Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 15

Results: 21
    1

    Cover Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt322
    Publication type:
    Article
    2
    3

    Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3174, doi. 10.1093/hmg/ddt169
    By:
    • Kirin, Mirna;
    • Chandra, Aman;
    • Charteris, David G.;
    • Hayward, Caroline;
    • Campbell, Susan;
    • Celap, Ivana;
    • Bencic, Goran;
    • Vatavuk, Zoran;
    • Kirac, Iva;
    • Richards, Allan J.;
    • Tenesa, Albert;
    • Snead, Martin P.;
    • Fleck, Brian W.;
    • Singh, Jaswinder;
    • Harsum, Steven;
    • MacLaren, Robert E.;
    • den Hollander, Anneke I.;
    • Dunlop, Malcolm G.;
    • Hoyng, Carel B.;
    • Wright, Alan F.
    Publication type:
    Article
    4

    Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3152, doi. 10.1093/hmg/ddt172
    By:
    • Cattin, Marie-Elodie;
    • Bertrand, Anne T.;
    • Schlossarek, Saskia;
    • Le Bihan, Marie-Catherine;
    • Skov Jensen, Søren;
    • Neuber, Christiane;
    • Crocini, Claudia;
    • Maron, Sophia;
    • Lainé, Jeanne;
    • Mougenot, Nathalie;
    • Varnous, Shaïda;
    • Fromes, Yves;
    • Hansen, Arne;
    • Eschenhagen, Thomas;
    • Decostre, Valérie;
    • Carrier, Lucie;
    • Bonne, Gisèle
    Publication type:
    Article
    5
    6

    Impaired viability of muscle precursor cells in muscular dystrophy with glycosylation defects and amelioration of its severe phenotype by limited gene expression.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3003, doi. 10.1093/hmg/ddt157
    By:
    • Kanagawa, Motoi;
    • Yu, Chih-Chieh;
    • Ito, Chiyomi;
    • Fukada, So-ichiro;
    • Hozoji-Inada, Masako;
    • Chiyo, Tomoko;
    • Kuga, Atsushi;
    • Matsuo, Megumi;
    • Sato, Kanoko;
    • Yamaguchi, Masahiko;
    • Ito, Takahito;
    • Ohtsuka, Yoshihisa;
    • Katanosaka, Yuki;
    • Miyagoe-Suzuki, Yuko;
    • Naruse, Keiji;
    • Kobayashi, Kazuhiro;
    • Okada, Takashi;
    • Takeda, Shin'ichi;
    • Toda, Tatsushi
    Publication type:
    Article
    7
    8
    9

    Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3038, doi. 10.1093/hmg/ddt160
    By:
    • Cicek, Mine S.;
    • Koestler, Devin C.;
    • Fridley, Brooke L.;
    • Kalli, Kimberly R.;
    • Armasu, Sebastian M.;
    • Larson, Melissa C.;
    • Wang, Chen;
    • Winham, Stacey J.;
    • Vierkant, Robert A.;
    • Rider, David N.;
    • Block, Matthew S.;
    • Klotzle, Brandy;
    • Konecny, Gottfried;
    • Winterhoff, Boris J.;
    • Hamidi, Habib;
    • Shridhar, Viji;
    • Fan, Jian-Bing;
    • Visscher, Daniel W.;
    • Olson, Janet E.;
    • Hartmann, Lynn C.
    Publication type:
    Article
    10

    CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3138, doi. 10.1093/hmg/ddt170
    By:
    • van Bon, Bregje W.M.;
    • Oortveld, Merel A.W.;
    • Nijtmans, Leo G.;
    • Fenckova, Michaela;
    • Nijhof, Bonnie;
    • Besseling, Judith;
    • Vos, Melissa;
    • Kramer, Jamie M.;
    • de Leeuw, Nicole;
    • Castells-Nobau, Anna;
    • Asztalos, Lenke;
    • Viragh, Erika;
    • Ruiter, Mariken;
    • Hofmann, Falko;
    • Eshuis, Lillian;
    • Collavin, Licio;
    • Huynen, Martijn A.;
    • Asztalos, Zoltan;
    • Verstreken, Patrik;
    • Rodenburg, Richard J.
    Publication type:
    Article
    11
    12

    Genome-wide association study in a Chinese population with diabetic retinopathy.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3165, doi. 10.1093/hmg/ddt161
    By:
    • Sheu, Wayne H.-H.;
    • Kuo, Jane Z.;
    • Lee, I-Te;
    • Hung, Yi-Jen;
    • Lee, Wen-Jane;
    • Tsai, Hin-Yeung;
    • Wang, J.-S.;
    • Goodarzi, Mark O.;
    • Klein, Ronald;
    • Klein, Barbara E. K.;
    • Ipp, Eli;
    • Lin, Shin-Yi;
    • Guo, Xiuqing;
    • Hsieh, Chang-Hsun;
    • Taylor, Kent D.;
    • Fu, Chia-Po;
    • Rotter, Jerome I.;
    • Chen, Yii-Der I.
    Publication type:
    Article
    13
    14
    15

    Contents Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt321
    Publication type:
    Article
    16

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt323
    Publication type:
    Article
    17

    Smooth muscle hyperplasia due to loss of smooth muscle α-actin is driven by activation of focal adhesion kinase, altered p53 localization and increased levels of platelet-derived growth factor receptor-β.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. 3123, doi. 10.1093/hmg/ddt167
    By:
    • Papke, Christina L.;
    • Cao, Jiumei;
    • Kwartler, Callie S.;
    • Villamizar, Carlos;
    • Byanova, Katerina L.;
    • Lim, Soon-Mi;
    • Sreenivasappa, Harini;
    • Fischer, Grant;
    • Pham, John;
    • Rees, Meredith;
    • Wang, Miranda;
    • Chaponnier, Christine;
    • Gabbiani, Giulio;
    • Khakoo, Aarif Y.;
    • Chandra, Joya;
    • Trache, Andreea;
    • Zimmer, Warren;
    • Milewicz, Dianna M.
    Publication type:
    Article
    18
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    21

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2013, v. 22, n. 15, p. NP, doi. 10.1093/hmg/ddt324
    Publication type:
    Article