Evidence map›Paper›PMID 17803899›Full record

ArticleCell2007

A fight for neurotransmission: SCRAPPER trashes RIM.

Frederick Dobie, Ann Marie Craig

Abstract readComment
In one paragraph

Article in Cell, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. SCRAPPER Selectively Contributes to Spontaneous Release and Presynaptic Long-Term Potentiation in the Anterior Cingulate Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Frederick DobieBrain Research Centre, Department of Psychiatry, University of British Columbia, Vancouver, BC, V6T 2B5, Canada.
Ann Marie Craig

Funding

Mechanisms of Central Neuron SynaptogenesisR01MH070860 · NIMH · UNIVERSITY OF BRITISH COLUMBIA · PI CRAIG, ANN M · 2005 to 2015
$2.3M
NIMH NIH HHS R01 MH070860
6 · The paper itself

Abstract

The presynaptic scaffold molecule RIM1alpha is important for regulating neurotransmitter release. In this issue, Yao et al. (2007) show in mice that an E3 ubiquitin ligase, SCRAPPER, targets a set of presynaptic proteins including RIM1alpha for degradation by the ubiquitin-proteasome system. Their results identify protein degradation as a mechanism for holding rapid synaptic communication in check.

Indexed as

Protein Processing, Post-TranslationalSynaptic TransmissionAnimalsBrainCells, CulturedExcitatory Postsynaptic PotentialsGenotypeGTP-Binding ProteinsHalf-LifeHumansKineticsMiceMice, KnockoutNeuronal PlasticityNeuronsPhenotypeGTP-Binding ProteinsProteasome Endopeptidase ComplexRims1 protein, mouseRNA, MessengerUbiquitinUbiquitin-Protein Ligases

Identifiers

PMID17803899
PMCPMC2821330

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.