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Pubblicazioni su CCM

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

Breve descrizione:
Loss-of-function mutations of the KRIT1 gene (CCM1) have been associated with the Cerebral Cavernous Malformation (CCM) disease, which is character...
Inviato da:
Francesco
Inviato il
30 Sep 2012
Scaricati:
15

KRIT1 Regulates the Homeostasis of Intracellular Reactive Oxygen Species

Breve descrizione:
KRIT1 is a gene responsible for Cerebral Cavernous Malformations (CCM), a major cerebrovascular disease characterized byabnormally enlarged and lea...
Inviato da:
admin
Inviato il
30 Sep 2012
Dimensioni del file:
1,451.52 Kb
Scaricati:
11
Autore del file:
Luca Goitre1, Fiorella Balzac1, Simona Degani1, Paolo Degan2, Saverio Marchi3, Paolo Pinton3, Saveri

Mutation Analysis of CCM1, CCM2 and CCM3 Genes in a Cohort of Italian Patients with Cerebral Cavernous Malformation

Breve descrizione:
Cerebral cavernous malformations (CCMs) are vascular lesions of the CNS characterizedby abnormally enlarged capillary cavities. CCMs can occur as s...
Inviato da:
admin
Inviato il
07 Sep 2011
Dimensioni del file:
1,257.68 Kb
Scaricati:
11
Autore del file:
Rosalia D’Angelo1*; Valeria Marini2*; Carmela Rinaldi1; Paola Origone2; Alessandra Dorcaratto3; Mari

Identification of Krit1B: a novel alternative splicing isoform of cerebral cavernous malformation gene-1

Breve descrizione:
Cerebral cavernous malformations (CCM) are vascular malformations, mostly located in the central nervous system, which occur in 0.1–0.5% of the p...
Inviato da:
admin
Inviato il
30 Sep 2012
Dimensioni del file:
1,243.58 Kb
Scaricati:
9
Autore del file:
Saverio Francesco Retta*, Maria Avolio, Floriana Francalanci, Simone Procida, Fiorella Balzac, Simon
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