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Number of items: 17.
B
Bras, J;
Guerreiro, R;
Darwent, L;
Parkkinen, L;
Ansorge, O;
Escott-Price, V;
Hernandez, DG;
... Hardy, J; + view all
(2014)
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies.
Hum Mol Genet
, 23
(23)
6139 - 6146.
10.1093/hmg/ddu334.
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Brown, CA;
Schmidt, C;
Poulter, M;
Hummerich, H;
Klöhn, PC;
Jat, P;
Mead, S;
... Lloyd, SE; + view all
(2014)
In-vitro screen of prion disease susceptibility genes using the scrapie cell assay.
Hum Mol Genet
, 23
(19)
pp. 5102-5108.
10.1093/hmg/ddu233.
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C
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Chan, AS;
Mowla, SN;
Arora, P;
Jat, PS;
(2014)
Tumour suppressors and cellular senescence.
IUBMB Life
, 66
(12)
pp. 812-822.
10.1002/iub.1335.
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E
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Escott-Price, V;
Bellenguez, C;
Wang, LS;
Choi, SH;
Harold, D;
Jones, L;
Holmans, P;
... Cardiovascular Health Study (CHS); + view all
(2014)
Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease.
PLoS One
, 9
(6)
, Article e94661. 10.1371/journal.pone.0094661.
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G
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Grizenkova, J;
Akhtar, S;
Brandner, S;
Collinge, J;
Lloyd, SE;
(2014)
Microglial Cx3cr1 knockout reduces prion disease incubation time in mice.
BMC Neurosci
, 15
, Article 44. 10.1186/1471-2202-15-44.
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H
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Hu, NW;
Nicoll, AJ;
Zhang, D;
Mably, AJ;
O'Malley, T;
Purro, SA;
Terry, C;
... Rowan, MJ; + view all
(2014)
mGlu5 receptors and cellular prion protein mediate amyloid-β-facilitated synaptic long-term depression in vivo.
Nature Communications
, 5
, Article 3374. 10.1038/ncomms4374.
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K
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Klyubin, I;
Nicoll, AJ;
Khalili-Shirazi, A;
Farmer, M;
Canning, S;
Mably, A;
Linehan, J;
... Collinge, J; + view all
(2014)
Peripheral Administration of a Humanized Anti-PrP Antibody Blocks Alzheimer's Disease Aβ Synaptotoxicity.
J Neurosci
, 34
(18)
6140 - 6145.
10.1523/JNEUROSCI.3526-13.2014.
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M
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Mahoney, CJ;
Ridgway, GR;
Malone, IB;
Downey, LE;
Beck, J;
Kinnunen, KM;
Schmitz, N;
... Warren, JD; + view all
(2014)
Profiles of white matter tract pathology in frontotemporal dementia.
Hum Brain Mapp
, 35
(8)
pp. 4163-4179.
10.1002/hbm.22468.
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Marbiah, MM;
Harvey, A;
West, BT;
Louzolo, A;
Banerjee, P;
Alden, J;
Grigoriadis, A;
... Klöhn, PC; + view all
(2014)
Identification of a gene regulatory network associated with prion replication.
The EMBO Journal
, 33
(14)
1503- 1614.
10.15252/embj.201387150.
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Mizielinska, S;
Grönke, S;
Niccoli, T;
Ridler, CE;
Clayton, EL;
Devoy, A;
Moens, T;
... Isaacs, AM; + view all
(2014)
C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins.
Science
10.1126/science.1256800.
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Moss, DJH;
Poulter, M;
Beck, J;
Hehir, J;
Polke, JM;
Campbell, T;
Adamson, G;
... Tabrizi, SJ; + view all
(2014)
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Neurology
, 82
(4)
pp. 292-299.
10.1212/WNL.0000000000000061.
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O
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Onoufriadis, A;
Shoemark, A;
Schmidts, M;
Patel, M;
Jimenez, G;
Liu, H;
Thomas, B;
... Mitchison, HM; + view all
(2014)
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central-pair agenesis due to radial spoke defects.
Hum Mol Genet
, 23
(13)
pp. 3362-3374.
10.1093/hmg/ddu046.
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Owen, J;
Beck, J;
Campbell, T;
Adamson, G;
Gorham, M;
Thompson, A;
Smithson, S;
... Mead, S; + view all
(2014)
Predictive testing for inherited prion disease: report of 22 years experience.
European Journal of Human Genetics
, 22
(12)
pp. 1351-1356.
10.1038/ejhg.2014.42.
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P
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Purro, SA;
Galli, S;
Salinas, PC;
(2014)
Dysfunction of Wnt signaling and synaptic disassembly in neurodegenerative diseases.
Journal of Molecular Cell Biology
, 6
(1)
pp. 75-80.
10.1093/jmcb/mjt049.
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S
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Sandberg, MK;
Al-Doujaily, H;
Sharps, B;
De Oliveira, MW;
Schmidt, C;
Richard-Londt, A;
Lyall, S;
... Collinge, J; + view all
(2014)
Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked.
Nat Commun
, 5
, Article 4347. 10.1038/ncomms5347.
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T
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Traeger, U;
Andre, R;
Lahiri, N;
Magnusson-Lind, A;
Weiss, A;
Grueninger, S;
McKinnon, C;
... Tabrizi, SJ; + view all
(2014)
HTT-lowering reverses Huntington's disease immune dysfunction caused by NF kappa B pathway dysregulation.
Brain
, 137
pp. 819-833.
10.1093/brain/awt355.
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Trevitt, CR;
Hosszu, LL;
Batchelor, M;
Panico, S;
Terry, C;
Nicoll, AJ;
Risse, E;
... Clarke, AR; + view all
(2014)
N-terminal domain of prion protein directs its oligomeric association.
J Biol Chem
, 289
(37)
25497 - 25508.
10.1074/jbc.M114.566588.
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