Evidence map›Paper›PMID 23900301›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Proteomic approaches and identification of novel therapeutic targets for alcoholism.

Giorgio Gorini, R Adron Harris, R Dayne Mayfield

Open access · bronzeAbstract readReview
In one paragraph

Review in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Article
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  5. Article
  6. Review
  7. Article
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  11. Review
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  15. Heteromeric Solute Carriers: Function, Structure, Pathology and Pharmacology.Advances in experimental medicine and biology · 2021
    Review
  16. Review
  17. Article
  18. Article
  19. Possible involvement of ACSS2 gene in alcoholism.Journal of neural transmission (Vienna, Austria : 1996) · 2017
    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

3 authors at 1 institution in 1 country.

Giorgio GoriniWaggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX, USA.
R Adron Harris
R Dayne Mayfield
The University of Texas at Austin · US

Funding

GENE EXPRESSION IN THE HUMAN ALCOHOLIC BRAINR01AA012404 · NIAAA · UNIVERSITY OF TEXAS AUSTIN · PI MAYFIELD, ROY DAYNE · 2000 to 2025
$10.7M
Brain Tissue Resource Centre for Alcohol ResearchR28AA012725 · NIAAA · UNIVERSITY OF SYDNEY · PI Greg Trevor Sutherland · 2012 to 2026
$7.0M
Next Generation Sequencing of Human Alcoholic BrainU01AA020926 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI Roy DAYNE MAYFIELD · 2011 to 2026
$6.7M
Next-gen sequencing: searching for mechanisms of alcohol and nicotine dependenceRC2AA019382 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI MAYFIELD, R. DAYNE · 2009 to 2010
$1.7M
Alcohol-responsive protein networks underlying excessive ethanol consumptionU01AA016648 · NIAAA · UNIVERSITY OF TEXAS AT AUSTIN · PI MAYFIELD, R. DAYNE · 2006 to 2010
$776k
NIAAA NIH HHS AA0107838NIAAA NIH HHS AA016648NIAAA NIH HHS AA019382NIAAA NIH HHS AA020926NIAAA NIH HHS R01 AA012404NIAAA NIH HHS R28 AA012725NIAAA NIH HHS RC2 AA019382NIAAA NIH HHS U01 AA016648NIAAA NIH HHS U01 AA020926
6 · The paper itself

Abstract

Recent studies have shown that gene regulation is far more complex than previously believed and does not completely explain changes at the protein level. Therefore, the direct study of the proteome, considerably different in both complexity and dynamicity to the genome/transcriptome, has provided unique insights to an increasing number of researchers. During the past decade, extraordinary advances in proteomic techniques have changed the way we can analyze the composition, regulation, and function of protein complexes and pathways underlying altered neurobiological conditions. When combined with complementary approaches, these advances provide the contextual information for decoding large data sets into meaningful biologically adaptive processes. Neuroproteomics offers potential breakthroughs in the field of alcohol research by leading to a deeper understanding of how alcohol globally affects protein structure, function, interactions, and networks. The wealth of information gained from these advances can help pinpoint relevant biomarkers for early diagnosis and improved prognosis of alcoholism and identify future pharmacological targets for the treatment of this addiction.

Indexed as

AlcoholismAnimalsBiomarkersBrainDrug DiscoveryGene Expression RegulationHumansIon ChannelsMolecular Targeted TherapyProteomicsSystems BiologyBiomarkersIon Channels

Identifiers

PMID23900301
PMCPMC3857647
OpenAlexW1995492336

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.