Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Emmanuelle C Genin

Showing results (11-20 of 28) with videos related to

Pageof 3
Sort By:
Neurobiology of Disease|April 7, 2024
CHCHD10<sup>S59L/+</sup> mouse model: Behavioral and neuropathological features of frontotemporal dementiaEmmanuelle C Genin, Pauline Pozzo di Borgo, Thomas Lorivel, et al.
Brain : a Journal of Neurology|June 3, 2022
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viabilityEmmanuelle C Genin, Sylvie Bannwarth, Baptiste Ropert, et al.
Annals of Neurology|June 23, 2015
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophyGodelieve Morel, Cécile Rouzier, Annabelle Chaussenot, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Biochimica Et Biophysica Acta|November 19, 2013
LXR antagonists induce ABCD2 expressionCatherine Gondcaille, Emmanuelle C Genin, Tatiana E Lopez, et al.
Neurobiology of Disease|August 10, 2018
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseasesEmmanuelle C Genin, Sylvie Bannwarth, Françoise Lespinasse, et al.
Acta Neuropathologica|March 16, 2019
Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10<sup>S59L/+</sup> mouseEmmanuelle C Genin, Blandine Madji Hounoum, Sylvie Bannwarth, et al.
EMBO Molecular Medicine|December 16, 2015
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosisEmmanuelle C Genin, Morgane Plutino, Sylvie Bannwarth, et al.
Brain : a Journal of Neurology|May 9, 2015
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Neurobiology of Disease|April 7, 2024
CHCHD10<sup>S59L/+</sup> mouse model: Behavioral and neuropathological features of frontotemporal dementiaEmmanuelle C Genin, Pauline Pozzo di Borgo, Thomas Lorivel, et al.
Brain : a Journal of Neurology|June 3, 2022
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viabilityEmmanuelle C Genin, Sylvie Bannwarth, Baptiste Ropert, et al.
Annals of Neurology|June 23, 2015
CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophyGodelieve Morel, Cécile Rouzier, Annabelle Chaussenot, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Biochimica Et Biophysica Acta|November 19, 2013
LXR antagonists induce ABCD2 expressionCatherine Gondcaille, Emmanuelle C Genin, Tatiana E Lopez, et al.
Neurobiology of Disease|August 10, 2018
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseasesEmmanuelle C Genin, Sylvie Bannwarth, Françoise Lespinasse, et al.
Acta Neuropathologica|March 16, 2019
Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10<sup>S59L/+</sup> mouseEmmanuelle C Genin, Blandine Madji Hounoum, Sylvie Bannwarth, et al.
EMBO Molecular Medicine|December 16, 2015
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosisEmmanuelle C Genin, Morgane Plutino, Sylvie Bannwarth, et al.
Brain : a Journal of Neurology|May 9, 2015
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Brain : a Journal of Neurology|January 11, 2015
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 3