Evidence map›Paper›PMID 32748522›Full record

ReviewWIREs mechanisms of disease2021

Single-cell proteomic analysis.

Thai Pham, Ankush Tyagi, Yu-Sheng Wang, Jia Guo

Open access · greenAbstract readReview
In one paragraph

Review in WIREs mechanisms of disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Emerging technologies in the spatial proteomics landscape.Analytical and bioanalytical chemistry · 2026
    Review
  2. Review
  3. Review
  4. Single-cell spatial proteomics.Histology and histopathology · 2025
    Review
  5. Article
  6. Uncovering biology by single-cell proteomics.Communications biology · 2023
    Review
  7. Robotic data acquisition with deep learning enables cell image-based prediction of transcriptomic phenotypes.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Multiplexed Single-Cell in Situ Protein Profiling.ACS measurement science au · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Multiplexed Single-CellFrontiers in molecular biosciences · 2021
    Review
  13. Article
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

4 authors at 1 institution in 1 country.

Thai PhamBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, Arizona, USA.
Ankush TyagiBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, Arizona, USA.
Yu-Sheng WangBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, Arizona, USA.
Jia GuoBiodesign Institute & School of Molecular Sciences, Arizona State University, Tempe, Arizona, USA.ORCID 0000-0001-8036-5349
Arizona State University · US

Funding

Novel in situ proteomics methods to classify cell types in Alzheimer’s brains - Administrative SupplementR01GM127633 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI GUO, JIA · 2018 to 2022
$1.8M
Imaging Functionally Distinct Eosinophil Subtypes Within Tissue Biopsies Using Gene Expression Profiling and an In Situ Hybridization Approach based on a Concurrent Multiple RNA Targeting StrategyR21AI132840 · NIAID · MAYO CLINIC ARIZONA · PI JACOBSEN, ELIZABETH A · 2018 to 2019
$463k
NIAID NIH HHS R21 AI132840NIGMS NIH HHS R01 GM127633
6 · The paper itself

Abstract

The ability to comprehensively profile proteins in every individual cell of complex biological systems is crucial to advance our understanding of normal physiology and disease pathogenesis. Conventional bulk cell experiments mask the cell heterogeneity in the population, while the single-cell imaging methods suffer from the limited multiplexing capacities. Recent advances in microchip-, mass spectrometry-, and reiterative staining-based technologies have enabled comprehensive protein profiling in single cells. These approaches will bring new insights into a variety of biological and biomedical fields, such as signaling network regulation, cell heterogeneity, tissue architecture, disease diagnosis, and treatment monitoring. In this article, we will review the recent advances in the development of single-cell proteomic technologies, describe their advantages, discuss the current limitations and challenges, and propose potential solutions. We will also highlight the wide applications of these technologies in biology and medicine. This article is categorized under: Cancer > Molecular and Cellular Physiology.

Indexed as

NeoplasmsProteomicsHumansMass SpectrometryProteinsSingle-Cell AnalysisProteinsimagingmass spectrometrymicrochipsystems biology

Identifiers

PMID32748522
PMCPMC7980505
OpenAlexW3047246440

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.