Physiology of mutations affecting learning and memory in Drosophila--the missing link between gene product and behavior

Within-species variation in long-term trajectories of growth, fecundity and mortality in the Collembola Folsomia candida.

Journal of evolutionary biology·2015

Walking deficits and centrophobism in an α-synuclein fly model of Parkinson's disease.

Genes, brain, and behavior·2014

Diversity, community composition, and dynamics of nonpigmented and late-pigmenting rapidly growing mycobacteria in an urban tap water production and distribution system.

Applied and environmental microbiology·2013

RNA interference in hippocampus demonstrates opposing roles for CREB and PP1alpha in contextual and temporal long-term memory.

Genes, brain, and behavior·2009

Effects of mutant Drosophila K+ channel subunits on habituation of the olfactory jump response.

Journal of neurogenetics·2007

The Drosophila nitric-oxide synthase gene (dNOS) encodes a family of proteins that can modulate NOS activity by acting as dominant negative regulators.

The Journal of biological chemistry·2001

Amygdala excitability across development: mechanisms, environmental influences, and behavioral outcomes.

Trends in neurosciences·2026

The Microglia-Astrocyte-Neuron Lactate Shuttle model.

Trends in neurosciences·2026

Beyond Bayesian integration: how meaning shapes placebo effects.

Trends in neurosciences·2026

Putting endocrine signaling on the neurodevelopmental map.

Trends in neurosciences·2026

Development sculpts dense neural circuits to enhance memory capacity.

Trends in neurosciences·2026

Alternative splicing dysregulation in CAG repeat expansion diseases.

Trends in neurosciences·2026

[Autism - Phenotypic variability].

Medicina·2026

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

Neurogenetics·2026

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Neural plasticity·2026

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Frontiers in genetics·2026

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

International journal of general medicine·2026

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

Physiology of mutations affecting learning and memory in Drosophila--the missing link between gene product and

Related Concept Videos

Within-species variation in long-term trajectories of growth, fecundity and mortality in the Collembola Folsomia candida.

Walking deficits and centrophobism in an α-synuclein fly model of Parkinson's disease.

Diversity, community composition, and dynamics of nonpigmented and late-pigmenting rapidly growing mycobacteria in an urban tap water production and distribution system.

RNA interference in hippocampus demonstrates opposing roles for CREB and PP1alpha in contextual and temporal long-term memory.

Effects of mutant Drosophila K+ channel subunits on habituation of the olfactory jump response.

The Drosophila nitric-oxide synthase gene (dNOS) encodes a family of proteins that can modulate NOS activity by acting as dominant negative regulators.

Amygdala excitability across development: mechanisms, environmental influences, and behavioral outcomes.

The Microglia-Astrocyte-Neuron Lactate Shuttle model.

Beyond Bayesian integration: how meaning shapes placebo effects.

Putting endocrine signaling on the neurodevelopmental map.

Development sculpts dense neural circuits to enhance memory capacity.

Alternative splicing dysregulation in CAG repeat expansion diseases.

[Autism - Phenotypic variability].

Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier.

A Novel Mutation in ACTG1 as the Probable Cause of Nonsyndromic Hearing Loss in Chinese Han Population.

Rare missense variants in NECTIN1 alter local protein structure and may contribute to non-syndromic cleft lip with or without palate.

Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.

Biallelic VPS41 Variants in Autosomal Recessive Spinocerebellar Ataxia 29 Resolved by Long-Read Sequencing and RNA Analysis.

Related Experiment Videos

Physiology of mutations affecting learning and memory in Drosophila--the missing link between gene product and...

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Physiology of mutations affecting learning and memory in Drosophila--the missing link between gene product and