Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Leclerc, Emilie"'
Autor:
Leclerc, Emilie, Mansur, Rodrigo B., Grassi-Oliveira, Rodrigo, Cordeiro, Quirino, Kapczinski, Flavio, McIntyre, Roger S., Brietzke, Elisa
Publikováno v:
In Journal of Affective Disorders February 2018 227:214-218
Autor:
Bourgeois, Capucine, Leclerc, Émilie A., Corbin, Cyrielle, Doussot, Joël, Serrano, Valérie, Vanier, Jean-Raymond, Seigneuret, Jean-Marc, Auguin, Daniel, Pichon, Chantal, Lainé, Éric, Hano, Christophe
Publikováno v:
In Comptes rendus - Chimie September 2016 19(9):1090-1100
Autor:
Lyons, L., Buckley, R., Harvey, R., Abitbol, Marie, Aberdein, Danielle, Alves, Paulo, Ohlsson Andersson, Asa, Bellone, Rebecca, Bergström, Tomas, Bilgen, Nuket, Boyko, Adam, Brockman, Jeffrey, Casal, Margret, Castelhano, Marta, Davis, Brian, Davison, Lucy, Distl, Ottmar, Dodman, Nicholas, Ellinwood, N. Matthew, Fogle, Jonathan, Forman, Oliver, Garrick, Dorian, Ginns, Edward, Häggström, Jens, Hasegawa, Daisuke, Haase, Bianca, Jagannathan, Vidhya, Lait, Philippa, Hernandez, Isabel, Hytönen, Marjo, Kaukonen, Maria, Kosho, Tomoki, Leclerc, Emilie, Lear, Teri, Leeb, Tosso, Li, Ronald H.L., Lohi, Hannes, Longeri, Maria, Magnuson, Mark, Malik, Richard, Mane, Shrinivasrao, Middleton, Rondo, Munday, John, Murphy, William, Myers, Alexandra, Pedersen, Niels, Peterson‐Jones, Simon, Rothschild, Max, Rusbridge, Clare, Schoenebeck, Jeffrey, Shapiro, Beth, Stern, Joshua, Swanson, William, Terio, Karen, Todhunter, Rory, Warren, Wesley, Wilcox, Elizabeth, Wildschutte, Julia, Yu, Yoshihiko
Publikováno v:
Animal Genetics
Animal Genetics, Wiley-Blackwell, 2021, 52 (3), pp.321-332. ⟨10.1111/age.13059⟩
Animal Genetics, Wiley-Blackwell, 2021, 52 (3), pp.321-332. ⟨10.1111/age.13059⟩
Summary Tabby patterns of fur coats are defining characteristics in wild and domestic felids. Historically, three autosomal alleles at one locus (Tabby): Abyssinian (Ta; a.k.a. ticked), mackerel (Tm; a.k.a. striped) and blotched (tb; a.k.a. classic,
Autor:
Asevedo, Elson, Gadelha, Ary, Noto, Cristiano, Mansur, Rodrigo B., Zugman, André, Belangero, Síntia I.N., Berberian, Arthur A., Scarpato, Bruno S., Leclerc, Emilie, Teixeira, Antônio L., Gama, Clarissa S., Bressan, Rodrigo A., Brietzke, Elisa
Publikováno v:
In Journal of Psychiatric Research October 2013 47(10):1376-1382
Publikováno v:
In Journal of Affective Disorders July 2013 149(1-3):247-252
The present invention relates to the use of a sequence chosen among Seq ID No 3, Seq ID No l, Seq ID No 2, Seq ID No 4, Seq ID No 5, Seq ID No 6, Seq ID No 7, Seq ID No 8, and functional variants thereof, as an odorant binding protein (OBP).
La
La
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b92dcecd063700885407ddafabefc219
https://hal.inrae.fr/hal-03781247
https://hal.inrae.fr/hal-03781247
Akademický článek
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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
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/
https://pub.epsilon.slu.se/24206/
Autor:
Buckley, Reuben M., Gandolfi, Barbara, Creighton, Erica K., Pyne, Connor A., Bouhan, Delia M., Leroy, Michelle L., Senter, David A., Gobble, Johnny R., Abitbol, Marie, Lyons, Leslie A., Aberdein, Danielle, Garrick, Dorian J., Munday, John S., Alves, Paulo C., Barsh, Gregory S., Kaelin, Christopher B., Bellone, Rebecca R., Bergström, Tomas F., Boyko, Adam R., Brockman, Jeffrey A., Casal, Margret L., Castelhano, Marta G., Todhunter, Rory J., Wilcox, Elizabeth A., Distl, Ottmar, Dodman, Nicholas H., Ellinwood, N. Matthew, Rothschild, Max F., Fogle, Jonathan E., Forman, Oliver P., Ginns, Edward I., Häggström, Jens, Harvey, Robert J., Hasegawa, Daisuke, Yu, Yoshihiko, Haase, Bianca, Helps, Christopher R., Hernandez, Isabel, Hytönen, Marjo K., Kaukonen, Maria, Lohi, Hannes, Kosho, Tomoki, Leclerc, Emilie, Lear, Teri L., Leeb, Tosso, Li, Ronald H.L., Longeri, Maria, Magnuson, Mark A., Malik, Richard, Mane, Shrinivasrao P., Murphy, William J., Pedersen, Niels C., Stern, Joshua A., Peterson-Jones, Simon M., Rusbridge, Clare, Shapiro, Beth, Swanson, William F., Terio, Karen A., Warren, Wesley C., Wildschutte, Julia H.
Publikováno v:
Genes
Genes, MDPI, 2020, 11 (6), pp.682. ⟨10.3390/genes11060682⟩
Volume 11
Issue 6
Genes, vol 11, iss 6
Genes, Vol 11, Iss 682, p 682 (2020)
Genes, MDPI, 2020, 11 (6), pp.682. ⟨10.3390/genes11060682⟩
Volume 11
Issue 6
Genes, vol 11, iss 6
Genes, Vol 11, Iss 682, p 682 (2020)
Publisher Copyright: © 2020 by the authors. Licensee MDPI, Basel, Switzerland. A variety of cat breeds have been developed via novelty selection on aesthetic, dermatological traits, such as coat colors and fur types. A recently developed breed, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e564138d24b7446d938cea336c702f1
https://hal.archives-ouvertes.fr/hal-02888652
https://hal.archives-ouvertes.fr/hal-02888652
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)
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,