Evidence map›Paper›PMID 8093671›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1993

Genetic and physical mapping of the biglycan gene on the mouse X chromosome.

A Chatterjee, C J Faust, G E Herman

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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 36% 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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Comparative mapping on the mouse X chromosome defines a myotubular myopathy equivalent region.Mammalian genome : official journal of the International Mammalian Genome Society · 1996
    Article
  5. A dinucleotide repeat in the mouse biglycan gene (EST) on the X chromosome.Mammalian genome : official journal of the International Mammalian Genome Society · 1994
    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.

A ChatterjeeInstitute for Molecular Genetics, Baylor College of Medicine, Houston, TX 77030.
C J Faust
G E Herman
Baylor College of Medicine · USBaylor Genetics · US

Funding

X-LINKED CHONDRODYSPLASIA PUNCTATA--MOLECULAR STUDIESR01AR039499 · NIAMS · BAYLOR COLLEGE OF MEDICINE · PI HERMAN, GAIL E. · 1991 to 1994
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PHYSICAL AND GENETIC MAPPING OF X CHROMOSOMER01HG000131 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI HERMAN, GAIL E. · 1991 to 1993
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NHGRI NIH HHS R01 HG00131NIAMS NIH HHS R01 AR39499
6 · The paper itself

Abstract

A human cDNA for biglycan (BGN) has recently been mapped to proximal Xq28. We have mapped the murine locus, Bgn, approximately 50 kb distal to DXPas8, using a combination of genetic mapping in an interspecific backcross of B6CBA-Aw-J/A-Bpa x Mus spretus and physical mapping using pulsed field gel electrophoresis and analysis of murine yeast artificial chromosomes (YACs) containing both DXPas8 and Bgn. Our mapping studies also appear to exclude Bgn as a candidate gene for the bare patches (Bpa) mutation and for the homologous human disorder X-linked dominant chondrodysplasia punctata (CDPX2).

Indexed as

Chromosome MappingX ChromosomeAnimalsBiglycanBlotting, SouthernChromosomes, FungalCrosses, GeneticExtracellular Matrix ProteinsFemaleGene LibraryGenetic LinkageHybrid CellsMaleMicePolymorphism, Restriction Fragment LengthProteoglycansBGN protein, humanBgn protein, mouseBiglycanExtracellular Matrix ProteinsProteoglycans

Identifiers

PMID8093671
OpenAlexW2058345438

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.