Works matching IS 09646906 AND DT 2012 AND VI 21 AND IP 9


Results: 22
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    Subscription Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. NP-b, doi. 10.1093/hmg/dds121
    Publication type:
    Article
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    Cover Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. NP-a, doi. 10.1093/hmg/dds120
    Publication type:
    Article
    8

    Contents Page.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. NP, doi. 10.1093/hmg/dds119
    Publication type:
    Article
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    Rescue from excitotoxicity and axonal degeneration accompanied by age-dependent behavioral and neuroanatomical alterations in caspase-6-deficient mice.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. 1954, doi. 10.1093/hmg/dds005
    By:
    • Uribe, Valeria;
    • Wong, Bibiana K.Y.;
    • Graham, Rona K.;
    • Cusack, Corey L.;
    • Skotte, Niels H.;
    • Pouladi, Mahmoud A.;
    • Xie, Yuanyun;
    • Feinberg, Konstantin;
    • Ou, Yimiao;
    • Ouyang, Yingbin;
    • Deng, Yu;
    • Franciosi, Sonia;
    • Bissada, Nagat;
    • Spreeuw, Amanda;
    • Zhang, Weining;
    • Ehrnhoefer, Dagmar E.;
    • Vaid, Kuljeet;
    • Miller, Freda D.;
    • Deshmukh, Mohanish;
    • Howland, David
    Publication type:
    Article
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    Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. 2132, doi. 10.1093/hmg/dds029
    By:
    • Abnet, Christian C.;
    • Wang, Zhaoming;
    • Song, Xin;
    • Hu, Nan;
    • Zhou, Fu-You;
    • Freedman, Neal D.;
    • Li, Xue-Min;
    • Yu, Kai;
    • Shu, Xiao-Ou;
    • Yuan, Jian-Min;
    • Zheng, Wei;
    • Dawsey, Sanford M.;
    • Liao, Linda M.;
    • Lee, Maxwell P.;
    • Ding, Ti;
    • Qiao, You-Lin;
    • Gao, Yu-Tang;
    • Koh, Woon-Puay;
    • Xiang, Yong-Bing;
    • Tang, Ze-Zhong
    Publication type:
    Article
    12

    Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. 2039, doi. 10.1093/hmg/dds022
    By:
    • Purevjav, Enkhsaikhan;
    • Arimura, Takuro;
    • Augustin, Sibylle;
    • Huby, Anne-Cecile;
    • Takagi, Ken;
    • Nunoda, Shinichi;
    • Kearney, Debra L.;
    • Taylor, Michael D.;
    • Terasaki, Fumio;
    • Bos, Johan M.;
    • Ommen, Steve R.;
    • Shibata, Hiroki;
    • Takahashi, Megumi;
    • Itoh-Satoh, Manatsu;
    • McKenna, William J.;
    • Murphy, Ross T.;
    • Labeit, Siegfried;
    • Yamanaka, Yoichi;
    • Machida, Noboru;
    • Park, Jeong-Euy
    Publication type:
    Article
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    Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases.

    Published in:
    Human Molecular Genetics, 2012, v. 21, n. 9, p. 1968, doi. 10.1093/hmg/dds006
    By:
    • Chelbi, Sonia T.;
    • Wilson, Melissa L.;
    • Veillard, Anne-Clémence;
    • Ingles, Sue A.;
    • Zhang, Jim;
    • Mondon, Françoise;
    • Gascoin-Lachambre, Géraldine;
    • Doridot, Ludivine;
    • Mignot, Thérèse-Marie;
    • Rebourcet, Régis;
    • Carbonne, Bruno;
    • Concordet, Jean-Paul;
    • Barbaux, Sandrine;
    • Vaiman, Daniel
    Publication type:
    Article
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