Asante EA - Search Results

1

Frontotemporal dementia caused by CHMP2B mutation is characterised by neuronal lysosomal storage pathology.

Clayton EL, Mizielinska S, Edgar JR, Nielsen TT, Marshall S, Norona FE, Robbins M, Damirji H, Holm IE, Johannsen P, Nielsen JE, Asante EA, Collinge J; FReJA consortium; Isaacs AM. Clayton EL, et al. Among authors: asante ea. Acta Neuropathol. 2015 Oct;130(4):511-23. doi: 10.1007/s00401-015-1475-3. Epub 2015 Sep 10. Acta Neuropathol. 2015. PMID: 26358247 Free PMC article.

2

Isolation and functional characterisation of the promoter region of the human prion protein gene.

Mahal SP, Asante EA, Antoniou M, Collinge J. Mahal SP, et al. Among authors: asante ea. Gene. 2001 May 2;268(1-2):105-14. doi: 10.1016/s0378-1119(01)00424-3. Gene. 2001. PMID: 11368906

3

Transgenic studies of the influence of the PrP structure on TSE diseases.

Asante EA, Collinge J. Asante EA, et al. Adv Protein Chem. 2001;57:273-311. doi: 10.1016/s0065-3233(01)57025-4. Adv Protein Chem. 2001. PMID: 11447693 Review. No abstract available.

4

Post-natal knockout of prion protein alters hippocampal CA1 properties, but does not result in neurodegeneration.

Mallucci GR, Ratté S, Asante EA, Linehan J, Gowland I, Jefferys JG, Collinge J. Mallucci GR, et al. Among authors: asante ea. EMBO J. 2002 Feb 1;21(3):202-10. doi: 10.1093/emboj/21.3.202. EMBO J. 2002. PMID: 11823413 Free PMC article.

5

Expression pattern of a mini human PrP gene promoter in transgenic mice.

Asante EA, Gowland I, Linehan JM, Mahal SP, Collinge J. Asante EA, et al. Neurobiol Dis. 2002 Jun;10(1):1-7. doi: 10.1006/nbdi.2002.0486. Neurobiol Dis. 2002. PMID: 12079398

6

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.

Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, Welch J, Hill AF, Lloyd SE, Wadsworth JD, Collinge J. Asante EA, et al. EMBO J. 2002 Dec 2;21(23):6358-66. doi: 10.1093/emboj/cdf653. EMBO J. 2002. PMID: 12456643 Free PMC article.

7

Pathogenic human prion protein rescues PrP null phenotype in transgenic mice.

Asante EA, Li YG, Gowland I, Jefferys JG, Collinge J. Asante EA, et al. Neurosci Lett. 2004 Apr 22;360(1-2):33-6. doi: 10.1016/j.neulet.2004.01.049. Neurosci Lett. 2004. PMID: 15082172

8

Human prion protein with valine 129 prevents expression of variant CJD phenotype.

Wadsworth JD, Asante EA, Desbruslais M, Linehan JM, Joiner S, Gowland I, Welch J, Stone L, Lloyd SE, Hill AF, Brandner S, Collinge J. Wadsworth JD, et al. Among authors: asante ea. Science. 2004 Dec 3;306(5702):1793-6. doi: 10.1126/science.1103932. Epub 2004 Nov 11. Science. 2004. PMID: 15539564

9

Phenotypic heterogeneity in inherited prion disease (P102L) is associated with differential propagation of protease-resistant wild-type and mutant prion protein.

Wadsworth JD, Joiner S, Linehan JM, Cooper S, Powell C, Mallinson G, Buckell J, Gowland I, Asante EA, Budka H, Brandner S, Collinge J. Wadsworth JD, et al. Among authors: asante ea. Brain. 2006 Jun;129(Pt 6):1557-69. doi: 10.1093/brain/awl076. Epub 2006 Apr 5. Brain. 2006. PMID: 16597650

10

Prion infectivity in variant Creutzfeldt-Jakob disease rectum.

Wadsworth JD, Joiner S, Fox K, Linehan JM, Desbruslais M, Brandner S, Asante EA, Collinge J. Wadsworth JD, et al. Among authors: asante ea. Gut. 2007 Jan;56(1):90-4. doi: 10.1136/gut.2006.091637. Epub 2006 Jun 8. Gut. 2007. PMID: 16763054 Free PMC article.

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