Malcolm K. Horne

A mouse model of spinal and bulbar muscular atrophy.

Proconvulsant-induced seizures in alpha(4) nicotinic acetylcholine receptor subunit knockout mice.

The role of interleukin-1, interleukin-6, and glia in inducing growth of neuronal terminal arbors in mice.

Neurochemical changes in dopamine D1, D3 and D1/D3 receptor knockout mice.

The Monash University Consortium: factors involved in the local implementation of clinical evidence into practice.

Glial responses associated with dopaminergic striatal reinnervation following lesions of the rat substantia nigra.

Merozoite surface proteins 4 and 5 of Plasmodium knowlesi have differing cellular localisation and association with lipid rafts.

Dietary polyphenols protect dopamine neurons from oxidative insults and apoptosis: investigations in primary rat mesencephalic cultures.

Postural changes after lesions of the substantia nigra pars reticulata in hemiparkinsonian monkeys.

Murine embryonic EGF-responsive ventral mesencephalic neurospheres display distinct regional specification and promote survival of dopaminergic neurons.

Null mutation of the alpha4 nicotinic receptor subunit increases the propensity of muscarinic-mediated neuronal bursting in mouse hippocampal slices.

Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.

Plasma alpha-synuclein is decreased in subjects with Parkinson's disease.

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.

Nicotine-induced dystonic arousal complex in a mouse line harboring a human autosomal-dominant nocturnal frontal lobe epilepsy mutation.

Neural tissue engineering of the CNS using hydrogels.

Quantified assessment of terminal density and innervation.

Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis.

Sprouting of dopamine terminals and altered dopamine release and uptake in Parkinsonian dyskinaesia.

Long-term administration of cocaine or serotonin reuptake inhibitors results in anatomical and neurochemical changes in noradrenergic, dopaminergic, and serotonin pathways.

Recruitment of mitochondria into apoptotic signaling correlates with the presence of inclusions formed by amyotrophic lateral sclerosis-associated SOD1 mutations.

Surface and bulk characterisation of electrospun membranes: problems and improvements.

Meloxicam reduces lipopolysaccharide-induced degeneration of dopaminergic neurons in the rat substantia nigra pars compacta.

Neurite infiltration and cellular response to electrospun polycaprolactone scaffolds implanted into the brain.

Three-dimensional nanofibrous scaffolds incorporating immobilized BDNF promote proliferation and differentiation of cortical neural stem cells.

Dopamine D2 receptor knockout mice develop features of Parkinson disease.

Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis.

Impairment in motor reprogramming in Friedreich ataxia reflecting possible cerebellar dysfunction.

Retrograde axonal tracing using manganese enhanced magnetic resonance imaging.

Implantation of functionalized thermally gelling xyloglucan hydrogel within the brain: associated neurite infiltration and inflammatory response.

Creating a ventral midbrain stem cell niche in an animal model for Parkinson's disease.

Neuronal activity regulates expression of tyrosine hydroxylase in adult mouse substantia nigra pars compacta neurons.

Aromatase and its inhibition in behaviour, obsessive compulsive disorder and parkinsonism.

Wnt5a regulates midbrain dopaminergic axon growth and guidance.

Reduced proliferation in the adult mouse subventricular zone increases survival of olfactory bulb interneurons.

Mutant FUS induces endoplasmic reticulum stress in amyotrophic lateral sclerosis and interacts with protein disulfide-isomerase.

Bim links ER stress and apoptosis in cells expressing mutant SOD1 associated with amyotrophic lateral sclerosis.

Antibodies to surface dopamine-2 receptor in autoimmune movement and psychiatric disorders.

Female mice lacking cholecystokinin 1 receptors have compromised neurogenesis, and fewer dopaminergic cells in the olfactory bulb.

Automated assessment of bradykinesia and dyskinesia in Parkinson's disease.

Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis.

Overexpression of survival motor neuron improves neuromuscular function and motor neuron survival in mutant SOD1 mice.

ALS-associated TDP-43 induces endoplasmic reticulum stress, which drives cytoplasmic TDP-43 accumulation and stress granule formation.

Environmental and behavioral modulation of the number of substantia nigra dopamine neurons in adult mice.

3D Electrospun scaffolds promote a cytotrophic phenotype of cultured primary astrocytes.

Mutant TDP-43 Deregulates AMPK activation by PP2A in ALS models.

Characterization of aromatase expression in the adult male and female mouse brain. I. Coexistence with oestrogen receptors α and β, and androgen receptors.

Mutant TDP-43 deregulates AMPK activation by PP2A in ALS models.