Evidence map›Paper›PMID 9335613›Full record

ArticleGenetics1997

Murine albino-deletion complex: high-resolution microsatellite map and genetically anchored YAC framework map.

B A Rikke, D K Johnson, T E Johnson

Abstract read
In one paragraph

Article in Genetics, 1997. 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
1.5field-weighted citation impact, top 16% 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, 15 citations in OpenAlex.

  1. Creating a "hopeful monster": mouse forward genetic screens.Methods in molecular biology (Clifton, N.J.) · 2011
    Article
  2. Overlapping deletions spanning the proximal two-thirds of the mouse t complex.Mammalian genome : official journal of the International Mammalian Genome Society · 2003
    Article
  3. Article
  4. Article
  5. Article
  6. 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.

B A RikkeInstitute for Behavioral Genetics, University of Colorado, Boulder 80309-0447, USA.
D K Johnson
T E Johnson
University of Colorado Boulder · USOak Ridge National Laboratory · US

Funding

TRANSGENIC MOUSE MODELS TO STUDY THE ROLE OF NEUROTENSIN RECEPTORP50AA003527 · NIAAA · UNIVERSITY OF COLORADO DENVER · PI DEITRICH, RICHARD A · 1985 to 2003
$5.9M
MAPPING OF GENES PREDISPOSING TO ALCOHOL SENSITIVITYR01AA008940 · NIAAA · UNIVERSITY OF COLORADO AT BOULDER · PI JOHNSON, THOMAS E. · 1992 to 2007
$3.0M
NIAAA NIH HHS AA-00195NIAAA NIH HHS AA-03527NIAAA NIH HHS AA-08940
6 · The paper itself

Abstract

The murine albino-deletion complex developed as part of the Oak Ridge specific-locus test covers 6-11 cM of chromosome 7. This complex has proven to be a valuable resource for localizing traits to a small target region for positional cloning. In this study, we mapped the endpoints of deletions in this complex using all of the available Mit simple-sequence length polymorphism (SSLP) markers. Concurrently, this mapping has determined the map order of nearly all of the SSLP markers, most of which were previously unresolved. The SSLP-based deletion map was confirmed and genetic distances were determined using the European Collaborative Interspecific Backcross panel of nearly a thousand mice. The average SSLP marker resolution is 0.3-0.4 cM, comparable to the cloning capacity of yeast artificial chromosomes (YACs). The SSLP markers were then used to construct a genetically anchored YAC framework map that further confirms the deletion map. We find that the largest deleted region distal to Tyr is about two to three times larger than the largest proximal deletion region, and the original C3H/101 regions flanking the deletions (moved to an St2A cch/cch background) are smaller than anticipated, which we suggest may result from increased recombination rates immediately flanking the deleted regions.

Indexed as

Chromosome MappingSequence DeletionAnimalsChromosomes, Artificial, YeastCloning, MolecularCrosses, GeneticDNA, SatelliteGenetic MarkersMiceMice, Inbred C3HPolymorphism, Single-Stranded ConformationalDNA, SatelliteGenetic Markers

Identifiers

PMID9335613
PMCPMC1208198
OpenAlexW2132394800

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.