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A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis.Myod and H19-Igf2 locus interactions are required for diaphragm formation in the mouse.Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys.Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide.Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathyA deletion in FOXN1 is associated with a syndrome characterized by congenital hypotrichosis and short life expectancy in Birman cats.A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeysThe Shepherds' Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian ShepherdsA COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic SyndromeHACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth.Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice.Breed differences in natriuretic peptides in healthy dogs.Effect of Breed on Plasma Endothelin-1 Concentration, Plasma Renin Activity, and Serum Cortisol Concentration in Healthy DogsTargeted Lipidomic Analysis of Myoblasts by GC-MS and LC-MS/MS.SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.Uterine contractions depend on KIT-positive interstitial cells in the mouse: genetic and pharmacological evidence.The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2.A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys.Progressive Structural Defects in Canine Centronuclear Myopathy Indicate a Role for HACD1 in Maintaining Skeletal Muscle Membrane Systems.Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient miceFeline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human diseaseNecroptosis mediates myofibre death in dystrophin-deficient miceInterbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogsInterbreed variation of biomarkers of lipid and glucose metabolism in dogsNIPAL4 deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapyAllelic heterogeneity of albinism in the domestic catGenetic heterogeneity of polydactyly in Maine Coon catsThe Dog Model in the Spotlight: Legacy of a Trustful CooperationAbsence of SARS-CoV-2 infection in cats and dogs in close contact with a cluster of COVID-19 patients in a veterinary campus
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P50
description
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Laurent Tiret
@ast
Laurent Tiret
@en
Laurent Tiret
@es
Laurent Tiret
@nl
Laurent Tiret
@sl
type
label
Laurent Tiret
@ast
Laurent Tiret
@en
Laurent Tiret
@es
Laurent Tiret
@nl
Laurent Tiret
@sl
prefLabel
Laurent Tiret
@ast
Laurent Tiret
@en
Laurent Tiret
@es
Laurent Tiret
@nl
Laurent Tiret
@sl
P1053
K-3877-2017
P106
P31
P3829
P496
0000-0001-8573-8335