Evidence map›Paper›PMID 41590853›Full record

ReviewJournal of cardiovascular development and disease2026

Precision Profiling of the Cardiovascular Post-Translationally Modified Proteome.

Thakorn Pruktanakul, Konstantinos Theofilatos

Abstract readReview
In one paragraph

Review in Journal of cardiovascular development and disease, 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

2 authors.

Thakorn PruktanakulKing's British Heart Foundation Centre, King's College London, London SE5 9NU, UK.ORCID 0000-0003-2613-1271
Konstantinos TheofilatosKing's British Heart Foundation Centre, King's College London, London SE5 9NU, UK.ORCID 0000-0001-6799-0553

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins exist as multiple chemical and sequence-specific proteoforms, each of which may serve as a critical mediator of physiological or pathological signalling. This diversity arises from processes such as alternative splicing of gene transcripts, translation into amino acid sequences, and various post-translational modifications (PTMs), leading to an exponential increase in biological complexity. This manuscript provides an overview of the mechanisms underlying proteoform generation in biological systems and highlights strategies for their analysis using mass spectrometry (MS)-based proteomics and bioinformatics. Additionally, it focuses on recent findings linking PTMs to cardiovascular disease (CVD), highlighting the MS-based methods and workflows that have been used to study uncommon PTMs and their role in CVD. This review provides a comprehensive collection of tools and knowledge to explore the breadth of proteoforms, particularly PTMs, within their specific areas of interest in cardiovascular physiology.

Indexed as

bioinformaticscardiovascular diseasemass spectrometrypost-translational modificationsproteoformsproteomics

Identifiers

PMID41590853
PMCPMC12842255

What Socratic holds

Textmetadata
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 Socratic graph.