Laurent Tiret
Laurent Tiret
Professor in comparative physiology and pharmacology, Alfort School of Veterinary Medicine, Paris
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Identification of genomic regions associated with phenotypic variation between dog breeds using selection mapping
A Vaysse, A Ratnakumar, T Derrien, E Axelsson, GR Pielberg, ...
PLoS Genet 7 (10), e1002316, 2011
Targeting of the EphA4 tyrosine kinase receptor affects dorsal/ventral pathfinding of limb motor axons
F Helmbacher, S Schneider-Maunoury, P Topilko, L Tiret, P Charnay
Development 127 (15), 3313-3324, 2000
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs
M Pelé, L Tiret, JL Kessler, S Blot, JJ Panthier
Human molecular genetics 14 (11), 1417-1427, 2005
Increased apoptosis of motoneurons and altered somatotopic maps in the brachial spinal cord of Hoxc-8-deficient mice
L Tiret, H Le Mouellic, M Maury, P Brulet
Development 125 (2), 279-291, 1998
MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers
AH Beggs, J Böhm, E Snead, M Kozlowski, M Maurer, K Minor, ...
Proceedings of the National Academy of Sciences 107 (33), 14697-14702, 2010
A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis
M Abitbol, JL Thibaud, NJ Olby, C Hitte, JP Puech, M Maurer, ...
Proceedings of the National Academy of Sciences 107 (33), 14775-14780, 2010
Inhibited gastrulation in mouse embryos overexpressing the leukemia inhibitory factor
F Conquet, N Peyrieras, L Tiret, P Brûlet
Proceedings of the National Academy of Sciences 89 (17), 8195-8199, 1992
Uterine contractions depend on KIT-positive interstitial cells in the mouse: genetic and pharmacological evidence
S Allix, E Reyes-Gomez, G Aubin-Houzelstein, D Noël, L Tiret, JJ Panthier, ...
Biology of reproduction 79 (3), 510-517, 2008
Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy
J Böhm, N Vasli, M Maurer, B Cowling, GD Shelton, W Kress, A Toussaint, ...
PLoS Genet 9 (6), e1003430, 2013
The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2
L Tiret, S Blot, JL Kessler, H Gaillot, M Breen, JJ Panthier
Human genetics 113 (4), 297-306, 2003
Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse
M Borensztein, P Monnier, Y Louault, MA Ripoche, L Tiret, Z Yao, ...
Development 140 (6), 1231-1239, 2013
Breed differences in natriuretic peptides in healthy dogs
K Sjöstrand, G Wess, I Ljungvall, J Häggström, AC Merveille, M Wiberg, ...
Journal of veterinary internal medicine 28 (2), 451-457, 2014
Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice
F Redelsperger, N Raddi, A Bacquin, C Vernochet, V Mariot, V Gache, ...
PLoS genetics 12 (9), e1006289, 2016
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth
J Blondelle, Y Ohno, V Gache, S Guyot, S Storck, N Blanchard-Gutton, ...
Journal of molecular cell biology 7 (5), 429-440, 2015
Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide
M Maurer, J Mary, L Guillaud, M Fender, M Pele, T Bilzer, N Olby, ...
PloS one 7 (10), e46408, 2012
Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys
R Legrand, L Tiret, M Abitbol
Genetics Selection Evolution 46 (1), 1-7, 2014
Necroptosis mediates myofibre death in dystrophin-deficient mice
JE Morgan, A Prola, V Mariot, V Pini, J Meng, C Hourde, J Dumonceaux, ...
Nature communications 9 (1), 1-10, 2018
A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys
M Abitbol, R Legrand, L Tiret
Genetics Selection Evolution 47 (1), 28, 2015
A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys
M Abitbol, R Legrand, L Tiret
Animal genetics 45 (6), 878-880, 2014
A deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats
M Abitbol, P Bossé, A Thomas, L Tiret
PLoS One 10 (3), e0120668, 2015
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