scholarly article | Q13442814 |
P2093 | author name string | Alexander R Kazarov | |
Arja Kaipainen | |||
Martin E Hemler | |||
Laura E Benjamin | |||
Yoshito Takeda | |||
Benjamin D Hopkins | |||
Catherine E Butterfield | |||
P2860 | cites work | Function of the tetraspanin CD151-alpha6beta1 integrin complex during cellular morphogenesis | Q24555041 |
Annexin II regulates fibrin homeostasis and neoangiogenesis in vivo | Q24623508 | ||
Akt1 regulates pathological angiogenesis, vascular maturation and permeability in vivo | Q24648140 | ||
Akt1 in endothelial cell and angiogenesis | Q24676614 | ||
PETA-3/CD151, a member of the transmembrane 4 superfamily, is localised to the plasma membrane and endocytic system of endothelial cells, associates with multiple integrins and modulates cell function | Q28137736 | ||
Eukaryotic expression cloning with an antimetastatic monoclonal antibody identifies a tetraspanin (PETA-3/CD151) as an effector of human tumor cell migration and metastasis | Q28142104 | ||
Laminin-10/11 and fibronectin differentially regulate integrin-dependent Rho and Rac activation via p130(Cas)-CrkII-DOCK180 pathway | Q28190218 | ||
Laminin-10/11 and fibronectin differentially prevent apoptosis induced by serum removal via phosphatidylinositol 3-kinase/Akt- and MEK1/ERK-dependent pathways | Q28206731 | ||
Complexes of tetraspanins with integrins: more than meets the eye | Q28210099 | ||
CD151 enhances cell motility and metastasis of cancer cells in the presence of focal adhesion kinase | Q28214450 | ||
Localization of the transmembrane 4 superfamily (TM4SF) member PETA-3 (CD151) in normal human tissues: comparison with CD9, CD63, and alpha5beta1 integrin | Q28235612 | ||
Tetraspanin functions and associated microdomains | Q28284176 | ||
Developmental regulation of the laminin alpha5 chain suggests a role in epithelial and endothelial cell maturation | Q28505309 | ||
SRC binding to the cytoskeleton, triggered by growth cone attachment to laminin, is protein tyrosine phosphatase-dependent | Q28578043 | ||
Characterization of mice lacking the tetraspanin superfamily member CD151 | Q28587010 | ||
Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival | Q28592841 | ||
Angiogenesis in life, disease and medicine | Q29614539 | ||
Endothelial/pericyte interactions | Q29619802 | ||
Tumorigenesis and the angiogenic switch | Q29619849 | ||
Basement membranes: structure, assembly and role in tumour angiogenesis | Q29622882 | ||
A critical role for tetraspanin CD151 in alpha3beta1 and alpha6beta4 integrin-dependent tumor cell functions on laminin-5 | Q30477393 | ||
Tetraspanin CD151 regulates alpha6beta1 integrin adhesion strengthening | Q30478308 | ||
Mapping of tetraspanin-enriched microdomains that can function as gateways for HIV-1. | Q30480407 | ||
Integrin signaling via the PI3-kinase-Akt pathway increases neuronal resistance to glutamate-induced apoptosis | Q32134580 | ||
Angiogenesis and vasculogenesis are impaired in the precocious-aging klotho mouse | Q33205670 | ||
The HMG-CoA reductase inhibitor simvastatin activates the protein kinase Akt and promotes angiogenesis in normocholesterolemic animals | Q33688733 | ||
Potentiation of the ligand-binding activity of integrin alpha3beta1 via association with tetraspanin CD151 | Q33837431 | ||
Laminin isoforms in tumor invasion, angiogenesis and metastasis | Q34706652 | ||
Role of Akt signaling in vascular homeostasis and angiogenesis | Q34712853 | ||
Platelets and cancer | Q34762260 | ||
A reevaluation of integrins as regulators of angiogenesis | Q34805783 | ||
Tetraspanin Proteins Mediate Cellular Penetration, Invasion, and Fusion Events and Define a Novel Type of Membrane Microdomain | Q35564822 | ||
Heterogeneity of Endothelial Cells from Different Organ Sites in T-Cell Subset Recruitment | Q35749118 | ||
Angiogenesis and signal transduction in endothelial cells | Q35874931 | ||
Integrins and angiogenesis | Q35962963 | ||
Expression and function of laminins in the embryonic and mature vasculature. | Q36178995 | ||
Angiogenesis: update 2005. | Q36230890 | ||
Rho, Rac, Pak and angiogenesis: old roles and newly identified responsibilities in endothelial cells | Q36255483 | ||
A Rac switch regulates random versus directionally persistent cell migration | Q36320639 | ||
Endothelial extracellular matrix: biosynthesis, remodeling, and functions during vascular morphogenesis and neovessel stabilization | Q36321628 | ||
Palmitoylation supports assembly and function of integrin-tetraspanin complexes | Q36322840 | ||
Integrins and angiogenesis: a sticky business | Q36330257 | ||
Cloning of the Mouse Laminin α4 cDNA. Expression in a Subset of Endothelium | Q36870573 | ||
Dose-dependent response of FGF-2 for lymphangiogenesis | Q37415307 | ||
Between molecules and morphology. Extracellular matrix and creation of vascular form. | Q40421562 | ||
Role of extracellular matrix in regulation of staurosporine-induced apoptosis in breast cancer cells. | Q40448713 | ||
Integrin engagement differentially modulates epithelial cell motility by RhoA/ROCK and PAK1. | Q40478610 | ||
Alpha 3 beta 1 integrin promotes keratinocyte cell survival through activation of a MEK/ERK signaling pathway | Q40530851 | ||
Specific interactions among transmembrane 4 superfamily (TM4SF) proteins and phosphoinositide 4-kinase | Q40847493 | ||
Regulation of endothelial cell motility by complexes of tetraspan molecules CD81/TAPA-1 and CD151/PETA-3 with alpha3 beta1 integrin localized at endothelial lateral junctions | Q41035046 | ||
p38 MAPK is a critical regulator of the constitutive and the beta4 integrin-regulated expression of IL-6 in human normal thymic epithelial cells. | Q42451854 | ||
Function of alpha3beta1-tetraspanin protein complexes in tumor cell invasion. Evidence for the role of the complexes in production of matrix metalloproteinase 2 (MMP-2). | Q42870963 | ||
Transmembrane-4 superfamily proteins associate with activated protein kinase C (PKC) and link PKC to specific beta(1) integrins | Q43590665 | ||
NSAIDs inhibit alpha V beta 3 integrin-mediated and Cdc42/Rac-dependent endothelial-cell spreading, migration and angiogenesis. | Q43726776 | ||
Association of the tetraspanin CD151 with the laminin-binding integrins alpha3beta1, alpha6beta1, alpha6beta4 and alpha7beta1 in cells in culture and in vivo | Q43909564 | ||
Retinal vascular development is mediated by endothelial filopodia, a preexisting astrocytic template and specific R-cadherin adhesion. | Q44198738 | ||
Angiogenesis in collagen I requires alpha2beta1 ligation of a GFP*GER sequence and possibly p38 MAPK activation and focal adhesion disassembly | Q44467145 | ||
Antiangiogenic and antitumor efficacy of EphA2 receptor antagonist | Q44761792 | ||
Matrix-specific activation of Src and Rho initiates capillary morphogenesis of endothelial cells | Q44788587 | ||
The tetraspanin superfamily member CD151 regulates outside-in integrin alphaIIbbeta3 signaling and platelet function. | Q44958582 | ||
Differential expression of pro- and antiangiogenic factors in mouse strain-dependent hypoxia-induced retinal neovascularization | Q46459264 | ||
The integrin alpha6beta1 modulation of PI3K and Cdc42 activities induces dynamic filopodium formation in human platelets | Q46756082 | ||
Regulation of skin microvasculature angiogenesis, cell migration, and permeability by a specific inhibitor of PKCalpha | Q46865497 | ||
Deletion of laminin-8 results in increased tumor neovascularization and metastasis in mice. | Q47324578 | ||
Laminin-1 promotes angiogenesis in synergy with fibroblast growth factor by distinct regulation of the gene and protein expression profile in endothelial cells. | Q47880744 | ||
The mouse aorta model: influence of genetic background and aging on bFGF- and VEGF-induced angiogenic sprouting | Q47889556 | ||
Tensional forces in fibrillar extracellular matrices control directional capillary sprouting. | Q48749055 | ||
CD151, the first member of the tetraspanin (TM4) superfamily detected on erythrocytes, is essential for the correct assembly of human basement membranes in kidney and skin | Q50335739 | ||
Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice. | Q52200996 | ||
MT1-MMP expression promotes tumor growth and angiogenesis through an up-regulation of vascular endothelial growth factor expression. | Q53876521 | ||
Integrin β4 signaling promotes tumor angiogenesis | Q57359862 | ||
Enhanced pathological angiogenesis in mice lacking β3 integrin or β3 and β5 integrins | Q61631829 | ||
Protein kinase C and downstream signaling pathways in a three-dimensional model of phorbol ester-induced angiogenesis | Q61815743 | ||
The Cdc42 and Rac1 GTPases are required for capillary lumen formation in three-dimensional extracellular matrices | Q64379046 | ||
A model of angiogenesis in the mouse cornea | Q71174063 | ||
Alpha 3 beta 1 integrin has a crucial role in kidney and lung organogenesis | Q71849956 | ||
Regulation of endothelial cell morphogenesis by integrins, mechanical forces, and matrix guidance pathways | Q72390027 | ||
Clinical significance of CD151 gene expression in non-small cell lung cancer | Q77372883 | ||
PKCalpha activates eNOS and increases arterial blood flow in vivo | Q81009178 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | angiogenesis | Q539568 |
P304 | page(s) | 1524-1532 | |
P577 | publication date | 2006-10-05 | |
P1433 | published in | Blood | Q885070 |
P1476 | title | Deletion of tetraspanin Cd151 results in decreased pathologic angiogenesis in vivo and in vitro | |
P478 | volume | 109 |