Browse by UCL Departments and Centres
![[up]](/style/images/multi_up.png)
Up a levelGroup by: Author | Type
Number of items: 17.
A
Asante, EA;
Grimshaw, A;
Smidak, M;
Jakubcova, T;
Tomlinson, A;
Jeelani, A;
Hamdan, S;
... Collinge, J; + view all
(2015)
Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.
PLOS Pathogens
, 11
(7)
, Article e1004953. 10.1371/journal.ppat.1004953.
|
 |
|
Asante, EA;
Smidak, M;
Grimshaw, A;
Houghton, R;
Tomlinson, A;
Jeelani, A;
Jakubcova, T;
... Collinge, J; + view all
(2015)
A naturally occurring variant of the human prion protein completely prevents prion disease.
Nature
, 522
pp. 478-481.
10.1038/nature14510.
|
|
B
|
Bras, J;
Darwent, L;
Orme, T;
Hardy, J;
Guerreiro, R;
Alonso, I;
Barbot, C;
... Costa, MM; + view all
(2015)
Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4.
American Journal of Human Genetics
, 96
(3)
474 - 479.
10.1016/j.ajhg.2015.01.005.
|
 |
C
|
Caine, D;
Tinelli, RJ;
Hyare, H;
De Vita, E;
Lowe, J;
Lukic, A;
Thompson, A;
... Mead, S; + view all
(2015)
The cognitive profile of prion disease: a prospective clinical and imaging study.
Ann Clin Transl Neurol
, 2
(5)
pp. 548-558.
10.1002/acn3.195.
|
|
Clayton, EL;
Mizielinska, S;
Edgar, JR;
Nielsen, TT;
Marshall, S;
Norona, FE;
Robbins, M;
... Isaacs, AM; + view all
(2015)
Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology.
Acta Neuropathologica
, 130
(4)
pp. 511-523.
10.1007/s00401-015-1475-3.
|
|
F
|
Fratta, P;
Polke, JM;
Newcombe, J;
Mizielinska, S;
Lashley, T;
Poulter, M;
Beck, J;
... Fisher, EM; + view all
(2015)
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion.
Neurobiology of Aging
, 36
(1)
546.e1-546.e7.
10.1016/j.neurobiolaging.2014.07.037.
|
K
|
Kun-Rodrigues, C;
Ganos, C;
Guerreiro, R;
Schneider, SA;
Schulte, C;
Lesage, S;
Darwent, L;
... Bras, J; + view all
(2015)
A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease.
Human Molecula Genetics
, 24
(23)
pp. 6711-6720.
10.1093/hmg/ddv376.
|
|
M
|
Mirabile, I;
Jat, PS;
Brandner, S;
Collinge, J;
(2015)
Identification of clinical target areas in the brainstem of prion-infected mice.
Neuropathology and Applied Neurobiology
, 41
(5)
pp. 613-630.
10.1111/nan.12189.
|
|
R
|
Risse, E;
Nicoll, AJ;
Taylor, WA;
Wright, D;
Badoni, M;
Yang, X;
Farrow, MA;
(2015)
Identification of a Compound That Disrupts Binding of Amyloid-β to the Prion Protein Using a Novel Fluorescence-based Assay.
Journal of Biological Chemistry
, 290
(27)
pp. 17020-17028.
10.1074/jbc.M115.637124.
|
|
|
Rohrer, JD;
Nicholas, JM;
Cash, DM;
van Swieten, J;
Dopper, E;
Jiskoot, L;
van Minkelen, R;
... Rossor, MN; + view all
(2015)
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.
Lancet Neurol
, 14
(3)
253 - 262.
10.1016/S1474-4422(14)70324-2.
|
|
|
Rossi, M;
Mead, S;
Collinge, J;
Rudge, P;
Vincent, A;
(2015)
Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob Disease.
Journal of Neurology, Neurosurgery, and Psychiatry
, 86
(6)
pp. 692-694.
10.1136/jnnp-2014-308695.
|
|
Rudge, P;
Jaunmuktane, Z;
Adlard, P;
Bjurstrom, N;
Caine, D;
Lowe, J;
Norsworthy, P;
... Collinge, J; + view all
(2015)
Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.
Brain
, 138
(Pt 11)
pp. 3386-3399.
10.1093/brain/awv235.
|
|
S
|
Sawyer, EB;
Edgeworth, JA;
Thomas, C;
Collinge, J;
Jackson, GS;
(2015)
Preclinical detection of infectivity and disease-specific PrP in blood throughout the incubation period of prion disease.
Scientific Reports
, 5
, Article 17742. 10.1038/srep17742.
|
|
|
Schmidt, C;
Fizet, J;
Properzi, F;
Batchelor, M;
Sandberg, MK;
Edgeworth, JA;
Afran, L;
... Collinge, J; + view all
(2015)
A systematic investigation of production of synthetic prions from recombinant prion protein.
Open Biology
, 5
(12)
, Article 150165. 10.1098/rsob.150165.
|
|
|
Schmidts, M;
Hou, Y;
Cortés, CR;
Mans, DA;
Huber, C;
Boldt, K;
Patel, M;
... Witman, GB; + view all
(2015)
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport.
Nature Communications
, 6
, Article 7074. 10.1038/ncomms8074.
|
T
|
Thompson, AG;
Uphill, J;
Lowe, J;
Porter, MC;
Lukic, A;
Carswell, C;
Rudge, P;
... Mead, S; + view all
(2015)
Genome-wide association study of behavioural and psychiatric features in human prion disease.
Transl Psychiatry
, 5
, Article e552. 10.1038/tp.2015.42.
|
|
W
|
Wenborn, A;
Terry, C;
Gros, N;
Joiner, S;
D'Castro, L;
Panico, S;
Sells, J;
... Wadsworth, JD; + view all
(2015)
A novel and rapid method for obtaining high titre intact prion strains from mammalian brain.
Scientific Reports
, 5
, Article 10062. 10.1038/srep10062.
|
|
