Evidence map›Paper›PMID 7506713›Full record

ArticleThe Journal of clinical investigation1994

Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.

T V Strong, K Boehm, F S Collins

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

105 citing papers in PubMed, 274 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Acquired dysfunction of CFTR underlies cystic fibrosis-like disease of the canine gallbladder.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  10. Article
  11. ThePolymers · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. ACS pharmacology & translational science · 2023
    Review
  18. Review
  19. Review
  20. Association between stool consistency and clinical variables among infants with cystic fibrosis: Findings from the BONUS study.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2022
    Article

45 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

T V StrongDepartment of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0650.
K Boehm
F S Collins
National Human Genome Research Institute · US

Funding

EXPERIMENTAL MODELS OF GENE THERAPY/PILOT PROGRAMP01DK042718 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILSON, JAMES M · 1990 to 1992
–
REVERSE GENETICS OF CF LOCUS USING CHROMOSOME JUMPINGR01DK039690 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COLLINS, FRANCIS S. · 1988 to 1993
–
NIDDK NIH HHS DK-39690NIDDK NIH HHS DK-42718
6 · The paper itself

Abstract

We have used in situ hybridization to localize expression of the cystic fibrosis transmembrane conductance regulator (CFTR) gene in the human gastrointestinal tract and associated organs. The stomach exhibits a low level of CFTR expression throughout gastric mucosa. In the small intestine, expression is relatively high in the mucosal epithelium, with a decreasing gradient of expression along the crypt to tip axis. The cells of the Brunner's glands express high levels of CFTR mRNA. In addition, there is a small subpopulation of highly positive cells scattered along the epithelium in the duodenum and jejunum, but not in the ileum. These cells do not represent endocrine cells, as determined by lack of colocalization with an endocrine-specific marker. The distribution of CFTR mRNA in the colon is similar to the small intestine, with highest level of expression in the epithelial cells at the base of the crypts. In the pancreas, CFTR is expressed at high levels in the small, intercalated ducts and at lower levels in the interlobular ducts. CFTR transcripts are expressed at uniformly high levels in the epithelium of the gallbladder. Throughout the gastrointestinal tract, CFTR expression is increased in mucosal epithelial cells that are near lymph nodules.

Indexed as

Antisense Elements (Genetics)Chloride ChannelsColonCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorEpitheliumGastric MucosaGene ExpressionHumansImmunohistochemistryIn Situ HybridizationIntestinal MucosaIntestine, SmallMembrane ProteinsRNA, MessengerRNA ProbesAntisense Elements (Genetics)CFTR protein, humanChloride ChannelsCystic Fibrosis Transmembrane Conductance RegulatorMembrane ProteinsRNA, MessengerRNA Probes

Identifiers

PMID7506713
PMCPMC293778
OpenAlexW2170265384

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.