Evidence map›Paper›PMID 25861030›Full record

ArticleInfection2015

A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease.

Rumi Taniguchi, Shin Koyano, Tatsuo Suzutani, Keiji Goishi, Yushi Ito, Ichiro Morioka, Hiroyuki Nakamura, Hideto Yamada, Akira Oka, Naoki Inoue

Abstract read
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In one paragraph

Article in Infection, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Frontiers in cellular and infection microbiology · 2017
    Article
  6. Article
  7. 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

10 authors at 6 institutions in 1 country.

Rumi TaniguchiDepartment of Virology I, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan.
Shin Koyano
Tatsuo Suzutani
Keiji Goishi
Yushi Ito
Ichiro Morioka
Hiroyuki Nakamura
Hideto Yamada
Akira Oka
Naoki Inoue
National Center For Child Health and Development · JPKobe University · JPNational Institute of Infectious Diseases · JPAsahikawa Medical University · JPFukushima Medical University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The potential risk factors for congenital cytomegalovirus (cCMV) infection or development of disease remain unclear. Here, we investigated the genetic polymorphisms in natural killer (NK) group 2, member D (NKG2D), an activating receptor expressed on NK cells, and in MHC class I-related chains A, the ligand of NKG2D, in 87 cCMV cases, and found that there was a significant association between cCMV disease and a single nucleotide polymorphism, Thr72Ala, in NKG2D.

Indexed as

Genetic Predisposition to DiseaseMutation, MissenseChildChild, PreschoolCytomegalovirus InfectionsFemaleHumansInfantInfant, NewbornMaleNK Cell Lectin-Like Receptor Subfamily KPolymorphism, Single NucleotideProspective StudiesKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily K

Identifiers

PMID25861030
OpenAlexW1993072278

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.