Laurent Tiret

Laurent Tiret

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Laurent Tiret

Laurent Tiret

Publications by authors named "Laurent Tiret"

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The Dog Model in the Spotlight: Legacy of a Trustful Cooperation.

J Neuromuscul Dis 2019 Aug 19. Epub 2019 Aug 19.

U955 - IMRB, Team 10 - Biology of the neuromuscular system, Inserm, UPEC, EFS, École nationale vétérinaire d'Alfort, Maisons-Alfort, 94700, France.

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http://dx.doi.org/10.3233/JND-190394DOI Listing
August 2019

NIPAL4 deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy.

Vet Med Sci 2019 05 11;5(2):112-117. Epub 2019 Feb 11.

U955 - IMRB, Team 10 - Biology of the neuromuscular system, Inserm, UPEC, Ecole nationale vétérinaire d'Alfort, Maisons-Alfort, France.

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http://dx.doi.org/10.1002/vms3.149DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498511PMC
May 2019

Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient mice.

Nat Commun 2018 10 2;9(1):4107. Epub 2018 Oct 2.

The Dubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.

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http://www.nature.com/articles/s41467-018-06636-w
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http://dx.doi.org/10.1038/s41467-018-06636-wDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168580PMC
October 2018

Necroptosis mediates myofibre death in dystrophin-deficient mice.

Nat Commun 2018 09 7;9(1):3655. Epub 2018 Sep 7.

The Dubowitz Neuromuscular Centre, Molecular Neurosciences Section, Developmental Neurosciences Programme, UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.

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http://www.nature.com/articles/s41467-018-06057-9
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http://dx.doi.org/10.1038/s41467-018-06057-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128848PMC
September 2018

Targeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS.

Methods Mol Biol 2017 ;1668:39-60

Institut Mondor de Recherche Biomédicale (IMRB), U955-E10 Biologie du Système Neuromusculaire, Université Paris-Est, Ecole Nationale Vétérinaire d'Alfort (EnvA), Maisons-Alfort, France.

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http://dx.doi.org/10.1007/978-1-4939-7283-8_4DOI Listing
June 2018

Allelic heterogeneity of albinism in the domestic cat.

Anim Genet 2017 Feb 15;48(1):127-128. Epub 2016 Sep 15.

INSERM U955-E10, IMRB, Université Paris-Est Créteil, Ecole Nationale Vétérinaire d'Alfort, 7 Avenue du Général de Gaulle, 94700, Maisons-Alfort, France.

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http://dx.doi.org/10.1111/age.12503DOI Listing
February 2017

Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems.

Am J Pathol 2017 Feb 8;187(2):441-456. Epub 2016 Dec 8.

Comparative Neuromuscular Diseases Laboratory, Department of Clinical Sciences and Services, Royal Veterinary College, London, United Kingdom.

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http://dx.doi.org/10.1016/j.ajpath.2016.10.002DOI Listing
February 2017

A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome.

PLoS One 2015 1;10(9):e0137019. Epub 2015 Sep 1.

Inserm, IMRB U955-E10, 94000, Créteil, France; Université Paris Est, Ecole nationale vétérinaire d'Alfort, 94700, Maisons-Alfort, & Faculté de médecine, 94000, Créteil, France; Etablissement Français du Sang, 94017, Créteil, France; APHP, Hôpitaux Universitaires Henri Mondor, DHU Pepsy & Centre de référence des maladies neuromusculaires GNMH, 94000 Créteil, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0137019PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4556666PMC
May 2016

A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats.

PLoS One 2015 17;10(3):e0120668. Epub 2015 Mar 17.

U955 IMRB, INSERM, Équipe 10, Créteil, France; BNMS-Génétique Médicale Comparée des Affections Neuromusculaires, École nationale vétérinaire d'Alfort, Maisons-Alfort, France.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0120668PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363148PMC
December 2015

HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth.

J Mol Cell Biol 2015 Oct 9;7(5):429-40. Epub 2015 Jul 9.

Inserm, IMRB U955-E10, 94000 Créteil, France Université Paris-Est, Ecole nationale vétérinaire d'Alfort (EnvA), 94700 Maisons-Alfort, France Université Paris-Est Créteil, Faculté de médecine, 94000 Créteil, France

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http://dx.doi.org/10.1093/jmcb/mjv049DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589950PMC
October 2015

A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys.

Genet Sel Evol 2015 Apr 8;47:28. Epub 2015 Apr 8.

Inra, Unité de Génétique Fonctionnelle et Médicale, Ecole nationale vétérinaire d'Alfort, Maisons-Alfort, 94700, France.

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http://dx.doi.org/10.1186/s12711-015-0112-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389795PMC
April 2015

Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys.

Genet Sel Evol 2014 Sep 25;46:65. Epub 2014 Sep 25.

UMR955 INRA-ENVA de Génétique Fonctionnelle et Médicale, Université Paris-Est, Institut National de la Recherche Agronomique, Ecole nationale vétérinaire d'Alfort, F-94700, Maisons-Alfort, France.

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http://dx.doi.org/10.1186/s12711-014-0065-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175617PMC
September 2014

Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse.

Development 2013 Mar 13;140(6):1231-9. Epub 2013 Feb 13.

Genetics and Development Department, Inserm U1016, CNRS UMR 8104, University of Paris Descartes, Institut Cochin, 75014 Paris, France.

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http://dx.doi.org/10.1242/dev.084665DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074262PMC
March 2013

A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.

Proc Natl Acad Sci U S A 2010 Aug 2;107(33):14775-80. Epub 2010 Aug 2.

Unité Mixte de Recherche 955 de Génétique Fonctionnelle et Médicale, Institut National de la Recherche Agronomique, and Unité Propre de Recherche de Neurobiologie, Université Paris-Est, Ecole Nationale Vétérinaire d'Alfort, F-94700 Maisons-Alfort, France.

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http://www.pnas.org/cgi/doi/10.1073/pnas.0914206107
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http://dx.doi.org/10.1073/pnas.0914206107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930459PMC
August 2010

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers.

Proc Natl Acad Sci U S A 2010 Aug 3;107(33):14697-702. Epub 2010 Aug 3.

Division of Genetics and Program in Genomics, The Manton Center for Orphan Disease Research at Children's Hospital Boston and Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1073/pnas.1003677107DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2930454PMC
August 2010

Uterine contractions depend on KIT-positive interstitial cells in the mouse: genetic and pharmacological evidence.

Biol Reprod 2008 Sep 14;79(3):510-7. Epub 2008 May 14.

Institut National de la Recherche Agronomique, UMR955 de Génétique Moléculaire et Cellulaire, Ecole Nationale Vétérinaire d'Alfort, 94704 Maisons-Alfort, France.

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http://dx.doi.org/10.1095/biolreprod.107.066373DOI Listing
September 2008

SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.

Hum Mol Genet 2005 Jun 13;14(11):1417-27. Epub 2005 Apr 13.

UMR 955 INRA-ENVA de Génétique Moléculaire et Cellulaire, Ecole Nationale Vétérinaire d'Alfort, 7 avenue du Général de Gaulle, 94704 Maisons-Alfort cedex, France.

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http://dx.doi.org/10.1093/hmg/ddi151DOI Listing
June 2005

The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2.

Hum Genet 2003 Sep 23;113(4):297-306. Epub 2003 Jul 23.

UMR 955 INRA-ENVA de Génétique Moléculaire et Cellulaire, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.

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http://dx.doi.org/10.1007/s00439-003-0984-7DOI Listing
September 2003