Evidence map›Paper›PMID 42190811›Full record

ReviewThe Journal of biological chemistry2026

Liprin-α family proteins and their cellular functions.

Abigail Mayer, Yang Zhang, Houhui Xia

Abstract readReview
In one paragraph

Review in The Journal of biological chemistry, 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.

Abigail MayerNeuroscience Graduate Program, Department of Neuroscience, University of Rochester Medical Center, Rochester, New York, USA. Electronic address: Abigail_Mayer8@outlook.com.
Yang ZhangDepartment of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York, USA.
Houhui XiaNeuroscience Graduate Program, Department of Neuroscience, University of Rochester Medical Center, Rochester, New York, USA; Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York, USA. Electronic address: Houhui_xia@urmc.rochester.edu.

Funding

Protein phosphatase 1 isoforms, human de novo mutations and synaptic functionsR01MH128279 · NIMH · UNIVERSITY OF ROCHESTER · PI HOUHUI XIA · 2023 to 2026
$2.3M
NIMH NIH HHS R01 MH128279
6 · The paper itself

Abstract

Scaffold proteins are critical for the spatial organization and assembly of subcellular compartments through interactions with specific binding partners. The liprin-α family of scaffold proteins are implicated in diverse cellular functions across both neuronal and non-neuronal cell types. All four liprin-α isoforms contribute to presynaptic active zone formation, promoting synaptic vesicle accumulation and neurotransmitter release. Additionally, there is evidence that liprin-α plays a role in postsynaptic cellular processes such as dendritic growth, spinogenesis, and AMPA receptor trafficking. Due to ubiquitous expression, liprin-α1 regulates cell adhesion and motility. This review summarizes liprin-α functions, emphasizing its interactors and associated signaling pathways. Liprin-α proteins participate in multivalent interactions and undergo liquid-liquid phase separation, a mechanism postulated to promote the formation of membrane-less compartments. This review further examines regulatory mechanisms that govern liprin-α function and phase separation.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsHumansPhase SeparationSignal TransductionAdaptor Proteins, Signal TransducingPPFIA1 protein, humanactive zonecell signalingfocal adhesionliprin-αliquid-liquid phase separationPhosphorylationprotein-protein interactionscaffolding proteinSynapsesynaptic transmission

Identifiers

PMID42190811
PMCPMC13311821

What OpenQuestion holds

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LicenceCC BY
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.