Works by Chen, Jian-Min


Results: 144
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    Functionally deficient TRPV6 variants contribute to hereditary and familial chronic pancreatitis.

    Published in:
    Human Mutation, 2022, v. 43, n. 2, p. 228, doi. 10.1002/humu.24315
    By:
    • Hamada, Shin;
    • Masson, Emmanuelle;
    • Chen, Jian‐Min;
    • Sakaguchi, Reiko;
    • Rebours, Vinciane;
    • Buscail, Louis;
    • Matsumoto, Ryotaro;
    • Tanaka, Yu;
    • Kikuta, Kazuhiro;
    • Kataoka, Fumiya;
    • Sasaki, Akira;
    • Le Rhun, Marc;
    • Audin, Hela;
    • Lachaux, Alain;
    • Caumont, Bernard;
    • Lorenzo, Diane;
    • Billiemaz, Kareen;
    • Besnard, Raphael;
    • Koch, Stéphane;
    • Lamireau, Thierry
    Publication type:
    Article
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    Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.

    Published in:
    Human Genetics, 2015, v. 134, n. 6, p. 589, doi. 10.1007/s00439-015-1539-4
    By:
    • Wang, Ye;
    • Su, Peiqiang;
    • Hu, Bin;
    • Zhu, Wenjuan;
    • Li, Qibin;
    • Yuan, Ping;
    • Li, Jiangchao;
    • Guan, Xinyuan;
    • Li, Fucheng;
    • Jing, Xiangyi;
    • Li, Ru;
    • Zhang, Yongling;
    • Férec, Claude;
    • Cooper, David;
    • Wang, Jun;
    • Huang, Dongsheng;
    • Chen, Jian-Min;
    • Wang, Yiming
    Publication type:
    Article
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