Evidence map›Paper›PMID 42334536›Full record

ReviewAdvances in experimental medicine and biology2026

Structural Insights into Ordered Multicomponent Assemblies in Cell Junctions.

Oliver James Harrison, Priyanka Mathews, Julia Brasch

Abstract readReview
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In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Oliver James HarrisonDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID https://orcid.org/0000-0002-6443-7645
Priyanka MathewsDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA.ORCID https://orcid.org/0009-0007-1915-5650
Julia BraschDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA. julia.brasch@biochem.utah.edu.ORCID https://orcid.org/0000-0002-1831-6244

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell junctions are essential structures of metazoan tissues that maintain cohesion and integrity and permit coordinated tissue rearrangements in development. Vertebrate junctions include stable structures, like adherens junctions, desmosomes, and focal adhesions, and transient, ultrastructurally less-defined complexes that mediate recognition and signaling. All are mediated by assemblies of cell adhesion and recognition proteins at the cell surface and cytoplasmic proteins that mediate signaling or linkage to the cytoskeleton. These multiple components must organize together to form large functional intercellular structures. Structural methods have provided deep insights into how these large structures assemble and revealed roles for intrinsic propensities of adhesion and recognition protein ectodomains to form ordered assemblies on membranes, often mirrored by their intracellular components. In this chapter, we discuss the structural and molecular principles underlying the assembly and organization of these large complexes and focus in detail on three important cadherin-mediated junctions: adherens junctions, desmosomes, and neuronal self-recognition complexes formed by clustered protocadherins. These examples highlight the highly specific and organized arrangements that contribute to junction assembly and how these mechanisms are closely tuned to the biological roles of specific junctions.

Indexed as

Adherens JunctionsCadherinsDesmosomesIntercellular JunctionsAnimalsCell AdhesionHumansSignal TransductionCadherinsAdherens junctionCadherinCell adhesionCell junctionClustered protocadherinCryo-EMCryo-ETDelta protocadherinDesmosomeMembrane assemblyProtein assemblyProtein interactionStructural biologyStructureX-ray crystallography

Identifiers

PMID42334536

What OpenQuestion holds

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Registered trials

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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.