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M E McCue

Showing results (21-30 of 33) with videos related to

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Animal Genetics|May 16, 2020
Assessment of the FAM174A 11G allele as a risk allele for equine metabolic syndromeM M Roy, E M Norton, A K Rendahl, et al.
Animal Genetics|September 30, 2008
A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horsesB Herszberg, M E McCue, T Larcher, et al.
Journal of Veterinary Internal Medicine|July 24, 2013
Coat color genotypes and risk and severity of melanoma in gray quarter horsesR B C Teixeira, A K Rendahl, S M Anderson, et al.
Scientific Reports|April 10, 2024
Predicted genetic burden and frequency of phenotype-associated variants in the horseS A Durward-Akhurst, J L Marlowe, R J Schaefer, et al.
Equine Veterinary Journal|October 7, 2009
A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breedsR L Stanley, M E McCue, S J Valberg, et al.
Chemosphere|December 4, 2018
Associations between endocrine disrupting chemicals and equine metabolic syndrome phenotypesS A Durward-Akhurst, N E Schultz, E M Norton, et al.
Animal Genetics|November 13, 2010
Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breedsM E McCue, S M Anderson, S J Valberg, et al.
Scientific Reports|November 1, 2019
A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Scientific Reports|February 27, 2020
Publisher Correction: A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Biochimica Et Biophysica Acta. General Subjects|September 5, 2016
A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthaseC A Maile, J R Hingst, K K Mahalingan, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Animal Genetics|May 16, 2020
Assessment of the FAM174A 11G allele as a risk allele for equine metabolic syndromeM M Roy, E M Norton, A K Rendahl, et al.
Animal Genetics|September 30, 2008
A GYS1 gene mutation is highly associated with polysaccharide storage myopathy in Cob Normand draught horsesB Herszberg, M E McCue, T Larcher, et al.
Journal of Veterinary Internal Medicine|July 24, 2013
Coat color genotypes and risk and severity of melanoma in gray quarter horsesR B C Teixeira, A K Rendahl, S M Anderson, et al.
Scientific Reports|April 10, 2024
Predicted genetic burden and frequency of phenotype-associated variants in the horseS A Durward-Akhurst, J L Marlowe, R J Schaefer, et al.
Equine Veterinary Journal|October 7, 2009
A glycogen synthase 1 mutation associated with equine polysaccharide storage myopathy and exertional rhabdomyolysis occurs in a variety of UK breedsR L Stanley, M E McCue, S J Valberg, et al.
Chemosphere|December 4, 2018
Associations between endocrine disrupting chemicals and equine metabolic syndrome phenotypesS A Durward-Akhurst, N E Schultz, E M Norton, et al.
Animal Genetics|November 13, 2010
Estimated prevalence of the Type 1 Polysaccharide Storage Myopathy mutation in selected North American and European breedsM E McCue, S M Anderson, S J Valberg, et al.
Scientific Reports|November 1, 2019
A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Scientific Reports|February 27, 2020
Publisher Correction: A large intragenic deletion in the CLCN1 gene causes Hereditary Myotonia in pigsC E T Araújo, C M C Oliveira, J D Barbosa, et al.
Biochimica Et Biophysica Acta. General Subjects|September 5, 2016
A highly prevalent equine glycogen storage disease is explained by constitutive activation of a mutant glycogen synthaseC A Maile, J R Hingst, K K Mahalingan, et al.
Pageof 4