Evidence map›Paper›PMID 18650496›Full record

ReviewJournal of cell science2008

Paxillin comes of age.

Nicholas O Deakin, Christopher E Turner

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of cell science, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 309 papers.

0numbers the graph read from it
0cells of the map it votes in
309citing papers in PubMed
11.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

309 citing papers in PubMed, 487 citations in OpenAlex.

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249 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Nicholas O DeakinDepartment of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA.
Christopher E Turner
SUNY Upstate Medical University · US

Funding

STRUCTURE AND FUNCTION OF PAXILLINR01GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1996 to 2017
$5.5M
ILK-Actopaxin Interactions in Cell SignalingR01HL070244 · NHLBI · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 2002 to 2010
$3.0M
STRUCTURE AND FUNCTION OF PAXILLINR29GM047607 · NIGMS · UPSTATE MEDICAL UNIVERSITY · PI TURNER, CHRISTOPHER E · 1991 to 1995
–
NHLBI NIH HHS HL070244NHLBI NIH HHS R01 HL070244NIGMS NIH HHS GM47607NIGMS NIH HHS R01 GM047607
6 · The paper itself

Abstract

Paxillin is a multi-domain scaffold protein that localizes to the intracellular surface of sites of cell adhesion to the extracellular matrix. Through the interactions of its multiple protein-binding modules, many of which are regulated by phosphorylation, paxillin serves as a platform for the recruitment of numerous regulatory and structural proteins that together control the dynamic changes in cell adhesion, cytoskeletal reorganization and gene expression that are necessary for cell migration and survival. In particular, paxillin plays a central role in coordinating the spatial and temporal action of the Rho family of small GTPases, which regulate the actin cytoskeleton, by recruiting an array of GTPase activator, suppressor and effector proteins to cell adhesions. When paxillin was first described 18 years ago, the amazing complexity of cell-adhesion organization, dynamics and signaling was yet to be realized. Herein we highlight our current understanding of how the multiple protein interactions of paxillin contribute to the coordination of cell-adhesion function.

Indexed as

AnimalsCell AdhesionCell MovementCell SurvivalCytoskeletonHumansModels, BiologicalPaxillinPhosphorylationrho GTP-Binding ProteinsPaxillinrho GTP-Binding Proteins

Identifiers

PMID18650496
PMCPMC2522309
OpenAlexW2108770100

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.