Powell C - Search Results

1

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations.

Urwin H, Authier A, Nielsen JE, Metcalf D, Powell C, Froud K, Malcolm DS, Holm I, Johannsen P, Brown J, Fisher EM, van der Zee J, Bruyland M; FReJA Consortium; Van Broeckhoven C, Collinge J, Brandner S, Futter C, Isaacs AM. Urwin H, et al. Among authors: powell c. Hum Mol Genet. 2010 Jun 1;19(11):2228-38. doi: 10.1093/hmg/ddq100. Epub 2010 Mar 10. Hum Mol Genet. 2010. PMID: 20223751 Free PMC article.

2

Progressive neuronal inclusion formation and axonal degeneration in CHMP2B mutant transgenic mice.

Ghazi-Noori S, Froud KE, Mizielinska S, Powell C, Smidak M, Fernandez de Marco M, O'Malley C, Farmer M, Parkinson N, Fisher EM, Asante EA, Brandner S, Collinge J, Isaacs AM. Ghazi-Noori S, et al. Among authors: powell c. Brain. 2012 Mar;135(Pt 3):819-32. doi: 10.1093/brain/aws006. Brain. 2012. PMID: 22366797

3

Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.

Isaacs AM, Powell C, Webb TE, Linehan JM, Collinge J, Brandner S. Isaacs AM, et al. Among authors: powell c. Neuropathol Appl Neurobiol. 2008 Aug;34(4):446-56. doi: 10.1111/j.1365-2990.2008.00963.x. Neuropathol Appl Neurobiol. 2008. PMID: 18657254 Free PMC article.

4

Molecular diagnosis of human prion disease.

Wadsworth JD, Powell C, Beck JA, Joiner S, Linehan JM, Brandner S, Mead S, Collinge J. Wadsworth JD, et al. Among authors: powell c. Methods Mol Biol. 2008;459:197-227. doi: 10.1007/978-1-59745-234-2_14. Methods Mol Biol. 2008. PMID: 18576157

5

Methods for Molecular Diagnosis of Human Prion Disease.

Wadsworth JDF, Adamson G, Joiner S, Brock L, Powell C, Linehan JM, Beck JA, Brandner S, Mead S, Collinge J. Wadsworth JDF, et al. Among authors: powell c. Methods Mol Biol. 2017;1658:311-346. doi: 10.1007/978-1-4939-7244-9_22. Methods Mol Biol. 2017. PMID: 28861799

6

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: powell c. Brain. 2006 Jun;129(Pt 6):1557-69. doi: 10.1093/brain/awl076. Epub 2006 Apr 5. Brain. 2006. PMID: 16597650

7

Chronic wasting disease prions are not transmissible to transgenic mice overexpressing human prion protein.

Sandberg MK, Al-Doujaily H, Sigurdson CJ, Glatzel M, O'Malley C, Powell C, Asante EA, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Sandberg MK, et al. Among authors: powell c. J Gen Virol. 2010 Oct;91(Pt 10):2651-7. doi: 10.1099/vir.0.024380-0. Epub 2010 Jul 7. J Gen Virol. 2010. PMID: 20610667 Free PMC article.

8

Magnetization transfer ratio may be a surrogate of spongiform change in human prion diseases.

Siddique D, Hyare H, Wroe S, Webb T, Macfarlane R, Rudge P, Collinge J, Powell C, Brandner S, So PW, Walker S, Mead S, Yousry T, Thornton JS. Siddique D, et al. Among authors: powell c. Brain. 2010 Oct;133(10):3058-68. doi: 10.1093/brain/awq243. Brain. 2010. PMID: 20881162

9

Effect of fixation on brain and lymphoreticular vCJD prions and bioassay of key positive specimens from a retrospective vCJD prevalence study.

Wadsworth JD, Dalmau-Mena I, Joiner S, Linehan JM, O'Malley C, Powell C, Brandner S, Asante EA, Ironside JW, Hilton DA, Collinge J. Wadsworth JD, et al. Among authors: powell c. J Pathol. 2011 Mar;223(4):511-8. doi: 10.1002/path.2821. Epub 2010 Dec 10. J Pathol. 2011. PMID: 21294124

10

Transmission Properties of Human PrP 102L Prions Challenge the Relevance of Mouse Models of GSS.

Asante EA, Grimshaw A, Smidak M, Jakubcova T, Tomlinson A, Jeelani A, Hamdan S, Powell C, Joiner S, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Asante EA, et al. Among authors: powell c. PLoS Pathog. 2015 Jul 2;11(7):e1004953. doi: 10.1371/journal.ppat.1004953. eCollection 2015 Jul. PLoS Pathog. 2015. PMID: 26135918 Free PMC article.

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