Louise C. Abbott

Decreased calretinin expression in cerebellar granule cells in the leaner mouse.

A line of Berlin Druckrey IV rats proposed as a new model for human hereditary ataxia.

Effects of early postnatal ethanol intubation on GABAergic synaptic proteins.

Neonatal cerebellar ataxia in Coton de Tulear dogs.

Altered neuronal nitric oxide synthase expression in the cerebellum of calcium channel mutant mice.

Homeostatic compensation maintains Ca2+ signaling functions in Purkinje neurons in the leaner mutant mouse.

Insulin-like growth factor-I improves cerebellar dysfunction but does not prevent cerebellar neurodegeneration in the calcium channel mutant mouse, leaner.

Differential expression of T-type calcium channels in P/Q-type calcium channel mutant mice with ataxia and absence epilepsy.

Neuronal nitric oxide synthase expression in cerebellar mutant mice.

Postnatal apoptosis in cerebellar granule cells of homozygous leaner (tg1a/tg1a) mice.

Developmental expression of neuronal nitric oxide synthase in P/Q-type voltage-gated calcium ion channel mutant mice, leaner and tottering.

Functional compensation by other voltage-gated Ca2+ channels in mouse basal forebrain neurons with Ca(V)2.1 mutations.

Inherited tertiary hypothyroidism in Sprague-Dawley rats.

Coordination deficits induced in young adult mice treated with methylmercury.

Changes in biochemical processes in cerebellar granule cells of mice exposed to methylmercury.

Analysis of calcium ion homeostasis and mitochondrial function in cerebellar granule cells of adult CaV 2.1 calcium ion channel mutant mice.

Chronic, low-dose prenatal exposure to methylmercury impairs motor and mnemonic function in adult C57/B6 mice.

Effects of quillaja saponin (Quillaja saponaria) on early embryonic zebrafish (Danio rerio) development.

Assessment of mercury concentrations in mouse brain using different routes of administration and different tissue preparations.

Alterations in intracellular calcium ion concentrations in cerebellar granule cells of the CACNA1A mutant mouse, leaner, during postnatal development.

Striatal expression of Homer1a is affected by genotype but not dystonic phenotype of tottering mice: a model of spontaneously occurring motor disturbances.

Multiscale exploration of mouse brain microstructures using the knife-edge scanning microscope brain atlas.