Results 81 to 90 of about 1,269 (145)

KRIT1 LOSS-OF-FUNCTION INDUCES ANGIOGENESIS AND MIGRATION IN A CCM CELLULAR MODEL

open access: yes, 2019
KRIT1 is a gene involved in Cerebral Cavernous Malformations (CCMs), a cerebrovascular disease characterized by thin-walled capillaries lacking of normal vessel structure that predispose to headaches, neurological deficits, seizures, stroke and ...
SCHIAVO, IRENE
core  

C329X in KRIT1 is a founder mutation among CCM patients in Sardinia

open access: yes, 2009
Cerebral cavernous malformations(CCMs)are CNS vascular anomalies associated with seizures,head- aches and hemorrhagic strokes and represent 10–20% of cerebral lesions.CCM is present in 0.1–0.5 of the population.This disorder most often occurs ...
LOI M   +8 more
core   +1 more source

A novel PDCD10 gene mutation in cerebral cavernous malformations: a case report and review of the literature

open access: yesJournal of Pain Research, 2019
Weiwei Yu, Haiqiang Jin, Qian You, Ding Nan, Yining HuangDepartment of Neurology, Peking University First Hospital, Beijing 100034, People’s Republic of ChinaAbstract: Cerebral cavernous malformations (CCMs) are one of the most common types of ...
Yu W, Jin H, You Q, Nan D, Huang Y
doaj  

Serebral kavernoz malformasyonlarda (celebral cavernous malformation, CCM) mutasyona uğrayan KRIT1’in anjiogenik sinyal yolunun moleküler mekanizması.

open access: yes, 2004
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 ...
Kayışlı, Özlem Güzeloğlu
core  

Proteomic analysis reveals KRIT1 as a modulator for the antioxidant effects of valproic acid in human bone-marrow mesenchymal stromal cells

open access: yes, 2015
Valproic acid (VPA) protects human bone marrow-mesenchymal stromal cells (hBM-MSCs) against oxidative stress and improves their migratory ability through increasing the secretion of trophic factors.
Goang-Won Cho (85423)   +5 more
core   +1 more source

The interaction with Nd1-L involves two different regions of KRIT1.

open access: yes, 2013
A. Schematic representation of the KRIT1 isoforms and deletion mutants used in the assay. B. Yeast two-hybrid analysis of the KRIT1-Nd1-L interaction. pGADT7-Nd1-L was used to co-transform AH109 yeast strain along with different fragments of KRIT1A and ...
Lorenza Trabalzini (308642)   +6 more
core   +1 more source

Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations

open access: yes, 2003
Cerebral cavernous malformations (CCMs) are congenital vascular anomalies of the central nervous system that can result in hemorrhagic stroke, seizures, recurrent headaches, and focal neurologic deficits.
Siegel, Adrian M.   +17 more
core   +1 more source

KRIT1-Mediated Regulation of the Cellular Response to Inflammation

open access: yes
Thesis (Ph.D.)--University of Rochester. School of Medicine & Dentistry. Dept. of Pharmacology and Physiology, 2023.Cerebral cavernous malformations (CCM) is a disease in which abnormal blood vessel formation compromises the structure and function of the
Glading, Angela J., Nobiletti, Nicholas
core  

Regulation of Endothelial Cell Behavior via KRIT1 Localization and Function

open access: yes
Thesis (Ph.D.)--University of Rochester. School of Medicine & Dentistry. Dept. of Pharmacology and Physiology, 2022.Stable endothelial barrier function is necessary for vascular homeostasis. Disruption of endothelial cell-cell contacts leads to a loss of
Glading, Angela J., Swamy, Harsha
core  

Identification of Nd1-L as a new interaction partner of KRIT1.

open access: yes, 2013
A. Small scale yeast two-hybrid analysis of the interaction of KRIT1 with the C17 clone. Yeast strain AH109 was cotransformed with GAL4DNA-BD and GAL4AD fusion constructs as indicated (left).
Lorenza Trabalzini (308642)   +6 more
core   +1 more source

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