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Plos One
|
June 29, 2018
The study design elements employed by researchers in preclinical animal experiments from two research domains and implications for automation of systematic reviews
Annette M O'Connor, Sarah C Totton, Jonah N Cullen, et al.
Genes
|
August 26, 2023
Current Classification of Canine Muscular Dystrophies and Identification of New Variants
G Diane Shelton, Katie M Minor, Steven G Friedenberg, et al.
Genes
|
November 27, 2025
Dystrophin-Deficient Muscular Dystrophy in a Family of Shiba Inu Dogs with a Complex Deletion Encompassing <i>DMD</i> Exon 5
Laura Mcleay, Simone Hardinge, Katie M Minor, et al.
Journal of Veterinary Internal Medicine
|
June 5, 2025
Identification of a Novel Mutation in the SERPINE1 Gene Causing Clinical Hyperfibrinolysis in English Springer Spaniel Dogs
Kelley Kilpatrick, Jonah N Cullen, Farah F Almeer, et al.
Journal of Veterinary Internal Medicine
|
February 26, 2026
Myopathy due to a creatine deficiency disorder in a family of mixed breed dogs with a glycine amidinotransferase gene mutation
Hugo Leonardi, Katie M Minor, Julien Fritz, et al.
BMC Veterinary Research
|
May 3, 2025
Genomic analyses in Cavalier King Charles spaniels identify loci associated with clinical signs of Chiari-like malformation and Syringomyelia
Courtney R Sparks, Jonah N Cullen, Michael W Vandewege, et al.
Journal of Veterinary Internal Medicine
|
December 2, 2021
Congenital muscular dystrophy in a dog with a LAMA2 gene deletion
G Diane Shelton, Katie M Minor, Stephanie Thomovsky, et al.
Animals : an Open Access Journal From MDPI
|
July 13, 2024
Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia
G Diane Shelton, James R Mickelson, Steven G Friedenberg, et al.
Journal of Veterinary Internal Medicine
|
May 9, 2026
Progressive abnormal gait in an adult Jack Russell Terrier with a homozygous frameshift variant in SETX (senataxin)
G Diane Shelton, Sofie F M Bhatti, Luc Van Ham, et al.
Animals : an Open Access Journal From MDPI
|
March 13, 2024
Variants in <i>CLCN1</i> and <i>PDE4C</i> Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs
G Diane Shelton, James R Mickelson, Steven G Friedenberg, et al.
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Search research articles
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Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Plos One
|
June 29, 2018
The study design elements employed by researchers in preclinical animal experiments from two research domains and implications for automation of systematic reviews
Annette M O'Connor, Sarah C Totton, Jonah N Cullen, et al.
Genes
|
August 26, 2023
Current Classification of Canine Muscular Dystrophies and Identification of New Variants
G Diane Shelton, Katie M Minor, Steven G Friedenberg, et al.
Genes
|
November 27, 2025
Dystrophin-Deficient Muscular Dystrophy in a Family of Shiba Inu Dogs with a Complex Deletion Encompassing <i>DMD</i> Exon 5
Laura Mcleay, Simone Hardinge, Katie M Minor, et al.
Journal of Veterinary Internal Medicine
|
June 5, 2025
Identification of a Novel Mutation in the SERPINE1 Gene Causing Clinical Hyperfibrinolysis in English Springer Spaniel Dogs
Kelley Kilpatrick, Jonah N Cullen, Farah F Almeer, et al.
Journal of Veterinary Internal Medicine
|
February 26, 2026
Myopathy due to a creatine deficiency disorder in a family of mixed breed dogs with a glycine amidinotransferase gene mutation
Hugo Leonardi, Katie M Minor, Julien Fritz, et al.
BMC Veterinary Research
|
May 3, 2025
Genomic analyses in Cavalier King Charles spaniels identify loci associated with clinical signs of Chiari-like malformation and Syringomyelia
Courtney R Sparks, Jonah N Cullen, Michael W Vandewege, et al.
Journal of Veterinary Internal Medicine
|
December 2, 2021
Congenital muscular dystrophy in a dog with a LAMA2 gene deletion
G Diane Shelton, Katie M Minor, Stephanie Thomovsky, et al.
Animals : an Open Access Journal From MDPI
|
July 13, 2024
Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia
G Diane Shelton, James R Mickelson, Steven G Friedenberg, et al.
Journal of Veterinary Internal Medicine
|
May 9, 2026
Progressive abnormal gait in an adult Jack Russell Terrier with a homozygous frameshift variant in SETX (senataxin)
G Diane Shelton, Sofie F M Bhatti, Luc Van Ham, et al.
Animals : an Open Access Journal From MDPI
|
March 13, 2024
Variants in <i>CLCN1</i> and <i>PDE4C</i> Associated with Muscle Hypertrophy, Dysphagia, and Gait Abnormalities in Young French Bulldogs
G Diane Shelton, James R Mickelson, Steven G Friedenberg, et al.
Page
of 4