Rohan de Silva
Rohan de Silva
Professor of Molecular Neuroscience, UCL Queen Square Institute of Neurology
Підтверджена електронна адреса в ucl.ac.uk
Назва
Посилання
Посилання
Рік
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
R Sherrington, EI Rogaev, Y Liang, EA Rogaeva, G Levesque, M Ikeda, ...
Nature 375 (6534), 754-760, 1995
47881995
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ...
Neuron 44 (4), 595-600, 2004
22572004
The precursor protein of non-Aβ component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system
A Iwai, E Masliah, M Yoshimoto, N Ge, L Flanagan, HAR De Silva, A Kittel, ...
Neuron 14 (2), 467-475, 1995
13781995
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism
DR Williams, R de Silva, DC Paviour, A Pittman, HC Watt, L Kilford, ...
Brain 128 (6), 1247-1258, 2005
6742005
Hyperphosphorylation and aggregation of tau in mice expressing normal human tau isoforms
C Andorfer, Y Kress, M Espinoza, R De Silva, KL Tucker, YA Barde, K Duff, ...
Journal of neurochemistry 86 (3), 582-590, 2003
6462003
Genetic variability in the regulation of gene expression in ten regions of the human brain
A Ramasamy, D Trabzuni, S Guelfi, V Varghese, C Smith, R Walker, T De, ...
Nature neuroscience 17 (10), 1418-1428, 2014
4912014
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
R Bandopadhyay, AE Kingsbury, MR Cookson, AR Reid, IM Evans, ...
Brain 127 (2), 420-430, 2004
4812004
Lewy-and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important?
Y Compta, L Parkkinen, SS O'Sullivan, J Vandrovcova, JL Holton, ...
Brain 134 (5), 1493-1505, 2011
4572011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
GU Höglinger, NM Melhem, DW Dickson, PMA Sleiman, LS Wang, L Klei, ...
Nature genetics 43 (7), 699, 2011
4322011
α-Synuclein gene haplotypes are associated with Parkinson’s disease
M Farrer, DM Maraganore, P Lockhart, A Singleton, TG Lesnick, ...
Human molecular genetics 10 (17), 1847-1851, 2001
3922001
The heritability and genetics of frontotemporal lobar degeneration
JD Rohrer, R Guerreiro, J Vandrovcova, J Uphill, D Reiman, J Beck, ...
Neurology 73 (18), 1451-1456, 2009
3742009
Microdeletion encompassing MAPT at chromosome 17q21. 3 is associated with developmental delay and learning disability
C Shaw-Smith, AM Pittman, L Willatt, H Martin, L Rickman, S Gribble, ...
Nature genetics 38 (9), 1032-1037, 2006
3622006
Tau protein hyperphosphorylation and aggregation in Alzheimer’s disease and other tauopathies, and possible neuroprotective strategies
G Šimić, M Babić Leko, S Wray, C Harrington, I Delalle, ...
Biomolecules 6 (1), 6, 2016
3492016
Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome
DR Williams, JL Holton, C Strand, A Pittman, R de Silva, AJ Lees, ...
Brain 130 (6), 1566-1576, 2007
3192007
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
JD Rohrer, T Lashley, JM Schott, JE Warren, S Mead, AM Isaacs, J Beck, ...
Brain 134 (9), 2565-2581, 2011
2832011
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration
AM Pittman, AJ Myers, P Abou-Sleiman, HC Fung, M Kaleem, L Marlowe, ...
Journal of medical genetics 42 (11), 837-846, 2005
2552005
Argyrophilic grain disease is a sporadic 4-repeat tauopathy
T Togo, N Sahara, SH Yen, N Cookson, T Ishizawa, M Hutton, R De Silva, ...
Journal of Neuropathology & Experimental Neurology 61 (6), 547-556, 2002
2472002
The H1c haplotype at the MAPT locus is associated with Alzheimer's disease
AJ Myers, M Kaleem, L Marlowe, AM Pittman, AJ Lees, HC Fung, ...
Human molecular genetics 14 (16), 2399-2404, 2005
2312005
The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts
AJ Myers, AM Pittman, AS Zhao, K Rohrer, M Kaleem, L Marlowe, A Lees, ...
Neurobiology of disease 25 (3), 561-570, 2007
2222007
Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule‐binding repeat domains as demonstrated by new specific …
R De Silva, T Lashley, G Gibb, D Hanger, A Hope, A Reid, ...
Neuropathology and applied neurobiology 29 (3), 288-302, 2003
2062003
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