Evidence map›Paper›PMID 25082861›Full record

ArticleBlood2014

Errant innate immune signaling in del(5q) MDS.

Daniel T Starczynowski

Abstract readComment
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Daniel T StarczynowskiCINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER.
Cincinnati Children's Hospital Medical Center · US

Funding

Identification and characterization of genes in del(5q) myelodysplastic syndromeR01HL111103 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI STARCZYNOWSKI, DANIEL · 2012 to 2016
$1.9M
Molecular Pathogenesis of MDSR01DK102759 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI STARCZYNOWSKI, DANIEL · 2014 to 2016
$701k
NHLBI NIH HHS R01 HL111103NIDDK NIH HHS R01 DK102759
6 · The paper itself

Abstract

In this issue of Blood, Keerthivasan et al have identified that the deletion of mDia1, a chromosome 5q gene, contributes to myelodysplastic syndromes (MDSs) by increasing innate immune signaling in granulocytes.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 5Gene Expression RegulationHeterozygoteImmunity, InnateAdaptor Proteins, Signal TransducingAnimalsCarrier ProteinsFemaleForminsGranulocytesHumansLipopolysaccharide ReceptorsMaleMyelodysplastic SyndromesAdaptor Proteins, Signal TransducingCarrier ProteinsDiap1 protein, mouseDIAPH1 protein, humanForminsLipopolysaccharide Receptors

Identifiers

PMID25082861
PMCPMC4118479
OpenAlexW2057124376

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.