Simon Lecointe

Simon Lecointe

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Simon Lecointe

Simon Lecointe

Publications by authors named "Simon Lecointe"

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Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve Dysplasia.

Biophys J 2019 Oct 31;117(8):1467-1475. Epub 2019 Aug 31.

Institute of Biomedicine, University of Turku, Turku, Finland; Turku Bioscience Centre, University of Turku, 20520 Turku, Finland. Electronic address:

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http://dx.doi.org/10.1016/j.bpj.2019.08.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817519PMC
October 2019

Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin A.

Structure 2019 01 18;27(1):102-112.e4. Epub 2018 Oct 18.

Department of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, 40014 Jyväskylä, Finland; Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Institute of Biomedicine, University of Turku, 20520 Turku, Finland; Turku Centre for Biotechnology, University of Turku, 20520 Turku, Finland. Electronic address:

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http://dx.doi.org/10.1016/j.str.2018.09.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6984350PMC
January 2019

The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway.

Biochim Biophys Acta Mol Cell Res 2017 Jul 18;1864(7):1142-1152. Epub 2017 Mar 18.

l'institut du thorax, INSERM, CNRS, UNIV Nantes, Nantes, France. Electronic address:

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http://dx.doi.org/10.1016/j.bbamcr.2017.03.008DOI Listing
July 2017

Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia.

Atherosclerosis 2016 07 11;250:52-6. Epub 2016 Apr 11.

INSERM, UMR1087, l'institut du thorax, Nantes, F-44000, France; CNRS, UMR 6291, Nantes, F-44000, France; Université de Nantes, Nantes, F-44000, France; CHU Nantes, l'institut du Thorax, Nantes, F-44000, France; CIC Thorax, CHU Nantes, l'institut du Thorax, Nantes, F-44000, France. Electronic address:

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http://dx.doi.org/10.1016/j.atherosclerosis.2016.04.010DOI Listing
July 2016

Fine-scale human genetic structure in Western France.

Eur J Hum Genet 2015 Jun 3;23(6):831-6. Epub 2014 Sep 3.

1] INSERM UMR 1087, Nantes, France [2] CNRS, UMR 6291 institut du thorax, Nantes, France [3] Université de Nantes, Nantes, France [4] CHU Nantes, l'institut du thorax, Service de Cardiologie, Nantes, France.

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http://dx.doi.org/10.1038/ejhg.2014.175DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795055PMC
June 2015

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

Nat Genet 2013 Sep 21;45(9):1044-9. Epub 2013 Jul 21.

Department of Clinical and Experimental Cardiology, Heart Failure Research Center, Academic Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1038/ng.2712DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869788PMC
September 2013