Hasil Pencarian - Monika M Welle

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  1. 1
    Canine Epithelial Skin Tumours: Expression of the Stem Cell Markers Lgr5, Lgr6 and Sox9 in Light of New Cancer Stem Cell Theories

    Canine Epithelial Skin Tumours: Expression of the Stem Cell Markers Lgr5, Lgr6 and Sox9 in Light of New Cancer Stem Cell Theories oleh Laura Bongiovanni, Chiara Brachelente, Eva Moreno, Monika M. Welle

    Diterbitkan 2020-05-01
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  2. 2
    Spatial Distribution of Stem Cell-Like Keratinocytes in Dissected Compound Hair Follicles of the Dog.

    Spatial Distribution of Stem Cell-Like Keratinocytes in Dissected Compound Hair Follicles of the Dog. oleh Dominique J Wiener, Marcus G Doherr, Eliane J Müller, Monika M Welle

    Diterbitkan 2016-01-01
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  3. 3
    DSP missense variant in a Scottish Highland calf with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects

    DSP missense variant in a Scottish Highland calf with congenital ichthyosis, alopecia, acantholysis of the tongue and corneal defects oleh Irene M. Häfliger, Caroline T. Koch, Astrid Michel, Silvia Rüfenacht, Mireille Meylan, Monika M. Welle, Cord Drögemüller

    Diterbitkan 2022-01-01
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  4. 4
    A complex histopathological challenge: suspicion of an osteoblastoma-like osteosarcoma arising from the second thoracic vertebra in a cat

    A complex histopathological challenge: suspicion of an osteoblastoma-like osteosarcoma arising from the second thoracic vertebra in a cat oleh Felix Giebels, Franck Forterre, Simona Vincenti, Urs Geissbuehler, Monika M. Welle, Roy Pool, Sabina Soldati, Arianna Maiolini

    Diterbitkan 2020-10-01
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  5. 5
    A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder

    A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder oleh Anina Bauer, Michela De Lucia, Vidhya Jagannathan, Giorgia Mezzalira, Margret L. Casal, Monika M. Welle, Tosso Leeb

    Diterbitkan 2017-09-01
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  6. 6
    A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype

    A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype oleh Dominik P. Waluk, Gila Zur, Ronnie Kaufmann, Monika M. Welle, Vidhya Jagannathan, Cord Drögemüller, Eliane J. Müller, Tosso Leeb, Arnaud Galichet

    Diterbitkan 2016-09-01
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  7. 7
    Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X.

    Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X. oleh Magdalena A T Brunner, Vidhya Jagannathan, Dominik P Waluk, Petra Roosje, Monika Linek, Lucia Panakova, Tosso Leeb, Dominique J Wiener, Monika M Welle

    Diterbitkan 2017-01-01
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  8. 8
    Bald thigh syndrome in sighthounds-Revisiting the cause of a well-known disease.

    Bald thigh syndrome in sighthounds-Revisiting the cause of a well-known disease. oleh 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

    Diterbitkan 2019-01-01
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  9. 9
    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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  10. 10
    A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH).

    A mutation in the FAM83G gene in dogs with hereditary footpad hyperkeratosis (HFH). oleh 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

    Diterbitkan 2014-01-01
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  11. 11
    A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome

    A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome oleh 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

    Diterbitkan 2017-04-01
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  12. 12
    Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK).

    Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK). oleh 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

    Diterbitkan 2020-01-01
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  13. 13
    An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture

    An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture oleh 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

    Diterbitkan 2016-09-01
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  14. 14
    MKLN1 splicing defect in dogs with lethal acrodermatitis.

    MKLN1 splicing defect in dogs with lethal acrodermatitis. oleh 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

    Diterbitkan 2018-03-01
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  15. 15
    Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene.

    Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) gene. oleh 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

    Diterbitkan 2014-01-01
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  16. 16
    A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation.

    A mutation in the SUV39H2 gene in Labrador Retrievers with hereditary nasal parakeratosis (HNPK) provides insights into the epigenetics of keratinocyte differentiation. oleh 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

    Diterbitkan 2013-01-01
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