Works matching IS 17574676 AND DT 2021 AND VI 13 AND IP 12


Results: 13
    1
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    P‐tau235: a novel biomarker for staging preclinical Alzheimer's disease.

    Published in:
    EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202115098
    By:
    • Lantero‐Rodriguez, Juan;
    • Snellman, Anniina;
    • Benedet, Andrea L;
    • Milà‐Alomà, Marta;
    • Camporesi, Elena;
    • Montoliu‐Gaya, Laia;
    • Ashton, Nicholas J;
    • Vrillon, Agathe;
    • Karikari, Thomas K;
    • Gispert, Juan Domingo;
    • Salvadó, Gemma;
    • Shekari, Mahnaz;
    • Toomey, Christina E;
    • Lashley, Tammaryn L;
    • Zetterberg, Henrik;
    • Suárez‐Calvet, Marc;
    • Brinkmalm, Gunnar;
    • Rosa Neto, Pedro;
    • Blennow, Kaj
    Publication type:
    Article
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    Uncovering a conserved vulnerability site in SARS‐CoV‐2 by a human antibody.

    Published in:
    EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202114544
    By:
    • Li, Tingting;
    • Cai, Hongmin;
    • Zhao, Yapei;
    • Li, Yanfang;
    • Lai, Yanling;
    • Yao, Hebang;
    • Liu, Liu Daisy;
    • Sun, Zhou;
    • van Vlissingen, Martje Fentener;
    • Kuiken, Thijs;
    • GeurtsvanKessel, Corine H;
    • Zhang, Ning;
    • Zhou, Bingjie;
    • Lu, Lu;
    • Gong, Yuhuan;
    • Qin, Wenming;
    • Mondal, Moumita;
    • Duan, Bowen;
    • Xu, Shiqi;
    • Richard, Audrey S
    Publication type:
    Article
    7

    Brain cross‐protection against SARS‐CoV‐2 variants by a lentiviral vaccine in new transgenic mice.

    Published in:
    EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202114459
    By:
    • Ku, Min‐Wen;
    • Authié, Pierre;
    • Bourgine, Maryline;
    • Anna, François;
    • Noirat, Amandine;
    • Moncoq, Fanny;
    • Vesin, Benjamin;
    • Nevo, Fabien;
    • Lopez, Jodie;
    • Souque, Philippe;
    • Blanc, Catherine;
    • Fert, Ingrid;
    • Chardenoux, Sébastien;
    • Lafosse, llta;
    • Cussigh, Delphine;
    • Hardy, David;
    • Nemirov, Kirill;
    • Guinet, Françoise;
    • Langa Vives, Francina;
    • Majlessi, Laleh
    Publication type:
    Article
    8

    Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes.

    Published in:
    EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202114397
    By:
    • Vidali, Silvia;
    • Gerlini, Raffaele;
    • Thompson, Kyle;
    • Urquhart, Jill E;
    • Meisterknecht, Jana;
    • Aguilar‐Pimentel, Juan Antonio;
    • Amarie, Oana V;
    • Becker, Lore;
    • Breen, Catherine;
    • Calzada‐Wack, Julia;
    • Chhabra, Nirav F;
    • Cho, Yi‐Li;
    • da Silva‐Buttkus, Patricia;
    • Feichtinger, René G;
    • Gampe, Kristine;
    • Garrett, Lillian;
    • Hoefig, Kai P;
    • Hölter, Sabine M;
    • Jameson, Elisabeth;
    • Klein‐Rodewald, Tanja
    Publication type:
    Article
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    BET1 variants establish impaired vesicular transport as a cause for muscular dystrophy with epilepsy.

    Published in:
    EMBO Molecular Medicine, 2021, v. 13, n. 12, p. 1, doi. 10.15252/emmm.202013787
    By:
    • Donkervoort, Sandra;
    • Krause, Niklas;
    • Dergai, Mykola;
    • Yun, Pomi;
    • Koliwer, Judith;
    • Gorokhova, Svetlana;
    • Geist Hauserman, Janelle;
    • Cummings, Beryl B;
    • Hu, Ying;
    • Smith, Rosemarie;
    • Uapinyoying, Prech;
    • Ganesh, Vijay S;
    • Ghosh, Partha S;
    • Monaghan, Kristin G;
    • Edassery, Seby L;
    • Ferle, Pia E;
    • Silverstein, Sarah;
    • Chao, Katherine R;
    • Snyder, Molly;
    • Ellingwood, Sara
    Publication type:
    Article
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