Cerebral cavernous malformation ccm

Results 201 to 210 of about 4,624 (210)

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Serebral kavernoz malformasyonlarla (Cerebral cavernous malformation, CCM) mutasyona uğrayan KRIT1`in anjiogenik sinyal yolunun moleküler mekanizması

2020
ÖZET Serebral kavemoz malforaıasyonlann (SKM) genetik temelim anlamaya yönelik yapılan moleküler genetik çalışmalar sonucunda hastalıkla ilişkili üç (Cerebral Cavernous Malformation 1-3) lokus tanımlanmış ve CCMİ lokusu içerisinde yer alan KRIT1 geni klonlanmıştır.
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

Integrin β1–Talin1 at focal adhesions underpin uncontrolled endothelial cell enlargement in live cerebral cavernous malformation vasculature