Evidence mapPaperPMID 7560076Full record

ArticleThe Journal of clinical investigation1995

Genetic factors in lipoprotein metabolism. Analysis of a genetic cross between inbred mouse strains NZB/BINJ and SM/J using a complete linkage map approach.

D A Purcell-Huynh, A Weinreb, L W Castellani, M Mehrabian, M H Doolittle, A J Lusis

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Quantitative trait loci that control body weight in DDD/Sgn and C57BL/6J inbred mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2017
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Establishment of consomic strains derived from A/J and SM/J mice for genetic analysis of complex traits.Mammalian genome : official journal of the International Mammalian Genome Society · 2012
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. A large-sample QTL study in mice: II. Body composition.Mammalian genome : official journal of the International Mammalian Genome Society · 2004
    Article
  17. Article
  18. Identification of a gene encoding an acyl CoA:diacylglycerol acyltransferase, a key enzyme in triacylglycerol synthesis.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  19. Article
  20. Srb1 maps to mouse chromosome 5 in a region harboring putative QTLs for plasma lipoprotein levels.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

6 authors at 1 institution in 1 country.

D A Purcell-HuynhDepartment of Microbiology and Molecular Genetics, University of California, Los Angeles 90024, USA.
A Weinreb
L W Castellani
M Mehrabian
M H Doolittle
A J Lusis
University of California, Los Angeles · US

Funding

MUTATIONS AFFECTING LIPOPROTEIN METABOLISMP01HL028481 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1985 to 2005
$13.6M
LIPOPROTEIN METABOLISM GENETIC CONTROL--MOUSE MODELR01HL042488 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1989 to 1994
LIPOPROTEIN METABOLISM GENETIC CONTROL--MOUSE MODELR37HL042488 · UNIVERSITY OF CALIFORNIA LOS ANGELES · 1994 to 1999
NHLBI NIH HHS HL-28481NHLBI NIH HHS HL-42488NIGMS NIH HHS GM08243
6 · The paper itself

Abstract

A genetic cross was constructed from two parental inbred strains of mice, NZB/BINJ and SM/J, which differ markedly in their plasma lipoprotein levels. Plasma lipid and apolipoprotein values were measured in 184 F2 progeny on a normal chow diet and on an atherogenic diet. Genetic markers were typed at 126 loci spanning all chromosomes except the Y. Statistical analysis revealed significant linkage or suggestive linkage of lipoprotein levels with markers on a number of chromosomes. Chromosome 1 markers were linked to levels of total cholesterol (lod 5.9) and high density lipoprotein (HDL) cholesterol (lod 8.1), chromosome 5 markers were linked to levels of total cholesterol (lod 6.7) and HDL cholesterol (lod 5.6), and chromosome 7 markers were linked to levels of total plasma triglycerides (lod 5.1) and free fatty acids (lod 5.6). Plasma apoAII levels were linked to the apoAII gene (lod score 19.6) and were highly correlated with plasma HDL cholesterol levels (r = 0.63, P = 0.0001), indicating that apoAII expression influences HDL cholesterol levels. Molecular studies suggested that structural differences in the apoAII polypeptide of the two strains may contribute to differences in clearance of the protein.

Indexed as

Chromosome MappingGenetic LinkageAmino Acid SequenceAnimalsApolipoprotein A-IIApolipoproteinsBase SequenceCrosses, GeneticFemaleGene Expression RegulationLipoproteinsMaleMiceMice, Inbred NZBMolecular Sequence DataRabbitsApolipoprotein A-IIApolipoproteinsLipoproteins

Identifiers

PMID7560076
PMCPMC185821
OpenAlexW2030046033

What Socratic 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 Socratic graph.