Browse by UCL people
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Number of items: 9.
Article
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.
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Asante, EA;
Linehan, JM;
Smidak, M;
Tomlinson, A;
Grimshaw, A;
Jeelani, A;
Jakubcova, T;
... Collinge, J; + view all
(2013)
Inherited Prion Disease A117V Is Not Simply a Proteinopathy but Produces Prions Transmissible to Transgenic Mice Expressing Homologous Prion Protein.
PLoS Pathog
, 9
(9)
, Article e1003643. 10.1371/journal.ppat.1003643.
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Asante, EA;
Linehan, JM;
Tomlinson, AD;
Jakubcova, T;
Hamdan, S;
Grimshaw, A;
Smidak, M;
... Collinge, J; + view all
(2020)
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.
PLOS Biology
, 18
(6)
, Article e3000725. 10.1371/journal.pbio.3000725.
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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.
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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.
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Fernández-Borges, N;
Carlos Espinosa, J;
Marín-Moreno, A;
Aguilar-Calvo, P;
Asante, EAA;
Kitamoto, T;
Mohri, S;
... Torres, JM; + view all
(2017)
Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.
Emerging Infectious Diseases
, 23
(9)
pp. 1522-1530.
10.3201/eid2309.161948.
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Freir, DB;
Nicoll, AJ;
Klyubin, I;
Panico, S;
Mc Donald, JM;
Risse, E;
Asante, EA;
... Collinge, J; + view all
(2011)
Interaction between prion protein and toxic amyloid beta assemblies can be therapeutically targeted at multiple sites.
Nature Communications
, 2
, Article 336. 10.1038/ncomms1341.
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Joiner, S;
Asante, EA;
Linehan, JM;
Brock, L;
Brandner, S;
Bellworthy, SJ;
Simmons, MM;
... Wadsworth, JDF; + view all
(2018)
Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein.
Journal of the Neurological Sciences
, 386
pp. 4-11.
10.1016/j.jns.2017.12.038.
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Wadsworth, JDF;
Joiner, S;
Linehan, JM;
Jack, K;
Al-Doujaily, H;
Costa, H;
Ingold, T;
... Collinge, J; + view all
(2021)
Humanised transgenic mice are resistant to chronic wasting disease prions from Norwegian reindeer and moose.
The Journal of Infectious Diseases
10.1093/infdis/jiab033.
(In press).
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