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G3 (Bethesda, Md.)
|
February 26, 2017
A Nonsense Variant in the <i>ST14</i> Gene in Akhal-Teke Horses with Naked Foal Syndrome
Anina Bauer, Theresa Hiemesch, Vidhya Jagannathan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 17, 2026
A canine <i>PLP1</i> missense variant differentiates oligodendrocyte maturation in connatal and classical Pelizaeus-Merzbacher disease
Rodrigo Gutierrez-Quintana, Paul Montague, Angie Rupp, et al.
Plos One
|
April 29, 2011
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle
Cord Drögemüller, Ursula Reichart, Torsten Seuberlich, et al.
G3 (Bethesda, Md.)
|
December 14, 2018
Complex Structural <i>PPT1</i> Variant Associated with Non-syndromic Canine Retinal Degeneration
Leonardo Murgiano, Doreen Becker, Dina Torjman, et al.
Plos Genetics
|
May 17, 2014
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH)
Michaela Drögemüller, Vidhya Jagannathan, Doreen Becker, et al.
Scientific Reports
|
November 5, 2023
Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever
Danika L Bannasch, Danielle T Oertle, Julia Vo, et al.
G3 (Bethesda, Md.)
|
March 2, 2018
A Nonsense Variant in the <i>ACADVL</i> Gene in German Hunting Terriers with Exercise Induced Metabolic Myopathy
Vincent Lepori, Franziska Mühlhause, Adrian C Sewell, et al.
Journal of Equine Veterinary Science
|
April 19, 2020
A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color
Gertrud Grilz-Seger, Simone Reiter, Markus Neuditschko, et al.
BMC Genetics
|
July 1, 2016
Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs
Katarina Tengvall, Sergey Kozyrev, Marcin Kierczak, et al.
Plos Genetics
|
June 22, 2023
Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes
Bianca Lourdes Frehner, Matthias Christen, Iris M Reichler, et al.
Page
of 31
Search research articles
Search
Showing results (251-260 of 310) with videos related to
Sort By:
Page
of 31
G3 (Bethesda, Md.)
|
February 26, 2017
A Nonsense Variant in the <i>ST14</i> Gene in Akhal-Teke Horses with Naked Foal Syndrome
Anina Bauer, Theresa Hiemesch, Vidhya Jagannathan, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 17, 2026
A canine <i>PLP1</i> missense variant differentiates oligodendrocyte maturation in connatal and classical Pelizaeus-Merzbacher disease
Rodrigo Gutierrez-Quintana, Paul Montague, Angie Rupp, et al.
Plos One
|
April 29, 2011
An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle
Cord Drögemüller, Ursula Reichart, Torsten Seuberlich, et al.
G3 (Bethesda, Md.)
|
December 14, 2018
Complex Structural <i>PPT1</i> Variant Associated with Non-syndromic Canine Retinal Degeneration
Leonardo Murgiano, Doreen Becker, Dina Torjman, et al.
Plos Genetics
|
May 17, 2014
A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH)
Michaela Drögemüller, Vidhya Jagannathan, Doreen Becker, et al.
Scientific Reports
|
November 5, 2023
Naturally occurring canine laminopathy leading to a dilated and fibrosing cardiomyopathy in the Nova Scotia Duck Tolling Retriever
Danika L Bannasch, Danielle T Oertle, Julia Vo, et al.
G3 (Bethesda, Md.)
|
March 2, 2018
A Nonsense Variant in the <i>ACADVL</i> Gene in German Hunting Terriers with Exercise Induced Metabolic Myopathy
Vincent Lepori, Franziska Mühlhause, Adrian C Sewell, et al.
Journal of Equine Veterinary Science
|
April 19, 2020
A Genome-Wide Association Analysis in Noriker Horses Identifies a SNP Associated With Roan Coat Color
Gertrud Grilz-Seger, Simone Reiter, Markus Neuditschko, et al.
BMC Genetics
|
July 1, 2016
Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs
Katarina Tengvall, Sergey Kozyrev, Marcin Kierczak, et al.
Plos Genetics
|
June 22, 2023
Autosomal recessive hyposegmentation of granulocytes in Australian Shepherd Dogs indicates a role for LMBR1L in myeloid leukocytes
Bianca Lourdes Frehner, Matthias Christen, Iris M Reichler, et al.
Page
of 31