A frameshift-deletion mutation in Reelin causes cerebellar hypoplasia in White Swiss Shepherd dogs von Littlejohn, Mathew D, Sneddon, Nick, Dittmer, Keren, Keehan, Mike, Stephen, Melissa, Drögemüller, Michaela, Garrick, Dorian

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A large deletion in the GP9 gene in Cocker Spaniel dogs with Bernard-Soulier syndrome von Gentilini, Fabio, Turba, Maria Elena, Giancola, Fiorella, Chiocchetti, Roberto, Bernardini, Chiara, Dajbychova, Markéta, Jagannathan, Vidhya, Drögemüller, Michaela, Drögemüller, Cord

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A Missense Change in the ATG4D Gene Links Aberrant Autophagy to a Neurodegenerative Vacuolar Storage Disease: e1005169 von Kyöstilä, Kaisa, Syrjä, Pernilla, Jagannathan, Vidhya, Chandrasekar, Gayathri, Jokinen, Tarja S, Seppälä, Eija H, Becker, Doreen, Drögemüller, Michaela, Dietschi, Elisabeth, Drögemüller, Cord, Lang, Johann, Steffen, Frank, Rohdin, Cecilia, Jäderlund, Karin H, Lappalainen, Anu K, Hahn, Kerstin, Wohlsein, Peter, Baumgärtner, Wolfgang, Henke, Diana, Oevermann, Anna, Kere, Juha, Lohi, Hannes, Leeb, Tosso

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A frameshift mutation in the cubilin gene (CUBN) in Beagles with Imerslund-Graesbeck syndrome (selective cobalamin malabsorption) von Drogemueller, Michaela, Jagannathan, Vidhya, Howard, Judith, Bruggmann, Remy, Drogemueller, Cord, Ruetten, Maja, Leeb, Tosso, Kook, Peter H

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A Mutation in the SUV39H2 Gene in Labrador Retrievers with Hereditary Nasal Parakeratosis (HNPK) Provides Insights into the Epigenetics of Keratinocyte Differentiation: e1003848 von Jagannathan, Vidhya, Bannoehr, Jeanette, Plattet, Philippe, Hauswirth, Regula, Drögemüller, Cord, Drögemüller, Michaela, Wiener, Dominique J, Doherr, Marcus, Owczarek-Lipska, Marta, Galichet, Arnaud, Welle, Monika M, Tengvall, Katarina, Bergvall, Kerstin, Lohi, Hannes, Rüfenacht, Silvia, Linek, Monika, Paradis, Manon, Müller, Eliane J, Roosje, Petra, Leeb, Tosso

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Magnetic resonance imaging and genetic investigation of a case of Rottweiler leukoencephalomyelopathy von Hirschvogel, Katrin, Matiasek, Kaspar, Flatz, Katharina, Drögemüller, Michaela, Drögemüller, Cord, Reiner, Bärbel, Fischer, Andrea

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Arachnomelia in Brown Swiss cattle maps to chromosome 5 von Drögemüller, Cord, Rossi, Marco, Gentile, Arcangelo, Testoni, Stefania, Jörg, Hannes, Stranzinger, Gerald, Drögemüller, Michaela, Glowatzki-Mullis, Marie-Louise, Leeb, Tosso

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A Deletion in the VLDLR Gene in Eurasier Dogs with Cerebellar Hypoplasia Resembling a Dandy-Walker-Like Malformation (DWLM): e0108917 von Gerber, Martina, Fischer, Andrea, Jagannathan, Vidhya, Drogemueller, Michaela, Drogemueller, Cord, Schmidt, Martin J, Bernardino, Filipa, Manz, Eberhard, Matiasek, Kaspar, Rentmeister, Kai

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Impaired Cell Cycle Regulation in a Natural Equine Model of Asthma: e0136103 von Pacholewska, Alicja, Jagannathan, Vidhya, Drogemueller, Michaela, Klukowska-Rotzler, Jolanta, Lanz, Simone, Hamza, Eman, Dermitzakis, Emmanouil T, Marti, Eliane, Leeb, Tosso, Gerber, Vincent

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The Transcriptome of Equine Peripheral Blood Mononuclear Cells: e0122011 von Pacholewska, Alicja, Drogemueller, Michaela, Klukowska-Rotzler, Jolanta, Lanz, Simone, Hamza, Eman, Dermitzakis, Emmanouil T, Marti, Eliane, Gerber, Vincent, Leeb, Tosso, Jagannathan, Vidhya

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Congenital Hepatic Fibrosis in the Franches-Montagnes Horse Is Associated with the Polycystic Kidney and Hepatic Disease 1 (PKHD1) Gene: e110125 von Drogemueller, Michaela, Jagannathan, Vidhya, Welle, Monika M, Graubner, Claudia, Straub, Reto, Gerber, Vinzenz, Burger, Dominik, Signer-Hasler, Heidi, Poncet, Pierre-Andre, Klopfenstein, Stephane

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Magnetic resonance imaging and genetic investigation of a case of rottweiler leukoencephalomyelopathy von Hirschvogel, Katrin, Matiasek, Kaspar, Flatz, Katharina, Drögemueller, Michaela, Drögemueller, Cord, Reiner, Bärbel, Fischer, Andrea

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