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Gary S Johnson

Showing results (11-20 of 52) with videos related to

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Biochemical and Biophysical Research Communications|January 5, 2005
A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosisMartin L Katz, Shahnawaz Khan, Tomoyuki Awano, et al.
Neurochemistry International|April 21, 2009
Involvement of oxidative pathways in cytokine-induced secretory phospholipase A2-IIA in astrocytesMichael D Jensen, Wenwen Sheng, Agnes Simonyi, et al.
Plos One|August 17, 2013
Genome-wide association study identifies a novel canine glaucoma locusSaija J Ahonen, Elina Pietilä, Cathryn S Mellersh, et al.
BMC Veterinary Research|July 28, 2012
A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduriaFabiana H G Farias, Rong Zeng, Gary S Johnson, et al.
Genes|November 27, 2024
<i>FAN1</i> Deletion Variant in Basenji Dogs with Fanconi SyndromeFabiana H G Farias, Tendai Mhlanga-Mutangadura, Juyuan Guo, et al.
Journal of the American Veterinary Medical Association|January 14, 2005
Clinical description and mode of inheritance of idiopathic epilepsy in English springer spanielsEdward E Patterson, P Jane Armstrong, Dennis P O'Brien, et al.
Gene|April 21, 2022
Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogsGarrett Bullock, Gary S Johnson, Tendai Mhlanga-Mutangadura, et al.
Journal of Biomedicine & Biotechnology|January 15, 2011
A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosisMartin L Katz, Fabiana H Farias, Douglas N Sanders, et al.
Acta Veterinaria Scandinavica|May 23, 2015
A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breedsCecilia Rohdin, Douglas Gilliam, Caroline A O'Leary, et al.
The Journal of Heredity|June 17, 2005
Genetic mapping of canine multiple system degeneration and ectodermal dysplasia lociDennis P O'Brien, Gary S Johnson, Robert D Schnabel, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Biochemical and Biophysical Research Communications|January 5, 2005
A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosisMartin L Katz, Shahnawaz Khan, Tomoyuki Awano, et al.
Neurochemistry International|April 21, 2009
Involvement of oxidative pathways in cytokine-induced secretory phospholipase A2-IIA in astrocytesMichael D Jensen, Wenwen Sheng, Agnes Simonyi, et al.
Plos One|August 17, 2013
Genome-wide association study identifies a novel canine glaucoma locusSaija J Ahonen, Elina Pietilä, Cathryn S Mellersh, et al.
BMC Veterinary Research|July 28, 2012
A L2HGDH initiator methionine codon mutation in a Yorkshire terrier with L-2-hydroxyglutaric aciduriaFabiana H G Farias, Rong Zeng, Gary S Johnson, et al.
Genes|November 27, 2024
<i>FAN1</i> Deletion Variant in Basenji Dogs with Fanconi SyndromeFabiana H G Farias, Tendai Mhlanga-Mutangadura, Juyuan Guo, et al.
Journal of the American Veterinary Medical Association|January 14, 2005
Clinical description and mode of inheritance of idiopathic epilepsy in English springer spanielsEdward E Patterson, P Jane Armstrong, Dennis P O'Brien, et al.
Gene|April 21, 2022
Lysosomal storage disease associated with a CNP sequence variant in Dalmatian dogsGarrett Bullock, Gary S Johnson, Tendai Mhlanga-Mutangadura, et al.
Journal of Biomedicine & Biotechnology|January 15, 2011
A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosisMartin L Katz, Fabiana H Farias, Douglas N Sanders, et al.
Acta Veterinaria Scandinavica|May 23, 2015
A KCNJ10 mutation previously identified in the Russell group of terriers also occurs in Smooth-Haired Fox Terriers with hereditary ataxia and in related breedsCecilia Rohdin, Douglas Gilliam, Caroline A O'Leary, et al.
The Journal of Heredity|June 17, 2005
Genetic mapping of canine multiple system degeneration and ectodermal dysplasia lociDennis P O'Brien, Gary S Johnson, Robert D Schnabel, et al.
Pageof 6