Fisher EM - Search Results

1

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.

Urwin H, Josephs KA, Rohrer JD, Mackenzie IR, Neumann M, Authier A, Seelaar H, Van Swieten JC, Brown JM, Johannsen P, Nielsen JE, Holm IE; FReJA Consortium; Dickson DW, Rademakers R, Graff-Radford NR, Parisi JE, Petersen RC, Hatanpaa KJ, White CL 3rd, Weiner MF, Geser F, Van Deerlin VM, Trojanowski JQ, Miller BL, Seeley WW, van der Zee J, Kumar-Singh S, Engelborghs S, De Deyn PP, Van Broeckhoven C, Bigio EH, Deng HX, Halliday GM, Kril JJ, Munoz DG, Mann DM, Pickering-Brown SM, Doodeman V, Adamson G, Ghazi-Noori S, Fisher EM, Holton JL, Revesz T, Rossor MN, Collinge J, Mead S, Isaacs AM. Urwin H, et al. Among authors: fisher em. Acta Neuropathol. 2010 Jul;120(1):33-41. doi: 10.1007/s00401-010-0698-6. Epub 2010 May 20. Acta Neuropathol. 2010. PMID: 20490813 Free PMC article.

2

An improved protocol for the analysis of SOD1 gene mutations, and a new mutation in exon 4.

Yulug IG, Katsanis N, de Belleroche J, Collinge J, Fisher EM. Yulug IG, et al. Among authors: fisher em. Hum Mol Genet. 1995 Jun;4(6):1101-4. doi: 10.1093/hmg/4.6.1101. Hum Mol Genet. 1995. PMID: 7655468 No abstract available.

3

Prions and the prion disorders.

Fisher E, Telling G, Collinge J. Fisher E, et al. Mamm Genome. 1998 Jul;9(7):497-502. doi: 10.1007/s003359900807. Mamm Genome. 1998. PMID: 9657843 Review.

4

Molecular genetic characterisation of frontotemporal dementia on chromosome 3.

Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V Jr, Taylor K, Cameron J, Munroe D, Johansson J, Rossor M, Fisher EM, Collinge J. Ashworth A, et al. Among authors: fisher em. Dement Geriatr Cogn Disord. 1999;10 Suppl 1:93-101. doi: 10.1159/000051222. Dement Geriatr Cogn Disord. 1999. PMID: 10436350

5

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Among authors: fisher em. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

6

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

Mead S, Mahal SP, Beck J, Campbell T, Farrall M, Fisher E, Collinge J. Mead S, et al. Am J Hum Genet. 2001 Dec;69(6):1225-35. doi: 10.1086/324710. Epub 2001 Nov 5. Am J Hum Genet. 2001. PMID: 11704923 Free PMC article.

7

Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in mice.

Lloyd SE, Uphill JB, Targonski PV, Fisher EM, Collinge J. Lloyd SE, et al. Among authors: fisher em. Neurogenetics. 2002 Oct;4(2):77-81. doi: 10.1007/s10048-002-0133-9. Neurogenetics. 2002. PMID: 12481985

8

Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.

Mead S, Stumpf MP, Whitfield J, Beck JA, Poulter M, Campbell T, Uphill JB, Goldstein D, Alpers M, Fisher EM, Collinge J. Mead S, et al. Among authors: fisher em. Science. 2003 Apr 25;300(5619):640-3. doi: 10.1126/science.1083320. Epub 2003 Apr 10. Science. 2003. PMID: 12690204

9

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: fisher em. Mamm Genome. 2004 May;15(5):383-9. doi: 10.1007/s00335-004-3041-5. Mamm Genome. 2004. PMID: 15170227

10

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: fisher em. 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

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