Evidence map›Paper›PMID 8535078›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1995

A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

K A Mills, Y Sunada, K P Campbell, K D Mathews

Abstract read
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 3 institutions in 1 country.

K A MillsDepartment of Pediatrics, University of Iowa Hospitals and Clinics, Iowa City 52242, USA.
Y Sunada
K P Campbell
K D Mathews
University of Iowa Hospitals and Clinics · USHoward Hughes Medical Institute · USUniversity of Iowa · US

Funding

IDENTIFICATION OF THE FACIOSCAPULOHUMERAL DYSTROPHY GENEK08NS001591 · NINDS · UNIVERSITY OF IOWA · PI MATHEWS, KATHERINE · 1993 to 1997
–
NINDS NIH HHS K08 NS 01591-01A1
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome MappingAnimalsBase SequenceDNA PrimersDystrophin-Associated ProteinsHindlimbMembrane ProteinsMiceMolecular Sequence DataMuscular Dystrophy, AnimalMutationDNA PrimersDystrophin-Associated ProteinsMembrane Proteinssyntrophin

Identifiers

PMID8535078
OpenAlexW2005382816

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.