Evidence map›Paper›PMID 8703133›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1996

The Ant1 gene maps near Klk3 on proximal mouse chromosome 8.

K A Mills, J W Ellison, K D Mathews

Abstract read
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    Article
  2. Fath, the murine homolog of the Drosophila fat tumor suppressor gene, maps to chromosome 8.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    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

3 authors at 2 institutions in 1 country.

K A MillsDepartment of Pediatrics, 220 MRC, University of Iowa Hospitals and Clinics, Iowa City, Iowa 52242, USA.
J W Ellison
K D Mathews
University of Iowa Hospitals and Clinics · USUniversity of California, San Francisco · US

Funding

IDENTIFICATION OF THE FACIOSCAPULOHUMERAL DYSTROPHY GENEK08NS001591 · NINDS · UNIVERSITY OF IOWA · PI MATHEWS, KATHERINE · 1993 to 1997
–
NINDS NIH HHS K08NS01591
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome MappingAllelesAnimalsBase SequenceChromosomes, Human, Pair 4Dinucleotide RepeatsDNA PrimersGenetic MarkersGenotypeHumansMiceMice, Inbred StrainsMitochondrial ADP, ATP TranslocasesMolecular Sequence DataPolymerase Chain ReactionPolymorphism, GeneticDNA PrimersGenetic MarkersMitochondrial ADP, ATP TranslocasesProteins

Identifiers

PMID8703133
OpenAlexW2088435354

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.