Evidence map›Paper›PMID 2303033›Full record

ArticleThe EMBO journal1990

Genetic ablation of a mouse gene expressed specifically in brain.

D M Kingsley, E M Rinchik, L B Russell, H P Ottiger, J G Sutcliffe, N G Copeland, N A Jenkins

Open access · greenAbstract read
In one paragraph

Article in The EMBO journal, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
  2. Article
  3. Pathophysiology of Retinopathy of Prematurity.Annual review of vision science · 2023
    Review
  4. Article
  5. Neurovascular abnormalities in retinopathy of prematurity and emerging therapies.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  6. Article
  7. Article
  8. Article
  9. Selectively targeting disease-restricted secretogranin III to alleviate choroidal neovascularization.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  10. Neurovascular regulation in diabetic retinopathy and emerging therapies.Cellular and molecular life sciences : CMLS · 2021
    Review
  11. Review
  12. Expression Pattern of theThe journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Article
  13. Article
  14. Article
  15. Review
  16. Secretogranin III: a diabetic retinopathy-selective angiogenic factor.Cellular and molecular life sciences : CMLS · 2018
    Review
  17. Secretogranin III promotes angiogenesis through MEK/ERK signaling pathway.Biochemical and biophysical research communications · 2018
    Article
  18. Article
  19. Article
  20. 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

7 authors at 1 institution in 1 country.

D M KingsleyMammalian Genetics Laboratory, NCI-Frederick Cancer Research Facility, MD 21701.
E M Rinchik
L B Russell
H P Ottiger
J G Sutcliffe
N G Copeland
N A Jenkins
Cancer Research Center · US

Funding

GENE EXPRESSION IN RAT BRAINR01GM032355 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SUTCLIFFE, J GREGOR · 1985 to 2010
$4.2M
PROVIDE BASIC CANCER RESEARCHN01CO074101 · CO · ADVANCED BIOSCIENCE LABORATORIES, INC. · PI VANDE WOUDE, GEORGE F · 1987 to 1994
–
MOLECULAR DESCRIPTION OF THE CORTEX AND HIPPOCAMPUSR01NS022111 · NINDS · SCRIPPS RESEARCH INSTITUTE · PI SUTCLIFFE, J GREGOR · 1985 to 1995
–
NCI NIH HHS N01-CO-74101NIGMS NIH HHS GM32355NINDS NIH HHS NS22111
6 · The paper itself

Abstract

The 1B1075 gene was initially identified from a cDNA clone of a rat brain messenger RNA expressed in particular subsets of CNS neurons and pituitary cells. Although the protein encoded by this gene is of unknown function, its sequence suggests that it may be related to secretogranin proteins, which are found in association with secretory granules in a variety of peptidergic endocrine and neuronal cells. Here we show that the mouse 1B1075 gene is located between the dilute (d) and short ear (se) genes on chromosome 9. Many different deletion mutations have previously been isolated in the genetic region that includes these genes. By producing mice carrying two deletions that overlap at the 1B1075 locus, the gene for this brain-specific message can be completely eliminated from otherwise viable animals. The animals missing the 1B1075 gene provide an important new tool for determining the function of this gene in the brain. In addition, these results provide a new molecular entry point for detailed characterization of other genes in the d-se region.

Indexed as

Chromosome DeletionGenesMutationAnimalsBrainChromosome MappingCrosses, GeneticDNADNA ProbesFemaleMaleMiceMice, Inbred C57BLNerve Tissue ProteinsNucleic Acid HybridizationDNADNA ProbesNerve Tissue Proteins

Identifiers

PMID2303033
PMCPMC551679
OpenAlexW2255508744

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.