Evidence map›Paper›PMID 30237319›Full record

ArticleDisease models & mechanisms2018

Mice doubly deficient in

Masanori Takahashi, Masaru Tamura, Shigeru Sato, Kiyoshi Kawakami

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Disease models & mechanisms, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Ventral body wall closure: Mechanistic insights from mouse models and translation to human pathology.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
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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.

Masanori TakahashiDivision of Biology, Center for Molecular Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
Masaru TamuraTechnology and Development Team for Mouse Phenotype Analysis, RIKEN BioResource Center, 3-1-1, Koyadai, Tsukuba, Ibaraki, 305-0074, Japan.
Shigeru SatoDivision of Biology, Center for Molecular Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan.
Kiyoshi KawakamiDivision of Biology, Center for Molecular Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke, Tochigi, 329-0498, Japan kkawakam@jichi.ac.jp.ORCID 0000-0002-0058-4072

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Omphalocele is a human congenital anomaly in ventral body wall closure and may be caused by impaired formation of the primary abdominal wall (PAW) and/or defects in abdominal muscle development. Here, we report that mice doubly deficient in homeobox genes

Indexed as

Abdominal WallAnimalsCell ProliferationEmbryo, MammalianHernia, UmbilicalHomeodomain ProteinsHumansMesodermMice, Inbred C57BLMice, KnockoutModels, BiologicalMusclesStem CellsTrans-ActivatorsHomeodomain ProteinsSix4 protein, mouseSix5 protein, mouseTrans-ActivatorsCoelomic epithelial cellsMesotheliumMouseOmphalocelePrimary body wallSix4/Six5

Identifiers

PMID30237319
PMCPMC6215434

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.