Evidence map›Paper›PMID 24766605›Full record

ReviewCell communication & adhesion2014

N-cadherin/catenin complex as a master regulator of intercalated disc function.

Alexia Vite, Glenn L Radice

Erratum issuedAbstract readReview
In one paragraph

Review in Cell communication & adhesion, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
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

48 citing papers in PubMed.

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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

2 authors.

Alexia ViteDepartment of Medicine, Center for Translational Medicine, Thomas Jefferson University , Philadelphia, PA , USA.
Glenn L Radice

Funding

Role of the cytoskeleton in cardiac regenerationR21HL111788 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI RADICE, GLENN LAWRENCE · 2012 to 2013
$417k
N-cadherin and Metastatic DisseminationR21CA176097 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RADICE, GLENN LAWRENCE · 2014 to 2015
$371k
NCI NIH HHS CA176097NCI NIH HHS R21 CA176097NHLBI NIH HHS HL111788NHLBI NIH HHS R21 HL111788
6 · The paper itself

Abstract

Intercellular adhesive junctions are essential for maintaining the physical integrity of tissues; this is particularly true for the heart that is under constant mechanical load. The correct functionality of the heart is dependent on the electrical and mechanical coordination of its constituent cardiomyocytes. The intercalated disc (ID) structure located at the termini of the rod-shaped adult cardiomyocyte contains various junctional proteins responsible for the integration of structural information and cell-cell communication. According to the classical description, the ID consists of three distinct junctional complexes: adherens junction (AJ), desmosome (Des), and gap junction (GJ) that work together to mediate mechanical and electrical coupling of cardiomyocytes. However, recent morphological and molecular studies indicate that AJ and Des components are capable of mixing together resulting in a "hybrid adhering junction" or "area composita." This review summarizes recent progress in understanding the in vivo function(s) of AJ components in cardiac homeostasis and disease.

Indexed as

Adherens JunctionsAnimalsCadherinsCateninsHumansMyocytes, CardiacCadherinsCateninsadherens junctionarrhythmogenic cardiomyopathycatenindesmosomeN-cadherin

Identifiers

PMID24766605
PMCPMC6054126

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.