Baker MC - Search Results

1

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype.

Rutherford NJ, Heckman MG, Dejesus-Hernandez M, Baker MC, Soto-Ortolaza AI, Rayaprolu S, Stewart H, Finger E, Volkening K, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Knopman DS, Kretzschmar HA, Neumann M, Caselli RJ, White CL 3rd, Mackenzie IR, Petersen RC, Strong MJ, Miller BL, Boeve BF, Uitti RJ, Boylan KB, Wszolek ZK, Graff-Radford NR, Dickson DW, Ross OA, Rademakers R. Rutherford NJ, et al. Among authors: baker mc. Neurobiol Aging. 2012 Dec;33(12):2950.e5-7. doi: 10.1016/j.neurobiolaging.2012.07.005. Epub 2012 Jul 26. Neurobiol Aging. 2012. PMID: 22840558 Free PMC article.

2

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, Hardy J, Lynch T, Bigio E, Hutton M. Baker M, et al. Hum Mol Genet. 1999 Apr;8(4):711-5. doi: 10.1093/hmg/8.4.711. Hum Mol Genet. 1999. PMID: 10072441

3

Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations.

Houlden H, Rizzu P, Stevens M, de Knijff P, van Duijn CM, van Swieten JC, Heutink P, Perez-Tur J, Thomas V, Baker M, Morris H, Rossor M, Jannsen JC, Petersen RC, Dodd P, Dark F, Boeve B, Dickson D, Davies P, Pickering-Brown S, Mann D, Adamson J, Lynch T, Payami H, Hardy J, et al. Houlden H, et al. Neurosci Lett. 1999 Feb 5;260(3):193-5. doi: 10.1016/s0304-3940(98)00931-8. Neurosci Lett. 1999. PMID: 10076900

4

Frequency of tau mutations in three series of non-Alzheimer's degenerative dementia.

Houlden H, Baker M, Adamson J, Grover A, Waring S, Dickson D, Lynch T, Boeve B, Petersen RC, Pickering-Brown S, Owen F, Neary D, Craufurd D, Snowden J, Mann D, Hutton M. Houlden H, et al. Ann Neurol. 1999 Aug;46(2):243-8. doi: 10.1002/1531-8249(199908)46:2<243::aid-ana14>3.0.co;2-l. Ann Neurol. 1999. PMID: 10443890

5

No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease.

Baker M, Graff-Radford D, Wavrant DeVrièze F, Graff-Radford N, Petersen RC, Kokmen E, Boeve B, Myllykangas L, Polvikoski T, Sulkava R, Verkoniemmi A, Tienari P, Haltia M, Hardy J, Hutton M, Perez-Tur J. Baker M, et al. Neurosci Lett. 2000 May 12;285(2):147-9. doi: 10.1016/s0304-3940(00)01057-0. Neurosci Lett. 2000. PMID: 10793248

6

Relationship of the extended tau haplotype to tau biochemistry and neuropathology in progressive supranuclear palsy.

Liu WK, Le TV, Adamson J, Baker M, Cookson N, Hardy J, Hutton M, Yen SH, Dickson DW. Liu WK, et al. Ann Neurol. 2001 Oct;50(4):494-502. doi: 10.1002/ana.1159. Ann Neurol. 2001. PMID: 11601500

7

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. Neurobiol Dis. 2002 Mar;9(2):269-73. doi: 10.1006/nbdi.2001.0473. Neurobiol Dis. 2002. PMID: 11895378

8

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. Arch Neurol. 2002 Apr;59(4):611-5. doi: 10.1001/archneur.59.4.611. Arch Neurol. 2002. PMID: 11939896

9

Familial frontotemporal dementia associated with a novel presenilin-1 mutation.

Tang-Wai D, Lewis P, Boeve B, Hutton M, Golde T, Baker M, Hardy J, Michels V, Ivnik R, Jack C, Petersen R. Tang-Wai D, et al. Dement Geriatr Cogn Disord. 2002;14(1):13-21. doi: 10.1159/000058328. Dement Geriatr Cogn Disord. 2002. PMID: 12053127

10

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.

Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Tsuboi Y, et al. Arch Neurol. 2002 Jun;59(6):943-50. doi: 10.1001/archneur.59.6.943. Arch Neurol. 2002. PMID: 12056930

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