Suchergebnisse - "Awad, Issam A"

PubPharm (13)

1

PIK3CA and CCM mutations fuel cavernomas through a cancer-like mechanism

enthalten in: Nature | 2021

von Ren, A. | Snellings, D. | Su, Y. | +25

2

A Brain-Targeted Orally Available ROCK2 Inhibitor Benefits Mild and Aggressive Cavernous Angioma Disease

enthalten in: Translational stroke research | 2020

von McKerracher, L. | Shenkar, R. | Abbinanti, M. | +13

3

Phenotypic characterization of murine models of cerebral cavernous malformations

enthalten in: Laboratory investigation; a journal of technical methods and pathology | 2019

von Zeineddine, H. | Girard, R. | Saadat, L. | +19

4

Rho Kinase Inhibition Blunts Lesion Development and Hemorrhage in Murine Models of Aggressive Pdcd10/Ccm3 Disease

enthalten in: Stroke | 2019

von Shenkar, R. | Peiper, A. | Pardo, H. | +16

5

The cerebral cavernous malformation disease causing gene KRIT1 participates in intestinal epithelial barrier maintenance and regulation

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2019

von Wang, Y. | Li, Y. | Zou, J. | +8

6

RhoA Kinase Inhibition With Fasudil Versus Simvastatin in Murine Models of Cerebral Cavernous Malformations

enthalten in: Stroke | 2017

von Shenkar, R. | Shi, C. | Austin, C. | +14

7

Micro-computed tomography in murine models of cerebral cavernous malformations as a paradigm for brain disease

enthalten in: Journal of neuroscience methods | 2016

von Girard, R. | Zeineddine, H. | Orsbon, C. | +17

8

Peripheral plasma vitamin D and non-HDL cholesterol reflect the severity of cerebral cavernous malformation disease

enthalten in: Biomarkers in medicine | 2016

von Girard, R. | Khanna, O. | Shenkar, R. | +12

9

Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2015

von Shenkar, R. | Shi, C. | Rebeiz, T. | +14

10

Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes : evidence for a common biochemical pathway for CCM pathogenesis

enthalten in: Human molecular genetics | 2014

von McDonald, D. | Shi, C. | Shenkar, R. | +8