Baker M - Search Results

1

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

Boeve BF, Baker M, Dickson DW, Parisi JE, Giannini C, Josephs KA, Hutton M, Pickering-Brown SM, Rademakers R, Tang-Wai D, Jack CR Jr, Kantarci K, Shiung MM, Golde T, Smith GE, Geda YE, Knopman DS, Petersen RC. Boeve BF, et al. Among authors: baker m. Brain. 2006 Nov;129(Pt 11):3103-14. doi: 10.1093/brain/awl268. Epub 2006 Oct 9. Brain. 2006. PMID: 17030535

2

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Baker M, et al. Ann Neurol. 1997 Nov;42(5):794-8. doi: 10.1002/ana.410420516. Ann Neurol. 1997. PMID: 9392579

3

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: baker 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

4

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.

Crook R, Verkkoniemi A, Perez-Tur J, Mehta N, Baker M, Houlden H, Farrer M, Hutton M, Lincoln S, Hardy J, Gwinn K, Somer M, Paetau A, Kalimo H, Ylikoski R, Pöyhönen M, Kucera S, Haltia M. Crook R, et al. Among authors: baker m. Nat Med. 1998 Apr;4(4):452-5. doi: 10.1038/nm0498-452. Nat Med. 1998. PMID: 9546792

5

Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.

Hardy J, Pérez-Tur J, Baker M, Farrer M, Crook R, Hutton M, Johnson WG, Gwinn K, Muenter M, Rocca WA, Maraganore D. Hardy J, et al. Among authors: baker m. Am J Med Genet. 1998 Mar 28;81(2):166-71. Am J Med Genet. 1998. PMID: 9613857

6

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P. Hutton M, et al. Among authors: baker m. Nature. 1998 Jun 18;393(6686):702-5. doi: 10.1038/31508. Nature. 1998. PMID: 9641683

7

Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.

Isaacs A, Baker M, Wavrant-De Vrièze F, Hutton M. Isaacs A, et al. Among authors: baker m. Genomics. 1998 Jul 1;51(1):152-4. doi: 10.1006/geno.1998.5360. Genomics. 1998. PMID: 9693047 No abstract available.

8

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

9

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. Among authors: baker m. Neurosci Lett. 1999 Feb 5;260(3):193-5. doi: 10.1016/s0304-3940(98)00931-8. Neurosci Lett. 1999. PMID: 10076900

10

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

Grover A, Houlden H, Baker M, Adamson J, Lewis J, Prihar G, Pickering-Brown S, Duff K, Hutton M. Grover A, et al. Among authors: baker m. J Biol Chem. 1999 May 21;274(21):15134-43. doi: 10.1074/jbc.274.21.15134. J Biol Chem. 1999. PMID: 10329720 Free article.

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