Zobrazeno 1 - 10
of 17
pro vyhledávání: '"K. Abada"'
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68584 (2013)
Huntington disease (HD) is frequently first diagnosed by the appearance of motor symptoms; the diagnosis is subsequently confirmed by the presence of expanded CAG repeats (> 35) in the HUNTINGTIN (HTT) gene. A BACHD rat model for HD carrying the huma
Externí odkaz:
https://doaj.org/article/2c172c906bdd4c9f8bacf6d62f81b888
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e71633 (2013)
Chorea and psychiatric symptoms are hallmarks of Huntington disease (HD), a neurodegenerative disorder, genetically characterized by the presence of expanded CAG repeats (>35) in the Huntingtin (HTT) gene. HD patients present psychiatric symptoms pri
Externí odkaz:
https://doaj.org/article/65d2942a76c84ae29e7dae14f109838d
Autor:
Nathalie Sans, Vera L. Pinheiro, Hélène Doat, Laurent Vuillard, Chantal Medina, Jean-Michel Blanc, Yah-Se K Abada, Aude Panatier, Thomas Papouin, Nicolas H. Piguel, Mireille Montcouquiol, Steve Dos-Santos Carvalho, Claudia Racca, Maïté M. Moreau, Ronan Peyroutou, Muna L Hilal, Jean-Paul Borg, Rivka A. Rachel, Stéphane H. R. Oliet, Marie-Josée Santoni
Publikováno v:
Cerebral Cortex
Cerebral Cortex, 2017, 27 (12), pp.5635-5651. ⟨10.1093/cercor/bhw333⟩
Cerebral Cortex, Oxford University Press (OUP), 2017, 27 (12), pp.5635-5651. ⟨10.1093/cercor/bhw333⟩
Cerebral Cortex, 2017, 27 (12), pp.5635-5651. ⟨10.1093/cercor/bhw333⟩
Cerebral Cortex, Oxford University Press (OUP), 2017, 27 (12), pp.5635-5651. ⟨10.1093/cercor/bhw333⟩
International audience; Planar cell polarity (PCP) signaling is well known to play a critical role during prenatal brain development; whether it plays specific roles at postnatal stages remains rather unknown. Here, we investigated the role of a key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7df21b783b823223154653de0ad69d
https://hal.science/hal-01789668
https://hal.science/hal-01789668
Autor:
Yah-se K. Abada, Marie-Claude Potier, Julie Bruyère, Benoît Delatour, Frédéric Saudou, Aurelia Ces
Publikováno v:
Alzheimer's & Dementia. 12
Publikováno v:
Egyptian Journal of Agricultural Sciences. 53:309-326
Autor:
K. Abada, M. Abdel-Aziz
Publikováno v:
Egyptian Journal of Agricultural Sciences. 53:115-128
Autor:
A. Chanot A, J.-C. Semet, C. Arnaud, A. Dali-Youcef, K. Abada, B. Gayzard, F. Lancelin, S. Pax-Chochois, N. Alves, A.-M. Curat, A. Caubisens, I. Sicre, N. Montjaux-Regis, C. Casper
Publikováno v:
Archives de Pédiatrie. 16:706-708
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68584 (2013)
PLoS ONE, 8(7):e68584. PUBLIC LIBRARY SCIENCE
PLoS ONE
PLoS ONE, 8(7):e68584. PUBLIC LIBRARY SCIENCE
PLoS ONE
Rationale: Huntington disease (HD) is frequently first diagnosed by the appearance of motor symptoms; the diagnosis is subsequently confirmed by the presence of expanded CAG repeats (> 35) in the HUNTINGTIN (HTT) gene. A BACHD rat model for HD carryi
Publikováno v:
Behavioral Brain Research, 238, 243-251. ELSEVIER SCIENCE BV
Rationale: Huntington's disease (HD) is characterized by progressive motor dysfunction, emotional disturbances and cognitive deficits. It is a genetic disease caused by an elongation of the polyglutamine repeats in the huntingtin gene. Whereas HD is
Autor:
A, Chanot A, J-C, Semet, C, Arnaud, A, Dali-Youcef, K, Abada, B, Gayzard, F, Lancelin, S, Pax-Chochois, N, Alves, A-M, Curat, A, Caubisens, I, Sicre, N, Montjaux-Regis, C, Casper
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 16(6)