Evidence map›Paper›PMID 28061846›Full record

ReviewJournal of biomedical science2017

MAP4K4 and IL-6

Huai-Chia Chuang, Tse-Hua Tan

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of biomedical science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. MAP4K3/GLK in autoimmune disease, cancer and aging.Journal of biomedical science · 2019
    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

2 authors at 1 institution in 1 country.

Huai-Chia ChuangImmunology Research Center, National Health Research Institutes, 35 Keyan Road, Zhunan, 35053, Taiwan.
Tse-Hua TanImmunology Research Center, National Health Research Institutes, 35 Keyan Road, Zhunan, 35053, Taiwan. ttan@nhri.org.tw.
National Health Research Institutes · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is a causal factor of type 2 diabetes (T2D); however, people without obesity (including lean, normal weight, or overweight) may still develop T2D. Non-obese T2D is prevalent in Asia and also frequently occurs in Europe. Recently, multiple evidences oppose the notion that either obesity or central obesity (visceral fat accumulation) promotes non-obese T2D. Several factors such as inflammation and environmental factors contribute to non-obese T2D. According to the data derived from gene knockout mice and T2D clinical samples in Asia and Europe, the pathogenesis of non-obese T2D has been unveiled recently. MAP4K4 downregulation in T cells results in enhancement of the IL-6

Indexed as

Interleukin-6Intracellular Signaling Peptides and ProteinsPolymorphism, Single NucleotideProtein Serine-Threonine KinasesAnimalsAsiaDiabetes Mellitus, Type 2Epigenesis, GeneticEuropeHumansMiceMice, KnockoutTh17 CellsIL6 protein, humanInterleukin-6Intracellular Signaling Peptides and ProteinsMAP4K4 protein, humanProtein Serine-Threonine KinasesLean type 2 diabetesMAP4K4Non-obese type 2 diabetesNormal-weight type 2 diabetesTh17 cellsType 2 diabetesVisceral fat accumulation

Identifiers

PMID28061846
PMCPMC5219747
OpenAlexW2571045402

What OpenQuestion 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 OpenQuestion graph.