Author details

Full Name

Carole DorÃ©

Affiliation

ORCID

Career Start Year

1999

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37400371	Tissue-Engineered Disease Modeling of Lymphangioleiomyomatosis Exposes a Therapeutic Vulnerability to HDAC Inhibition.	Adv Sci (Weinh)	2023
31813826	Transcriptomically Guided Mesendoderm Induction of Human Pluripotent Stem Cells Using a Systematically Defined Culture Scheme.	Stem Cell Reports	2019
29561844	Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset.	PLoS Genet	2018
29893190	Metformin Preconditioning of Human Induced Pluripotent Stem Cell-Derived Neural Stem Cells Promotes Their Engraftment and Improves Post-Stroke Regeneration and Recovery.	Stem Cells Dev	2018
30461330	A cost-effectiveness analysis comparing the originator follitropin alfa to its biosimilars in patients undergoing a medically assisted reproduction program from a French perspective.	J Med Econ	2018
28830860	Human Pluripotent Stem Cell-Derived <i>TSC2</i>-Haploinsufficient Smooth Muscle Cells Recapitulate Features of Lymphangioleiomyomatosis.	Cancer Res	2017
28597562	Reprogramming progeria fibroblasts re-establishes a normal epigenetic landscape.	Aging Cell	2017
26715668	Redundant Regulation of Cdk1 Tyrosine Dephosphorylation in Saccharomyces cerevisiae.	Genetics	2016
26587833	Competition between Heterochromatic Loci Allows the Abundance of the Silencing Protein, Sir4, to Regulate de novo Assembly of Heterochromatin.	PLoS Genetics	2015
23751495	A Wee1 checkpoint inhibits anaphase onset.	Journal of Cell Biology	2013
20802492	Tah18 transfers electrons to Dre2 in cytosolic iron-sulfur protein biogenesis.	Nature Chemical Biology	2010
17805225	Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.	Eur J Hum Genet	2008
16311595	Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.	Nat Genet	2006
16301213	Mapping common regulatory variants to human haplotypes.	Hum Mol Genet	2005
16251468	Survey of allelic expression using EST mining.	Genome Res	2005
14737177	Susceptibility to leprosy is associated with PARK2 and PACRG.	Nature	2004
15523652	Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism.	Hum Mutat	2004
12068375	Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.	Am J Hum Genet	2002
11978666	5' flanking variants of resistin are associated with obesity.	Diabetes	2002
12438653	Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.	Proc Natl Acad Sci U S A	2002
10655055	ARSACS, a spastic ataxia common in northeastern QuÃ©bec, is caused by mutations in a new gene encoding an 11.5-kb ORF.	Nat Genet	2000
10610707	Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): high-resolution physical and transcript map of the candidate region in chromosome region 13q11.	Genomics	1999