Works matching DE "CENTROSOMES"


Results: 1182
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    Correction.

    Published in:
    Plant Cell, 2015, v. 27, n. 6, p. 1816, doi. 10.1105/tpc.15.00416
    Publication type:
    Article
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    Centrosomes: Til O-GlcNAc Do Us Apart.

    Published in:
    Frontiers in Endocrinology, 2021, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.621888
    By:
    • Yuan, Aiyun;
    • Tang, Xiangyan;
    • Li, Jing
    Publication type:
    Article
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    Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease.

    Published in:
    Nature Medicine, 2010, v. 16, n. 2, p. 198, doi. 10.1038/nm.2088
    By:
    • Stein, Stefan;
    • Ott, Marion G.;
    • Schultze-Strasser, Stephan;
    • Jauch, Anna;
    • Burwinkel, Barbara;
    • Kinner, Andrea;
    • Schmidt, Manfred;
    • Krämer, Alwin;
    • Schwäble, Joachim;
    • Glimm, Hanno;
    • Koehl, Ulrike;
    • Preiss, Carolin;
    • Ball, Claudia;
    • Martin, Hans;
    • Göhring, Gudrun;
    • Schwarzwaelder, Kerstin;
    • Hofmann, Wolf-Karsten;
    • Karakaya, Kadin;
    • Tchatchou, Sandrine;
    • Yang, Rongxi
    Publication type:
    Article
    48

    The oral-facial-digital syndrome gene C2CD3 encodes a positive regulator of centriole elongation.

    Published in:
    Nature Genetics, 2014, v. 46, n. 8, p. 905, doi. 10.1038/ng.3031
    By:
    • Thauvin-Robinet, Christel;
    • Lee, Jaclyn S;
    • Lopez, Estelle;
    • Herranz-Pérez, Vicente;
    • Shida, Toshinobu;
    • Franco, Brunella;
    • Jego, Laurence;
    • Ye, Fan;
    • Pasquier, Laurent;
    • Loget, Philippe;
    • Gigot, Nadège;
    • Aral, Bernard;
    • Lopes, Carla A M;
    • St-Onge, Judith;
    • Bruel, Ange-Line;
    • Thevenon, Julien;
    • González-Granero, Susana;
    • Alby, Caroline;
    • Munnich, Arnold;
    • Vekemans, Michel
    Publication type:
    Article
    49

    Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.

    Published in:
    Nature Genetics, 2013, v. 45, n. 6, p. 639, doi. 10.1038/ng.2613
    By:
    • Poirier, Karine;
    • Lebrun, Nicolas;
    • Broix, Loic;
    • Tian, Guoling;
    • Saillour, Yoann;
    • Boscheron, Cécile;
    • Parrini, Elena;
    • Valence, Stephanie;
    • Pierre, Benjamin Saint;
    • Oger, Madison;
    • Lacombe, Didier;
    • Geneviève, David;
    • Fontana, Elena;
    • Darra, Franscesca;
    • Cances, Claude;
    • Barth, Magalie;
    • Bonneau, Dominique;
    • Bernadina, Bernardo Dalla;
    • N'Guyen, Sylvie;
    • Gitiaux, Cyril
    Publication type:
    Article
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    Mutations in CEP57 cause mosaic variegated aneuploidy syndrome.

    Published in:
    Nature Genetics, 2011, v. 43, n. 6, p. 527, doi. 10.1038/ng.822
    By:
    • Snape, Katie;
    • Hanks, Sandra;
    • Ruark, Elise;
    • Barros-Núñez, Patricio;
    • Elliott, Anna;
    • Murray, Anne;
    • Lane, Andrew H.;
    • Shannon, Nora;
    • Callier, Patrick;
    • Chitayat, David;
    • Clayton-Smith, Jill;
    • FitzPatrick, David R;
    • Gisselsson, David;
    • Jacquemont, Sebastien;
    • Asakura-Hay, Keiko;
    • Micale, Mark A.;
    • Tolmie, John;
    • Turnpenny, Peter D.;
    • Wright, Michael;
    • Douglas, Jenny
    Publication type:
    Article