Evidence map›Paper›PMID 38353121›Full record

ArticleDisease models & mechanisms2024

Shared features in ear and kidney development - implications for oto-renal syndromes.

Scarlet Xiaoyan Wang, Andrea Streit

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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  4. Review
  5. 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

2 authors at 1 institution in 1 country.

Scarlet Xiaoyan WangCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK.
Andrea StreitCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK.ORCID 0000-0001-7664-7917
King's College London · GB

Funding

NIHR Biomedical Research Centre at Guy's and St Thomas' NHS Foundation Trust and King's College London IS-BRC-1215-20006
6 · The paper itself

Abstract

The association between ear and kidney anomalies has long been recognized. However, little is known about the underlying mechanisms. In the last two decades, embryonic development of the inner ear and kidney has been studied extensively. Here, we describe the developmental pathways shared between both organs with particular emphasis on the genes that regulate signalling cross talk and the specification of progenitor cells and specialised cell types. We relate this to the clinical features of oto-renal syndromes and explore links to developmental mechanisms.

Indexed as

Branchio-Oto-Renal SyndromeKidney DiseasesEmbryonic DevelopmentHumansKidneyOrganogenesisCongenital anomaliesEarEmbryo developmentKidneyOrganogenesis

Identifiers

PMID38353121
PMCPMC10886756
OpenAlexW4391824942

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.