Fisher EM - Search Results

1

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

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

Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21.

Katsanis N, Beck JA, Fisher EM. Katsanis N, et al. Among authors: fisher em. Hum Genet. 1997 Sep;100(3-4):477-80. doi: 10.1007/s004390050537. Hum Genet. 1997. PMID: 9272176

4

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.

5

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

6

The kinesin light chain gene: its mapping and exclusion in mouse and human forms of inherited motor neuron degeneration.

Hafezparast M, Witherden A, Nicholson S, Bermingham N, Mackin J, ten Asbroek A, Ball S, Peters J, Baas F, Martin JE, Fisher EM. Hafezparast M, et al. Among authors: fisher em. Neurosci Lett. 1999 Sep 24;273(1):49-52. doi: 10.1016/s0304-3940(99)00620-5. Neurosci Lett. 1999. PMID: 10505649

7

Genealogies of mouse inbred strains.

Beck JA, Lloyd S, Hafezparast M, Lennon-Pierce M, Eppig JT, Festing MF, Fisher EM. Beck JA, et al. Among authors: fisher em. Nat Genet. 2000 Jan;24(1):23-5. doi: 10.1038/71641. Nat Genet. 2000. PMID: 10615122

8

Identification of multiple quantitative trait loci linked to prion disease incubation period in mice.

Lloyd SE, Onwuazor ON, Beck JA, Mallinson G, Farrall M, Targonski P, Collinge J, Fisher EM. Lloyd SE, et al. Among authors: fisher em. Proc Natl Acad Sci U S A. 2001 May 22;98(11):6279-83. doi: 10.1073/pnas.101130398. Epub 2001 May 15. Proc Natl Acad Sci U S A. 2001. PMID: 11353827 Free PMC article.

9

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.

10

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

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