Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hubert Aviolat"'
Autor:
Neil Aronin, Hubert Aviolat, Maria Iuliano, Ningzhe Zhang, Ellen Sapp, Kimberly B. Kegel-Gleason, Lisa M. Ellerby, Patrick Reeves, Leah W. Gatune, Jonathan Alexander, Petr Vodicka, Adelaide Tousley, Elizabeth Weisman, Xueyi Li, Marian DiFiglia, Anastasia Khvorova
Publikováno v:
Journal of Huntington's Disease
Background Previous studies suggest that Huntingtin, the protein mutated in Huntington's disease (HD), is required for actin based changes in cell morphology, and undergoes stimulus induced targeting to plasma membranes where it interacts with phosph
Autor:
Yvon Trottier, Hélène Nierengarten, Pascal Villa, Hubert Aviolat, Yves Nominé, Anna Bonhoure, Frank Ruffenach, Fabrice A.C. Klein, David Hoffmann, Sophie Gioria, Christine Ruhlmann
Publikováno v:
Journal of Molecular Biology
Journal of Molecular Biology, Elsevier, 2018, 430 (24), pp.5257-5279. ⟨10.1016/j.jmb.2018.09.009⟩
Journal of Molecular Biology, Elsevier, 2018, 430 (24), pp.5257-5279. ⟨10.1016/j.jmb.2018.09.009⟩
Numerous proteins can coalesce into amyloid self-assemblies, which are responsible for a class of diseases called amyloidoses, but which can also fulfill important biological functions and are of great interest for biotechnology. Amyloid aggregation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57f27f6b16e16ad96b54669461ec8833
https://hal.archives-ouvertes.fr/hal-02006902
https://hal.archives-ouvertes.fr/hal-02006902
Autor:
Hubert Aviolat, Gabrielle Zeder-Lutz, Danièle Altschuh, Aurélien Davranche, Yvon Trottier, Fabrice A.C. Klein, Didier Busso
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (14), pp.2795-2806. ⟨10.1093/hmg/ddr178⟩
Human Molecular Genetics, 2011, 20 (14), pp.2795-2806. ⟨10.1093/hmg/ddr178⟩
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (14), pp.2795-2806. ⟨10.1093/hmg/ddr178⟩
Human Molecular Genetics, 2011, 20 (14), pp.2795-2806. ⟨10.1093/hmg/ddr178⟩
International audience; Huntington's disease (HD) is caused by the expansion mutation above a length threshold of a polyglutamine (polyQ) stretch in the huntingtin (Htt) protein. Mutant Htt (mHtt) pathogenicity is proposed to rely on its malfunction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b1bed132f8815fa345a0293a044c605
https://hal.archives-ouvertes.fr/hal-03503123
https://hal.archives-ouvertes.fr/hal-03503123