Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Leuthard, Fabienne"'
Autor:
Kiener, Sarah, Apostolopoulos, Neoklis, Schissler, Jennifer, Hass, Pascal-Kolja, Leuthard, Fabienne, Jagannathan, Vidhya, Schuppisser, Carole, Soto, Sara, Welle, Monika, Mayer, Ursula, Leeb, Tosso, Fischer, Nina M, Kaessmeyer, Sabine
Publikováno v:
Kiener, Sarah; Apostolopoulos, Neoklis; Schissler, Jennifer; Hass, Pascal-Kolja; Leuthard, Fabienne; Jagannathan, Vidhya; Schuppisser, Carole; Soto, Sara; Welle, Monika; Mayer, Ursula; Leeb, Tosso; Fischer, Nina M; Kaessmeyer, Sabine (2022). Independent COL5A1 Variant in Cats with Ehlers-Danlos Syndrome. Genes, 13(5), p. 797. MDPI, Molecular Diversity Preservation International 10.3390/genes13050797
We investigated four cats with similar clinical skin-related signs strongly suggestive of Ehlers-Danlos syndrome (EDS). Cases no. 1 and 4 were unrelated and the remaining two cases, no. 2 and 3, were reportedly siblings. Histopathological changes wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1aa03e17ca193fbe55112a611ddd49b
Autor:
O’Toole, Donal, Häfliger, Irene M., Leuthard, Fabienne, Schumaker, Brant, Steadman, Lynn, Murphy, Brian, Drögemüller, Cord, Leeb, Tosso
Publikováno v:
Animals
Volume 11
Issue 3
O’Toole, Donal; Häfliger, Irene M.; Leuthard, Fabienne; Schumaker, Brant; Steadman, Lynn; Murphy, Brian; Drögemüller, Cord; Leeb, Tosso (2021). X-Linked Hypohidrotic Ectodermal Dysplasia in Crossbred Beef Cattle Due to a Large Deletion in EDA. Animals, 11(3), p. 657. MDPI 10.3390/ani11030657
Animals : an open access journal from MDPI, vol 11, iss 3
Animals, Vol 11, Iss 657, p 657 (2021)
Volume 11
Issue 3
O’Toole, Donal; Häfliger, Irene M.; Leuthard, Fabienne; Schumaker, Brant; Steadman, Lynn; Murphy, Brian; Drögemüller, Cord; Leeb, Tosso (2021). X-Linked Hypohidrotic Ectodermal Dysplasia in Crossbred Beef Cattle Due to a Large Deletion in EDA. Animals, 11(3), p. 657. MDPI 10.3390/ani11030657
Animals : an open access journal from MDPI, vol 11, iss 3
Animals, Vol 11, Iss 657, p 657 (2021)
X-linked hypohidrotic ectodermal dysplasia-1 (ECTD1) in people results in a spectrum of abnormalities, most importantly hypotrichosis, anodontia/oligodontia, and absent or defective ectodermally derived glands. Five Red Angus-Simmental calves born ov
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,
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
Congenital hemidysplasia with ichthyosiform nevus and limb defects syndrome in humans is a genodermatosis characterized by inflammatory linear verrucous epidermal nevi (ILVEN), often showing a striking lateralization pattern. It is caused by variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03955ad7a4491bb8e82ba3f7d8257794
Autor:
Anderegg, Linda, Im Hof Gut, Michelle, Hetzel, Udo, Howerth, Elizabeth W, Leuthard, Fabienne Nadja, Kyöstilä, Kaisa, Lohi, Hannes, Pettitt, Louise, Mellersh, Cathryn, Minor, Katie M, Mickelson, James R, Batcher, Kevin, Bannasch, Danika, Jagannathan, Vidya, Leeb, Tosso
Primary ciliary dyskinesia (PCD) is a hereditary defect of motile cilia in humans and several domestic animal species. Typical clinical findings are chronic recurrent infections of the respiratory tract and fertility problems. We analyzed an Alaskan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::611f33cc6d547cefce683296a1fa2f3a
Autor:
Leeb, Tosso, Leuthard, Fabienne, Jagannathan, Vidya, Kiener, Sarah, Letko, Anna, Roosje, Petra, Welle, Monika M., Gailbreath, Katherine L, Cannon, Andrea, Linek, Monika, Banovic, Frane, Olivry, Thierry, White, Stephen D, Batcher, Kevin, Bannasch, Danika, Minor, Katie M, Mickelson, James R, Hytönen, Marjo K, Lohi, Hannes, Mauldin, Elizabeth A, Casal, Margret L
Cutaneous lupus erythematosus (CLE) in humans encompasses multiple subtypes that exhibit a wide array of skin lesions and, in some cases, are associated with the development of systemic lupus erythematosus (SLE). We investigated dogs with exfoliative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76eb4184e9fde729ac7a855fe074b9e8