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Prevalence of an angiotensin-converting enzyme gene variant in dogs

Canine medicine and genetics, 2021-07, Vol.8 (1), p.1-6, Article 6

2021

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Genotype imputation in the domestic dog

Mammalian genome, 2016-10, Vol.27 (9-10), p.485-494

2016

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Lymphocyte Subsets in the Adrenal Glands of Dogs With Primary Hypoadrenocorticism

Veterinary pathology, 2018-01, Vol.55 (1), p.177-181

2018

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Evaluation of genes associated with human myxomatous mitral valve disease in dogs with familial myxomatous mitral valve degeneration

The veterinary journal (1997), 2018-02, Vol.232, p.16-19

2018

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Use of a vascular closure device during percutaneous arterial access in a dog with impaired hemostasis

Journal of veterinary emergency and critical care (San Antonio, Tex. : 2000), 2017-07, Vol.27 (4), p.465-471

2017

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RNA sequencing of whole blood in dogs with primary immune-mediated hemolytic anemia (IMHA) reveals novel insights into disease pathogenesis

PloS one, 2020-10, Vol.15 (10), p.e0240975-e0240975

2020

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Restoring cortical control of functional movement in a human with quadriplegia

Nature (London), 2016-05, Vol.533 (7602), p.247-250

2016

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A scoping review of autoantibodies as biomarkers for canine autoimmune disease

Journal of veterinary internal medicine, 2022-03, Vol.36 (2), p.363-378

2022

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A review of CD4+ T cell differentiation and diversity in dogs

Veterinary immunology and immunopathology, 2024-09, Vol.275, p.110816, Article 110816

2024

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Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoire

PloS one, 2022-07, Vol.17 (7), p.e0270710-e0270710

2022

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GWAS using low-pass whole genome sequence reveals a novel locus in canine congenital idiopathic megaesophagus

Mammalian genome, 2023-09, Vol.34 (3), p.464-472

2023

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Whole Animal Genome Sequencing: user-friendly, rapid, containerized pipelines for processing, variant discovery, and annotation of short-read whole genome sequencing data

G3 : genes - genomes - genetics, 2023-08, Vol.13 (8)

2023

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Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy

Journal of veterinary internal medicine, 2023-11, Vol.37 (6), p.2504-2509

2023

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A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat

Orphanet journal of rare diseases, 2021-02, Vol.16 (1), p.108-7, Article 108

2021

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Congenital muscular dystrophy in a dog with a LAMA2 gene deletion

Journal of veterinary internal medicine, 2022-01, Vol.36 (1), p.279-284

2022

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A case‐control survey study of environmental risk factors for primary hypoadrenocorticism in dogs

Journal of veterinary internal medicine, 2023-11, Vol.37 (6), p.2073-2083

2023

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Targeted sequencing of candidate gene regions for myelofibrosis in dogs

Journal of veterinary internal medicine, 2022-07, Vol.36 (4), p.1237-1247

2022

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A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death

Human genetics, 2019-05, Vol.138 (5), p.515-524

2019

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Current Classification of Canine Muscular Dystrophies and Identification of New Variants

Genes, 2023-07, Vol.14 (8), p.1557

2023

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Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia

Animals (Basel), 2024-06, Vol.14 (13), p.1946

2024

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Acquired dysfunction of CFTR underlies cystic fibrosis-like disease of the canine gallbladder

American journal of physiology: Gastrointestinal and liver physiology, 2024-10, Vol.327 (4), p.G513-G530

2024

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A defect in the NOG gene increases susceptibility to spontaneous superficial chronic corneal epithelial defects (SCCED) in boxer dogs

BMC veterinary research, 2021-07, Vol.17 (1), p.1-254, Article 254

2021

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A novel missense mutation of the NAT10 gene in a juvenile Schnauzer dog with chronic respiratory tract infections

Journal of veterinary internal medicine, 2021-05, Vol.35 (3), p.1542-1546

2021

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The R9H phospholamban mutation is associated with highly penetrant dilated cardiomyopathy and sudden death in a spontaneous canine model

Gene, 2019-05, Vol.697, p.118-122

2019

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Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs

Animals (Basel), 2024-02, Vol.14 (5), p.722

2024

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Prevalence of an angiotensin-converting enzyme gene variant in dogs

Genotype imputation in the domestic dog

Lymphocyte Subsets in the Adrenal Glands of Dogs With Primary Hypoadrenocorticism

Evaluation of genes associated with human myxomatous mitral valve disease in dogs with familial myxomatous mitral valve degeneration

Use of a vascular closure device during percutaneous arterial access in a dog with impaired hemostasis

RNA sequencing of whole blood in dogs with primary immune-mediated hemolytic anemia (IMHA) reveals novel insights into disease pathogenesis

Restoring cortical control of functional movement in a human with quadriplegia

A scoping review of autoantibodies as biomarkers for canine autoimmune disease

A review of CD4+ T cell differentiation and diversity in dogs

Development and application of a next-generation sequencing protocol and bioinformatics pipeline for the comprehensive analysis of the canine immunoglobulin repertoire

GWAS using low-pass whole genome sequence reveals a novel locus in canine congenital idiopathic megaesophagus

Whole Animal Genome Sequencing: user-friendly, rapid, containerized pipelines for processing, variant discovery, and annotation of short-read whole genome sequencing data

Novel COL6A3 frameshift variant in American Staffordshire Terrier dogs with Ullrich‐like congenital muscular dystrophy

A deleterious mutation in the ALMS1 gene in a naturally occurring model of hypertrophic cardiomyopathy in the Sphynx cat

Congenital muscular dystrophy in a dog with a LAMA2 gene deletion

A case‐control survey study of environmental risk factors for primary hypoadrenocorticism in dogs

Targeted sequencing of candidate gene regions for myelofibrosis in dogs

A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death

Current Classification of Canine Muscular Dystrophies and Identification of New Variants

Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia

Acquired dysfunction of CFTR underlies cystic fibrosis-like disease of the canine gallbladder

A defect in the NOG gene increases susceptibility to spontaneous superficial chronic corneal epithelial defects (SCCED) in boxer dogs

A novel missense mutation of the NAT10 gene in a juvenile Schnauzer dog with chronic respiratory tract infections

The R9H phospholamban mutation is associated with highly penetrant dilated cardiomyopathy and sudden death in a spontaneous canine model

Variants in CLCN1 and PDE4C Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs

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