Evidence map›Paper›PMID 28600349›Full record

ArticleDisease models & mechanisms2017

A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen.

Ashlee J Conway, Fiona C Brown, Robert O Fullinfaw, Benjamin T Kile, Stephen M Jane, David J Curtis

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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  6. BALB.NCT-Molecular genetics and metabolism reports · 2023
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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 3 institutions in 1 country.

Ashlee J ConwayAustralian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia.
Fiona C BrownAustralian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia.
Robert O FullinfawPorphyria Reference Laboratory, Biochemistry Department, Royal Melbourne Hospital, Parkville 3050, Australia.
Benjamin T KileACRF Chemical Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville 3052, Australia.ORCID 0000-0002-8836-8947
Stephen M JaneAustralian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia.ORCID 0000-0003-2968-359X
David J CurtisAustralian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia david.curtis@monash.edu.ORCID 0000-0001-9497-0996
Alfred Health · AUThe Royal Melbourne Hospital · AUWalter and Eliza Hall Institute of Medical Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A genome-wide ethyl-N-nitrosourea (ENU) mutagenesis screen in mice was performed to identify novel regulators of erythropoiesis. Here, we describe a mouse line, RBC16, which harbours a dominantly inherited mutation in the

Indexed as

Anemia, HypochromicAnimalsBase SequenceBiosynthetic PathwaysCoproporphyria, HereditaryCoproporphyrinogen OxidaseDisease Models, AnimalEthylnitrosoureaFastingFecesFemaleHemeMaleMice, Mutant StrainsMutagenesisMutationCoproporphyrinogen OxidaseEthylnitrosoureaHemePhenobarbitalAnaemiaCPOXEthyl-N-nitrosoureaHereditary coproporphyria

Identifiers

PMID28600349
PMCPMC5560062
OpenAlexW2624485373

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.