Hutton M - Search Results

1

Heritability of plasma amyloid beta in typical late-onset Alzheimer's disease pedigrees.

Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Adamson J, Schaid DJ, Blangero J, Hutton M, Younkin SG. Ertekin-Taner N, et al. Among authors: hutton m. Genet Epidemiol. 2001 Jul;21(1):19-30. doi: 10.1002/gepi.1015. Genet Epidemiol. 2001. PMID: 11443731

2

Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.

Ertekin-Taner N, Ronald J, Asahara H, Younkin L, Hella M, Jain S, Gnida E, Younkin S, Fadale D, Ohyagi Y, Singleton A, Scanlin L, de Andrade M, Petersen R, Graff-Radford N, Hutton M, Younkin S. Ertekin-Taner N, et al. Among authors: hutton m. Hum Mol Genet. 2003 Dec 1;12(23):3133-43. doi: 10.1093/hmg/ddg343. Epub 2003 Oct 14. Hum Mol Genet. 2003. PMID: 14559775 Free PMC article.

3

Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene.

Ertekin-Taner N, Ronald J, Feuk L, Prince J, Tucker M, Younkin L, Hella M, Jain S, Hackett A, Scanlin L, Kelly J, Kihiko-Ehman M, Neltner M, Hersh L, Kindy M, Markesbery W, Hutton M, de Andrade M, Petersen RC, Graff-Radford N, Estus S, Brookes AJ, Younkin SG. Ertekin-Taner N, et al. Among authors: hutton m. Hum Mol Genet. 2005 Feb 1;14(3):447-60. doi: 10.1093/hmg/ddi041. Epub 2004 Dec 22. Hum Mol Genet. 2005. PMID: 15615772

4

Plasma amyloid beta protein is elevated in late-onset Alzheimer disease families.

Ertekin-Taner N, Younkin LH, Yager DM, Parfitt F, Baker MC, Asthana S, Hutton ML, Younkin SG, Graff-Radford NR. Ertekin-Taner N, et al. Among authors: hutton ml. Neurology. 2008 Feb 19;70(8):596-606. doi: 10.1212/01.WNL.0000278386.00035.21. Epub 2007 Oct 3. Neurology. 2008. PMID: 17914065

5

Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.

Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Baker M, Adamson J, Ronald J, Blangero J, Hutton M, Younkin SG. Ertekin-Taner N, et al. Among authors: hutton m. Science. 2000 Dec 22;290(5500):2303-4. doi: 10.1126/science.290.5500.2303. Science. 2000. PMID: 11125143

6

Early onset familial Alzheimer Disease with spastic paraparesis, dysarthria, and seizures and N135S mutation in PSEN1.

Rudzinski LA, Fletcher RM, Dickson DW, Crook R, Hutton ML, Adamson J, Graff-Radford NR. Rudzinski LA, et al. Among authors: hutton ml. Alzheimer Dis Assoc Disord. 2008 Jul-Sep;22(3):299-307. doi: 10.1097/WAD.0b013e3181732399. Alzheimer Dis Assoc Disord. 2008. PMID: 18580586 Free PMC article.

7

Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes.

Short RA, Graff-Radford NR, Adamson J, Baker M, Hutton M. Short RA, et al. Among authors: hutton m. Arch Neurol. 2002 Apr;59(4):611-5. doi: 10.1001/archneur.59.4.611. Arch Neurol. 2002. PMID: 11939896

8

A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43).

Eckman CB, Mehta ND, Crook R, Perez-tur J, Prihar G, Pfeiffer E, Graff-Radford N, Hinder P, Yager D, Zenk B, Refolo LM, Prada CM, Younkin SG, Hutton M, Hardy J. Eckman CB, et al. Among authors: hutton m. Hum Mol Genet. 1997 Nov;6(12):2087-9. doi: 10.1093/hmg/6.12.2087. Hum Mol Genet. 1997. PMID: 9328472

9

Increased Abeta42(43) from cell lines expressing presenilin 1 mutations.

Mehta ND, Refolo LM, Eckman C, Sanders S, Yager D, Perez-Tur J, Younkin S, Duff K, Hardy J, Hutton M. Mehta ND, et al. Among authors: hutton m. Ann Neurol. 1998 Feb;43(2):256-8. doi: 10.1002/ana.410430217. Ann Neurol. 1998. PMID: 9485068

10

A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notch.

Amtul Z, Lewis PA, Piper S, Crook R, Baker M, Findlay K, Singleton A, Hogg M, Younkin L, Younkin SG, Hardy J, Hutton M, Boeve BF, Tang-Wai D, Golde TE. Amtul Z, et al. Among authors: hutton m. Neurobiol Dis. 2002 Mar;9(2):269-73. doi: 10.1006/nbdi.2001.0473. Neurobiol Dis. 2002. PMID: 11895378

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