Hutton M - Search Results

1

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease.

Hutton M, Busfield F, Wragg M, Crook R, Perez-Tur J, Clark RF, Prihar G, Talbot C, Phillips H, Wright K, Baker M, Lendon C, Duff K, Martinez A, Houlden H, Nichols A, Karran E, Roberts G, Roques P, Rossor M, Venter JC, Adams MD, Cline RT, Phillips CA, Goate A, et al. Hutton M, et al. Neuroreport. 1996 Feb 29;7(3):801-5. doi: 10.1097/00001756-199602290-00029. Neuroreport. 1996. PMID: 8733749

2

Apolipoprotein E alleles but neither apolipoprotein B nor apolipoprotein AI/CIII alleles are associated with late onset, familial Alzheimer's disease.

Houlden H, Crook R, Duff K, Hutton M, Collinge J, Roques P, Rossor M, Hardy J. Houlden H, et al. Among authors: hutton m. Neurosci Lett. 1995 Mar 31;188(3):202-4. doi: 10.1016/0304-3940(95)11422-s. Neurosci Lett. 1995. PMID: 7609909

3

Polymorphism in AACT gene may lower age of onset of Alzheimer's disease.

Talbot C, Houlden H, Craddock N, Crook R, Hutton M, Lendon C, Prihar G, Morris JC, Hardy J, Goate A. Talbot C, et al. Among authors: hutton m. Neuroreport. 1996 Jan 31;7(2):534-6. doi: 10.1097/00001756-199601310-00038. Neuroreport. 1996. PMID: 8730823 Clinical Trial.

4

Structure and alternative splicing of the presenilin-2 gene.

Prihar G, Fuldner RA, Perez-Tur J, Lincoln S, Duff K, Crook R, Hardy J, Philips CA, Venter C, Talbot C, Clark RF, Goate A, Li J, Potter H, Karran E, Roberts GW, Hutton M, Adams MD. Prihar G, et al. Among authors: hutton m. Neuroreport. 1996 Jul 8;7(10):1680-4. doi: 10.1097/00001756-199607080-00031. Neuroreport. 1996. PMID: 8904781

5

A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's disease.

Perez-Tur J, Croxton R, Wright K, Phillips H, Zehr C, Crook R, Hutton M, Hardy J, Karran E, Roberts GW, Lancaster S, Haltia T. Perez-Tur J, et al. Among authors: hutton m. Neurodegeneration. 1996 Sep;5(3):207-12. doi: 10.1006/neur.1996.0028. Neurodegeneration. 1996. PMID: 8910898

6

Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation.

Crook R, Ellis R, Shanks M, Thal LJ, Perez-Tur J, Baker M, Hutton M, Haltia T, Hardy J, Galasko D. Crook R, et al. Among authors: hutton m. Ann Neurol. 1997 Jul;42(1):124-8. doi: 10.1002/ana.410420121. Ann Neurol. 1997. PMID: 9225696

7

The role of presenilin 1 in the genetics of Alzheimer's disease.

Clark RF, Hutton M, Talbot C, Wragg M, Lendon C, Busfield F, Han SW, Perez-Tur J, Adams M, Fuldner R, Roberts G, Karran E, Hardy J, Goate A. Clark RF, et al. Among authors: hutton m. Cold Spring Harb Symp Quant Biol. 1996;61:551-8. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246481

8

ApoE genotype is a risk factor in nonpresenilin early-onset Alzheimer's disease families.

Houlden H, Crook R, Backhovens H, Prihar G, Baker M, Hutton M, Rossor M, Martin JJ, Van Broeckhoven C, Hardy J. Houlden H, et al. Among authors: hutton m. Am J Med Genet. 1998 Feb 7;81(1):117-21. doi: 10.1002/(sici)1096-8628(19980207)81:1<117::aid-ajmg19>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9514597

9

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease. Alzheimer's Disease Collaborative Group.

Wragg M, Hutton M, Talbot C. Wragg M, et al. Among authors: hutton m. Lancet. 1996 Feb 24;347(9000):509-12. doi: 10.1016/s0140-6736(96)91140-x. Lancet. 1996. PMID: 8596269

10

Increased amyloid-beta42(43) in brains of mice expressing mutant presenilin 1.

Duff K, Eckman C, Zehr C, Yu X, Prada CM, Perez-tur J, Hutton M, Buee L, Harigaya Y, Yager D, Morgan D, Gordon MN, Holcomb L, Refolo L, Zenk B, Hardy J, Younkin S. Duff K, et al. Among authors: hutton m. Nature. 1996 Oct 24;383(6602):710-3. doi: 10.1038/383710a0. Nature. 1996. PMID: 8878479

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