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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

Ena-vasodilator stimulated phosphoprotein

Evl, Ena/VASP-like, Ena/VASP-like protein
Top mentioned proteins: VASP, Actin, V1a, Zyxin, alpha-actin
Papers on Evl
Estrogen and androgen regulate actin-remodeling and endocytosis-related genes during rat spermiation.
Balasinor et al., Mumbai, India. In Mol Cell Endocrinol, Apr 2015
This was accompanied by reduction in intratesticular testosterone levels and increase in intratesticular estrogen along with deregulation of genes involved in cytoskeleton remodeling (Arpc1b, Evl and Capg) and endocytosis (Picalm, Eea1 and Stx5a).
Identification of specific gene modules in mouse lung tissue exposed to cigarette smoke.
Meng et al., Tianjin, China. In Asian Pac J Cancer Prev, 2014
Seven hub genes were identified as well, including Fip1l1, Anp32a, Acsl4, Evl, Sdc1, Arap3 and Cd52.
Cardioprotective Effects of Quercetin in Cardiomyocyte under Ischemia/Reperfusion Injury.
Chan et al., Taiwan. In Evid Based Complement Alternat Med, 2012
Although 17 identified proteins were altered in H2O2-induced cells, these proteins such as alpha-soluble NSF attachment protein ( α -SNAP), Ena/VASP-like protein (Evl), and isopentenyl-diphosphate delta-isomerase 1 (Idi-1) were reverted by pretreatment with quercetin, which correlates with kinase activation, DNA repair, lipid, and protein metabolism.
Biochemical analysis of the human ENA/VASP-family proteins, MENA, VASP and EVL, in homologous recombination.
Kurumizaka et al., Tokyo, Japan. In J Biochem, 2011
ENA/VASP-family proteins are functionally redundant in homologous recombination, and MENA, VASP and EVL may be involved in the DSB repair pathway in humans
DNA microarray analysis of the epithelial-mesenchymal transition of mesothelial cells in a rat model of peritoneal dialysis.
Kusano et al., Tochigi, Japan. In Adv Perit Dial, 2010
A DNA microarray analysis revealed that the expression of 168 genes had increased by more than a factor of 4. The upregulated genes included those that code for extracellular matrix components (such as types III and lV collagen, among others), cell division cycle 42 (Cdc42), an enabled/vasodilator-stimulated phosphoprotein-like protein [Ena/VASP (Evl)], and actin-related protein 2/3 complex subunits (Arp2/3).
Single-stranded DNA catenation mediated by human EVL and a type I topoisomerase.
Kurumizaka et al., Tokyo, Japan. In Nucleic Acids Res, 2010
EVL, with either E. coli topoisomerase I or human topoisomerase IIIalpha, catalyzed ssDNA catenation.
ENA/VASP downregulation triggers cell death by impairing axonal maintenance in hippocampal neurons.
Ceriani et al., Buenos Aires, Argentina. In Mol Cell Neurosci, 2010
Altogether these observations demonstrate that ENA/VASP proteins are implicated in the establishment and maintenance of the axonal structure and that a change on their expression levels triggers neuronal degeneration.
Identification and expression analysis of splice variants of mouse enabled homologue during development and in adult tissues.
Ampe et al., Gent, Belgium. In Bmc Mol Biol, 2009
BACKGROUND: The Enabled/Vasodilator stimulated phosphoprotein (Ena/VASP) gene family comprises three genes in vertebrates: Vasp, Enabled homologue (Enah) and Ena-VASP like (Evl).
Biochemical analysis of the human EVL domains in homologous recombination.
Kurumizaka et al., Tokyo, Japan. In Febs J, 2009
EVH2 domain, which is highly conserved among the ENA/VASP family proteins, may be responsible for the recombination function of EVL.
Recombination activator function of the novel RAD51- and RAD51B-binding protein, human EVL.
Kurumizaka et al., Tokyo, Japan. In J Biol Chem, 2009
EVL protein is a novel recombination factor that may be required for repairing specific DNA lesions, and that may cause tumor malignancy by its inappropriate expression.
EVL (Ena/VASP-like) expression is up-regulated in human breast cancer and its relative expression level is correlated with clinical stages.
Cao et al., Shanghai, China. In Oncol Rep, 2008
EVL may be implicated in invasion and/or metastasis of human breast cancer.
Tes, a specific Mena interacting partner, breaks the rules for EVH1 binding.
Way et al., London, United Kingdom. In Mol Cell, 2008
Here we show that the LIM3 domain of Tes, which lacks the FPPPP motif, binds to the EVH1 domain of Mena, but not to those of VASP or Evl.
Miniature protein ligands for EVH1 domains: interplay between affinity, specificity, and cell motility.
Schepartz et al., New Haven, United States. In Biochemistry, 2007
The Ena/VASP family proteins-Mena, VASP, and Evl-are believed to control cell motility by serving as a direct link between signaling events and the actin cytoskeleton.
Regulation of otic vesicle and hair cell stereocilia morphogenesis by Ena/VASP-like (Evl) in Xenopus.
Miller et al., Minneapolis, United States. In J Cell Sci, 2007
Ena/VASP-like (Evl) is an actin binding protein involved in the regulation of cytoskeletal dynamics and organization.
Positional cloning, association analysis and expression studies provide convergent evidence that the cadherin gene FAT contains a bipolar disorder susceptibility allele.
Schofield et al., Sydney, Australia. In Mol Psychiatry, 2006
Expression of Fat, Catnb (beta-catenin), and the three genes (Enah, Evl and Vasp) encoding the Ena/VASP proteins, were investigated in mice following administration of the mood-stabilizing drugs, lithium and valproate.
Cloning and developmental expression of Xenopus Enabled (Xena).
Miller et al., Minneapolis, United States. In Dev Dyn, 2005
The vertebrate Ena/VASP family is composed of three genes: Ena (Enabled), VASP (Vasodilator Stimulated Phosphoprotein), and Evl (Ena/VASP-Like).
Molecular cloning and expression of Ena/Vasp-like (Evl) during Xenopus development.
Miller et al., Minneapolis, United States. In Gene Expr Patterns, 2005
3 alternatively spliced isoforms; transcripts for each isoform are 1st detectable at low levels at stage 18, show increased abundance by stage 23, & persist throughout the remainder of embryogenesis
Increased spreading, Rac/p21-activated kinase (PAK) activity, and compromised cell motility in cells deficient in vasodilator-stimulated phosphoprotein (VASP).
Simm et al., Würzburg, Germany. In J Biol Chem, 2002
Here, we report that VASP-deficient fibroblasts, despite normal mammalian Enabled (Mena) and Ena-VASP-like (Evl) expression levels, are highly spread.
The N-terminal domain of Homer/Vesl is a new class II EVH1 domain.
Heinz et al., Braunschweig, Germany. In J Mol Biol, 2001
Our functional data, substantiated by structural data, demonstrate that the ligand-binding of the Vesl EVH1 domain differs from the interaction characteristics of the previously examined EVH1 domains of the Evl/Mena proteins.
Mena, a relative of VASP and Drosophila Enabled, is implicated in the control of microfilament dynamics.
Soriano et al., Seattle, United States. In Cell, 1996
We have identified two murine proteins, Mena and Evl, that are highly related to Enabled as well as VASP (Vasodilator-Stimulated Phosphoprotein).
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