Lista de obras - Laurent Tiret - Dominio Público Uruguay

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Absence of SARS-CoV-2 infection in cats and dogs in close contact with a cluster of COVID-19 patients in a veterinary campus

artículo científico publicado en 2020

Allelic heterogeneity of albinism in the domestic cat

scientific article published on 15 September 2016

Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy

artículo científico publicado en 2013

Breed differences in natriuretic peptides in healthy dogs.

artículo científico publicado en 2014

Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide

artículo científico publicado en 2012

Differential physiological role of BIN1 isoforms in skeletal muscle development, function and regeneration

artículo científico publicado en 2020

Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis

artículo científico publicado en 2022

Effect of Breed on Plasma Endothelin-1 Concentration, Plasma Renin Activity, and Serum Cortisol Concentration in Healthy Dogs

artículo científico publicado en 2016

Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease

article

Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice

artículo científico publicado en 2016

Genetic heterogeneity of polydactyly in Maine Coon cats

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Inhibited gastrulation in mouse embryos overexpressing the leukemia inhibitory factor ⬇️

artículo científico publicado el 1 de septiembre de 1992

Interbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogs

artículo científico publicado en 2018

Interbreed variation of biomarkers of lipid and glucose metabolism in dogs

artículo científico publicado en 2018

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

artículo científico publicado el 3 de agosto de 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 2019

Necroptosis mediates myofibre death in dystrophin-deficient mice

scientific article published in Nature Communications

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

artículo científico publicado en 2016

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

artículo científico publicado en 2018

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

artículo científico publicado en 2005

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

artículo científico publicado en 2017

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

scientific article published on 01 January 2019

The Shepherds' Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian Shepherds

artículo científico publicado en 2015

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

artículo científico publicado en 2003

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

Lista de obras de Laurent Tiret

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

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

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

A missense mutation in melanocortin 1 receptor is associated with the red coat colour in donkeys

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

Absence of SARS-CoV-2 infection in cats and dogs in close contact with a cluster of COVID-19 patients in a veterinary campus

Allelic heterogeneity of albinism in the domestic cat

Altered splicing of the BIN1 muscle-specific exon in humans and dogs with highly progressive centronuclear myopathy

Breed differences in natriuretic peptides in healthy dogs.

Centronuclear myopathy in Labrador retrievers: a recent founder mutation in the PTPLA gene has rapidly disseminated worldwide

Differential physiological role of BIN1 isoforms in skeletal muscle development, function and regeneration

Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis

Effect of Breed on Plasma Endothelin-1 Concentration, Plasma Renin Activity, and Serum Cortisol Concentration in Healthy Dogs

Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease

Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice

Genetic heterogeneity of polydactyly in Maine Coon cats

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

Inhibited gastrulation in mouse embryos overexpressing the leukemia inhibitory factor ⬇️

Interbreed variation in serum serotonin (5-hydroxytryptamine) concentration in healthy dogs

Interbreed variation of biomarkers of lipid and glucose metabolism in dogs

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

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

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

Necroptosis mediates myofibre death in dystrophin-deficient mice

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 mice

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

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

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

The Shepherds' Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian Shepherds

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

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

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