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Frederic Rousseau

Showing results (191-200 of 205) with videos related to

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Neurology|November 20, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohortIlse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.
The Journal of Pathology|December 31, 2016
Nuclear inclusion bodies of mutant and wild-type p53 in cancer: a hallmark of p53 inactivation and proteostasis remodelling by p53 aggregationFrederik De Smet, Mirian Saiz Rubio, Daphne Hompes, et al.
Cell|December 22, 2023
LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neuronsBaptiste Libé-Philippot, Amélie Lejeune, Keimpe Wierda, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature|November 17, 2022
Medin co-aggregates with vascular amyloid-β in Alzheimer's diseaseJessica Wagner, Karoline Degenhardt, Marleen Veit, et al.
The Journal of Allergy and Clinical Immunology|April 24, 2020
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropeniaErika Van Nieuwenhove, John S Barber, Julika Neumann, et al.
Cell|June 14, 2016
Restricted Location of PSEN2/γ-Secretase Determines Substrate Specificity and Generates an Intracellular Aβ PoolRagna Sannerud, Cary Esselens, Paulina Ejsmont, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Human Mutation|July 14, 2019
Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variantsLaura Kasak, Constantina Bakolitsa, Zhiqiang Hu, et al.
Pageof 21

Showing results (191-200 of 205) with videos related to

Sort By:
Pageof 21
Neurology|November 20, 2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohortIlse Gijselinck, Sara Van Mossevelde, Julie van der Zee, et al.
The Journal of Pathology|December 31, 2016
Nuclear inclusion bodies of mutant and wild-type p53 in cancer: a hallmark of p53 inactivation and proteostasis remodelling by p53 aggregationFrederik De Smet, Mirian Saiz Rubio, Daphne Hompes, et al.
Cell|December 22, 2023
LRRC37B is a human modifier of voltage-gated sodium channels and axon excitability in cortical neuronsBaptiste Libé-Philippot, Amélie Lejeune, Keimpe Wierda, et al.
Human Mutation|March 9, 2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementiaJulie van der Zee, Isabelle Le Ber, Sebastian Maurer-Stroh, et al.
Molecular Cell|March 18, 2017
Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule DynamicsSteven Boeynaems, Elke Bogaert, Denes Kovacs, et al.
Nature|November 17, 2022
Medin co-aggregates with vascular amyloid-β in Alzheimer's diseaseJessica Wagner, Karoline Degenhardt, Marleen Veit, et al.
The Journal of Allergy and Clinical Immunology|April 24, 2020
Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropeniaErika Van Nieuwenhove, John S Barber, Julika Neumann, et al.
Cell|June 14, 2016
Restricted Location of PSEN2/γ-Secretase Determines Substrate Specificity and Generates an Intracellular Aβ PoolRagna Sannerud, Cary Esselens, Paulina Ejsmont, et al.
Acta Neuropathologica|March 16, 2019
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitabilityRita Cacace, Bavo Heeman, Sara Van Mossevelde, et al.
Human Mutation|July 14, 2019
Assessing computational predictions of the phenotypic effect of cystathionine-beta-synthase variantsLaura Kasak, Constantina Bakolitsa, Zhiqiang Hu, et al.
Pageof 21