A model of high affinity glutamic acid transport by cortical synaptosomes from the Long-Evans rat

Effects of cocaine on sodium dependent dopamine uptake in rat striatal synaptosomes.

Neurochemical research·1994

A model of the sodium dependence of dopamine uptake in rat striatal synaptosomes.

Neurochemical research·1993

Effects of veratridine and cocaine on the kinetics of synaptosomal dopamine release.

Pharmacology·1993

Dopamine uptake in five structures of the brain: comparison of rate, sodium dependence and sensitivity to cocaine.

Neuropharmacology·1993

The effect of cocaine on membrane potential, on membrane depolarization by veratridine or elevated [K]o and on sodium/potassium permeability ratios in synaptosomes from the limbic cortex of the rat.

Neuropharmacology·1993

Aphasic subjects' comprehension of synthetic and natural speech.

The Journal of speech and hearing disorders·1990

Establishment of a Common Marmoset Lineage Carrying a Frameshift Mutation in SETD1A, a Schizophrenia Risk Gene.

Journal of neurochemistry·2026

Neuroinflammation and Graft Survival in Pluripotent Stem Cell-Derived Therapies for the Central Nervous System.

Journal of neurochemistry·2026

AHA1 Regulates Aβ Production via Modulation of APP Abundance and γ-Secretase Assembly.

Journal of neurochemistry·2026

Hippocampal Astrocytes Impact Postnatal Development of Inhibitory Connections, Parvalbumin Levels, Social, and Spatial Navigation Behaviors in a Mouse Model of Fragile X Syndrome.

Journal of neurochemistry·2026

Estradiol Replacement Modulates Synaptic Transmission-Related Proteins in the Hippocampus of Ovariectomized Rats: An Exploratory Proteomic Approach.

Journal of neurochemistry·2026

Distinct Adrenal Medulla Activity in Germ-Free Versus Conventional Male Rats Under Acute and Chronic Stress.

Journal of neurochemistry·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

A model of high affinity glutamic acid transport by cortical synaptosomes from the Long-Evans rat

Related Concept Videos

Effects of cocaine on sodium dependent dopamine uptake in rat striatal synaptosomes.

A model of the sodium dependence of dopamine uptake in rat striatal synaptosomes.

Effects of veratridine and cocaine on the kinetics of synaptosomal dopamine release.

Dopamine uptake in five structures of the brain: comparison of rate, sodium dependence and sensitivity to cocaine.

The effect of cocaine on membrane potential, on membrane depolarization by veratridine or elevated [K]o and on sodium/potassium permeability ratios in synaptosomes from the limbic cortex of the rat.

Aphasic subjects' comprehension of synthetic and natural speech.

Establishment of a Common Marmoset Lineage Carrying a Frameshift Mutation in SETD1A, a Schizophrenia Risk Gene.

Neuroinflammation and Graft Survival in Pluripotent Stem Cell-Derived Therapies for the Central Nervous System.

AHA1 Regulates Aβ Production via Modulation of APP Abundance and γ-Secretase Assembly.

Hippocampal Astrocytes Impact Postnatal Development of Inhibitory Connections, Parvalbumin Levels, Social, and Spatial Navigation Behaviors in a Mouse Model of Fragile X Syndrome.

Estradiol Replacement Modulates Synaptic Transmission-Related Proteins in the Hippocampus of Ovariectomized Rats: An Exploratory Proteomic Approach.

Distinct Adrenal Medulla Activity in Germ-Free Versus Conventional Male Rats Under Acute and Chronic Stress.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

A model of high affinity glutamic acid transport by cortical synaptosomes from the Long-Evans rat

Related Concept Videos

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