Hasil Pencarian - Elisabeth Dietschi

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  1. 1
    Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the F9 gene promoter

    Christmas disease in a Hovawart family resembling human hemophilia B Leyden is caused by a single nucleotide deletion in a highly conserved transcription factor binding site of the... oleh Bertram Brenig, Lilith Steingräber, Shuwen Shan, Fangzheng Xu, Marc Hirschfeld, Reiner Andag, Mirjam Spengeler, Elisabeth Dietschi, Reinhard Mischke, Tosso Leeb

    Diterbitkan 2019-11-01
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  2. 2
    A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses.

    A Non-Synonymous HMGA2 Variant Decreases Height in Shetland Ponies and Other Small Horses. oleh Mirjam Frischknecht, Vidhya Jagannathan, Philippe Plattet, Markus Neuditschko, Heidi Signer-Hasler, Iris Bachmann, Alicja Pacholewska, Cord Drögemüller, Elisabeth Dietschi, Christine Flury, Stefan Rieder, Tosso Leeb

    Diterbitkan 2015-01-01
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  3. 3
    A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism.

    A COL11A2 mutation in Labrador retrievers with mild disproportionate dwarfism. oleh Mirjam Frischknecht, Helena Niehof-Oellers, Vidhya Jagannathan, Marta Owczarek-Lipska, Cord Drögemüller, Elisabeth Dietschi, Gaudenz Dolf, Bernd Tellhelm, Johann Lang, Katriina Tiira, Hannes Lohi, Tosso Leeb

    Diterbitkan 2013-01-01
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  4. 4
    A de novo variant in the ASPRV1 gene in a dog with ichthyosis.

    A de novo variant in the ASPRV1 gene in a dog with ichthyosis. oleh Anina Bauer, Dominik P Waluk, Arnaud Galichet, Katrin Timm, Vidhya Jagannathan, Beyza S Sayar, Dominique J Wiener, Elisabeth Dietschi, Eliane J Müller, Petra Roosje, Monika M Welle, Tosso Leeb

    Diterbitkan 2017-03-01
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  5. 5
    A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1)

    A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1) oleh Nico Mauri, Miriam Kleiter, Michael Leschnik, Sandra Högler, Elisabeth Dietschi, Michaela Wiedmer, Joëlle Dietrich, Diana Henke, Frank Steffen, Simone Schuller, Corinne Gurtner, Nadine Stokar-Regenscheit, Donal O’Toole, Thomas Bilzer, Christiane Herden, Anna Oevermann, Vidhya Jagannathan, Tosso Leeb

    Diterbitkan 2017-02-01
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  6. 6
    LGI2 truncation causes a remitting focal epilepsy in dogs.

    LGI2 truncation causes a remitting focal epilepsy in dogs. oleh Eija H Seppälä, Tarja S Jokinen, Masaki Fukata, Yuko Fukata, Matthew T Webster, Elinor K Karlsson, Sami K Kilpinen, Frank Steffen, Elisabeth Dietschi, Tosso Leeb, Ranja Eklund, Xiaochu Zhao, Jennifer J Rilstone, Kerstin Lindblad-Toh, Berge A Minassian, Hannes Lohi

    Diterbitkan 2011-07-01
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  7. 7
    A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2)

    A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2) oleh Nico Mauri, Miriam Kleiter, Elisabeth Dietschi, Michael Leschnik, Sandra Högler, Michaela Wiedmer, Joëlle Dietrich, Diana Henke, Frank Steffen, Simone Schuller, Corinne Gurtner, Nadine Stokar-Regenscheit, Donal O’Toole, Thomas Bilzer, Christiane Herden, Anna Oevermann, Vidhya Jagannathan, Tosso Leeb

    Diterbitkan 2017-08-01
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  8. 8
    A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12.

    A Multi-Breed Genome-Wide Association Analysis for Canine Hypothyroidism Identifies a Shared Major Risk Locus on CFA12. oleh Matteo Bianchi, Stina Dahlgren, Jonathan Massey, Elisabeth Dietschi, Marcin Kierczak, Martine Lund-Ziener, Katarina Sundberg, Stein Istre Thoresen, Olle Kämpe, Göran Andersson, William E R Ollier, Åke Hedhammar, Tosso Leeb, Kerstin Lindblad-Toh, Lorna J Kennedy, Frode Lingaas, Gerli Rosengren Pielberg

    Diterbitkan 2015-01-01
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  9. 9
    An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.

    An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome. oleh Thomas W Marchant, Elisabeth Dietschi, Ulrich Rytz, Peter Schawalder, Vidhya Jagannathan, Sheida Hadji Rasouliha, Corinne Gurtner, Andreas S Waldvogel, Ronan S Harrington, Michaela Drögemüller, Jeffrey Kidd, Elaine A Ostrander, Amanda Warr, Mick Watson, David Argyle, Gert Ter Haar, Dylan N Clements, Tosso Leeb, Jeffrey J Schoenebeck

    Diterbitkan 2019-05-01
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  10. 10
    A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease.

    A missense change in the ATG4D gene links aberrant autophagy to a neurodegenerative vacuolar storage disease. oleh Kaisa Kyöstilä, Pernilla Syrjä, Vidhya Jagannathan, Gayathri Chandrasekar, Tarja S Jokinen, Eija H Seppälä, Doreen Becker, Michaela Drögemüller, Elisabeth Dietschi, Cord Drögemüller, Johann Lang, Frank Steffen, Cecilia Rohdin, Karin H Jäderlund, Anu K Lappalainen, Kerstin Hahn, Peter Wohlsein, Wolfgang Baumgärtner, Diana Henke, Anna Oevermann, Juha Kere, Hannes Lohi, Tosso Leeb

    Diterbitkan 2015-04-01
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