User profiles for Régen Drouin
Regen DrouinUniversité de Sherbrooke Verified email at USherbrooke.ca Cited by 6729 |
Sizing the ends: normal length of human telomeres
O Samassekou, M Gadji, R Drouin, JU Yan - Annals of Anatomy …, 2010 - Elsevier
The ends of human chromosomes are constituted of telomeres, a nucleoprotein complex.
They are mainly formed by the entanglement of repeat DNA and telomeric and non-telomeric …
They are mainly formed by the entanglement of repeat DNA and telomeric and non-telomeric …
UVA‐induced cyclobutane pyrimidine dimers form predominantly at thymine–thymine dipyrimidines and correlate with the mutation spectrum in rodent cells
PJ Rochette, JP Therrien, R Drouin… - Nucleic acids …, 2003 - academic.oup.com
Ligation‐mediated PCR was employed to quantify cyclobutane pyrimidine dimer (CPD)
formation at nucleotide resolution along exon 2 of the adenine phosphoribosyltransferase (aprt) …
formation at nucleotide resolution along exon 2 of the adenine phosphoribosyltransferase (aprt) …
Fetal–maternal exchange of multipotent stem/progenitor cells: microchimerism in diagnosis and disease
T Klonisch, R Drouin - Trends in molecular medicine, 2009 - cell.com
The biological concept of microchimerism, the bidirectional trafficking and stable long-term
persistence of small numbers of allogeneic (fetal and maternal) cells in a genetically different …
persistence of small numbers of allogeneic (fetal and maternal) cells in a genetically different …
[HTML][HTML] Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord
A Montpetit, S Côté, E Brustein, CA Drouin… - PLoS …, 2008 - journals.plos.org
Adaptor protein (AP) complexes regulate clathrin-coated vesicle assembly, protein cargo
sorting, and vesicular trafficking between organelles in eukaryotic cells. Because disruption of …
sorting, and vesicular trafficking between organelles in eukaryotic cells. Because disruption of …
P53 transcriptional activities: a general overview and some thoughts
JF Millau, N Bastien, R Drouin - Mutation Research/Reviews in Mutation …, 2009 - Elsevier
P53 is a master transcriptional regulator controlling several main cellular pathways. Its role
is to adapt gene expression programs in order to maintain cellular homeostasis and genome …
is to adapt gene expression programs in order to maintain cellular homeostasis and genome …
SW480, a p53 double-mutant cell line retains proficiency for some p53 functions
During certain types of cellular stress, the p53 tumor suppressor protein binds to DNA and
transactivates a variety of genes that regulate critical responses including apoptosis, cell cycle …
transactivates a variety of genes that regulate critical responses including apoptosis, cell cycle …
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry disease
Fabry disease is a complex, multisystemic and clinically heterogeneous disease, in which
the urinary excretion of globotriaosylceramide (Gb 3 ), the principal substrate of the deficient …
the urinary excretion of globotriaosylceramide (Gb 3 ), the principal substrate of the deficient …
ABC50, a novel human ATP-binding cassette protein found in tumor necrosis factor-α-stimulated synoviocytes
M Richard, R Drouin, AD Beaulieu - Genomics, 1998 - Elsevier
We have used the recently developed technique of differential display polymerase chain
reaction to seek for new genes modulated by tumor necrosis factor-α (TNF-α) in cultured …
reaction to seek for new genes modulated by tumor necrosis factor-α (TNF-α) in cultured …
Influence of cytosine methylation on ultraviolet-induced cyclobutane pyrimidine dimer formation in genomic DNA
The ultraviolet (UV) component of sunlight is the main cause of skin cancer. More than 50%
of all non-melanoma skin cancers and >90% of squamous cell carcinomas in the US carry a …
of all non-melanoma skin cancers and >90% of squamous cell carcinomas in the US carry a …
Genetic cooperation between the Werner syndrome protein and poly (ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal …
…, J Lavoie, I Gaudreault, M Bronsard, R Drouin - The American journal of …, 2003 - Elsevier
Werner syndrome is a rare disorder characterized by the premature onset of a number of
age-related diseases. The gene responsible for Werner syndrome encodes a DNA helicase/…
age-related diseases. The gene responsible for Werner syndrome encodes a DNA helicase/…