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Bassem A Hassan

Showing results (81-90 of 90) with videos related to

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Nature Communications|September 1, 2025
Temporal transcriptional regulation of mitochondrial morphology primes activity-dependent circuit connectivityIryna Mohylyak, Maheva Andriatsilavo, Mercedes Bengochea, et al.
Elife|October 10, 2022
Transient regulation of focal adhesion via Tensin3 is required for nascent oligodendrocyte differentiationEmeric Merour, Hatem Hmidan, Corentine Marie, et al.
Cell|January 30, 2016
Post-translational Control of the Temporal Dynamics of Transcription Factor Activity Regulates NeurogenesisXiao-Jiang Quan, Liqun Yuan, Luca Tiberi, et al.
Frontiers in Molecular Neuroscience|January 31, 2018
Regulation of Adult CNS Axonal Regeneration by the Post-transcriptional Regulator Cpeb1Wilson Pak-Kin Lou, Alvaro Mateos, Marta Koch, et al.
Life Science Alliance|January 31, 2023
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performanceMira Brazane, Dilyana G Dimitrova, Julien Pigeon, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Nature Genetics|December 25, 2012
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemiaKim De Keersmaecker, Zeynep Kalender Atak, Ning Li, et al.
American Journal of Human Genetics|September 23, 2025
Heterozygous pathogenic variants in the splicing factor SF1 lead to a large spectrum of neurodevelopmental disordersJohnny Bou-Rouphael, Auriane Cospain, Thomas Courtin, et al.
Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
<i>PSMF1</i> variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathwaysFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
Nature Communications|September 1, 2025
Temporal transcriptional regulation of mitochondrial morphology primes activity-dependent circuit connectivityIryna Mohylyak, Maheva Andriatsilavo, Mercedes Bengochea, et al.
Elife|October 10, 2022
Transient regulation of focal adhesion via Tensin3 is required for nascent oligodendrocyte differentiationEmeric Merour, Hatem Hmidan, Corentine Marie, et al.
Cell|January 30, 2016
Post-translational Control of the Temporal Dynamics of Transcription Factor Activity Regulates NeurogenesisXiao-Jiang Quan, Liqun Yuan, Luca Tiberi, et al.
Frontiers in Molecular Neuroscience|January 31, 2018
Regulation of Adult CNS Axonal Regeneration by the Post-transcriptional Regulator Cpeb1Wilson Pak-Kin Lou, Alvaro Mateos, Marta Koch, et al.
Life Science Alliance|January 31, 2023
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performanceMira Brazane, Dilyana G Dimitrova, Julien Pigeon, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Nature Genetics|December 25, 2012
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemiaKim De Keersmaecker, Zeynep Kalender Atak, Ning Li, et al.
American Journal of Human Genetics|September 23, 2025
Heterozygous pathogenic variants in the splicing factor SF1 lead to a large spectrum of neurodevelopmental disordersJohnny Bou-Rouphael, Auriane Cospain, Thomas Courtin, et al.
Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
<i>PSMF1</i> variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathwaysFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Nature Communications|April 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethalityFrancesca Magrinelli, Christelle Tesson, Plamena R Angelova, et al.
Pageof 9