Evidence map›Paper›PMID 8142895›Full record

ReviewProtein science : a publication of the Protein Society1994

G proteins: critical control points for transmembrane signals.

E J Neer

Open access · bronzeAbstract readReview
In one paragraph

Review in Protein science : a publication of the Protein Society, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.5field-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

24 citing papers in PubMed, 131 citations in OpenAlex.

  1. The NaThe Journal of veterinary medical science · 2026
    Review
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  11. Retinal ON bipolar cells express a new PCP2 splice variant that accelerates the light response.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  12. Article
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  15. Light response of retinal ON bipolar cells requires a specific splice variant of Galpha(o).The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  16. Review
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  20. Activation of protein kinase A-independent pathways by Gs alpha in Drosophila.Proceedings of the National Academy of Sciences of the United States of America · 1996
    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

1 author at 1 institution in 1 country.

E J NeerDepartment of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Brigham and Women's Hospital · US

Funding

Protein interactions in cardiovascular signalingR01GM036259 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI MICHEL, THOMAS · 1985 to 2009
$4.6M
REGULATION OF CELLULAR LEVELS OF G PROTEIN SUBUNITSR01GM046370 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NEER, EVA J. · 1991 to 1993
–
ADENYLATE CYCLASE AND THE PLASMA MEMBRANER37GM036259 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI NEER, EVA J. · 1989 to 1998
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NIGMS NIH HHS GM36259NIGMS NIH HHS GM46370
6 · The paper itself

Abstract

Heterotrimeric GTP-binding proteins (G proteins) that are made up of alpha and beta gamma subunits couple many kinds of cell-surface receptors to intracellular effector enzymes or ion channels. Every cell contains several types of receptors, G proteins, and effectors. The specificity with which G protein subunits interact with receptors and effectors defines the range of responses a cell is able to make to an external signal. Thus, the G proteins act as a critical control point that determines whether a signal spreads through several pathways or is focused to a single pathway. In this review, I will summarize some features of the structure and function of mammalian G protein subunits, discuss the role of both alpha and beta gamma subunits in regulation of effectors, the role of the beta gamma subunit in macromolecular assembly, and the mechanisms that might make some responses extremely specific and others rather diffuse.

Indexed as

Signal TransductionAnimalsCell MembraneGTP-Binding ProteinsMacromolecular SubstancesReceptors, Cell SurfaceGTP-Binding ProteinsMacromolecular SubstancesReceptors, Cell Surface

Identifiers

PMID8142895
PMCPMC2142477
OpenAlexW2162301608

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.