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Production of endoglin-specific heavy chain antibody fragments (VHHs) microarrays for whole-cell SPR imaging
(Elsevier, 2022)
Cell-based Surface Plasmon Resonance imaging (SPRi) with anti-endoglin VHH antibodies microarray on a gold-covered biochip was used to characterize the binding to endoglin expressed on the surface membrane of SC cells. ...
Endoglin increases eNOS expression by modulating Smad2 protein levels and Smad2-dependent TGF-β signaling
(2007)
The endothelial nitric oxide synthase (eNOS) is a critical regulator of cardiovascular homeostasis, whose dysregulation leads to different vascular pathologies. Endoglin is a component of the transforming growth factor ...
Endoglin regulates cyclooxygenase-2 expression and activity
(LIPPINCOTT WILLIAMS & WILKINS, 2006-08-04)
The endoglin heterozygous (Eng(+/-)) mouse, which serves as a model of hereditary hemorrhagic telangiectasia (HHT), was shown to express reduced levels of endothelial NO synthase (eNOS) with impaired activity. Because of ...
The TGF-β co-receptor endoglin modulates the expression and transforming potential of H-Ras
(Oxford University Press, 2010)
Endoglin is a coreceptor for transforming growth factor-β (TGF-β) that acts as a suppressor of malignancy during mouse skin carcinogenesis. Because in this model system H-Ras activation drives tumor initiation and progression, ...
The tgf-beta co-receptor endoglin modulates the expression and transforming potential of h-ras
(OXFORD UNIV PRESS, 2010)
Hypertension and vascular endothelial growth factors
(2015-01-01)
The members of vascular endothelial growth factors (VEGF) are the principal regulators of angiogenesis and vascular biology. The specific growth factor of the endothelial cells is VEGF, which produces nitric oxide (NO) ...
Markers of vascular differentiation, proliferation and tissue remodeling in juvenile nasopharyngeal angiofibromas
(SPANDIDOS PUBL LTD, 2010)
Juvenile nasopharingeal angiofibroma (JNA) is a histologically benign locally aggressive tumor characterized by irregular vessels embedded. in a fibrous stroma. Excessive vascularity results in bleeding complications, and ...
Mutation study of spanish patients with hereditary hemorrhagic telangiectasia and expression analysis of endoglin and ALK1
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes. The first large ...