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Michaela Drögemüller

Showing results (1-10 of 36) with videos related to

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Genes|June 28, 2023
<i>PKD1</i> Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney DiseaseMichaela 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 leukoencephalomyelopathyKatrin Hirschvogel, Kaspar Matiasek, Katharina Flatz, et al.
Tierarztliche Praxis. Ausgabe K, Kleintiere/Heimtiere|October 26, 2016
Neuronal ceroid lipofuscinosis in an adult American Staffordshire TerrierAnna 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 dogsMichaela 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 reactionJanez 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 dogsMathew 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 diseaseManuel R Schmidli, Bettina Fuhrer, Nadine Kurt, et al.
G3 (Bethesda, Md.)|October 7, 2015
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular DystrophyFrank 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 diseaseCord Drögemüller, Michaela Drögemüller, Tosso Leeb, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Genes|June 28, 2023
<i>PKD1</i> Nonsense Variant in a Lagotto Romagnolo Family with Polycystic Kidney DiseaseMichaela 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 leukoencephalomyelopathyKatrin Hirschvogel, Kaspar Matiasek, Katharina Flatz, et al.
Tierarztliche Praxis. Ausgabe K, Kleintiere/Heimtiere|October 26, 2016
Neuronal ceroid lipofuscinosis in an adult American Staffordshire TerrierAnna 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 dogsMichaela 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 reactionJanez 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 dogsMathew 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 diseaseManuel R Schmidli, Bettina Fuhrer, Nadine Kurt, et al.
G3 (Bethesda, Md.)|October 7, 2015
A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular DystrophyFrank 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 diseaseCord Drögemüller, Michaela Drögemüller, Tosso Leeb, et al.
Pageof 4