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Tosso Leeb

Showing results (261-270 of 310) with videos related to

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Plos One|March 3, 2020
Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK)Jeanette Bannoehr, Pierre Balmer, Michael H Stoffel, et al.
Veterinary Pathology|June 7, 2017
Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D MutationPernilla Syrjä, Tahira Anwar, Tarja Jokinen, et al.
Plos Genetics|March 23, 2018
MKLN1 splicing defect in dogs with lethal acrodermatitisAnina Bauer, Vidhya Jagannathan, Sandra Högler, et al.
G3 (Bethesda, Md.)|July 25, 2016
An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat TextureLeonardo Murgiano, Dominik P Waluk, Rachel Towers, et al.
Plos Genetics|September 4, 2019
NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesiaLinda Anderegg, Michelle Im Hof Gut, Udo Hetzel, et al.
Genes|June 2, 2021
Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference GenomeVidhya Jagannathan, Christophe Hitte, Jeffrey M Kidd, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2024
Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal DystrophyShawna R Cook, Cleo Schwarz, Julien Guevar, et al.
Plos One|October 9, 2014
Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) geneMichaela Drögemüller, Vidhya Jagannathan, Monika M Welle, et al.
Genes|July 15, 2020
Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED)Jasmin Nessler, Petra Hug, Paul J J Mandigers, et al.
Plos Genetics|December 1, 2025
Two genes, one culprit - a functional candidate validation of a SPATA7 deletion in dogs with day blindness/retinal degenerationLeonardo Murgiano, Jessica K Niggel, Kei Takahashi, et al.
Pageof 31

Showing results (261-270 of 310) with videos related to

Sort By:
Pageof 31
Plos One|March 3, 2020
Abnormal keratinocyte differentiation in the nasal planum of Labrador Retrievers with hereditary nasal parakeratosis (HNPK)Jeanette Bannoehr, Pierre Balmer, Michael H Stoffel, et al.
Veterinary Pathology|June 7, 2017
Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D MutationPernilla Syrjä, Tahira Anwar, Tarja Jokinen, et al.
Plos Genetics|March 23, 2018
MKLN1 splicing defect in dogs with lethal acrodermatitisAnina Bauer, Vidhya Jagannathan, Sandra Högler, et al.
G3 (Bethesda, Md.)|July 25, 2016
An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat TextureLeonardo Murgiano, Dominik P Waluk, Rachel Towers, et al.
Plos Genetics|September 4, 2019
NME5 frameshift variant in Alaskan Malamutes with primary ciliary dyskinesiaLinda Anderegg, Michelle Im Hof Gut, Udo Hetzel, et al.
Genes|June 2, 2021
Dog10K_Boxer_Tasha_1.0: A Long-Read Assembly of the Dog Reference GenomeVidhya Jagannathan, Christophe Hitte, Jeffrey M Kidd, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2024
Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal DystrophyShawna R Cook, Cleo Schwarz, Julien Guevar, et al.
Plos One|October 9, 2014
Congenital hepatic fibrosis in the Franches-Montagnes horse is associated with the polycystic kidney and hepatic disease 1 (PKHD1) geneMichaela Drögemüller, Vidhya Jagannathan, Monika M Welle, et al.
Genes|July 15, 2020
Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED)Jasmin Nessler, Petra Hug, Paul J J Mandigers, et al.
Plos Genetics|December 1, 2025
Two genes, one culprit - a functional candidate validation of a SPATA7 deletion in dogs with day blindness/retinal degenerationLeonardo Murgiano, Jessica K Niggel, Kei Takahashi, et al.
Pageof 31