Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Navarro Hilfiker, Sabine"'
[EN] The present invention describes the direct relationship between the phosphorylation of the parkin protein and the formation of intracellular aggregates in neurons. Consequently inhibitors of casein kinase 1 and Cdk5 can be useful pharmaceutical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1106::6e08bce22ebd931b53efa813136d9dc6
http://hdl.handle.net/10261/27848
http://hdl.handle.net/10261/27848
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
[EN] The present invention describes the direct relationship between the phosphorylation of the parkin protein and the formation of intracellular aggregates in neurons. Consequently inhibitors of casein kinase 1 and Cdk5 can be useful pharmaceutical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::6e08bce22ebd931b53efa813136d9dc6
http://hdl.handle.net/10261/27848
http://hdl.handle.net/10261/27848
Autor:
Lara Ordóñez, Antonio Jesús
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
In the present doctoral thesis, we demonstrate that the LRRK2-mediated centrosomal cohesion deficits are not only caused by accumulation of phospho-RAB8A but also of phospho-RAB10. Using CRISPR-Cas9 approaches, we identify that the LRRK2-mediated cen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6fb204a5e247f0b5e0217e7905eb9a69
http://hdl.handle.net/10481/74781
http://hdl.handle.net/10481/74781
Autor:
Madero Pérez, Jesús
Publikováno v:
Digibug: Repositorio Institucional de la Universidad de Granada
Universidad de Granada (UGR)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Universidad de Granada (UGR)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Mutations in the leucine rich repeat kinase 2 (LRRK2) gene are the most common cause of familial Parkinson’s disease (PD), with autosomal-dominant inheritance, and variants in this gene also confer risk to develop sporadic PD. Whilst the cellular a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cc2e5cb5688dc869d3c57b75c0afa061
http://hdl.handle.net/10481/67459
http://hdl.handle.net/10481/67459
Autor:
Rivero Ríos, María del Pilar
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digibug. Repositorio Institucional de la Universidad de Granada
instname
Digibug. Repositorio Institucional de la Universidad de Granada
Mutations in the gene encoding for leucine-rich repeat kinase 2 (LRRK2) are a common cause of hereditary Parkinson´s disease (PD), and some variants also confer risk to develop sporadic PD. LRRK2 has been reported to regulate various intracellular v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cf5f41df91821d951a83a22706e61b94
http://hdl.handle.net/10261/213678
http://hdl.handle.net/10261/213678
Autor:
Fernández Fernández, Elena
Tesis Consejo Superior de Investigaciones Científicas. Instituto de Parasitología y Biomedicina López Neyra
Tesis Univ. Granada. Departamento de Bioquímica y Biología Molecular. Leída el 9 de octubre de 2009
Tesis Univ. Granada. Departamento de Bioquímica y Biología Molecular. Leída el 9 de octubre de 2009
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f4096598bfacac7c289d529d5755469b
http://hdl.handle.net/10481/2708
http://hdl.handle.net/10481/2708
Autor:
Blanca Ramírez, Marian
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
En esta tesis, primero demostramos que la mayoría de los mutantes patogénicos, así como su versión farmacológicamente inhibida de la actividad kinasa, intensifican la asociación de LRRK2 con un grupo de MTs estables, mostrando un fenotipo filam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::09b340a88c015adcf74637f5778ac818
http://hdl.handle.net/10481/48377
http://hdl.handle.net/10481/48377
Autor:
Gómez Suaga, Patricia María
Publikováno v:
Digibug. Repositorio Institucional de la Universidad de Granada
instname
instname
Although the majority of PD cases are idiopathic, the identification of diseasecausing mutations helps in our understanding of the molecular mechanisms involved in neuronal demise. Mutations in LRRK2 (leucine-rich repeat kinase 2) are found associate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::240a6fb24a156e4e6eb62a1e3c5bd53c
http://hdl.handle.net/10481/45093
http://hdl.handle.net/10481/45093
Autor:
Rubio de la Torre Gil, Elena
Resumen e Introducción escritos en español
Tesis Univ. Granada. Departamento de Medicina. Leída el 10 de junio de 2009
Tesis Univ. Granada. Departamento de Medicina. Leída el 10 de junio de 2009
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::934358788d1ee09d61e34dc8b62c63da
http://hdl.handle.net/10481/2392
http://hdl.handle.net/10481/2392