Evidence map›Paper›PMID 29651291›Full record

ReviewFrontiers in immunology2018

Cutting an NKG2D Ligand Short: Cellular Processing of the Peculiar Human NKG2D Ligand ULBP4.

Tobias Zöller, Mareike Wittenbrink, Meike Hoffmeister, Alexander Steinle

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-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

14 citing papers in PubMed, 23 citations in OpenAlex.

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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.

Tobias ZöllerInstitute for Molecular Medicine, Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
Mareike WittenbrinkInstitute for Molecular Medicine, Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
Meike HoffmeisterInstitute of Biochemistry II, Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
Alexander SteinleInstitute for Molecular Medicine, Goethe University Frankfurt am Main, Frankfurt am Main, Germany.
Goethe University Frankfurt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stress-induced cell surface expression of MHC class I-related glycoproteins of the MIC and ULBP families allows for immune recognition of dangerous "self cells" by human cytotoxic lymphocytes

Indexed as

AutoantigensCarrier ProteinsCytotoxicity, ImmunologicHistocompatibility Antigens Class IHumansImmune EvasionLymphocytesMembrane ProteinsNK Cell Lectin-Like Receptor Subfamily KOrgan SpecificityProtein Processing, Post-TranslationalVirus DiseasesAutoantigensCarrier ProteinsHistocompatibility Antigens Class IMembrane ProteinsMHC class I-related chain AMICB antigenNK Cell Lectin-Like Receptor Subfamily KRAET1E protein, humanantibodiesNK cellsNKG2DsheddingULBP4

Identifiers

PMID29651291
PMCPMC5884875
OpenAlexW2795059696

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.