Comparative analysis of vertebrate EIF2AK2 (PKR) genes and assignment of the equine gene to ECA15q24–q25 and the bovine gene to BTA11q12–q15

Autor: Zharkikh Andrey A, Lear Teri L, Perelygin Andrey A, Brinton Margo A

Publikováno v: Genetics Selection Evolution, Vol 38, Iss 5, Pp 551-563 (2006)

Abstract The structures of the canine, rabbit, bovine and equine EIF2AK2 genes were determined. Each of these genes has a 5' non-coding exon as well as 15 coding exons. All of the canine, bovine and equine EIF2AK2 introns have consensus donor and acc

Externí odkaz: https://doaj.org/article/0e98324b000e4b918a624f67b098679d

Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits

Autor: Genova, Francesca, Nonnis, Simona, Maffioli, Elisa, Tedeschi, Gabriella, Strillacci, Maria Giuseppina, Carisetti, Michela, Sironi, Giuseppe, Cupaioli, Francesca Anna, Di Nanni, Noemi, Mezzelani, Alessandra, Mosca, Ettore, Helps, Christopher R., Leegwater, Peter A.J., Dorso, Laetitia, Buckley, Reuben M., Aberdein, Danielle, Alves, Paulo C., Andersson, Asa Ohlsson, Barsh, Gregory S., Bellone, Rebecca R., Bergström, Tomas F., Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Haase, Bianca, Häggström, Jens, Harvey, Robert J., Hasegawa, Daisuke, Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kaelin, Christopher B., Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Magnuson, Mark A., Malik, Richard, Mane, Shrinivasrao P., Munday, John S., Murphy, William J., Pedersen, Niels C., Peterson-Jones, Simon M., Rothschild, Max F., Rusbridge, Clare, Shapiro, Beth, Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H., Yu, Yoshihiko, Lyons, Leslie A., Longeri, Maria

Publikováno v: Scientific reports (Nature Publishing Group) 11 (2021). doi:10.1038/s41598-021-87168-0
info:cnr-pdr/source/autori:Genova, Francesca; Nonnis, Simona; Maffioli, Elisa; Tedeschi, Gabriella; Strillacci, Maria Giuseppina; Carisetti, Michela; Sironi, Giuseppe; Cupaioli, Francesca Anna; Di Nanni, Noemi; Mezzelani, Alessandra; Mosca, Ettore; Helps, Christopher R.; Leegwater, Peter A.J.; Dorso, Laetitia; Buckley, Reuben M.; Aberdein, Danielle; Alves, Paulo C.; Andersson, Asa Ohlsson; Barsh, Gregory S.; Bellone, Rebecca R.; Bergström, Tomas F.; Boyko, Adam R.; Brockman, Jeffrey A.; Casal, Margret L.; Castelhano, Marta G.; Distl, Ottmar; Dodman, Nicholas H.; Ellinwood, N. Matthew; Fogle, Jonathan E.; Forman, Oliver P.; Garrick, Dorian J.; Ginns, Edward I.; Haase, Bianca; Häggström, Jens; Harvey, Robert J.; Hasegawa, Daisuke; Hernandez, Isabel; Hytönen, Marjo K.; Kaukonen, Maria; Kaelin, Christopher B.; Kosho, Tomoki; Leclerc, Emilie; Lear, Teri L.; Leeb, Tosso; Li, Ronald H.L.; Lohi, Hannes; Magnuson, Mark A.; Malik, Richard; Mane, Shrinivasrao P.; Munday, John S.; Murphy, William J.; Pedersen, Niels C.; Peterson-Jones, Simon M.; Rothschild, Max F.; Rusbridge, Clare; Shapiro, Beth; Stern, Joshua A.; Swanson, William F.; Terio, Karen A.; Todhunter, Rory J.; Warren, Wesley C.; Wilcox, Elizabeth A.; Wildschutte, Julia H.; Yu, Yoshihiko; Lyons, Leslie A.; Longeri, Maria/titolo:Multi-omic analyses in Abyssinian cats with primary renal amyloid deposits/doi:10.1038%2Fs41598-021-87168-0/rivista:Scientific reports (Nature Publishing Group)/anno:2021/pagina_da:/pagina_a:/intervallo_pagine:/volume:11

The amyloidoses constitute a group of diseases occurring in humans and animals that are characterized by abnormal deposits of aggregated proteins in organs, affecting their structure and function. In the Abyssinian cat breed, a familial form of renal

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::59eda4fd77009d3874997accfa4773b7
https://pub.epsilon.slu.se/24206/

A Deletion in GDF7 is Associated with a Heritable Forebrain Commissural Malformation Concurrent with Ventriculomegaly and Interhemispheric Cysts in Cats

Autor: Yu, Yoshihiko, Creighton, Erica K., Buckley, Reuben M., Lyons, Leslie A., Aberdein, Danielle, Alves, Paulo C., Barsh, Gregory S., Bellone, Rebecca R., Bergström, Tomas F., Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Fogle, Jonathan E., Forman, Oliver P., Garrick, Dorian J., Ginns, Edward I., Häggström, Jens, Harvey, Robert J., Hasegawa, Daisuke, Haase, Bianca, Helps, Christopher R., Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Kaelin, Christopher B., Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivasrao P., Munday, John S., Murphy, William J., Pedersen, Niels C., Peterson-Jones, Simon M., Rothschild, Max F., Rusbridge, Clare, Shapiro, Beth, Stern, Joshua A., Swanson, William F., Terio, Karen A., Todhunter, Rory J., Warren, Wesley C., Wilcox, Elizabeth A., Wildschutte, Julia H.

Publikováno v: Genes
Genes, vol 11, iss 6
Volume 11
Issue 6
Genes, Vol 11, Iss 672, p 672 (2020)

Publisher Copyright: © 2020 by the authors. An inherited neurologic syndrome in a family of mixed-breed Oriental cats has been characterized as forebrain commissural malformation, concurrent with ventriculomegaly and interhemispheric cysts. However,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd4448affe349042df7fc2a78a3af6c1
http://europepmc.org/articles/PMC7349246

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