Evidence map›Paper›PMID 7524330›Full record

ArticleThe American journal of pathology1994

Cell type-specific deficiency of c-kit gene expression in mutant mice of mi/mi genotype.

K Isozaki, T Tsujimura, S Nomura, E Morii, U Koshimizu, Y Nishimune, Y Kitamura

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In one paragraph

Article in The American journal of pathology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-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

15 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  5. Article
  6. Development of mast cells: analysis with mutant mice.International journal of hematology · 2007
    Review
  7. Article
  8. Article
  9. Transcription factor MITF regulates cardiac growth and hypertrophy.The Journal of clinical investigation · 2006
    Article
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  11. Article
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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 1 institution in 1 country.

K IsozakiDepartment of Pathology, Medical School, Osaka University, Japan.
T Tsujimura
S Nomura
E Morii
U Koshimizu
Y Nishimune
Y Kitamura
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mi locus of mice encodes a novel member of the basic-helix-loop-helix-leucine zipper protein family of transcription factors (hereafter called mi factor). In addition to microphthalmus, osteopetrosis, and lack of melanocytes, mice of mi/mi genotype are deficient in mast cells. Since the c-kit receptor tyrosine kinase plays an important role in the development of mast cells, and since the c-kit expression by cultured mast cells from mi/mi mice is deficient in both mRNA and protein levels, the mast cell deficiency of mi/mi mice has been attributed at least in part to the deficient expression of c-kit. However, it remained to be examined whether the c-kit expression was also deficient in tissues of mi/mi mice. In the present study, we examined the c-kit expression by mi/mi skin mast cells using in situ hybridization and immunohistochemistry. Moreover, we examined the c-kit expression by various cells other than mast cells in tissues of mi/mi mice. We found that the c-kit expression was deficient in mast cells but not in erythroid precursors, testicular germ cells, and neurons of mi/mi mice. This suggested that the regulation of the c-kit transcription by the mi factor was dependent on cell types. Mice of mi/mi genotype appeared to be a useful model to analyze the function of transcription factors in the whole-animal level.

Indexed as

Gene ExpressionAnimalsAnimals, NewbornErythroid Precursor CellsFetusGenotypeGerm CellsMaleMast CellsMiceMice, Inbred C57BLMice, Mutant StrainsNeuronsProto-Oncogene ProteinsProto-Oncogene Proteins c-kitReceptor Protein-Tyrosine KinasesProto-Oncogene ProteinsProto-Oncogene Proteins c-kitReceptor Protein-Tyrosine KinasesReceptors, Colony-Stimulating FactorRNA, Messenger

Identifiers

PMID7524330
PMCPMC1887326
OpenAlexW1468755370

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.