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Dr. St George-Hyslop’s research centres around mapping, cloning and functional characterization of genes associated with human neurodegenerative diseases with a specific emphasis on Alzheimer ’s disease. Unraveling this neurodegenerative process will be helpful in designing potential therapeutics and providing insight into other neurodegenerative diseases such as Parkinson’s disease, Frontotemporal Dementia, Amyotrophic lateral sclerosis (ALS) or Motor Neuron Disease and Prion diseases.
The. George-Hyslop group also is interested is understanding the role of the presenilin complex in neurodegenerative disease and characterizing the individual components of this complex and how they function.
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Researcher Information
Professor
Department of Medicine
Website
Tanz Neuroscience Building University of Toronto
6 Queen's Park Crescent West
Toronto, Ontario
Canada M5S 3H2
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Dr. St George-Hyslop is a Professor in the Department of Medicine, Division of Neurology, at the University of Toronto. He is an internationally acclaimed geneticist and physician and received his M.D from University of Ottawa in 1976.and an F.R.C.P.(C) in internal medicine and in neurology from the Royal College of Physicians of Canada. Further, he did post-graduate work in internal medicine and neurology at the University of Toronto. He conducted post-doctoral research at Harvard Medical School where he also became an instructor in molecular genetics and neurology from 1987 to 1991. In 1991, he was appointed to the Faculty of Medicine at the University of Toronto as an Assistant Professor of Medicine and was promoted to Professor in 1996. He became a Director of the Centre for Research in Neurodegenerative Diseases in 1995.
Dr. St George-Hyslop is also a practicing neurologist and attends in the ward at the University Health Network teaching hospitals.
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Researcher Information
Professor
Department of Medicine
Website
Tanz Neuroscience Building University of Toronto
6 Queen's Park Crescent West
Toronto, Ontario
Canada M5S 3H2
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Yang DS, Stavrides P, Mohan PS, Kaushik S, Kumar A, Ohno M, Schmidt SD, Wesson DW, Bandyopadhyay U, Jiang Y, Pawlik M, Peterhoff CM, Yang AJ, Wilson DA, St George-Hyslop P, Westaway D, Mathews PM, Levy E, Cuervo AM, Nixon RA. Therapeutic effects of remediating autophagy failure in a mouse model of Alzheimer disease by enhancing lysosomal proteolysis. Autophagy. 2011,7,7.
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Wakasaya Y, Kawarabayashi T, Watanabe M, Yamamoto-Watanabe Y, Takamura A, Kurata T, Murakami T, Abe K, Yamada K, Wakabayashi K, Sasaki A, Westaway D, Hyslop PS, Matsubara E, Shoji M. Factors responsible for neurofibrillary tangles and neuronal cell losses in tauopathy. J Neurosci Res. 2011,89,4:576-84.
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Reitz C, Tokuhiro S, Clark LN, Conrad C, Vonsattel JP, Hazrati LN, Palotás A, Lantigua R, Medrano M, Z Jiménez-Velázquez I, Vardarajan B, Simkin I, Haines JL, Pericak-Vance MA, Farrer LA, Lee JH, Rogaeva E, George-Hyslop PS, Mayeux R. SORCS1 alters amyloid precursor protein processing and variants may increase Alzheimer's disease risk. Ann Neurol. 2011,69,1:47-64.
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Ehsani S, Huo H, Salehzadeh A, Pocanschi CL, Watts JC, Wille H, Westaway D, Rogaeva E, St George-Hyslop PH, Schmitt-Ulms G. Family reunion--the ZIP/prion gene family. Prog Neurobiol. 2011 Mar;93(3):405-20.
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Yang DS, Stavrides P, Mohan PS, Kaushik S, Kumar A, Ohno M, Schmidt SD, Wesson D, Bandyopadhyay U, Jiang Y, Pawlik M, Peterhoff CM, Yang AJ, Wilson DA, St George-Hyslop P, Westaway D, Mathews PM, Levy E, Cuervo AM, Nixon RA. Reversal of autophagy dysfunction in the TgCRND8 mouse model of Alzheimer's disease ameliorates amyloid pathologies and memory deficits. Brain. 2011,134,Pt 1:258-77
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Researcher Information
Professor
Department of Medicine
Website
Tanz Neuroscience Building University of Toronto
6 Queen's Park Crescent West
Toronto, Ontario
Canada M5S 3H2
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YOU MAY ALSO BE INTERESTED IN:
CATEGORIES
Application Area
Human health,
Instrumentation and tools
Disciplinary Focus
Experimental biology and chemistry,
Informatics, theoretical biology and computer science
Core Technology
Nucleic acids:
DNA sequencing,
Genotyping
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