Evidence map›Paper›PMID 35487100›Full record

ReviewCurrent opinion in chemical biology2022

Small-molecule discovery in the pancreatic beta cell.

Bridget K Wagner

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. The Omnipresence of DYRK1A in Human Diseases.International journal of molecular sciences · 2022
    Review
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 at 1 institution in 1 country.

Bridget K WagnerChemical Biology and Therapeutics Science Program, Broad Institute, Cambridge, MA 02142, USA. Electronic address: bwagner@broadinstitute.org.
Broad Institute · US

Funding

One-compound, one-islet: A high-throughput platform for small-molecule discoveryU01DK123717 · NIDDK · BROAD INSTITUTE, INC. · PI KULKARNI, ROHIT N., WAGNER, BRIDGET K · 2019 to 2022
$3.1M
Interrogating the ubiquitin pathway to understand and treat cytokine-induced beta-cell death in type 1 diabetesR01DK129464 · NIDDK · BROAD INSTITUTE, INC. · PI CHOUDHARY, AMIT, KULKARNI, ROHIT N. · 2021 to 2024
$2.1M
NIDDK NIH HHS R01 DK129464NIDDK NIH HHS U01 DK123717
6 · The paper itself

Abstract

The pancreatic beta cell is the only cell type in the body responsible for insulin secretion, and thus plays a unique role in the control of glucose homeostasis. The loss of beta-cell mass and function plays an important role in both type 1 and type 2 diabetes. Thus, using chemical biology to identify small molecules targeting the beta cell could be an important component to developing future therapeutics for diabetes. This strategy provides an attractive path toward increasing beta-cell numbers in vivo. A regenerative strategy involves enhancing proliferation, differentiation, or neogenesis. On the other hand, protecting beta cells from cell death, or improving maturity and function, could preserve beta-cell mass. Here, we discuss the current state of chemical matter available to study beta-cell regeneration, and how they were discovered.

Indexed as

Diabetes Mellitus, Type 2Insulin-Secreting CellsCell DifferentiationHumans

Identifiers

PMID35487100
PMCPMC9188675
OpenAlexW4224924595

What Socratic 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 Socratic graph.