Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Jagannathan, Vidya"'
Autor:
Christen, Matthias, Bongers, Jos, Mathis, Déborah, Jagannathan, Vidya, Quintana, Rodrigo Gutierrez, Leeb, Tosso
Publikováno v:
Christen, Matthias; Bongers, Jos; Mathis, Déborah; Jagannathan, Vidya; Quintana, Rodrigo Gutierrez; Leeb, Tosso (2022). ACADM Frameshift Variant in Cavalier King Charles Spaniels with Medium-Chain Acyl-CoA Dehydrogenase Deficiency. Genes, 13(10), p. 1847. MDPI 10.3390/genes13101847
A 3-year-old, male neutered Cavalier King Charles Spaniel (CKCS) presented with complex focal seizures and prolonged lethargy. The aim of the study was to investigate the clinical signs, metabolic changes and underlying genetic defect. Blood and urin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8940e816375af05e07c940e2d32261c
Autor:
Gerber, Nadja, Brunner, Magdalena A. T., Jagannathan, Vidya, Leeb, Tosso, Gerhards, Nora M., Welle, Monika M., Dettwiler, Martina
Publikováno v:
Gerber, Nadja; Brunner, Magdalena A. T.; Jagannathan, Vidya; Leeb, Tosso; Gerhards, Nora M.; Welle, Monika M.; Dettwiler, Martina (2021). Transcriptional Differences between Canine Cutaneous Epitheliotropic Lymphoma and Immune-Mediated Dermatoses. Genes, 12(2) MDPI, Molecular Diversity Preservation International 10.3390/genes12020160
Genes, 12(2), 1-16
Genes
Genes 12 (2021) 2
Genes, Vol 12, Iss 160, p 160 (2021)
Volume 12
Issue 2
Genes, 12(2), 1-16
Genes
Genes 12 (2021) 2
Genes, Vol 12, Iss 160, p 160 (2021)
Volume 12
Issue 2
Canine cutaneous epitheliotropic T-cell lymphoma (CETL) and immune-mediated T-cell predominant dermatoses (IMD) share several clinical and histopathological features, but differ substantially in prognosis. The discrimination of ambiguous cases may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95939fa9071e600fd1e68e94858c8adc
Autor:
Nessler, Jasmin, Hug, Petra, Mandigers, Paul J J, Leegwater, Peter A J, Jagannathan, Vidya, Das, Anibh M, Rosati, Marco, Matiasek, Kaspar, Sewell, Adrian C, Kornberg, Marion, Hoffmann, Marina, Wolf, Petra, Fischer, Andrea, Tipold, Andrea, Leeb, Tosso
Publikováno v:
Genes
Volume 11
Issue 7
Genes, Vol 11, Iss 774, p 774 (2020)
Nessler, Jasmin; Hug, Petra; Mandigers, Paul J J; Leegwater, Peter A J; Jagannathan, Vidya; Das, Anibh M; Rosati, Marco; Matiasek, Kaspar; Sewell, Adrian C; Kornberg, Marion; Hoffmann, Marina; Wolf, Petra; Fischer, Andrea; Tipold, Andrea; Leeb, Tosso (2020). Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED). Genes, 11(7) MDPI, Molecular Diversity Preservation International 10.3390/genes11070774
Volume 11
Issue 7
Genes, Vol 11, Iss 774, p 774 (2020)
Nessler, Jasmin; Hug, Petra; Mandigers, Paul J J; Leegwater, Peter A J; Jagannathan, Vidya; Das, Anibh M; Rosati, Marco; Matiasek, Kaspar; Sewell, Adrian C; Kornberg, Marion; Hoffmann, Marina; Wolf, Petra; Fischer, Andrea; Tipold, Andrea; Leeb, Tosso (2020). Mitochondrial PCK2 Missense Variant in Shetland Sheepdogs with Paroxysmal Exercise-Induced Dyskinesia (PED). Genes, 11(7) MDPI, Molecular Diversity Preservation International 10.3390/genes11070774
Four female Shetland Sheepdogs with hypertonic paroxysmal dyskinesia, mainly triggered by exercise and stress, were investigated in a retrospective multi-center investigation aiming to characterize the clinical phenotype and its underlying molecular
Autor:
Kiener, Sarah, Kehl, Alexandra, Loechel, Robert, Langbein-Detsch, Ines, Müller, Elisabeth, Bannasch, Danika, Jagannathan, Vidya, Leeb, Tosso
Publikováno v:
Genes, Vol 11, Iss 636, p 636 (2020)
Genes
Volume 11
Issue 6
Genes, vol 11, iss 6
Kiener, Sarah; Kehl, Alexandra; Loechel, Robert; Langbein-Detsch, Ines; Müller, Elisabeth; Bannasch, Danika; Jagannathan, Vidya; Leeb, Tosso (2020). Novel Brown Coat Color (Cocoa) in French Bulldogs Results from a Nonsense Variant in HPS3. Genes, 11(6) MDPI, Molecular Diversity Preservation International 10.3390/genes11060636
Genes
Volume 11
Issue 6
Genes, vol 11, iss 6
Kiener, Sarah; Kehl, Alexandra; Loechel, Robert; Langbein-Detsch, Ines; Müller, Elisabeth; Bannasch, Danika; Jagannathan, Vidya; Leeb, Tosso (2020). Novel Brown Coat Color (Cocoa) in French Bulldogs Results from a Nonsense Variant in HPS3. Genes, 11(6) MDPI, Molecular Diversity Preservation International 10.3390/genes11060636
Brown or chocolate coat color in many mammalian species is frequently due to variants at the B locus or TYRP1 gene. In dogs, five different TYRP1 loss-of-function alleles have been described, which explain the vast majority of dogs with brown coat co
Autor:
Linek, Monika, Doelle, Maren, Leeb, Tosso, Bauer, Anina, Leuthard, Fabienne, Henkel, Jan, Bannasch, Danika, Jagannathan, Vidya, Welle, Monika M.
Publikováno v:
Genes
Volume 11
Issue 5
Genes, Vol 11, Iss 481, p 481 (2020)
Genes, vol 11, iss 5
Linek, Monika; Doelle, Maren; Leeb, Tosso; Bauer, Anina; Leuthard, Fabienne; Henkel, Jan; Bannasch, Danika; Jagannathan, Vidya; Welle, Monika M. (2020). ATP2A2 SINE Insertion in an Irish Terrier with Darier Disease and Associated Infundibular Cyst Formation. Genes, 11(5) MDPI, Molecular Diversity Preservation International 10.3390/genes11050481
Volume 11
Issue 5
Genes, Vol 11, Iss 481, p 481 (2020)
Genes, vol 11, iss 5
Linek, Monika; Doelle, Maren; Leeb, Tosso; Bauer, Anina; Leuthard, Fabienne; Henkel, Jan; Bannasch, Danika; Jagannathan, Vidya; Welle, Monika M. (2020). ATP2A2 SINE Insertion in an Irish Terrier with Darier Disease and Associated Infundibular Cyst Formation. Genes, 11(5) MDPI, Molecular Diversity Preservation International 10.3390/genes11050481
A 4-month-old female Irish Terrier presented with a well demarcated ulcerative and crusting lesion in the right ear canal. Histological analysis revealed epidermal hyperplasia with severe acantholysis affecting all suprabasal layers of the epidermis,
Autor:
Saif, Rashid, Henkel, Jan, Jagannathan, Vidya, Drögemüller, Cord, Flury, Christine, Leeb, Tosso
Publikováno v:
Saif, Rashid; Henkel, Jan; Jagannathan, Vidya; Drögemüller, Cord; Flury, Christine; Leeb, Tosso (2020). The LCORL Locus is under Selection in Large-Sized Pakistani Goat Breeds. Genes, 11(2) MDPI, Molecular Diversity Preservation International 10.3390/genes11020168
Genes, Vol 11, Iss 2, p 168 (2020)
Genes
Genes, Vol 11, Iss 2, p 168 (2020)
Genes
Goat domestication and human selection for valued traits have formed diverse breeds with characteristic phenotypes. This process led to the fixation of causative genetic variants controlling breed-specific traits within regions of reduced genetic div
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc216374408c68ca49d3b5126aa22e5c
https://boris.unibe.ch/140089/1/Saif_2020_Genes_11_168.pdf
https://boris.unibe.ch/140089/1/Saif_2020_Genes_11_168.pdf
Autor:
Murgiano, Leonardo, Becker, Doreen, Torjman, Dina, Niggel, Jessica K, Milano, Ausra, Cullen, Cheryl, Feng, Rui, Wang, Fan, Jagannathan, Vidya, Pearce-Kelling, Sue, Katz, Martin L, Leeb, Tosso, Aguirre, Gustavo D
Publikováno v:
Murgiano, Leonardo; Becker, Doreen; Torjman, Dina; Niggel, Jessica K; Milano, Ausra; Cullen, Cheryl; Feng, Rui; Wang, Fan; Jagannathan, Vidya; Pearce-Kelling, Sue; Katz, Martin L; Leeb, Tosso; Aguirre, Gustavo D (2019). Complex Structural Variant Associated with Non-syndromic Canine Retinal Degeneration. G3 Genes Genomes Genetics, 9(2), pp. 425-437. Genetics Society of America 10.1534/g3.118.200859
Rod and cone photoreceptors are specialized retinal neurons that have a fundamental role in visual perception, capturing light and transducing it into a neuronal signal. Aberrant functioning of rod and/or cone photoreceptors can ultimately lead to pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::722aa502623f72edfb5ad7360b2a1386
White spotting phenotypes in horses may be caused by developmental alterations impairing melanoblast differentiation, survival, migration and/or proliferation. Candidate genes for white-spotting phenotypes in horses include EDNRB, KIT, MITF, PAX3 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::505b5c1568e71ba845a1e5610842d046
The Ehlers-Danlos syndromes (EDSs) are a heterogeneous group of inherited connective tissue disorders characterized by skin hyperextensibility, joint hypermobility and tissue fragility. Inherited disorders similar to human EDS have been reported in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e0ef7d2da9c1ce6b493701217759913