Publications by authors named "Severine Leclerc"

13Publications

Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics.

Cell Mol Gastroenterol Hepatol 2019 24;7(2):411-431. Epub 2018 Oct 24.

Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte Justine Research Center, Université de Montréal, Montréal, Québec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.jcmgh.2018.10.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369230PMC
May 2019

Dataset of expression in cardiac, gastrointestinal, hepatic and neuronal tissue in mouse.

Data Brief 2017 Aug 1;13:731-737. Epub 2017 Jul 1.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Canada.

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http://dx.doi.org/10.1016/j.dib.2017.06.046DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512188PMC
August 2017

Characterization of Sgo1 expression in developing and adult mouse.

Gene Expr Patterns 2017 11 29;25-26:36-45. Epub 2017 Apr 29.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Montreal, QC, Canada; Université de Montréal, Montreal, QC, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.gep.2017.04.004DOI Listing
November 2017

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

Can J Cardiol 2016 Jan 13;32(1):135.e1-7. Epub 2015 Apr 13.

Cardiovascular Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montréal, Québec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.cjca.2015.04.004DOI Listing
January 2016

Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm.

Nat Genet 2014 Nov 5;46(11):1245-9. Epub 2014 Oct 5.

1] Cardiovascular Genetics, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Centre, Université de Montréal, Montreal, Quebec, Canada. [2] Department of Pediatrics, Université de Montréal, Montreal, Quebec, Canada. [3] Department of Biochemistry, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1038/ng.3113DOI Listing
November 2014

Genetic interaction between members of the Vangl family causes neural tube defects in mice.

Proc Natl Acad Sci U S A 2008 Mar 22;105(9):3449-54. Epub 2008 Feb 22.

Department of Biochemistry, McGill University, Montreal, QC, Canada H3G 1Y6.

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http://dx.doi.org/10.1073/pnas.0712126105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2265143PMC
March 2008

Expression of heat-shock protein 70 during limb development and regeneration in the axolotl.

Dev Dyn 2005 Aug;233(4):1525-34

Department of Biochemistry, Université de Montréal, Québec, Canada.

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http://dx.doi.org/10.1002/dvdy.20458DOI Listing
August 2005

Drug transport into the mammalian brain: the nasal pathway and its specific metabolic barrier.

J Drug Target 2002 Jun;10(4):285-96

Laboratoire de Pharmacologie, UMR No 7561 CNRS-Université Henri-Poincaré-Nancy 1, Faculté de Médecine, Vandoeuvre-lès-Nancy, France.

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http://dx.doi.org/10.1080/713714452DOI Listing
June 2002