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Christian Poitras

Showing results (21-30 of 27) with videos related to

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Nature Communications|January 12, 2026
DOT1L activity limits transcription elongation velocity and favors RNAPII pausing to facilitate mutagenesis by AIDPoorani Ganesh Subramani, Noé Seija, Jana Ridani, et al.
Molecular Brain|June 22, 2019
The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesisKarine Choquet, Maxime Pinard, Sharon Yang, et al.
Molecular Cell|July 24, 2007
Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzymeCélia Jeronimo, Diane Forget, Annie Bouchard, et al.
Frontiers in Molecular Neuroscience|April 4, 2024
Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organizationNicolas Chofflet, Yusuke Naito, Anthony John Pastore, et al.
Molecular Brain|April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutationKarine Choquet, Sharon Yang, Robyn D Moir, et al.
HGG Advances|January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseAlexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Nature Communications|January 12, 2026
DOT1L activity limits transcription elongation velocity and favors RNAPII pausing to facilitate mutagenesis by AIDPoorani Ganesh Subramani, Noé Seija, Jana Ridani, et al.
Molecular Brain|June 22, 2019
The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesisKarine Choquet, Maxime Pinard, Sharon Yang, et al.
Molecular Cell|July 24, 2007
Systematic analysis of the protein interaction network for the human transcription machinery reveals the identity of the 7SK capping enzymeCélia Jeronimo, Diane Forget, Annie Bouchard, et al.
Frontiers in Molecular Neuroscience|April 4, 2024
Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organizationNicolas Chofflet, Yusuke Naito, Anthony John Pastore, et al.
Molecular Brain|April 15, 2017
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutationKarine Choquet, Sharon Yang, Robyn D Moir, et al.
HGG Advances|January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseAlexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.
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