Xiuzhi, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2018)
Published in Intractable & Rare Diseases Research (01.02.2018)
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Journal Article
Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patients
Lu, Yanqin, Ren, Xiuzhi, Wang, Yanzhou, Li, Tianyou, Li, Fuhui, Wang, Shifu, Xu, Chao, Wu, Guohua, Li, Hu, Li, Gongchao, Zhao, Fei, Wang, Ziqiang, Mo, Xinkai, Han, Jinxiang
Published in Clinical endocrinology (Oxford) (01.04.2014)
Published in Clinical endocrinology (Oxford) (01.04.2014)
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Journal Article
Splice receptor-site mutation c.697-2A>G of the COL1A1 gene in a Chinese family with osteogenesis imperfecta
Zhai, Naixiang, Lu, Yanqin, Wang, Yanzhou, Zhang, Shie, Peng, Chuanming, Zhang, Shanshan, Li, Tianyou, Chen, Mei, Liu, Junlong, Fang, Fengling, Ren, Xiuzhi, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.05.2019)
Published in Intractable & Rare Diseases Research (01.05.2019)
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Journal Article
A preparation method for the treatment of Cr(VI) composite adsorbent Ca-AC
Qin, Minjie, He, Zhaoju, Liu, Shen, Zhu, Li, Lu, Yanqin
Published in MATEC Web of Conferences (01.01.2018)
Published in MATEC Web of Conferences (01.01.2018)
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Journal Article
Conference Proceeding
Effects of targeted modulation of miR-762 on expression of the IFITM5 gene in Saos-2 cells
Mo, Xinkai, Lu, Yanqin, Han, Jinxiang
Published in Intractable & Rare Diseases Research (01.02.2014)
Published in Intractable & Rare Diseases Research (01.02.2014)
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Journal Article