Rosemary M. Clark

发表

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.

Inhibitory dysfunction in amyotrophic lateral sclerosis: future therapeutic opportunities.

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

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.

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.

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.

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.

Pathogenic or protective? Neuropeptide Y in amyotrophic lateral sclerosis

Rosemary M. Clark, J. Hoyle, T. Dickson, 2020, Journal of neurochemistry.

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.