Brandner S - 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: brandner s. 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

A 38-year-old man with a 9 month history of neurological and cognitive impairment.

Collinge J, Brandner S, Kennedy A, Rossor M, Smith P, Stevens J, Rudge P. Collinge J, et al. Among authors: brandner s. Lancet Neurol. 2003 Mar;2(3):189-94. doi: 10.1016/s1474-4422(03)00325-9. Lancet Neurol. 2003. PMID: 12849240 No abstract available.

3

Depleting neuronal PrP in prion infection prevents disease and reverses spongiosis.

Mallucci G, Dickinson A, Linehan J, Klöhn PC, Brandner S, Collinge J. Mallucci G, et al. Among authors: brandner s. Science. 2003 Oct 31;302(5646):871-4. doi: 10.1126/science.1090187. Science. 2003. PMID: 14593181

4

Identification and characterization of a novel mouse prion gene allele.

Lloyd SE, Thompson SR, Beck JA, Linehan JM, Wadsworth JD, Brandner S, Collinge J, Fisher EM. Lloyd SE, et al. Among authors: brandner s. Mamm Genome. 2004 May;15(5):383-9. doi: 10.1007/s00335-004-3041-5. Mamm Genome. 2004. PMID: 15170227

5

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice.

Lloyd SE, Linehan JM, Desbruslais M, Joiner S, Buckell J, Brandner S, Wadsworth JDF, Collinge J. Lloyd SE, et al. Among authors: brandner s. J Gen Virol. 2004 Aug;85(Pt 8):2471-2478. doi: 10.1099/vir.0.79889-0. J Gen Virol. 2004. PMID: 15269389

6

Analysis of 2000 consecutive UK tonsillectomy specimens for disease-related prion protein.

Frosh A, Smith LC, Jackson CJ, Linehan JM, Brandner S, Wadsworth JD, Collinge J. Frosh A, et al. Among authors: brandner s. Lancet. 2004 Oct 2-8;364(9441):1260-2. doi: 10.1016/S0140-6736(04)17143-2. Lancet. 2004. PMID: 15464187

7

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: brandner s. Science. 2004 Dec 3;306(5702):1793-6. doi: 10.1126/science.1103932. Epub 2004 Nov 11. Science. 2004. PMID: 15539564

8

Prion disease incubation time is not affected in mice heterozygous for a dynein mutation.

Hafezparast M, Brandner S, Linehan J, Martin JE, Collinge J, Fisher EM. Hafezparast M, et al. Among authors: brandner s. Biochem Biophys Res Commun. 2005 Jan 7;326(1):18-22. doi: 10.1016/j.bbrc.2004.10.206. Biochem Biophys Res Commun. 2005. PMID: 15567146

9

An enzyme-detergent method for effective prion decontamination of surgical steel.

Jackson GS, McKintosh E, Flechsig E, Prodromidou K, Hirsch P, Linehan J, Brandner S, Clarke AR, Weissmann C, Collinge J. Jackson GS, et al. Among authors: brandner s. J Gen Virol. 2005 Mar;86(Pt 3):869-878. doi: 10.1099/vir.0.80484-0. J Gen Virol. 2005. PMID: 15722550

10

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia.

Skibinski G, Parkinson NJ, Brown JM, Chakrabarti L, Lloyd SL, Hummerich H, Nielsen JE, Hodges JR, Spillantini MG, Thusgaard T, Brandner S, Brun A, Rossor MN, Gade A, Johannsen P, Sørensen SA, Gydesen S, Fisher EM, Collinge J. Skibinski G, et al. Among authors: brandner s. Nat Genet. 2005 Aug;37(8):806-8. doi: 10.1038/ng1609. Epub 2005 Jul 24. Nat Genet. 2005. PMID: 16041373

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