Evidence map›Paper›PMID 41051712›Full record

ReviewAdvances in neurobiology2025

Drosophila as an Animal Model To Determine the Functional and Behavioral Significance of Dopamine Transporter Genetic Variations Associated with Brain Disorders.

Samuel J Mabry, Angela M Carter, Aurelio Galli

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in neurobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Samuel J MabryUAB Department of Surgery, Birmingham, AL, USA.
Angela M Carter *UAB Department of Surgery, Birmingham, AL, USA.
Aurelio Galli *UAB Department of Surgery, Birmingham, AL, USA. agalli@uabmc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drosophila melanogaster, commonly referred to as the "fruit fly," has been a long-utilized animal model in multiple areas of biological research. It is estimated that 75% of human genes, which are associated with disease, have homologues in Drosophila. The conservation of biological systems, the genetic tractability, short generation time, and a broad array of available behavioral assessments make Drosophila an especially robust model organism for neuroscience investigations. The dopamine (DA) system, in particular, is highly conserved between mammals and Drosophila. Mutations of the DA transporter (DAT), a negative regulator of DA neurotransmission, have been associated with multiple different neuropsychiatric and neurodegenerative disorders, including autism spectrum disorders (ASDs), attention deficit hyperactivity disorder (ADHD), and Parkinson's disease (PD). Utilization of Drosophila models demonstrates specific structural and functional alterations in mutated DAT that manifest as unique behavioral phenotypes. Ultimately, combining techniques ranging from biochemistry, electrochemistry, and complex behavioral analyses facilitated a deeper understanding of how transporter function and dysfunction can translate to neurological and neuropsychiatric disorders.

Indexed as

Behavior, AnimalBrain DiseasesDisease Models, AnimalDopamine Plasma Membrane Transport ProteinsDrosophila melanogasterAnimalsHumansDopamine Plasma Membrane Transport ProteinsAnomalous dopamine efflux (ADE)Autism spectrum disorder (ASD)Complex behaviorDopamine transporter (DAT)Dopamine transporter deficiency syndrome (DTDS)DrosophilaParkinson’s disease (PD)

Identifiers

PMID41051712

What OpenQuestion holds

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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.