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Michael Landon

Affiliations: 
Pathology University of Nottingham, Nottingham, England, United Kingdom 
Area:
Alzheimer disease
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"Michael Landon"
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http://www.mgwater.com/lyso.shtml

Cross-listing: Neurotree

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Mark Anthony Smith grad student 1986-1990 Nottingham

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Lowe J, McDermott H, Landon M, et al. (1990) Ubiquitin carboxyl-terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseases. The Journal of Pathology. 161: 153-60
Landon M, Smith MA, Clarke K, et al. (1989) Immunoaffinity chromatographic purification of amyloid-related proteins from Alzheimer's disease brain tissue. Progress in Clinical and Biological Research. 317: 903-12
Landon M, Kidd M. (1989) Amyloid in Alzheimer's disease. Biochemical Society Transactions. 17: 69-72
Allsop D, Wong CW, Ikeda S, et al. (1988) Immunohistochemical evidence for the derivation of a peptide ligand from the amyloid beta-protein precursor of Alzheimer disease Proceedings of the National Academy of Sciences of the United States of America. 85: 2790-2794
Roberts GW, Lofthouse R, Allsop D, et al. (1988) CNS amyloid proteins in neurodegenerative diseases. Neurology. 38: 1534-40
Allsop D, Landon M, Kidd M, et al. (1986) Monoclonal antibodies raised against a subsequence of senile plaque core protein react with plaque cores, plaque periphery and cerebrovascular amyloid in Alzheimer's disease. Neuroscience Letters. 68: 252-6
Allsop D, Kidd M, Landon M, et al. (1986) Isolated senile plaque cores in Alzheimer's disease and Down's syndrome show differences in morphology. Journal of Neurology, Neurosurgery, and Psychiatry. 49: 886-892
Kidd M, Allsop D, Landon M. (1985) Senile plaque amyloid, paired helical filaments, and cerebrovascular amyloid in Alzheimer's disease are all deposits of the same protein. The Lancet. 325: 278
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