Works matching IS 10614036 AND DT 2000 AND VI 24 AND IP 1


Results: 26
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    2

    TOUCHINGbase.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 11
    Publication type:
    Article
    3
    4

    The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 15, doi. 10.1038/71626
    By:
    • de Winter, Johan P.;
    • Rooimans, Martin A.;
    • van der Weel, Laura;
    • van Berkel, Carola G.M.;
    • Alon, Noa;
    • Bosnoyan-Collins, Lucine;
    • de Groot, Jan;
    • Zhi, Yu;
    • Waisfisz, Quinten;
    • Pronk, Jan C.;
    • Arwert, Fré;
    • Mathew, Christopher G.;
    • Scheper, Rik J.;
    • Hoatlin, Maureen E.;
    • Buchwald, Manuel;
    • Joenje, Hans
    Publication type:
    Article
    5
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    10
    11

    Control of endodermal endocrine development by Hes-1.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 36, doi. 10.1038/71657
    By:
    • Jensen, Jan;
    • Pedersen, Erna Engholm;
    • Galante, Philip;
    • Hald, Jacob;
    • Heller, R. Scott;
    • Ishibashi, Makoto;
    • Kageyama, Ryoichiro;
    • Guillemot, Francois;
    • Serup, Palle;
    • Madsen, Ole D.
    Publication type:
    Article
    12
    13

    Genealogies of mouse inbred strains.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 23, doi. 10.1038/71641
    By:
    • Beck, Jon A.;
    • Lloyd, Sarah;
    • Hafezparast, Majid;
    • Lennon-Pierce, Moyha;
    • Eppig, Janan T.;
    • Festing, Michael F.W.;
    • Fisher, Elizabeth M.C.
    Publication type:
    Article
    14

    Grass-roots genomics.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 5, doi. 10.1038/71681
    By:
    • Johnston, Mark;
    • Fields, Stanley
    Publication type:
    Article
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    Mediating mismatch repair.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 6, doi. 10.1038/71698
    By:
    • Jiricny, Josef
    Publication type:
    Article
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    19

    A mouse model for spinal muscular atrophy.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 66, doi. 10.1038/71709
    By:
    • Hsieh-Li, Hsiu Mei;
    • Chang, Jan-Gowth;
    • Jong, Yuh-Jyh;
    • Wu, Mei-Hsiang;
    • Wang, Nancy M.;
    • Tsai, Chang Hai;
    • Li, Hung
    Publication type:
    Article
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    22

    Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 79, doi. 10.1038/71732
    By:
    • Sohocki, Melanie M.;
    • Bowne, Sara J.;
    • Sullivan, Lori S.;
    • Blackshaw, Seth;
    • Cepko, Constance L.;
    • Payne, Annette M.;
    • Bhattacharya, Shomi S.;
    • Khaliq, Shagufta;
    • Qasim Mehdi, S.;
    • Birch, David G.;
    • Harrison, Wilbur R.;
    • Elder, Frederick F.B.;
    • Heckenlively, John R.;
    • Daiger, Stephen P.
    Publication type:
    Article
    23

    Learning from lentiviruses.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 8, doi. 10.1038/71740
    By:
    • Emerman, Michael
    Publication type:
    Article
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    26

    Cardiac defects and renal failure in mice with targeted mutations in Pkd2.

    Published in:
    Nature Genetics, 2000, v. 24, n. 1, p. 75, doi. 10.1038/71724
    By:
    • Wu, Guanqing;
    • Markowitz, Glen S.;
    • Li, Li;
    • D'Agati, Vivette D.;
    • Factor, Stephen M.;
    • Geng, Lin;
    • Tibara, Sonia;
    • Tuchman, Jay;
    • Cai, Yiqiang;
    • Hoon Park, Jong;
    • van Adelsberg, Janet;
    • Hou, Harry;
    • Kucherlapati, Raju;
    • Edelmann, Winfried;
    • Somlo, Stefan
    Publication type:
    Article