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Diane Forget

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Molecular & Cellular Proteomics : MCP|September 22, 2010
The protein interaction network of the human transcription machinery reveals a role for the conserved GTPase RPAP4/GPN1 and microtubule assembly in nuclear import and biogenesis of RNA polymerase IIDiane Forget, Andrée-Anne Lacombe, Philippe Cloutier, et al.
The Journal of Biological Chemistry|March 23, 2019
Leukodystrophy-associated <i>POLR3A</i> mutations down-regulate the RNA polymerase III transcript and important regulatory RNA <i>BC200</i>Karine Choquet, Diane Forget, Elisabeth Meloche, 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.
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.
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.
Molecular and Cellular Biology|July 30, 2004
RPAP1, a novel human RNA polymerase II-associated protein affinity purified with recombinant wild-type and mutated polymerase subunitsCélia Jeronimo, Marie-France Langelier, Mahel Zeghouf, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 26, 2019
Ser-Phosphorylation of PCSK9 (Proprotein Convertase Subtilisin-Kexin 9) by Fam20C (Family With Sequence Similarity 20, Member C) Kinase Enhances Its Ability to Degrade the LDLR (Low-Density Lipoprotein Receptor)Ali Ben Djoudi Ouadda, Marie-Soleil Gauthier, Delia Susan-Resiga, et al.
American Journal of Human Genetics|March 27, 2018
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating LeukodystrophyMarisa I Mendes, Mariana Gutierrez Salazar, Kether Guerrero, 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 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Molecular & Cellular Proteomics : MCP|September 22, 2010
The protein interaction network of the human transcription machinery reveals a role for the conserved GTPase RPAP4/GPN1 and microtubule assembly in nuclear import and biogenesis of RNA polymerase IIDiane Forget, Andrée-Anne Lacombe, Philippe Cloutier, et al.
The Journal of Biological Chemistry|March 23, 2019
Leukodystrophy-associated <i>POLR3A</i> mutations down-regulate the RNA polymerase III transcript and important regulatory RNA <i>BC200</i>Karine Choquet, Diane Forget, Elisabeth Meloche, 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.
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.
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.
Molecular and Cellular Biology|July 30, 2004
RPAP1, a novel human RNA polymerase II-associated protein affinity purified with recombinant wild-type and mutated polymerase subunitsCélia Jeronimo, Marie-France Langelier, Mahel Zeghouf, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 26, 2019
Ser-Phosphorylation of PCSK9 (Proprotein Convertase Subtilisin-Kexin 9) by Fam20C (Family With Sequence Similarity 20, Member C) Kinase Enhances Its Ability to Degrade the LDLR (Low-Density Lipoprotein Receptor)Ali Ben Djoudi Ouadda, Marie-Soleil Gauthier, Delia Susan-Resiga, et al.
American Journal of Human Genetics|March 27, 2018
Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating LeukodystrophyMarisa I Mendes, Mariana Gutierrez Salazar, Kether Guerrero, 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 2