Evidence map›Paper›PMID 39930241›Full record

ReviewAdvances in experimental medicine and biology2025

Critical Roles of SEA Domains.

Ezequiel M Salido

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2025. 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

1 author.

Ezequiel M SalidoDepartment of Biochemistry and Molecular Medicine, Ophthalmology and Visual Sciences, West Virginia University, Morgantown, WV, USA. ezequiel.salido@hsc.wvu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This mini-review delves into the multifaceted roles of SEA (sea urchin sperm protein, enterokinase, and agrin) domains, ubiquitous protein modules critical to the structure, and function of a wide range of membrane-associated and secreted proteins in organisms from yeast to humans. We explore the structural and functional characteristics of SEA domains based on their two types of fundamental characteristics: proteolytic and non-proteolytic SEA domains. We also examine the significance of SEA domains in different protein families, particularly in mucins and extracellular matrix proteins, emphasizing their roles in glycosylation, cell adhesion, and signal transduction. The review also highlights the crucial impact of SEA domains in health and disease contexts, with a focus on their implications in cancer progression and retinal health. Mutations within these domains are linked to a range of pathologies, including various cancers and congenital disorders, underscoring their clinical importance. Through this review, we aim to provide a deeper understanding of SEA domains, shedding light on their diverse biological functions and their potential as targets for therapeutic interventions in diseases where they play a pivotal role.

Indexed as

Protein DomainsAnimalsExtracellular Matrix ProteinsGlycosylationHumansMucinsNeoplasmsSignal TransductionExtracellular Matrix ProteinsMucinsExtracellular matrixIMPG1IMPG2Interphotoreceptor matrixProteoglycanProteolysisSEA domain

Identifiers

What OpenQuestion holds

Textmetadata
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.