Works matching DE "DYSTROGLYCAN"


Results: 127
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    Cover.

    Published in:
    Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 1, p. i, doi. 10.1002/mgg3.570
    By:
    • Bailey, Mitchell;
    • Miller, Nicole
    Publication type:
    Article
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    Abnormal promoter DNA hypermethylation of the integrin, nidogen, and dystroglycan genes in breast cancer.

    Published in:
    Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-81851-y
    By:
    • Strelnikov, Vladimir V.;
    • Kuznetsova, Ekaterina B.;
    • Tanas, Alexander S.;
    • Rudenko, Viktoria V.;
    • Kalinkin, Alexey I.;
    • Poddubskaya, Elena V.;
    • Kekeeva, Tatiana V.;
    • Chesnokova, Galina G.;
    • Trotsenko, Ivan D.;
    • Larin, Sergey S.;
    • Kutsev, Sergey I.;
    • Zaletaev, Dmitry V.;
    • Nemtsova, Marina V.;
    • Simonova, Olga A.
    Publication type:
    Article
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    Structural flexibility of human α-dystroglycan.

    Published in:
    FEBS Open Bio, 2017, v. 7, n. 8, p. 1064, doi. 10.1002/2211-5463.12259
    By:
    • Covaceuszach, Sonia;
    • Bozzi, Manuela;
    • Bigotti, Maria Giulia;
    • Sciandra, Francesca;
    • Konarev, Petr Valeryevich;
    • Brancaccio, Andrea;
    • Cassetta, Alberto
    Publication type:
    Article
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    This Week in The Journal.

    Published in:
    Journal of Neuroscience, 2016, v. 36, n. 40, p. i
    By:
    • Esch, Teresa
    Publication type:
    Article
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    COLQ variant associated with Devon Rex and Sphynx feline hereditary myopathy.

    Published in:
    Animal Genetics, 2015, v. 46, n. 6, p. 711, doi. 10.1111/age.12350
    By:
    • Gandolfi, Barbara;
    • Grahn, Robert A.;
    • Creighton, Erica K.;
    • Williams, D. Colette;
    • Dickinson, Peter J.;
    • Sturges, Beverly K.;
    • Guo, Ling T.;
    • Shelton, G. Diane;
    • Leegwater, Peter A. J.;
    • Longeri, Maria;
    • Malik, Richard;
    • Lyons, Leslie A.
    Publication type:
    Article
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    ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 1, p. 269
    By:
    • Cirak, Sebahattin;
    • Foley, Aileen Reghan;
    • Herrmann, Ralf;
    • Willer, Tobias;
    • Yau, Shu;
    • Stevens, Elizabeth;
    • Torelli, Silvia;
    • Brodd, Lina;
    • Kamynina, Alisa;
    • Vondracek, Petr;
    • Roper, Helen;
    • Longman, Cheryl;
    • Korinthenberg, Rudolf;
    • Marrosu, Gianni;
    • Nürnberg, Peter;
    • Michele, Daniel E.;
    • Plagnol, Vincent;
    • Hurles, Matt;
    • Moore, Steven A.;
    • Sewry, Caroline A.
    Publication type:
    Article
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    Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness.

    Published in:
    Skeletal Muscle, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13395-018-0170-1
    By:
    • Johnson, Katherine;
    • Bertoli, Marta;
    • Phillips, Lauren;
    • Töpf, Ana;
    • Van den Bergh, Peter;
    • Vissing, John;
    • Witting, Nanna;
    • Nafissi, Shahriar;
    • Jamal-Omidi, Shirin;
    • Łusakowska, Anna;
    • Kostera-Pruszczyk, Anna;
    • Potulska-Chromik, Anna;
    • Deconinck, Nicolas;
    • Wallgren-Pettersson, Carina;
    • Strang-Karlsson, Sonja;
    • Colomer, Jaume;
    • Claeys, Kristl G.;
    • De Ridder, Willem;
    • Baets, Jonathan;
    • von der Hagen, Maja
    Publication type:
    Article
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