Evidence map›Paper›PMID 8093670›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1993

Linkage of Agt and Actsk-1 to distal mouse chromosome 8 loci: a new conserved linkage.

J P Abonia, K J Abel, R L Eddy, R W Elliott, V M Chapman, T B Shows, K W Gross

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.Mammalian genome : official journal of the International Mammalian Genome Society · 1997
    Article
  2. Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.Mammalian genome : official journal of the International Mammalian Genome Society · 1994
    Article
  3. Re-localization of Actsk-1 to mouse chromosome 8, a new region of homology with human chromosome 1.Mammalian genome : official journal of the International Mammalian Genome Society · 1993
    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

7 authors at 2 institutions in 1 country.

J P AboniaDepartment of Molecular and Cellular Biology, Roswell Park Cancer Institute, New York State Department of Health, Buffalo 14263.
K J Abel
R L Eddy
R W Elliott
V M Chapman
T B Shows
K W Gross
Roswell Park Comprehensive Cancer Center · USNew York State Department of Health · US

Funding

ANDROGEN RESPONSIVE GENES OF SUBMAXILLARY GLANDR01GM030248 · NIGMS · ROSWELL PARK CANCER INSTITUTE · PI GROSS, KENNETH W · 1985 to 1989
–
TRANSGENIC MODEL STUDIES OF BLOOD PRESSURE REGULATIONR01HL035792 · NHLBI · ROSWELL PARK CANCER INSTITUTE · PI GROSS, KENNETH W · 1985 to 1994
–
NHLBI NIH HHS HL35792NIGMS NIH HHS GM30248
6 · The paper itself

Abstract

Angiotensinogen is an alpha 2-globulin involved in the maintenance of blood pressure and electrolyte balance. We have refined the position of the mouse angiotensinogen locus (Agt) on Chromosome (Chr) 8 and have also confirmed the assignment of the human angiotensinogen locus (AGT) to Chr 1. The segregation of several restriction fragment length variants (RFLVs) was followed in two interspecific backcross sets and in four recombinant inbred (RI) mouse sets. Analysis of the segregation patterns closely linked Agt to Aprt and Emv-2, which places the angiotensinogen locus on the distal end of mouse Chr 8. Additionally, a literature search has revealed that the strain distribution pattern (SDP) for the mouse skeletal alpha-actin locus 1 (Actsk-1, previously Acta1, Acta, or Acts) is nearly identical to the SDP for Agt in two RI sets. On the basis of this information we were able to reassign Actsk-1 to mouse Chr 8. By screening a panel of human-mouse somatic cell hybrids, we confirmed that the human angiotensinogen locus lies on Chr 1. This information describes a new region of conserved linkage homology between mouse Chr 8 and human Chr 1. It also defines the end of a large region of conserved linkage homology between mouse Chr 8 and human Chr 16.

Indexed as

Chromosome MappingChromosomes, Human, Pair 1Genetic LinkageActinsAngiotensinogenAnimalsBase SequenceBlotting, SouthernChromosomes, Human, Pair 16Crosses, GeneticDNA ProbesHumansHybrid CellsMiceMice, Inbred StrainsMolecular Sequence DataActinsAngiotensinogenDNA Probes

Identifiers

PMID8093670
OpenAlexW2030051154

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.