Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 22


Results: 24
    1

    Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. 4544
    By:
    • Orozco, Gisela;
    • Hinks, Anne;
    • Eyre, Steve;
    • Ke, Xiayi;
    • Gibbons, Laura J.;
    • Bowes, John;
    • Flynn, Edward;
    • Martin, Paul;
    • Wilson, Anthony G.;
    • Bax, Deborah E.;
    • Morgan, Ann W.;
    • Emery, Paul;
    • Steer, Sophia;
    • Hocking, Lynne;
    • Reid, David M.;
    • Wordsworth, Paul;
    • Harrison, Pille;
    • Thomson, Wendy;
    • Barton, Anne;
    • Worthington, Jane
    Publication type:
    Article
    2
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    Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. 4462, doi. 10.1093/hmg/ddq377
    By:
    • Poirier, Karine;
    • Saillour, Yoann;
    • Bahi-Buisson, Nadia;
    • Jaglin, Xavier H.;
    • Fallet-Bianco, Catherine;
    • Nabbout, Rima;
    • Castelnau-Ptakhine, Laetitia;
    • Roubertie, Agathe;
    • Attie-Bitach, Tania;
    • Desguerre, Isabelle;
    • Genevieve, David;
    • Barnerias, Christine;
    • Keren, Boris;
    • Lebrun, Nicolas;
    • Boddaert, Nathalie;
    • Encha-Razavi, Féréchté;
    • Chelly, Jamel
    Publication type:
    Article
    5
    6

    Identification of AF4/FMR2 family, member 3 (AFF3) as a novel rheumatoid arthritis susceptibility locus and confirmation of two further pan-autoimmune susceptibility genes.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. 4543
    By:
    • Barton, Anne;
    • Eyre, Steve;
    • Ke, Xiayi;
    • Hinks, Anne;
    • Bowes, John;
    • Flynn, Edward;
    • Martin, Paul;
    • Wilson, Anthony G.;
    • Morgan, Ann W.;
    • Emery, Paul;
    • Steer, Sophia;
    • Hocking, Lynne J.;
    • Reid, David M.;
    • Harrison, Pille;
    • Wordsworth, Paul;
    • Thomson, Wendy;
    • Worthington, Jane
    Publication type:
    Article
    7
    8

    Cover Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. NP, doi. 10.1093/hmg/ddq441
    Publication type:
    Article
    9
    10

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. NP, doi. 10.1093/hmg/ddq444
    Publication type:
    Article
    11

    Contents Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. NP, doi. 10.1093/hmg/ddq438
    Publication type:
    Article
    12

    Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasis.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. 4437, doi. 10.1093/hmg/ddq370
    By:
    • Burbulla, Lena F.;
    • Schelling, Carina;
    • Kato, Hiroki;
    • Rapaport, Doron;
    • Woitalla, Dirk;
    • Schiesling, Carola;
    • Schulte, Claudia;
    • Sharma, Manu;
    • Illig, Thomas;
    • Bauer, Peter;
    • Jung, Stephan;
    • Nordheim, Alfred;
    • Schöls, Ludger;
    • Riess, Olaf;
    • Krüger, Rejko
    Publication type:
    Article
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    A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. 4385, doi. 10.1093/hmg/ddq361
    By:
    • Braunstein, Kerstin E.;
    • Eschbach, Judith;
    • Ròna-Vörös, Krisztina;
    • Soylu, Rana;
    • Mikrouli, Elli;
    • Larmet, Yves;
    • René, Frédérique;
    • De Aguilar, Jose-Luis Gonzalez;
    • Loeffler, Jean-Philippe;
    • Müller, Hans-Peter;
    • Bucher, Selina;
    • Kaulisch, Thomas;
    • Niessen, Heiko G.;
    • Tillmanns, Julia;
    • Fischer, Kristina;
    • Schwalenstöcker, Birgit;
    • Kassubek, Jan;
    • Pichler, Bernd;
    • Stiller, Detlef;
    • Petersen, Åsa
    Publication type:
    Article
    22
    23

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2010, v. 19, n. 22, p. NP, doi. 10.1093/hmg/ddq447
    Publication type:
    Article
    24