Showing 1 - 18 results of 18 for search 'Monika M. Welle', query time: 0.05s
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Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis by Dominique J. Wiener, Kátia R. Groch, Magdalena A.T. Brunner, Tosso Leeb, Vidhya Jagannathan, Monika M. Welle
Published 2020-08-01
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DSP missense variant in a Scottish Highland calf with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects by Irene M. Häfliger, Caroline T. Koch, Astrid Michel, Silvia Rüfenacht, Mireille Meylan, Monika M. Welle, Cord Drögemüller
Published 2022-01-01
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A complex histopathological challenge: suspicion of an osteoblastoma-like osteosarcoma arising from the second thoracic vertebra in a cat by Felix Giebels, Franck Forterre, Simona Vincenti, Urs Geissbuehler, Monika M. Welle, Roy Pool, Sabina Soldati, Arianna Maiolini
Published 2020-10-01
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A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype by Dominik P. Waluk, Gila Zur, Ronnie Kaufmann, Monika M. Welle, Vidhya Jagannathan, Cord Drögemüller, Eliane J. Müller, Tosso Leeb, Arnaud Galichet
Published 2016-09-01
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Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X. by Magdalena A T Brunner, Vidhya Jagannathan, Dominik P Waluk, Petra Roosje, Monika Linek, Lucia Panakova, Tosso Leeb, Dominique J Wiener, Monika M Welle
Published 2017-01-01
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Bald thigh syndrome in sighthounds-Revisiting the cause of a well-known disease. by Magdalena A T Brunner, Silvia Rüfenacht, Anina Bauer, Susanne Erpel, Natasha Buchs, Sophie Braga-Lagache, Manfred Heller, Tosso Leeb, Vidhya Jagannathan, Dominique J Wiener, Monika M Welle
Published 2019-01-01
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Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek by Silvie Neradilová, Alexandria M. Schauer, Jessica J. Hayward, Magdalena A. T. Brunner, Magdalena Bohutínská, Vidhya Jagannathan, Laurie B. Connell, Adam R. Boyko, Monika M. Welle, Barbora Černá Bolfíková
Published 2022-04-01
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A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). by Michaela Drögemüller, Vidhya Jagannathan, Doreen Becker, Cord Drögemüller, Claude Schelling, Jocelyn Plassais, Cécile Kaerle, Caroline Dufaure de Citres, Anne Thomas, Eliane J Müller, Monika M Welle, Petra Roosje, Tosso Leeb
Published 2014-01-01
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A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome by Anina Bauer, Theresa Hiemesch, Vidhya Jagannathan, Markus Neuditschko, Iris Bachmann, Stefan Rieder, Sofia Mikko, M. Cecilia Penedo, Nadja Tarasova, Martina Vitková, Nicolò Sirtori, Paola Roccabianca, Tosso Leeb, Monika M. Welle
Published 2017-04-01
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Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK). by Jeanette Bannoehr, Pierre Balmer, Michael H Stoffel, Vidhya Jagannathan, Véronique Gaschen, Kathrin Kühni, Beyza Sayar, Michaela Drögemüller, Denise Howald, Dominique J Wiener, Tosso Leeb, Monika M Welle, Eliane J Müller, Petra J Roosje
Published 2020-01-01
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An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture by Leonardo Murgiano, Dominik P. Waluk, Rachel Towers, Natalie Wiedemar, Joëlle Dietrich, Vidhya Jagannathan, Michaela Drögemüller, Pierre Balmer, Tom Druet, Arnaud Galichet, M. Cecilia Penedo, Eliane J. Müller, Petra Roosje, Monika M. Welle, Tosso Leeb
Published 2016-09-01
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MKLN1 splicing defect in dogs with lethal acrodermatitis. by Anina Bauer, Vidhya Jagannathan, Sandra Högler, Barbara Richter, Neil A McEwan, Anne Thomas, Edouard Cadieu, Catherine André, Marjo K Hytönen, Hannes Lohi, Monika M Welle, Petra Roosje, Cathryn Mellersh, Margret L Casal, Tosso Leeb
Published 2018-03-01
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Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. by Michaela Drögemüller, Vidhya Jagannathan, Monika M Welle, Claudia Graubner, Reto Straub, Vinzenz Gerber, Dominik Burger, Heidi Signer-Hasler, Pierre-André Poncet, Stéphane Klopfenstein, Ruedi von Niederhäusern, Jens Tetens, Georg Thaller, Stefan Rieder, Cord Drögemüller, Tosso Leeb
Published 2014-01-01
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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. by Vidhya Jagannathan, Jeanette Bannoehr, Philippe Plattet, Regula Hauswirth, Cord Drögemüller, Michaela Drögemüller, Dominique J Wiener, Marcus Doherr, Marta Owczarek-Lipska, Arnaud Galichet, Monika M Welle, Katarina Tengvall, Kerstin Bergvall, Hannes Lohi, Silvia Rüfenacht, Monika Linek, Manon Paradis, Eliane J Müller, Petra Roosje, Tosso Leeb
Published 2013-01-01
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