Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Andrew R. Reid"'
Autor:
Rina Bandopadhyay, Ann E. Kingsbury, Miratul M. Muqit, Kirsten Harvey, Andrew R. Reid, Linda Kilford, Simone Engelender, Michael G. Schlossmacher, Nicholas W. Wood, David S. Latchman, Robert J. Harvey, Andrew J. Lees
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 2, Pp 401-411 (2005)
Lewy bodies (LBs) are the characteristic inclusions of Parkinson's disease brain but the mechanism responsible for their formation is obscure. Lewy bodies (LBs) are composed of a number of proteins of which alpha-synuclein (α-SYN) is a major constit
Externí odkaz:
https://doaj.org/article/6f0ed25c8e0f4630918b13e818439830
Autor:
Michael G. Schlossmacher, Linda Kilford, Kirsten Harvey, David S. Latchman, Rina Bandopadhyay, Robert J. Harvey, Miratul M. K. Muqit, Simone Engelender, Ann E. Kingsbury, Nicholas W. Wood, Andrew R. Reid, Andrew J. Lees
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 2, Pp 401-411 (2005)
Lewy bodies (LBs) are the characteristic inclusions of Parkinson's disease brain but the mechanism responsible for their formation is obscure. Lewy bodies (LBs) are composed of a number of proteins of which alpha-synuclein (alpha-SYN) is a major cons
Autor:
Andrew D. Hope, Rina Bandopadhyay, Andrew J. Lees, R de Silva, G M Gibb, Brian H. Anderton, C Strand, T Jowett, T Revesz, Nicola Wood, Nadeem A. Khan, Tammaryn Lashley, Diane P. Hanger, JL Holton, Andrew R. Reid, Michelle A. Utton
Publikováno v:
Neuropathology and Applied Neurobiology. 29:288-302
Pathological inclusions containing fibrillar aggregates of hyperphosphorylated tau protein are a characteristic feature in the tauopathies, which include Alzheimer's disease, frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17)
Publikováno v:
Journal of Neurocytology. 30:35-44
Evidence from a variety of sources suggests that pericytes have contractile properties and may therefore function in the regulation of capillary blood flow. However, it has been suggested that contractility is not a ubiquitous function of pericytes,
Autor:
Rohan de Silva, Hiroyashi Ariga, Ann E. Kingsbury, Andrew J. Lees, Andrew D. Hope, A.J. Leonard, John Hardy, Patrick M. Abou-Sleiman, Alan M. Pittman, Nicholas W. Wood, Mark R. Cookson, Tamas Revesz, Rina Bandopadhyay, Ian M. Evans, C Strand, Rosa M. Canet-Avilés, Andrew R. Reid, Daniel G. Healy, Tammaryn Lashley, Chris McLendon, David Miller
Publikováno v:
Brain : a journal of neurology. 127(Pt 2)
Two mutations in the DJ-1 gene on chromosome1p36 have been identified recently to cause early-onset, autosomal recessive Parkinson's disease. As no information is available regarding the distribution of DJ-1 protein in the human brain, in this study