Rosemary M Clark

Differential NPY-Y1 Receptor Density in the Motor Cortex of ALS Patients and Familial Model of ALS

J. Chuckowree, C. Mclean, T. Dickson, 2021, Brain sciences.

Amyotrophic lateral sclerosis mutant TDP-43 may cause synaptic dysfunction through altered dendritic spine function

C. Blizzard, T. Dickson, Tongcui Jiang, 2019, Disease Models & Mechanisms.

Synapse Dysfunction of Layer V Pyramidal Neurons Precedes Neurodegeneration in a Mouse Model of TDP-43 Proteinopathies

K. Young, B. J. Turner, C. Blizzard, 2016, Cerebral cortex.

Intranasal neuropeptide Y1 receptor antagonism improves motor deficits in symptomatic SOD1 ALS mice.

J. Chuckowree, C. Blizzard, Courtney M Clark, 2023, Annals of clinical and translational neurology.

Reduced Excitability and Increased Neurite Complexity of Cortical Interneurons in a Familial Mouse Model of Amyotrophic Lateral Sclerosis

C. Blizzard, T. Dickson, M. Brizuela, 2018, Front. Cell. Neurosci..

Calretinin and Neuropeptide Y interneurons are differentially altered in the motor cortex of the SOD1G93A mouse model of ALS

K. Young, C. Blizzard, A. King, 2017, Scientific Reports.

Inhibitory dysfunction in amyotrophic lateral sclerosis: future therapeutic opportunities.

C. Blizzard, T. Dickson, Rosemary M. Clark, 2015, Neurodegenerative disease management.

Amyloid β precursor protein regulates neuron survival and maturation in the adult mouse brain

K. Young, M. Bolós, C. L. Cullen, 2016, Molecular and Cellular Neuroscience.