Identification of the Kelch Family Protein Nd1-L as a Novel Molecular Interactor of KRIT1

Loss-of-function mutations of the KRIT1 gene (CCM1) have been associated with the Cerebral Cavernous Malformation (CCM) disease, which is characterized by serious alterations of brain capillary architecture. The KRIT1 protein contains multiple interaction domains and motifs, suggesting that it might...

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Detalles Bibliográficos
Autores principales: Guazzi, Paolo, Goitre, Luca, Ferro, Elisa, Cutano, Valentina, Martino, Chiara, Trabalzini, Lorenza, Retta, Saverio Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435375/
https://www.ncbi.nlm.nih.gov/pubmed/22970292
http://dx.doi.org/10.1371/journal.pone.0044705

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435375/
https://www.ncbi.nlm.nih.gov/pubmed/22970292
http://dx.doi.org/10.1371/journal.pone.0044705

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