Beck JA - Search Results

1

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: beck ja. Hum Genet. 1997 Sep;100(3-4):477-80. doi: 10.1007/s004390050537. Hum Genet. 1997. PMID: 9272176

2

Genealogies of mouse inbred strains.

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

3

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: beck ja. 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.

4

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. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

5

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.

6

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

7

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion.

Fratta P, Polke JM, Newcombe J, Mizielinska S, Lashley T, Poulter M, Beck J, Preza E, Devoy A, Sidle K, Howard R, Malaspina A, Orrell RW, Clarke J, Lu CH, Mok K, Collins T, Shoaii M, Nanji T, Wray S, Adamson G, Pittman A, Renton AE, Traynor BJ, Sweeney MG, Revesz T, Houlden H, Mead S, Isaacs AM, Fisher EM. Fratta P, et al. Neurobiol Aging. 2015 Jan;36(1):546.e1-7. doi: 10.1016/j.neurobiolaging.2014.07.037. Epub 2014 Aug 1. Neurobiol Aging. 2015. PMID: 25179228 Free PMC article.

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: beck ja. Science. 2003 Apr 25;300(5619):640-3. doi: 10.1126/science.1083320. Epub 2003 Apr 10. Science. 2003. PMID: 12690204

9

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia.

Fratta P, Poulter M, Lashley T, Rohrer JD, Polke JM, Beck J, Ryan N, Hensman D, Mizielinska S, Waite AJ, Lai MC, Gendron TF, Petrucelli L, Fisher EM, Revesz T, Warren JD, Collinge J, Isaacs AM, Mead S. Fratta P, et al. Acta Neuropathol. 2013 Sep;126(3):401-9. doi: 10.1007/s00401-013-1147-0. Epub 2013 Jul 2. Acta Neuropathol. 2013. PMID: 23818065 Free PMC article.

10

Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease.

Beck JA, Poulter M, Campbell TA, Uphill JB, Adamson G, Geddes JF, Revesz T, Davis MB, Wood NW, Collinge J, Tabrizi SJ. Beck JA, et al. Hum Mol Genet. 2004 Jun 15;13(12):1219-24. doi: 10.1093/hmg/ddh134. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115757

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