Works matching IS 15537390 AND DT 2015 AND VI 11 AND IP 3

Results: 91
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    Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005062
    By:
    • Brault, Véronique;
    • Duchon, Arnaud;
    • Romestaing, Caroline;
    • Sahun, Ignasi;
    • Pothion, Stéphanie;
    • Karout, Mona;
    • Borel, Christelle;
    • Dembele, Doulaye;
    • Bizot, Jean-Charles;
    • Messaddeq, Nadia;
    • Sharp, Andrew J.;
    • Roussel, Damien;
    • Antonarakis, Stylianos E;
    • Dierssen, Mara;
    • Hérault, Yann
    Publication type:
    Article
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    Mitochondrial Dysfunction Reveals the Role of mRNA Poly(A) Tail Regulation in Oculopharyngeal Muscular Dystrophy Pathogenesis.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005092
    By:
    • Chartier, Aymeric;
    • Klein, Pierre;
    • Pierson, Stéphanie;
    • Barbezier, Nicolas;
    • Gidaro, Teresa;
    • Casas, François;
    • Carberry, Steven;
    • Dowling, Paul;
    • Maynadier, Laurie;
    • Bellec, Maëlle;
    • Oloko, Martine;
    • Jardel, Claude;
    • Moritz, Bodo;
    • Dickson, George;
    • Mouly, Vincent;
    • Ohlendieck, Kay;
    • Butler-Browne, Gillian;
    • Trollet, Capucine;
    • Simonelig, Martine
    Publication type:
    Article
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    Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder Exstrophy.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005024
    By:
    • Draaken, Markus;
    • Knapp, Michael;
    • Pennimpede, Tracie;
    • Schmidt, Johanna M.;
    • Ebert, Anne-Karolin;
    • Rösch, Wolfgang;
    • Stein, Raimund;
    • Utsch, Boris;
    • Hirsch, Karin;
    • Boemers, Thomas M.;
    • Mangold, Elisabeth;
    • Heilmann, Stefanie;
    • Ludwig, Kerstin U.;
    • Jenetzky, Ekkehart;
    • Zwink, Nadine;
    • Moebus, Susanne;
    • Herrmann, Bernhard G.;
    • Mattheisen, Manuel;
    • Nöthen, Markus M.;
    • Ludwig, Michael
    Publication type:
    Article
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    Escape from X Inactivation Varies in Mouse Tissues.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005079
    By:
    • Berletch, Joel B.;
    • Ma, Wenxiu;
    • Yang, Fan;
    • Shendure, Jay;
    • Noble, William S.;
    • Disteche, Christine M.;
    • Deng, Xinxian
    Publication type:
    Article
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    A Meta-analysis of Gene Expression Signatures of Blood Pressure and Hypertension.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005035
    By:
    • Huan, Tianxiao;
    • Esko, Tõnu;
    • Peters, Marjolein J.;
    • Pilling, Luke C.;
    • Schramm, Katharina;
    • Schurmann, Claudia;
    • Chen, Brian H.;
    • Liu, Chunyu;
    • Joehanes, Roby;
    • Johnson, Andrew D.;
    • Yao, Chen;
    • Ying, Sai-xia;
    • Courchesne, Paul;
    • Milani, Lili;
    • Raghavachari, Nalini;
    • Wang, Richard;
    • Liu, Poching;
    • Reinmaa, Eva;
    • Dehghan, Abbas;
    • Hofman, Albert
    Publication type:
    Article
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    Clonality and Evolutionary History of Rhabdomyosarcoma.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005075
    By:
    • Chen, Li;
    • Shern, Jack F.;
    • Wei, Jun S.;
    • Yohe, Marielle E.;
    • Song, Young K.;
    • Hurd, Laura;
    • Liao, Hongling;
    • Catchpoole, Daniel;
    • Skapek, Stephen X.;
    • Barr, Frederic G.;
    • Hawkins, Douglas S.;
    • Khan, Javed
    Publication type:
    Article
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    Exome Sequencing in an Admixed Isolated Population Indicates NFXL1 Variants Confer a Risk for Specific Language Impairment.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1004925
    By:
    • Villanueva, Pía;
    • Nudel, Ron;
    • Hoischen, Alexander;
    • Fernández, María Angélica;
    • Simpson, Nuala H.;
    • Gilissen, Christian;
    • Reader, Rose H.;
    • Jara, Lillian;
    • Echeverry, Maria Magdalena;
    • Francks, Clyde;
    • Baird, Gillian;
    • Conti-Ramsden, Gina;
    • O’Hare, Anne;
    • Bolton, Patrick F.;
    • Hennessy, Elizabeth R.;
    • null, null;
    • Palomino, Hernán;
    • Carvajal-Carmona, Luis;
    • Veltman, Joris A.;
    • Cazier, Jean-Baptiste
    Publication type:
    Article
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    Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005059
    By:
    • Wolf, Zena T.;
    • Brand, Harrison A.;
    • Shaffer, John R.;
    • Leslie, Elizabeth J.;
    • Arzi, Boaz;
    • Willet, Cali E.;
    • Cox, Timothy C.;
    • McHenry, Toby;
    • Narayan, Nicole;
    • Feingold, Eleanor;
    • Wang, Xioajing;
    • Sliskovic, Saundra;
    • Karmi, Nili;
    • Safra, Noa;
    • Sanchez, Carla;
    • Deleyiannis, Frederic W. B.;
    • Murray, Jeffrey C.;
    • Wade, Claire M.;
    • Marazita, Mary L.;
    • Bannasch, Danika L.
    Publication type:
    Article
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    HDAC4-Myogenin Axis As an Important Marker of HD-Related Skeletal Muscle Atrophy.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005021
    By:
    • Mielcarek, Michal;
    • Toczek, Marta;
    • Smeets, Cleo J. L. M.;
    • Franklin, Sophie A.;
    • Bondulich, Marie K.;
    • Jolinon, Nelly;
    • Muller, Thomas;
    • Ahmed, Mhoriam;
    • Dick, James R. T.;
    • Piotrowska, Izabela;
    • Greensmith, Linda;
    • Smolenski, Ryszard T.;
    • Bates, Gillian P.
    Publication type:
    Article
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