Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 4


Results: 29
    1
    2
    3
    4
    5
    6
    7
    8
    9
    10
    11
    12

    Touching base.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 407, doi. 10.1038/ng0406-407
    By:
    • Axton, Myles;
    • Niemitz, Emily;
    • Vogan, Kyle
    Publication type:
    Article
    13

    Research Highlights.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 409, doi. 10.1038/ng0406-409
    By:
    • Axton, Myles;
    • Niemitz, Emily;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
    14

    Erratum: Mutations in different components of FGF signaling in LADD syndrome.

    Published in:
    2006
    By:
    • Rohmann, Edyta;
    • Brunner, Han G;
    • Kayserili, Hülya;
    • Uyguner, Oya;
    • Nürnberg, Gudrun;
    • Lew, Erin D.;
    • Dobbie, Angus;
    • Eswarakumar, Veraragavan P.;
    • Uzumcu, Abdullah;
    • Ulubil-Emeroglu, Melike;
    • Leroy, Jules G.;
    • Yun Li;
    • Becker, Christian;
    • Lehnerdt, Kai;
    • Cremers, Cor W. R. J.;
    • Yüksel-Apak, Memnune;
    • Nürnberg, Peter;
    • Kubisch, Christian;
    • Schlessinger, Joseph;
    • van Bokhoven, Hans
    Publication type:
    Correction Notice
    15

    ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 411, doi. 10.1038/ng1742
    By:
    • Greenway, Matthew J.;
    • Andersen, Peter M.;
    • Russ, Carsten;
    • Ennis, Sean;
    • Cashman, Susan;
    • Donaghy, Colette;
    • Patterson, Victor;
    • Swingler, Robert;
    • Kieran, Dairin;
    • Prehn, Jochen;
    • Morrison, Karen E.;
    • Green, Andrew;
    • Acharya, K. Ravi;
    • Brown Jr., Robert H.;
    • Hardiman, Orla
    Publication type:
    Article
    16
    17
    18
    19
    20
    21

    Mutations in different components of FGF signaling in LADD syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 414, doi. 10.1038/ng1757
    By:
    • Rohmann, Edyta;
    • Brunner, Han G.;
    • Kayserili, Hülya;
    • Uyguner, Oya;
    • Nürnberg, Gudrun;
    • Lew, Erin D.;
    • Dobbie, Angus;
    • Eswarakumar, Veraragavan P.;
    • Uzumcu, Abdullah;
    • Ulubil-Emeroglu, Melike;
    • Leroy, Jules G.;
    • Yun Li;
    • Becker, Christian;
    • Lehnerdt, Kai;
    • Cremers, Cor W. R. J.;
    • Yüksel-Apak, Memnune;
    • Nürnberg, Peter;
    • Kubisch, Christian;
    • Schlessinger, Joseph;
    • van Bokhoven, Hans
    Publication type:
    Article
    22
    23

    The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 431, doi. 10.1038/ng1760
    By:
    • Yuin-Han Loh;
    • Qiang Wu;
    • Joon-Lin Chew;
    • Vega, Vinsensius B.;
    • Weiwei Zhang;
    • Xi Chen;
    • Bourque, Guillaume;
    • George, Joshy;
    • Leong, Bernard;
    • Liu, Jun;
    • Kee-Yew Wong;
    • Sung, Ken W.;
    • Lee, Charlie W. H.;
    • Xiao-Dong Zhao;
    • Kuo-Ping Chiu;
    • Lipovich, Leonard;
    • Kuznetsov, Vladimir A.;
    • Robson, Paul;
    • Stanton, Lawrence W.;
    • Chia-Lin Wei
    Publication type:
    Article
    24
    25
    26
    27

    Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 441, doi. 10.1038/ng1767
    By:
    • Palmer, Colin N. A.;
    • Irvine, Alan D.;
    • Terron-Kwiatkowski, Ana;
    • Yiwei Zhao;
    • Haihui Liao;
    • Lee, Simon P.;
    • Goudie, David R.;
    • Sandilands, Aileen;
    • Campbell, Linda E.;
    • Smith, Frances J. D.;
    • O'Regan, Gráinne M.;
    • Watson, Rosemarie M.;
    • Cecil, Jo E.;
    • Bale, Sherri J.;
    • Compton, John G.;
    • DiGiovanna, John J.;
    • Fleckman, Philip;
    • Lewis-Jones, Sue;
    • Arseculeratne, Gehan;
    • Sergeant, Ann
    Publication type:
    Article
    28

    Genetic clonal diversity predicts progression to esophageal adenocarcinoma.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 468, doi. 10.1038/ng1768
    By:
    • Maley, Carlo C.;
    • Galipeau, Patricia C.;
    • Finley, Jennifer C.;
    • Wongsurawat, V. Jon;
    • Xiaohong Li;
    • Sanchez, Carissa A.;
    • Paulson, Thomas G.;
    • Blount, Patricia L.;
    • Risques, Rosa-Ana;
    • Rabinovitch, Peter S.;
    • Reid, Brian J.
    Publication type:
    Article
    29

    Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 452, doi. 10.1038/ng1764
    By:
    • Coucke, Paul J.;
    • Willaert, Andy;
    • Wessels, Marja W.;
    • Callewaert, Bert;
    • Zoppi, Nicoletta;
    • De Backer, Julie;
    • Fox, Joyce E.;
    • Mancini, Grazia M. S.;
    • Kambouris, Marios;
    • Gardella, Rita;
    • Facchetti, Fabio;
    • Willems, Patrick J.;
    • Forsyth, Ramses;
    • Dietz, Harry C.;
    • Barlati, Sergio;
    • Colombi, Marina;
    • Loeys, Bart;
    • De Paepe, Anne
    Publication type:
    Article