Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 21

Results: 23
    1

    Large common deletions associate with mortality at old age.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4290, doi. 10.1093/hmg/ddr340
    By:
    • Kuningas, Maris;
    • Estrada, Karol;
    • Hsu, Yi-Hsiang;
    • Nandakumar, Kannabiran;
    • Uitterlinden, André G.;
    • Lunetta, Kathryn L.;
    • van Duijn, Cornelia M.;
    • Karasik, David;
    • Hofman, Albert;
    • Murabito, Joanne;
    • Rivadeneira, Fernando;
    • Kiel, Douglas P.;
    • Tiemeier, Henning
    Publication type:
    Article
    2
    3

    Subscription Page.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr467
    Publication type:
    Article
    4

    LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4209, doi. 10.1093/hmg/ddr348
    By:
    • Herzig, Martin C.;
    • Kolly, Carine;
    • Persohn, Elke;
    • Theil, Diethilde;
    • Schweizer, Tatjana;
    • Hafner, Thomas;
    • Stemmelen, Christine;
    • Troxler, Thomas J.;
    • Schmid, Peter;
    • Danner, Simone;
    • Schnell, Christian R.;
    • Mueller, Matthias;
    • Kinzel, Bernd;
    • Grevot, Armelle;
    • Bolognani, Federico;
    • Stirn, Martina;
    • Kuhn, Rainer R.;
    • Kaupmann, Klemens;
    • van der Putten, P. Herman;
    • Rovelli, Giorgio
    Publication type:
    Article
    5
    6

    Cover Page.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr465
    Publication type:
    Article
    7
    8

    Editorial Board.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr466
    Publication type:
    Article
    9

    European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4268, doi. 10.1093/hmg/ddr303
    By:
    • Rafnar, Thorunn;
    • Vermeulen, Sita H.;
    • Sulem, Patrick;
    • Thorleifsson, Gudmar;
    • Aben, Katja K.;
    • Witjes, J. Alfred;
    • Grotenhuis, Anne J.;
    • Verhaegh, Gerald W.;
    • Hulsbergen-van de Kaa, Christina A.;
    • Besenbacher, Soren;
    • Gudbjartsson, Daniel;
    • Stacey, Simon N.;
    • Gudmundsson, Julius;
    • Johannsdottir, Hrefna;
    • Bjarnason, Hjordis;
    • Zanon, Carlo;
    • Helgadottir, Hafdis;
    • Jonasson, Jon Gunnlaugur;
    • Tryggvadottir, Laufey;
    • Jonsson, Eirikur
    Publication type:
    Article
    10

    Positional identification of variants of Adamts16 linked to inherited hypertension.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4297, doi. 10.1093/hmg/ddr286
    By:
    • Joe, Bina;
    • Saad, Yasser;
    • Dhindaw, Seema;
    • Lee, Norman H.;
    • Frank, Bryan C.;
    • Achinike, Ovokeraye H.;
    • Luu, Truong V.;
    • Gopalakrishnan, Kathirvel;
    • Toland, Edward J.;
    • Farms, Phyllis;
    • Yerga-Woolwine, Shane;
    • Manickavasagam, Ezhilarasi;
    • Rapp, John P.;
    • Garrett, Michael R.;
    • Coe, David;
    • Apte, Suneel S.;
    • Rankinen, Tuomo;
    • Pérusse, Louis;
    • Ehret, Georg B.;
    • Ganesh, Santhi K.
    Publication type:
    Article
    11

    MeCP2 Rett mutations affect large scale chromatin organization.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4187, doi. 10.1093/hmg/ddr346
    By:
    • Agarwal, Noopur;
    • Becker, Annette;
    • Jost, K. Laurence;
    • Haase, Sebastian;
    • Thakur, Basant K.;
    • Brero, Alessandro;
    • Hardt, Tanja;
    • Kudo, Shinichi;
    • Leonhardt, Heinrich;
    • Cardoso, M. Cristina
    Publication type:
    Article
    12
    13
    14

    A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4282, doi. 10.1093/hmg/ddr342
    By:
    • Garcia-Closas, Montserrat;
    • Ye, Yuanqing;
    • Rothman, Nathaniel;
    • Figueroa, Jonine D.;
    • Malats, Núria;
    • Dinney, Colin P.;
    • Chatterjee, Nilanjan;
    • Prokunina-Olsson, Ludmila;
    • Wang, Zhaoming;
    • Lin, Jie;
    • Real, Francisco X.;
    • Jacobs, Kevin B.;
    • Baris, Dalsu;
    • Thun, Michael;
    • De Vivo, Immaculata;
    • Albanes, Demetrius;
    • Purdue, Mark P.;
    • Kogevinas, Manolis;
    • Kamat, Ashish M.;
    • Lerner, Seth P.
    Publication type:
    Article
    15
    16
    17
    18
    19
    20

    Contents Page.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. NP, doi. 10.1093/hmg/ddr464
    Publication type:
    Article
    21
    22
    23

    Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies.

    Published in:
    Human Molecular Genetics, 2011, v. 20, n. 21, p. 4175, doi. 10.1093/hmg/ddr344
    By:
    • De Vos, Winnok H.;
    • Houben, Frederik;
    • Kamps, Miriam;
    • Malhas, Ashraf;
    • Verheyen, Fons;
    • Cox, Juliën;
    • Manders, Erik M.M.;
    • Verstraeten, Valerie L.R.M.;
    • van Steensel, Maurice A.M.;
    • Marcelis, Carlo L.M.;
    • van den Wijngaard, Arthur;
    • Vaux, David J.;
    • Ramaekers, Frans C.S.;
    • Broers, Jos L.V.
    Publication type:
    Article