Evidence map›Paper›PMID 21867767›Full record

ReviewNitric oxide : biology and chemistry2011

RNA splicing in regulation of nitric oxide receptor soluble guanylyl cyclase.

Iraida G Sharina, Gilbert J Cote, Emil Martin, Marie-Francoise Doursout, Ferid Murad

Abstract readReview
In one paragraph

Review in Nitric oxide : biology and chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Role of sGC-dependent NO signalling and myocardial infarction risk.Journal of molecular medicine (Berlin, Germany) · 2015
    Review
  8. Alternative splicing impairs soluble guanylyl cyclase function in aortic aneurysm.American journal of physiology. Heart and circulatory physiology · 2014
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
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

5 authors at 3 institutions in 1 country.

Iraida G SharinaDepartment of Internal Medicine, University of Texas Health Science Center, Houston, TX, USA. Iraida.G.Sharina@uth.tmc.edu
Gilbert J Cote
Emil Martin
Marie-Francoise Doursout
Ferid Murad
The University of Texas Health Science Center at Houston · USGeorge Washington University · USThe University of Texas MD Anderson Cancer Center · US

Funding

Soluble guanylyl cyclase modulation by endogenous elements and exogenous factorsR01HL088128 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MARTIN, EMIL · 2008 to 2012
$2.1M
NHLBI NIH HHS 3R01HL088128-02S1NHLBI NIH HHS HL088128NHLBI NIH HHS R01 HL088128
6 · The paper itself

Abstract

Soluble guanylyl cyclase (sGC) is a key protein in the nitric oxide (NO)/-cGMP signaling pathway. sGC activity is involved in a number of important physiological processes including smooth muscle relaxation, neurotransmission and platelet aggregation and adhesion. Regulation of sGC expression and activity emerges as a crucial factor in control of sGC function in normal and pathological conditions. Recently accumulated evidence strongly indicates that the regulation of sGC expression is a complex process modulated on several levels including transcription, post-transcriptional regulation, translation and protein stability. Presently our understanding of mechanisms governing regulation of sGC expression remains very limited and awaits systematic investigation. Among other ways, the expression of sGC subunits is modulated at the levels of mRNA abundance and transcript diversity. In this review we summarize available information on different mechanisms (including transcriptional activation, mRNA stability and alternative splicing) involved in the modulation of mRNA levels of sGC subunits in response to various environmental clues. We also summarize and cross-reference the information on human sGC splice forms available in the literature and in genomic databases. This review highlights the fact that the study of the biological role and regulation of sGC splicing will bring new insights to our understanding of NO/cGMP biology.

Indexed as

RNA SplicingAnimalsGuanylate CyclaseHumansReceptors, Cytoplasmic and NuclearRNA, MessengerSignal TransductionSoluble Guanylyl CyclaseGuanylate CyclaseReceptors, Cytoplasmic and NuclearRNA, MessengerSoluble Guanylyl Cyclase

Identifiers

PMID21867767
PMCPMC3190046
OpenAlexW2105910460

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.