Evidence map›Paper›PMID 8431641›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society1993

Mapping of the human homologs of the murine paired-box-containing genes.

A J Pilz, S Povey, P Gruss, C M Abbott

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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Molecular and genetic basis of inherited nephrotic syndrome.International journal of nephrology · 2011
    Article
  5. Transcriptional inhibition of intestinal NHE8 expression by glucocorticoids involves Pax5.American journal of physiology. Gastrointestinal and liver physiology · 2010
    Article
  6. The stumbler mutation maps to proximal mouse chromosome 2.Mammalian genome : official journal of the International Mammalian Genome Society · 1994
    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

4 authors.

A J PilzDepartment of Genetics and Biometry, University College London, UK.
S Povey
P Gruss
C M Abbott

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in paired-box-containing (Pax) genes have recently been found to be the primary lesions underlying human genetic disorders such as Waardenburg's Syndrome type 1 and mouse developmental mutants such as undulated (un), splotch (Sp), and small eye (Sey). In addition, PAX-6 is a strong candidate gene for aniridia in man. Eight independent Pax genes have been isolated in the mouse. All eight map to distinct regions of the mouse genome; they do not appear to be clustered in the same way as some groups of homeobox-containing genes. We have now mapped the human homologs of all eight of these genes; PAX genes are found on human Chromosomes (Chr) 1, 2, 7, 9, 10, 11, and 20.

Indexed as

Chromosomes, HumanAnimalsBase SequenceChromosome MappingDNA-Binding ProteinsDNA, Single-StrandedHumansHybrid CellsMiceMolecular Sequence DataDNA-Binding ProteinsDNA, Single-Stranded

Identifiers

PMID8431641

What OpenQuestion holds

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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.