Cerebral cavernous malformation ccm

Results 191 to 200 of about 1,916 (204)

Some of the next articles are maybe not open access.

The cerebral cavernous malformation proteins CCM2L and CCM2 prevent the activation of the MAP kinase MEKK3

Proceedings of the National Academy of Sciences of the United States of America, 2015
Tanya N Mayadas
exaly

2011
openaire +1 more source

KRIT1, a disease gene responsible for cerebral cavernous malformations (CCM), is involved in cell defences against oxidative stress  

2011
KRIT1 is a gene responsible for Cerebral Cavernous Malformations (CCM), a major cerebrovascular disease characterized by abnormally enlarged and leaky capillaries that predispose to seizures, focal neurological deficits, and fatal intracerebral haemorrhage. Comprehensive analysis of the KRIT1 gene in CCM patients has suggested that KRIT1 functions need
GOITRE, Luca +6 more
openaire +2 more sources

Cerebral cavernous malformation is a vascular disease associated with activated RhoA signaling

Biological Chemistry, 2013
Gary L Johnson
exaly

Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 2020
Concetta Scimone, Luigi Donato, Simona Alibrandi +2 more
exaly

CCM proteins are key players in redox signaling and oxidative stress regulation in Cerebral Cavernous Malformations

2023
Finetti F., Paradisi L., Trabalzini L.
openaire +2 more sources

Clinical characteristics and risk factors of cerebral cavernous malformation-related epilepsy

Epilepsy and Behavior, 2023
exaly

[Genetics of cerebral cavernous malformations (CCM)].

Deutsche medizinische Wochenschrift (1946), 2007
openaire +1 more source

Implication of PTEN loss in the neoangiogenesis of cerebral cavernous malformations (CCMs)

2007
Zhu, Y +5 more
openaire +1 more source