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Delphine Bohl

Showing results (31-40 of 38) with videos related to

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Nature Communications|March 30, 2024
A conserved NR5A1-responsive enhancer regulates SRY in testis-determinationDenis Houzelstein, Caroline Eozenou, Carlos F Lagos, et al.
Cellular and Molecular Life Sciences : CMLS|May 15, 2023
Neurofilament accumulations in amyotrophic lateral sclerosis patients' motor neurons impair axonal initial segment integrityCynthia Lefebvre-Omar, Elise Liu, Carine Dalle, et al.
Neurobiology of Aging|July 19, 2017
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysisElisa Teyssou, Laura Chartier, Maria-Del-Mar Amador, et al.
Nature Communications|August 26, 2025
ALS/FTD-linked TBK1 deficiency in microglia induces an aged-like microglial signature and drives social recognition deficits in miceIsadora Lenoel, Matthieu Ribon, Félicie Lorenc, 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.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Brain : a Journal of Neurology|October 31, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease modelsBaptiste Ropert, Sylvie Bannwarth, Emmanuelle C Genin, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Nature Communications|March 30, 2024
A conserved NR5A1-responsive enhancer regulates SRY in testis-determinationDenis Houzelstein, Caroline Eozenou, Carlos F Lagos, et al.
Cellular and Molecular Life Sciences : CMLS|May 15, 2023
Neurofilament accumulations in amyotrophic lateral sclerosis patients' motor neurons impair axonal initial segment integrityCynthia Lefebvre-Omar, Elise Liu, Carine Dalle, et al.
Neurobiology of Aging|July 19, 2017
Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysisElisa Teyssou, Laura Chartier, Maria-Del-Mar Amador, et al.
Nature Communications|August 26, 2025
ALS/FTD-linked TBK1 deficiency in microglia induces an aged-like microglial signature and drives social recognition deficits in miceIsadora Lenoel, Matthieu Ribon, Félicie Lorenc, 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.
Nature Communications|October 13, 2017
HDAC6 inhibition reverses axonal transport defects in motor neurons derived from FUS-ALS patientsWenting Guo, Maximilian Naujock, Laura Fumagalli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunitiesFrançois Muratet, Elisa Teyssou, Aude Chiot, et al.
Brain : a Journal of Neurology|October 31, 2024
Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease modelsBaptiste Ropert, Sylvie Bannwarth, Emmanuelle C Genin, et al.
Pageof 4