Evidence map›Paper›PMID 23979929›Full record

ArticleG3 (Bethesda, Md.)2013

Characterization of two ENU-induced mutations affecting mouse skeletal morphology.

Shauna M Dauphinee, Megan M Eva, Kyoko E Yuki, Melissa Herman, Silvia M Vidal, Danielle Malo

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

6 citing papers in PubMed, 12 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

6 authors at 1 institution in 1 country.

Shauna M DauphineeDepartment of Human Genetics, McGill University, Montreal, Quebec H3G 0B1, Canada.
Megan M Eva
Kyoko E Yuki
Melissa Herman
Silvia M Vidal
Danielle Malo
McGill University · CA

Funding

CIHR 87520-1
6 · The paper itself

Abstract

Using the N-ethyl-N-nitrosourea (ENU) mutagenesis screen, we have identified two skeletal morphology mutants, Skm1 and Skm2. Positional cloning and candidate gene sequencing localized the causative point mutations within the genes coding for natriuretic peptide receptor C (NPR-C) and filamin b (FLNB), respectively. Mice that carry a mutation in Npr3 exhibit a skeletal overgrowth phenotype, resulting in an elongated body and kyphosis. Skm2 mice, carrying a mutation in Flnb, present with scoliosis and lordosis. These mutant mice will serve as useful models for the study of vertebral malformations.

Indexed as

Mutation, MissenseAmino Acid SequenceAnimalsBone and BonesEthylnitrosoureaFilaminsMiceMolecular Sequence DataMutagensReceptors, Atrial Natriuretic FactorSpinal Curvaturesatrial natriuretic factor receptor CEthylnitrosoureaFilaminsMutagensReceptors, Atrial Natriuretic Factor

Identifiers

PMID23979929
PMCPMC3789799
OpenAlexW2147359903

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.