VNTR polymorphism for the human dopamine transporter gene (DAT1)

Disrupted hippocampal neuregulin-1/ErbB3 signaling and dentate gyrus granule cell alterations in suicide.

Translational psychiatry·2017

Disrupted hippocampal neuregulin-1/ErbB3 signaling and dentate gyrus granule cell alterations in suicide.

Translational psychiatry·2017

Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism.

Molecular psychiatry·2015

The absence of VGLUT3 predisposes to cocaine abuse by increasing dopamine and glutamate signaling in the nucleus accumbens.

Molecular psychiatry·2015

GABAB receptor cell-surface export is controlled by an endoplasmic reticulum gatekeeper.

Molecular psychiatry·2015

Brain organic cation transporter 2 controls response and vulnerability to stress and GSK3β signaling.

Molecular psychiatry·2014

A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

Human molecular genetics·2026

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Human molecular genetics·2026

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

Human molecular genetics·2026

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

Human molecular genetics·2026

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Human molecular genetics·2026

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

Human molecular genetics·2026

Magnesium deficiency and long-term incident dementia among COVID-19 survivors: a propensity score-matched cohort study.

Frontiers in nutrition·2026

Sociodemographic disadvantage and low healthcare access as contributing factors to high maternal death in Papua, Indonesia: multilevel analysis of census population data.

Rural and remote health·2026

Impact of reducing nicotine in cigarettes on mortality, economic costs and major depression in the USA.

Tobacco control·2026

Seasonal variations of Triatoma dimidiata demography and Trypanosoma cruzi transmission within its multi-host community in the Yucatan Peninsula, Mexico: Insights from an integrative SIR eco-epidemiological modelling.

PLoS neglected tropical diseases·2026

Trajectory of Kidney Function in T1D over Time: A Scoping Review.

Diabetes therapy : research, treatment and education of diabetes and related disorders·2026

Temporal trends in colorectal cancer mortality in Greece, 2014-2022: a Joinpoint regression analysis.

Annals of gastroenterology·2026

Related Experiment Videos

VNTR polymorphism for the human dopamine transporter gene (DAT1)

Related Concept Videos

Disrupted hippocampal neuregulin-1/ErbB3 signaling and dentate gyrus granule cell alterations in suicide.

Disrupted hippocampal neuregulin-1/ErbB3 signaling and dentate gyrus granule cell alterations in suicide.

Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism.

The absence of VGLUT3 predisposes to cocaine abuse by increasing dopamine and glutamate signaling in the nucleus accumbens.

GABAB receptor cell-surface export is controlled by an endoplasmic reticulum gatekeeper.

Brain organic cation transporter 2 controls response and vulnerability to stress and GSK3β signaling.

A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

Magnesium deficiency and long-term incident dementia among COVID-19 survivors: a propensity score-matched cohort study.

Sociodemographic disadvantage and low healthcare access as contributing factors to high maternal death in Papua, Indonesia: multilevel analysis of census population data.

Impact of reducing nicotine in cigarettes on mortality, economic costs and major depression in the USA.

Seasonal variations of Triatoma dimidiata demography and Trypanosoma cruzi transmission within its multi-host community in the Yucatan Peninsula, Mexico: Insights from an integrative SIR eco-epidemiological modelling.

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VNTR polymorphism for the human dopamine transporter gene (DAT1)

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