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Genes
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June 28, 2023
<i>PKD1</i> Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease
Michaela Drögemüller, Nadine Klein, Rikke Lill Steffensen, et al.
BMC Veterinary Research
|
March 28, 2013
Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy
Katrin Hirschvogel, Kaspar Matiasek, Katharina Flatz, et al.
Tierarztliche Praxis. Ausgabe K, Kleintiere/Heimtiere
|
October 26, 2016
Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier
Anna Nolte, Aimara Bello, Michaela Drögemüller, et al.
Human Genetics
|
November 14, 2014
A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs
Michaela Drögemüller, Vidhya Jagannathan, Gaudenz Dolf, et al.
Parasitology Research
|
February 14, 2004
Microchip capillary electrophoresis-based genetic comparison of closely related cyathostomin nematode parasites of horses using randomly amplified polymorphic DNA polymerase chain reaction
Janez Posedi, Michaela Drögemüller, Thomas Schnieder, et al.
Animal Genetics
|
June 19, 2023
A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs
Mathew D Littlejohn, Nick Sneddon, Keren Dittmer, et al.
Animal Genetics
|
October 30, 2013
A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption)
Michaela Drögemüller, Vidhya Jagannathan, Judith Howard, et al.
BMC Veterinary Research
|
May 18, 2018
Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease
Manuel R Schmidli, Bettina Fuhrer, Nadine Kurt, et al.
G3 (Bethesda, Md.)
|
October 7, 2015
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy
Frank Steffen, Thomas Bilzer, Jan Brands, et al.
Genomics
|
September 13, 2008
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease
Cord Drögemüller, Michaela Drögemüller, Tosso Leeb, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
Genes
|
June 28, 2023
<i>PKD1</i> Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney Disease
Michaela Drögemüller, Nadine Klein, Rikke Lill Steffensen, et al.
BMC Veterinary Research
|
March 28, 2013
Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy
Katrin Hirschvogel, Kaspar Matiasek, Katharina Flatz, et al.
Tierarztliche Praxis. Ausgabe K, Kleintiere/Heimtiere
|
October 26, 2016
Neuronal ceroid lipofuscinosis in an adult American Staffordshire Terrier
Anna Nolte, Aimara Bello, Michaela Drögemüller, et al.
Human Genetics
|
November 14, 2014
A single codon insertion in the PICALM gene is not associated with subvalvular aortic stenosis in Newfoundland dogs
Michaela Drögemüller, Vidhya Jagannathan, Gaudenz Dolf, et al.
Parasitology Research
|
February 14, 2004
Microchip capillary electrophoresis-based genetic comparison of closely related cyathostomin nematode parasites of horses using randomly amplified polymorphic DNA polymerase chain reaction
Janez Posedi, Michaela Drögemüller, Thomas Schnieder, et al.
Animal Genetics
|
June 19, 2023
A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs
Mathew D Littlejohn, Nick Sneddon, Keren Dittmer, et al.
Animal Genetics
|
October 30, 2013
A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Gräsbeck syndrome (selective cobalamin malabsorption)
Michaela Drögemüller, Vidhya Jagannathan, Judith Howard, et al.
BMC Veterinary Research
|
May 18, 2018
Inflammatory pattern of the infrapatellar fat pad in dogs with canine cruciate ligament disease
Manuel R Schmidli, Bettina Fuhrer, Nadine Kurt, et al.
G3 (Bethesda, Md.)
|
October 7, 2015
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy
Frank Steffen, Thomas Bilzer, Jan Brands, et al.
Genomics
|
September 13, 2008
Identification of a missense mutation in the bovine ATP2A1 gene in congenital pseudomyotonia of Chianina cattle: an animal model of human Brody disease
Cord Drögemüller, Michaela Drögemüller, Tosso Leeb, et al.
Page
of 4