Chantal Garand

Quebec, QC G1V0A6, Canada

Last Updated: 09/26/2026

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Found 13 publications

ARHGEF17/TEM4 regulates the cell cycle through control of G1 progression.

ARHGEF17/TEM4 regulates the cell cycle through control of G1 progression.

Journal: The Journal of cell biology
Published: April 23, 2024

The substrate quality of CK2 target sites has a determinant role on their function and evolution.

The substrate quality of CK2 target sites has a determinant role on their function and evolution.

Journal: Cell systems
Published: July 03, 2023

Considerations for studying phosphorylation of the mitotic checkpoint pseudokinase BUBR1.

Considerations for studying phosphorylation of the mitotic checkpoint pseudokinase BUBR1.

Journal: Methods in enzymology
Published: May 07, 2022

A quantitative and semiautomated method for determining misaligned and lagging chromosomes during mitosis.

A quantitative and semiautomated method for determining misaligned and lagging chromosomes during mitosis.

Journal: Molecular biology of the cell
Published: October 21, 2020

BUBR1 Pseudokinase Domain Promotes Kinetochore PP2A-B56 Recruitment, Spindle Checkpoint Silencing, and Chromosome Alignment.

BUBR1 Pseudokinase Domain Promotes Kinetochore PP2A-B56 Recruitment, Spindle Checkpoint Silencing, and Chromosome Alignment.

Journal: Cell reports
Published: October 23, 2019

Mps1 Phosphorylates Its N-Terminal Extension to Relieve Autoinhibition and Activate the Spindle Assembly Checkpoint.

Mps1 Phosphorylates Its N-Terminal Extension to Relieve Autoinhibition and Activate the Spindle Assembly Checkpoint.

Journal: Current biology : CB
Published: December 08, 2017

Vitamin C modulates the metabolic and cytokine profiles, alleviates hepatic endoplasmic reticulum stress, and increases the life span of Gulo-/- mice.

Vitamin C modulates the metabolic and cytokine profiles, alleviates hepatic endoplasmic reticulum stress, and increases the life span of Gulo-/- mice.

Journal: Aging
Published: February 29, 2016

Different non-synonymous polymorphisms modulate the interaction of the WRN protein to its protein partners and its enzymatic activities.

Different non-synonymous polymorphisms modulate the interaction of the WRN protein to its protein partners and its enzymatic activities.

Journal: Oncotarget
Published: October 30, 2015

Impact of vitamin C on the cardiometabolic and inflammatory profiles of mice lacking a functional Werner syndrome protein helicase.

Impact of vitamin C on the cardiometabolic and inflammatory profiles of mice lacking a functional Werner syndrome protein helicase.

Journal: Experimental gerontology
Published: August 12, 2015

Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.

Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.

Journal: PloS one
Published: July 14, 2015

Down regulation of miR-124 in both Werner syndrome DNA helicase mutant mice and mutant Caenorhabditis elegans wrn-1 reveals the importance of this microRNA in accelerated aging.

Down regulation of miR-124 in both Werner syndrome DNA helicase mutant mice and mutant Caenorhabditis elegans wrn-1 reveals the importance of this microRNA in accelerated aging.

Journal: Aging
Published: October 19, 2012

The non-synonymous polymorphism at position 114 of the WRN protein affects cholesterol efflux in vitro and correlates with cholesterol levels in vivo.

The non-synonymous polymorphism at position 114 of the WRN protein affects cholesterol efflux in vitro and correlates with cholesterol levels in vivo.

Journal: Experimental gerontology
Published: October 08, 2012
Showing 1-12 of 13

Last Updated: 09/26/2026