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Wyszukujesz frazę ""Adriaenssens, Elias"" wg kryterium: Autor


Tytuł :
BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes
Autorzy :
Adriaenssens, Elias
Tedesco, Barbara
Mediani, Laura
Asselbergh, Bob
Crippa, Valeria
Antoniani, Francesco
Carra, SerenaAff3, IDs4159802065664z_cor7
Poletti, AngeloAff2, IDs4159802065664z_cor8
Timmerman, VincentAff1, IDs4159802065664z_cor9
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Źródło :
Scientific Reports. 10(1)
Czasopismo naukowe
Tytuł :
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction.
Autorzy :
Lent, Jonas Van
Verstraelen, Peter
Asselbergh, Bob
Adriaenssens, Elias
Mateiu, Ligia
Verbist, Christophe
Winter, Vicky De
Eggermont, Kristel
Bosch, Ludo Van Den
Vos, Winnok H De
Timmerman, Vincent
Van Lent, Jonas
De Winter, Vicky
Van Den Bosch, Ludo
De Vos, Winnok H
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Źródło :
Brain: A Journal of Neurology; Aug2021, Vol. 144 Issue 8, p2471-2485, 15p
Czasopismo naukowe
Tytuł :
Induced pluripotent stem cell-derived motor neurons of CMT type 2 patients reveal progressive mitochondrial dysfunction.
Autorzy :
Van Lent J; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.; Neurogenetics Laboratory, Institute Born Bunge, Antwerp, 2610, Belgium.
Verstraelen P; Laboratory of Cell Biology and Histology, Department of Veterinary Sciences, University of Antwerp, Antwerp, 2610, Belgium.
Asselbergh B; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerp, 2610, Belgium.; Neuromics Support Facility, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.
Adriaenssens E; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.; Neurogenetics Laboratory, Institute Born Bunge, Antwerp, 2610, Belgium.
Mateiu L; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerp, 2610, Belgium.
Verbist C; Laboratory of Molecular Cellular and Network Excitability, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.
De Winter V; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.; Neurogenetics Laboratory, Institute Born Bunge, Antwerp, 2610, Belgium.
Eggermont K; Department of Neurosciences, Experimental Neurology, and Leuven Brain Institute, KU Leuven‒University of Leuven, Leuven, 3000, Belgium.; VIB-Center for Brain and Disease Research, Laboratory of Neurobiology, Leuven, 3000, Belgium.
Van Den Bosch L; Department of Neurosciences, Experimental Neurology, and Leuven Brain Institute, KU Leuven‒University of Leuven, Leuven, 3000, Belgium.; VIB-Center for Brain and Disease Research, Laboratory of Neurobiology, Leuven, 3000, Belgium.
De Vos WH; Laboratory of Cell Biology and Histology, Department of Veterinary Sciences, University of Antwerp, Antwerp, 2610, Belgium.
Timmerman V; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, 2610, Belgium.; Neurogenetics Laboratory, Institute Born Bunge, Antwerp, 2610, Belgium.
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Źródło :
Brain : a journal of neurology [Brain] 2021 Sep 04; Vol. 144 (8), pp. 2471-2485.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
A weakened interface in the P182L variant of HSP27 associated with severe Charcot-Marie-Tooth neuropathy causes aberrant binding to interacting proteins.
Autorzy :
Alderson TR; Chemistry Research Laboratory, University of Oxford, Oxford, UK.; Laboratory of Chemical Physics, National Institutes of Health, Bethesda, MD, USA.
Adriaenssens E; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
Asselbergh B; Neuromics Support Facility, VIB Center for Molecular Neurology, VIB, Antwerpen, Belgium.; Neuromics Support Facility, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Pritišanac I; Molecular Medicine Program, The Hospital for Sick Children, Toronto, ON, Canada.
Van Lent J; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
Gastall HY; Chemistry Research Laboratory, University of Oxford, Oxford, UK.
Wälti MA; Laboratory of Chemical Physics, National Institutes of Health, Bethesda, MD, USA.
Louis JM; Laboratory of Chemical Physics, National Institutes of Health, Bethesda, MD, USA.
Timmerman V; Peripheral Neuropathy Research Group, Department of Biomedical Sciences, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
Baldwin AJ; Chemistry Research Laboratory, University of Oxford, Oxford, UK.
Lp Benesch J; Chemistry Research Laboratory, University of Oxford, Oxford, UK.
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Źródło :
The EMBO journal [EMBO J] 2021 Apr 15; Vol. 40 (8), pp. e103811. Date of Electronic Publication: 2021 Mar 01.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Novel insights in the disease biology of mutant small heat shock proteins in neuromuscular diseases.
Autorzy :
Adriaenssens E; Peripheral Neuropathy Research Group, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
Geuens T; Peripheral Neuropathy Research Group, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
Baets J; Neurogenetics Group, Center for Molecular Neurology, VIB, Antwerpen, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerpen, Belgium.; Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Antwerpen, Belgium.
Echaniz-Laguna A; Department of Neurology, Neuromuscular Disease Center (CERNEST), Strasbourg University Hospital, Strasbourg, France.
Timmerman V; Peripheral Neuropathy Research Group, Institute Born Bunge, University of Antwerp, Antwerpen, Belgium.
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Źródło :
Brain : a journal of neurology [Brain] 2017 Oct 01; Vol. 140 (10), pp. 2541-2549.
Typ publikacji :
Journal Article
MeSH Terms :
HSP27 Heat-Shock Proteins/*genetics
Heat-Shock Proteins/*genetics
Mutation/*genetics
Neuromuscular Diseases/*genetics
Protein-Serine-Threonine Kinases/*genetics
Aged ; Aged, 80 and over ; Humans ; Male ; Models, Molecular ; Molecular Chaperones
Czasopismo naukowe

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