Evidence map›Paper›PMID 17960477›Full record

ReviewNeurochemical research2008

Molecular genetics of monoamine transporters: relevance to brain disorders.

K Haddley, A S Vasiliou, F R Ali, U M Paredes, V J Bubb, J P Quinn

Abstract readReview
PubMed Publisher
In one paragraph

Review in Neurochemical research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 71 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

K HaddleyPhysiology Laboratory, School of Biomedical Science, University of Liverpool, Liverpool, L69 3BX, England.
A S Vasiliou
F R Ali
U M Paredes
V J Bubb
J P Quinn
University of Liverpool · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D016754/1Medical Research Council G0701003
6 · The paper itself

Abstract

We have demonstrated in both the human serotonin transporter gene (5HTT) and the dopamine transporter gene (DAT1) that specific polymorphic variants termed Variable Number Tandem Repeats (VNTRs), which correlate with predisposition to a number of neurological and psychiatric disorders, act as transcriptional regulatory domains. We have demonstrated that these domains can act as both tissue-specific and stimulus-inducible regulators of gene expression. As such they can act to be mechanistically associated with the progression or initiation of a behavioural disorder by altering the level of transporter mRNA, which in turn regulates the concentration of transporter in specific cells or in response to a challenge; chemical, environmental or physiological. The synergistic actions of such transcriptional domains will modulate gene expression. Our hypothesis is that these VNTR variants are one mechanism by which nurture can modify concentrations of neurotransmitters in a differential manner.

Indexed as

AllelesAnimalsBase SequenceBrain DiseasesDopamine Plasma Membrane Transport ProteinsHumansMolecular Sequence DataPolymorphism, Single NucleotideSerotonin Plasma Membrane Transport ProteinsVesicular Monoamine Transport ProteinsDopamine Plasma Membrane Transport ProteinsSerotonin Plasma Membrane Transport ProteinsSLC6A3 protein, humanVesicular Monoamine Transport Proteins

Identifiers

PMID17960477
OpenAlexW2031597287

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.