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The cnm locus, a canine homologue of human autosomal forms of centronuclear myopathy, maps to chromosome 2.
- Published in:
- Human Genetics, 2003, v. 113, n. 4, p. 297, doi. 10.1007/s00439-003-0984-7
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- Article
Fasting triglyceride concentrations are associated with markers of lipid metabolism and glucose homeostasis in healthy, non-obese dogs in lean and overweight condition.
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- Frontiers in Veterinary Science, 2024, p. 1, doi. 10.3389/fvets.2024.1406322
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- Article
Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy.
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- Science Translational Medicine, 2023, v. 15, n. 685, p. 1, doi. 10.1126/scitranslmed.add5275
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- Article
Genetic heterogeneity of polydactyly in Maine Coon cats.
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- Journal of Feline Medicine & Surgery, 2020, v. 22, n. 12, p. 1103, doi. 10.1177/1098612X20905061
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- Article
Interbreed variation of biomarkers of lipid and glucose metabolism in dogs.
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- Veterinary Clinical Pathology, 2018, v. 47, n. 4, p. 582, doi. 10.1111/vcp.12673
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- Article
Feline low-grade alimentary lymphoma: an emerging entity and a potential animal model for human disease.
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- BMC Veterinary Research, 2018, v. 14, n. 1, p. N.PAG, doi. 10.1186/s12917-018-1635-5
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- Article
Genetic Evidence That Captured Retroviral Envelope syncytins Contribute to Myoblast Fusion and Muscle Sexual Dimorphism in Mice.
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- PLoS Genetics, 2016, v. 12, n. 9, p. 1, doi. 10.1371/journal.pgen.1006289
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- Article
Altered Splicing of the BIN1 Muscle-Specific Exon in Humans and Dogs with Highly Progressive Centronuclear Myopathy.
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- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003430
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- Article
A missense mutation in the agouti signaling protein gene (ASIP) is associated with the no light points coat phenotype in donkeys.
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- Genetics Selection Evolution, 2015, v. 47, p. 99, doi. 10.1186/s12711-015-0112-x
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- Article
Two recessive mutations in FGF5 are associated with the long-hair phenotype in donkeys.
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- Genetics Selection Evolution, 2014, v. 46, p. 1, doi. 10.1186/s12711-014-0065-5
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- Article
Assignation of highly polymorphic markers on a canine purebred pedigree.
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- Mammalian Genome, 2000, v. 11, n. 8, p. 703, doi. 10.1007/s003350010143
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- Article
X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterisation.
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- Skeletal Muscle, 2020, v. 10, n. 1, p. 1, doi. 10.1186/s13395-020-00239-0
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- Article
The Shepherds’ Tale: A Genome-Wide Study across 9 Dog Breeds Implicates Two Loci in the Regulation of Fructosamine Serum Concentration in Belgian Shepherds.
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- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0123173
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- Article
A Deletion in FOXN1 Is Associated with a Syndrome Characterized by Congenital Hypotrichosis and Short Life Expectancy in Birman Cats.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120668
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- Article
Centronuclear Myopathy in Labrador Retrievers: A Recent Founder Mutation in the PTPLA Gene Has Rapidly Disseminated Worldwide.
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- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046408
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- Article
Receptor interacting protein kinase‐3 mediates both myopathy and cardiomyopathy in preclinical animal models of Duchenne muscular dystrophy.
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- Journal of Cachexia, Sarcopenia & Muscle, 2023, v. 14, n. 6, p. 2520, doi. 10.1002/jcsm.13265
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- Article
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dog.
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- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1905, doi. 10.1093/hmg/ddi201
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- Article
SINE exonic insertion in the PTPLA gene leads to multiple splicing defects and segregates with the autosomal recessive centronuclear myopathy in dogs.
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- Human Molecular Genetics, 2005, v. 14, n. 11, p. 1417, doi. 10.1093/hmg/ddi151
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- Article
NIPAL4 deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy.
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- Veterinary Medicine & Science, 2019, v. 5, n. 2, p. 112, doi. 10.1002/vms3.149
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- Article
Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis.
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- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01355-2
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- Article
Genome wide association study of 40 clinical measurements in eight dog breeds.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-63457-y
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- Article
Feline chimerism revealed by DNA profiling.
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- Animal Genetics, 2020, v. 51, n. 4, p. 631, doi. 10.1111/age.12957
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- Article
Allelic heterogeneity of albinism in the domestic cat.
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- Animal Genetics, 2017, v. 48, n. 1, p. 127, doi. 10.1111/age.12503
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- Article
Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient mice.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06636-w
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- Article
Necroptosis mediates myofibre death in dystrophin-deficient mice.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06057-9
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- Article
A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome.
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- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0137019
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- Article