Publications by authors named "Carole Dore"

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Greening the lab: fighting climate change to enhance mental health.
Paul R Albert, Marie Marotel, Carole Doré, Rebecca C Auer

J Psychiatry Neurosci· April 2025

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Tissue-Engineered Disease Modeling of Lymphangioleiomyomatosis Exposes a Therapeutic Vulnerability to HDAC Inhibition.
Adam Pietrobon, Julien Yockell-Lelièvre, Nicole Melong, Laura J Smith, Sean P Delaney

Adv Sci (Weinh)· September 2023

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Transcriptomically Guided Mesendoderm Induction of Human Pluripotent Stem Cells Using a Systematically Defined Culture Scheme.
Richard L Carpenedo, Sarah Y Kwon, R Matthew Tanner, Julien Yockell-Lelièvre, Chandarong Choey, Theodore J Perkins

Stem Cell Reports· December 2019

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A cost-effectiveness analysis comparing the originator follitropin alfa to its biosimilars in patients undergoing a medically assisted reproduction program from a French perspective.
Michaël Grynberg, Claire Murphy, Carole Doré, Laurence Fresneau, Ségolène Paillet

J Med Econ· December 2018

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Metformin Preconditioning of Human Induced Pluripotent Stem Cell-Derived Neural Stem Cells Promotes Their Engraftment and Improves Post-Stroke Regeneration and Recovery.
Fares Ould-Brahim, Sailendra Nath Sarma, Charvi Syal, Kevin Jiaqi Lu, Matthew Seegobin

Stem Cells Dev· August 2018

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Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset.
Noel Lianga, Carole Doré, Erin K Kennedy, Elaine Yeh, Elizabeth C Williams

PLoS Genet· March 2018

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Human Pluripotent Stem Cell-Derived -Haploinsufficient Smooth Muscle Cells Recapitulate Features of Lymphangioleiomyomatosis.
Lisa M Julian, Sean P Delaney, Ying Wang, Alexander A Goldberg, Carole Doré

Cancer Res· October 2017

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Reprogramming progeria fibroblasts re-establishes a normal epigenetic landscape.
Zhaoyi Chen, Wing Y Chang, Alton Etheridge, Hilmar Strickfaden, Zhigang Jin, Theodore J Perkins

Aging Cell· August 2017

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Redundant Regulation of Cdk1 Tyrosine Dephosphorylation in Saccharomyces cerevisiae.
Erin K Kennedy, Michael Dysart, Noel Lianga, Elizabeth C Williams, Sophie Pilon

Genetics· March 2016

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Competition between Heterochromatic Loci Allows the Abundance of the Silencing Protein, Sir4, to Regulate de novo Assembly of Heterochromatin.
Michelle L Larin, Katherine Harding, Elizabeth C Williams, Noel Lianga, Carole Doré

PLoS Genet· November 2015

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A Wee1 checkpoint inhibits anaphase onset.
Noel Lianga, Elizabeth C Williams, Erin K Kennedy, Carole Doré, Sophie Pilon

J Cell Biol· June 2013

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Tah18 transfers electrons to Dre2 in cytosolic iron-sulfur protein biogenesis.
Daili J A Netz, Martin Stümpfig, Carole Doré, Ulrich Mühlenhoff, Antonio J Pierik

Nat Chem Biol· October 2010

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Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
James C Engert, Mathieu Lemire, Janet Faith, Diane Brisson, T Mary Fujiwara

Eur J Hum Genet· January 2008

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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Jordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, Carole Doré, Janet L Atkinson

Nat Genet· January 2006

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Mapping common regulatory variants to human haplotypes.
Tomi Pastinen, Bing Ge, Scott Gurd, Tiffany Gaudin, Carole Dore

Hum Mol Genet· December 2005

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Survey of allelic expression using EST mining.
Bing Ge, Scott Gurd, Tiffany Gaudin, Carole Dore, Pierre Lepage

Genome Res· November 2005

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Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism.
Jordan P Lerner-Ellis, C Melissa Dobson, Timothy Wai, David Watkins, Jamie C Tirone

Hum Mutat· December 2004

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Susceptibility to leprosy is associated with PARK2 and PACRG.
Marcelo T Mira, Alexandre Alcaïs, Van Thuc Nguyen, Milton O Moraes, Celestino Di Flumeri

Nature· February 2004

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Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.
C Melissa Dobson, Timothy Wai, Daniel Leclerc, Aaron Wilson, Xuchu Wu

Proc Natl Acad Sci U S A· November 2002

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Hyperhomocysteinemia due to methionine synthase deficiency, cblG: structure of the MTR gene, genotype diversity, and recognition of a common mutation, P1173L.
David Watkins, Ming Ru, Hye-Yeon Hwang, Caroline D Kim, Angus Murray

Am J Hum Genet· July 2002

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5' flanking variants of resistin are associated with obesity.
James C Engert, Marie-Claude Vohl, Scott M Williams, Pierre Lepage, J C Loredo-Osti

Diabetes· May 2002

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