Evidence map›Paper›PMID 35156158›Full record

ReviewGlycoconjugate journal2022

Gangliosides in T cell development and function of mice.

Jin-Ichi Inokuchi, Masakazu Nagafuku

Abstract readReview
PubMed Publisher
In one paragraph

Review in Glycoconjugate journal, 2022. 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
0.2field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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 at 2 institutions in 2 countries.

Jin-Ichi InokuchiDivision of Glycopathology, Institute of Molecular Biomembrane and Glycobiology (IMBG), Tohoku Medical and Pharmaceutical University (TMPU), Tohoku, Japan. jin@tohoku-mpu.ac.jp.ORCID 0000-0002-0703-5746
Masakazu NagafukuDivision of Glycopathology, Institute of Molecular Biomembrane and Glycobiology (IMBG), Tohoku Medical and Pharmaceutical University (TMPU), Tohoku, Japan.
Collaborative Research Group · AUTohoku Medical and Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular diversity of glycosphingolipids (GSLs) that arouse during the course of evolution clearly plays an essential role in maintenance of biological homeostasis. Why is such a wide variety of GSLs necessary, and what gave rise to the expression mechanisms that are selective and specific to individual cells, tissues, or organs? What is the biological significance of these mechanisms? The same questions apply to GSLs involved in T cell development and activation. Primary CD4

Indexed as

CD8-Positive T-LymphocytesGangliosidesAnimalsCell DifferentiationGlycosphingolipidsLymphocyte ActivationMiceGangliosidesGlycosphingolipidsCD4 + T cellCD8 + T cellD-PDMPGangliosidesImmunological synapseLipid raftT cell receptor (TCR)

Identifiers

PMID35156158
OpenAlexW4212964035

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.