Results 161 to 170 of about 1,834 (180)

KRIT1 helps cells to prevent oxidative stress.

2010
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 hemorrhage.
GOITRE, Luca, BALZAC, Fiorella, DEGANI, Simona, Degan P., RETTA, Saverio Francesco   +4 more
openaire   +2 more sources

Novel insights into the implication of KRIT1 in the maintenance of ROS homeostasis

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, Braggion S., Cutano V., Martino C., Forni M., RETTA, Saverio Francesco   +5 more
openaire   +1 more source

Multiple cerebral cavernomata - KRIT1 mutation

2022
openaire   +1 more source

KRIT1: A Traffic Warden at the Busy Crossroads Between Redox Signaling and the Pathogenesis of Cerebral Cavernous Malformation Disease

Antioxidants and Redox Signaling, 2023
Andrea Perrelli, Saverio Francesco Retta, Angela J. Glading   +2 more
exaly  

KRIT1 Protein Depletion Modifies Endothelial Cell Behavior via Increased Vascular Endothelial Growth Factor (VEGF) Signaling

Journal of Biological Chemistry, 2014
Angela J. Glading, Íngrid H Sarelius
exaly  

Association of Krev-1/rap1a With Krit1, a Novel Ankyrin Repeat-Containing Protein Encoded by a Gene Mapping to 7q21-22

Oncogene, 1997
Ilya G Serebriiskii, Joseph R Testa, Erica Golemis   +2 more
exaly  

Mutation and Expression Analysis of the KRIT1 Gene Associated With Cerebral Cavernous Malformations (CCM1)

Acta Neuropathologica, 2002
Hildegard Kehrer-Sawatzki, Horst Hameister, Hans-Peter Richter   +2 more
exaly  

Review for "KRIT1 nuclear localization does not impair KRIT1-dependent regulation of endothelial barrier permeability and cell homeostasis"

  +5 more sources

Cocrystal Structure of the ICAP1 PTB Domain in Complex With a KRIT1 Peptide

Acta Crystallographica Section F: Structural Biology Communications, 2013
Weizhi Liu, Titus J Boggon
exaly  

Identification of a Novel KRIT1 Mutation in an Italian Family With Cerebral Cavernous Malformation by the Protein Truncation Test

Journal of the Neurological Sciences, 2003
Loretta Ferrera, Giuseppe Viale, Paola Origone   +2 more
exaly