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Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C4T mutation in CLCN7

Xiang Chen Kun Zhang Janet Hock Chunyu Wang Xijie Yu

骨研究（英文版）2016，Vol.4Issue(4)：232-240,9.

骨研究（英文版）2016，Vol.4Issue(4)：232-240,9.DOI:10.1038/boneres.2016.35

Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C4T mutation in CLCN7

Xiang Chen ¹Kun Zhang ¹Janet Hock ²Chunyu Wang ¹Xijie Yu¹

作者信息

1. Laboratory of Endocrinology and Metabolism, Department of Endocrinology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China
2. The Polis Center, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA
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Xiang Chen,Kun Zhang,Janet Hock,Chunyu Wang,Xijie Yu..Enhanced but hypofunctional osteoclastogenesis in an autosomal dominant osteopetrosis type II case carrying a c.1856C4T mutation in CLCN7[J].骨研究（英文版）,2016,4(4):232-240,9.

基金项目

This work was supported by grants from the National Natural Science Foundation of China (Nos.81572639,81370969 and 81072190 to X Yu), the Ministry of Education of the People's Republic of China (No.20130181110066 to X Yu), and the Chengdu Bureau of Science and Technology (No.2014-HM01-00382-SF to X Yu). Xiang Chen and Xijie Yu designed this study. Xiang Chen performed gene detection and cel culture experiments. Kun Zhang and Chunyu Wang performed cell culture experiments. Xiang Chen, Xijie Yu, and Janet M Hock analyzed the data and wrote the paper （Nos.81572639,81370969 and 81072190 to X Yu）

骨研究（英文版）

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ISSN：2095-4700

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