Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Ann E, Kingsbury"'
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:
Ann E. Kingsbury, Janice L. Holton, Alan E. Renton, Sean S. O'Sullivan, Carles Vilariño-Güell, Nicholas W. Wood, Simone Sharma, Tamas Revesz, R. Kumaran, Rina Bandopadhyay, Tammaryn Lashley, Andrew J. Lees, Constantinos Kallis
Publikováno v:
Neuropathology and Applied Neurobiology. 37:777-790
Aims: Mutations in the gene encoding leucine-rich repeat kinase-2 (LRRK2) have been established as a common genetic cause of Parkinson's disease (PD). The distribution of LRRK2 mRNA and protein in the human brain has previously been described, althou
Autor:
Rina Bandopadhyay, Laura Silveira-Moriyama, Constantinos Kallis, Ann E. Kingsbury, Andrew J. Lees, William Sterlacci, Werner Poewe, Hans Maeir, H Ayling
Publikováno v:
Movement Disorders. 25:2508-2515
The lower brain stem of 25 pathologically-confirmed Parkinson's disease (PD) cases was examined by alpha synuclein immunohistochemistry to characterize pathological accumulation of alpha synuclein (Lewy-type α-synucleinopathy, LTS) in the medulla ob
Autor:
David J. Burn, David R. Williams, Janice L. Holton, Huw R. Morris, Graham Hughes, Andrew J. Lees, Ann E. Kingsbury, Aviva Petrie, H Ayling, Alistair Church, Tamas Revesz, Laura Silveira-Moriyama
Publikováno v:
Movement Disorders. 25:570-577
Previous studies suggested that olfaction is normal in progressive supranuclear palsy (PSP). We applied the University of Pennsylvania Smell Identification Test (UPSIT) to 36 patients with PSP who scored more than 18 on the Mini Mental State Examinat
Publikováno v:
European Journal of Pharmacology. 604:45-50
We have recently observed that the corticotrophin releasing factor (CRF) related peptide urocortin reverses key features of nigrostriatal damage in two paradigms of Parkinson's disease. Here we have studied whether these effects are supported by a re
Autor:
Nicholas W. Wood, Cristina Sampaio, Vincenzo Bonifati, Leonor Correia Guedes, Egberto Reis Barbosa, Aviva Petrie, Joaquim J. Ferreira, Karen Shaw, Tamas Revesz, Ann E. Kingsbury, Patrick M. Abou-Sleiman, Janice L. Holton, H Ayling, Laura Silveira-Moriyama, Niall Quinn, Andrew J. Lees
Publikováno v:
Neurology, 71(13), 1021-1026. Lippincott Williams & Wilkins
Background: Mutations in PARK8 (LRRK2) are associated with autosomal dominant parkinsonism and Parkinson disease (PD). Hyposmia is present in at least 80% of patients with PD and an accumulation of alpha-synuclein (alpha-syn) is seen in the olfactory
Autor:
Andrew J. Lees, Rohan de Silva, David M. A. Mann, David R. Williams, Ravindran Kumaran, Ian C. Coulter, Rina Bandopadhyay, Tamas Revesz, Tammaryn Lashley, Ann E. Kingsbury
Publikováno v:
Neurobiology of Disease, Vol 28, Iss 1, Pp 122-132 (2007)
Mutations in the DJ-1 gene are associated with autosomal recessive Parkinson's disease (PD), but its role in disease pathogenesis is unknown. This study examines DJ-1 immunoreactivity (DJ-1 IR) in a variety of neurodegenerative disorders, Alzheimer's
Autor:
Andrew J. Lees, Ann E. Kingsbury, Amjad Abuirmeileh, Hardial S. Chowdrey, Ian C. Locke, Richard A. Knight, Rebecca Lever, Peter S. Whitton, Christopher S. Biggs
Publikováno v:
European Journal of Neuroscience. 26:417-423
The potential neuroprotective action of the corticotrophin-releasing factor-related peptide urocortin (UCN) was investigated in the rat 6-hydroxydopamine (6-OHDA) and lipopolysaccharide (LPS) paradigms of Parkinson's disease. UCN (20 fmol) was either
Autor:
Alice Kaganovich, Elisa Greggio, Andrew J. Lees, Jeff Blackinton, Alexandra Beilina, Robert J. Harvey, Kirsten Harvey, Sashi Kesavapany, Rina Bandopadhyay, Andrew B. Singleton, Ann E. Kingsbury, Kelly Jean Thomas, David Miller, Patrick A. Lewis, Mark R. Cookson, Shushant Jain, Rili Ahmad, Marcel P. van der Brug
Publikováno v:
Neurobiology of Disease, Vol 23, Iss 2, Pp 329-341 (2006)
Mutations in the LRRK2 gene, coding for dardarin, cause dominantly inherited Parkinson's disease (PD). Dardarin is a large protein, and mutations are found throughout the gene including the kinase domain. However, it is not clear if kinase activity i
Publikováno v:
Movement Disorders. 21:2208-2211
Increased numbers of dopaminergic neurons are described in the striatum of patients with Parkinson's disease. In postmortem striatal tissue from Parkinson's disease patients with short disease duration (≤8 years), the number of dopaminergic neurons