Results 111 to 120 of about 2,366 (190)

Классификационные стратегические подходы в лечении врожденных сосудистых мальформаций: взгляд сосудистого хирурга [PDF]

, 2014
ВРОЖДЕННЫЕ СОСУДИСТЫЕ МАЛЬФОРМАЦИИНЕРВНОЙ СИСТЕМЫ МАЛЬФОРМАЦИИСОСУДИСТЫЕ МАЛЬФОРМАЦИИСОСУДИСТЫЕ ХИРУРГИЧЕСКИЕ ОПЕРАЦИИАНГИОДИСПЛАЗИЯГЕМАНГИОМА ...
Чернуха, Л. М., Каширова, Е. В., Тодосьев, А. В.   +2 more
core  

Ras-like small GTPases in platelet biology [PDF]

, 2002
In a human body, the behaviour of each cell is controlled by signals like hormones or growth factors. A cell receives such messages by means of specific receptors. These transmit the messages to other proteins in the cell and so on. Such cascades control
Bruyn, K.M.T. (Kimball Marinus Theodor) de
core   +1 more source

An estimate of maintenance efficiency in Brown-Proschan imperfect repair model with bathtub failure intensity [PDF]

, 2012
Purpose: Estimate the maintenance efficiency in the Brown-Proschan model with the bathtub failure intensity. Design/methodology/approach: Empirical research through which we propose a framework to establish the characteristics of failure process and ...
Krit, Makram, Rebai, Abdelwaheb
core  

Association of uncertain significance genetic variants with myocardial mechanics and morphometrics in patients with nonischemic dilated cardiomyopathy

BMC Cardiovascular Disorders
Background Careful interpretation of the relation between phenotype changes of the heart and gene variants detected in dilated cardiomyopathy (DCM) is important for patient care and monitoring.
Karolina Mėlinytė-Ankudavičė, Marius Šukys, Gabrielė Kasputytė, Ričardas Krikštolaitis, Eglė Ereminienė, Grytė Galnaitienė, Vaida Mizarienė, Gintarė Šakalytė, Tomas Krilavičius, Renaldas Jurkevičius   +9 more
doaj   +1 more source

KRIT1 Gene [PDF]

, 2020
openaire   +1 more source

KRIT1 wt Allele [PDF]

, 2020
openaire   +1 more source

The Molecular Pathogenesis Of Cerebral Cavernous Malformations [PDF]

, 2018
Cerebral cavernous malformation (CCM) is a human genetic, cerebrovascular disease that is caused by loss of function mutations in three non-homologous protein coding genes: KRIT1, CCM2, and PDCD10. These proteins form a heterotrimeric CCM adaptor complex
Tang, Alan Tien
core   +1 more source

KRIT1 ankyrin repeat containing (KRIT1; CCM1); cerebral cavernous malformation 2 (CCM2); programmed cell death 10 (PDCD10; CCM3) [PDF]

Science-Business eXchange, 2010
openaire   +1 more source

Targeted Reversible Covalent Modification of a Noncatalytic Lysine of the Krev Interaction Trapped 1 Protein Enables Site-Directed Screening for Protein-Protein Interaction Inhibitors. [PDF]

ACS Pharmacol Transl Sci, 2023
Francisco KR, Bruystens J, Varricchio C, McCurdy S, Wu J, Lopez-Ramirez MA, Ginsberg M, Caffrey CR, Brancale A, Gingras AR, Hixon MS, Ballatore C.   +11 more
europepmc   +1 more source

The Role of Immune Infiltration and Oxidative Stress in the Progression of Cerebral Cavernous Malformation. [PDF]

Brain Behav
Zhu X, Yao Y, Yu T, Xiao X.
europepmc   +1 more source