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Benoit Coulombe

Showing results (61-70 of 82) with videos related to

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American Journal of Human Genetics|January 8, 2021
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Journal of Clinical Lipidology|April 28, 2018
Posttranslational modification of proprotein convertase subtilisin/kexin type 9 is differentially regulated in response to distinct cardiometabolic treatments as revealed by targeted proteomicsMarie-Soleil Gauthier, Zuhier Awan, Annie Bouchard, et al.
American Journal of Human Genetics|April 8, 2022
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Nucleic Acids Research|February 19, 2008
LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associatedBrian J Krueger, Célia Jeronimo, Bibhuti Bhusan Roy, et al.
Biochimica Et Biophysica Acta|May 19, 2010
Conformational coupling, bridge helix dynamics and active site dehydration in catalysis by RNA polymeraseSteve A Seibold, Badri Nath Singh, Chunfen Zhang, 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.
Nucleic Acids Research|June 10, 2022
ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasiaLinjiang Lao, Isabelle Bourdeau, Lucia Gagliardi, et al.
Genome Biology|January 15, 2024
ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humansHongyu Luo, Linjiang Lao, Kit Sing Au, et al.
Methods (San Diego, Calif.)|March 16, 2015
A semi-automated mass spectrometric immunoassay coupled to selected reaction monitoring (MSIA-SRM) reveals novel relationships between circulating PCSK9 and metabolic phenotypes in patient cohortsMarie-Soleil Gauthier, Joëlle R Pérusse, Zuhier Awan, 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.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|January 8, 2021
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Journal of Clinical Lipidology|April 28, 2018
Posttranslational modification of proprotein convertase subtilisin/kexin type 9 is differentially regulated in response to distinct cardiometabolic treatments as revealed by targeted proteomicsMarie-Soleil Gauthier, Zuhier Awan, Annie Bouchard, et al.
American Journal of Human Genetics|April 8, 2022
De novo variants in POLR3B cause ataxia, spasticity, and demyelinating neuropathyDjurdja Djordjevic, Maxime Pinard, Marie-Soleil Gauthier, et al.
Nucleic Acids Research|February 19, 2008
LARP7 is a stable component of the 7SK snRNP while P-TEFb, HEXIM1 and hnRNP A1 are reversibly associatedBrian J Krueger, Célia Jeronimo, Bibhuti Bhusan Roy, et al.
Biochimica Et Biophysica Acta|May 19, 2010
Conformational coupling, bridge helix dynamics and active site dehydration in catalysis by RNA polymeraseSteve A Seibold, Badri Nath Singh, Chunfen Zhang, 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.
Nucleic Acids Research|June 10, 2022
ARMC5 is part of an RPB1-specific ubiquitin ligase implicated in adrenal hyperplasiaLinjiang Lao, Isabelle Bourdeau, Lucia Gagliardi, et al.
Genome Biology|January 15, 2024
ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humansHongyu Luo, Linjiang Lao, Kit Sing Au, et al.
Methods (San Diego, Calif.)|March 16, 2015
A semi-automated mass spectrometric immunoassay coupled to selected reaction monitoring (MSIA-SRM) reveals novel relationships between circulating PCSK9 and metabolic phenotypes in patient cohortsMarie-Soleil Gauthier, Joëlle R Pérusse, Zuhier Awan, 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.
Pageof 9