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

ELL associated factor 2

U19, Eaf2, FESTA
Top mentioned proteins: CAN, MEN, AGE, HAD, V1a
Papers on U19
The Effect of Body Mass on Eccentric Knee Flexor Strength Assessed With an Instrumented Nordic Hamstring Device (Nordbord) in Football Players.
Poulos et al., Saint-Germain-en-Laye, France. In Int J Sports Physiol Perform, Jan 2016
METHODS: Data from 81 soccer players (U17, U19, U21, senior 4th French division and professionals) and 41 Australian Football League (AFL) players were used for analysis.
The reliability, validity and sensitivity of a novel soccer-specific reactive repeated-sprint test (RRST).
Bradley et al., Leeds, United Kingdom. In Eur J Appl Physiol, Dec 2015
RESULTS: Test-retest coefficient of variation in elite U16 and sub-elite U19 players was 0.71 and 0.84 %, respectively.
ELL Protein-associated Factor 2 (EAF2) Inhibits Transforming Growth Factor β Signaling through a Direct Interaction with Smad3.
Xiao et al., Wuhan, China. In J Biol Chem, Nov 2015
A series of in vitro and in vivo studies has shown that EAF2 can affect multiple signaling pathways involved in cellular processes.
Use of the RSA/RCOD Index to Identify Training Priority in Soccer Players.
Ngo et al., Hong Kong, Hong Kong. In J Strength Cond Res, Oct 2015
To compare the RSA/RCOD index among different age groups, RSA and RCOD were measured from 20 under-16 players (U16), 20 under-19 players (U19), and 17 first-team professional players (PRO) from a football (soccer) club that has regular participation in the UEFA Champions League.
Perceptual Learning on Simultaneity and Temporal Order Judgments.
Achtman et al., In J Vis, Oct 2015
INTRODUCTION: Prior research on bilateral-stream Rapid Serial Visual Presentation (RSVP) displays reveals that participants often perceive left visual field (LVF) targets significantly sooner than right visual field (RVF) targets (Matthews, Welch, Festa & Clement, 2013).
FOXA1 modulates EAF2 regulation of AR transcriptional activity, cell proliferation, and migration in prostate cancer cells.
Wang et al., Shanghai, China. In Prostate, Jul 2015
BACKGROUND: ELL-associated factor 2 (EAF2) is an androgen-regulated tumor suppressor in the prostate.
The Yo-Yo intermittent recovery test level 1 is reliable in young high-level soccer players.
Vaeyens et al., Gent, Belgium. In Biol Sport, Mar 2015
Players were divided into three age groups (U15, U17 and U19) and completed three YYIR1 in three consecutive weeks.
Typical weekly workload of under 15, under 17, and under 19 elite Portuguese football players.
Sampaio et al., Vila Real, Portugal. In J Sports Sci, 2014
This study aims to describe the time-motion and physiological performance profiles of footballers whose ages are under 15 (U15), under 17 (U17), and under 19 (U19) during a typical week of a competitive season.
FOXP1 directly represses transcription of proapoptotic genes and cooperates with NF-κB to promote survival of human B cells.
Spaargaren et al., Amsterdam, Netherlands. In Blood, 2014
Low expression of these genes, encoding the BH3-only proteins BIK and Harakiri, the p53-regulatory proteins TP63, RASSF6, and TP53INP1, and AIM2 and EAF2, is associated with poor survival in DLBCL patients.
Effects of shock-absorbing insoles during transition from natural grass to artificial turf in young soccer players: a randomized controlled trial.
Madeleine et al., In J Am Podiatr Med Assoc, 2014
METHODS: In a prospective randomized controlled study, 75 players were included from the youth teams of U15, U17, and U19.
Serious neck injuries in U19 rugby union players: an audit of admissions to spinal injury units in Great Britain and Ireland.
Hutchison et al., Perth, United Kingdom. In Br J Sports Med, 2012
OBJECTIVES: To obtain data regarding admissions of U19 rugby players to spinal injury units in Great Britain and Ireland and to compare this with a recent peak in presentation in Scotland.
Niche crosstalk: intercellular signals at the hair follicle.
Christiano et al., Durham, United Kingdom. In Cell, 2011
A recent series of papers, including Festa et al. (2011) in this issue, has revealed unexpected interdependent relationships among cell populations residing in and around the hair follicle.
EAF2 loss enhances angiogenic effects of Von Hippel-Lindau heterozygosity on the murine liver and prostate.
Wang et al., Pittsburgh, United States. In Angiogenesis, 2011
cooperation of VHL and EAF2 may be critical for angiogenic regulation of the liver and prostate, and concurrent loss of these two tumor suppressors may result in a pro-angiogenic phenotype.
NCI60 cancer cell line panel data and RNAi analysis help identify EAF2 as a modulator of simvastatin and lovastatin response in HCT-116 cells.
Tuzmen et al., Toronto, Canada. In Plos One, 2010
the role of the EAF2 in response to simvastatin and lovastatin in HCT-116 colon cancer cells
Inhibition of 5alpha-reductase enhances testosterone-induced expression of U19/Eaf2 tumor suppressor during the regrowth of LNCaP xenograft tumor in nude mice.
Wang et al., Pittsburgh, United States. In Prostate, 2010
Inhibition of 5alpha-reductase during prostatic tumor regrowth enhances the expression of U19/Eaf2, an androgen-regulated tumor suppressor.
Tumor suppressor U19/EAF2 regulates thrombospondin-1 expression via p53.
Wang et al., Pittsburgh, United States. In Oncogene, 2010
Data show that the expression of TSP-1 is down-regulated in the prostate and liver of U19/EAF2 knockout mouse.
Negative feedback regulation of Wnt4 signaling by EAF1 and EAF2/U19.
Xiao et al., Wuhan, China. In Plos One, 2009
Findings provide the first convincing line of evidence that EAF and Wnt4 form an auto-regulatory negative feedback loop in vivo.
Elder mistreatment.
Fulmer, New York City, United States. In Annu Rev Nurs Res, 2001
Neglect, as a subcategory of EM, accounts for the majority of cases (Fulmer, Paveza, Abraham, & Fairchild, 2000; Pavlik, Hyman, Festa, & Bitondo Dyer, 2001; Fulmer & Gurland, 1996).
Nuclear snRNA and nuclear function (discovery of 5' cap structures in RNA).
Ro-Choi, Houston, United States. In Crit Rev Eukaryot Gene Expr, 1998
They have crucial roles in gene expression, such as transcription (U3 snoRNA), processing (U3, U8, U13, U14, U22, and 7-2/MRP), methylation (U14-16, U18, U20-21, and U24-63), pseudouridylation (E2, E3, U19, U23, and U64-72), and hnRNA splicing (U1, U2, U4, U5, and U6 snRNA).
Generation and regulation of developing immortalized neural cell lines.
Mehler et al., New York City, United States. In Methods, 1998
murine hippocampal and cerebellar cells using temperature-sensitive alleles (A58/U19) of the simian virus (SV) 40 large tumor (T) antigen.
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