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Items: 1 to 20 of 151

1.

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.

Pittman AM, Myers AJ, Abou-Sleiman P, Fung HC, Kaleem M, Marlowe L, Duckworth J, Leung D, Williams D, Kilford L, Thomas N, Morris CM, Dickson D, Wood NW, Hardy J, Lees AJ, de Silva R.

J Med Genet. 2005 Nov;42(11):837-46. Epub 2005 Mar 25.

2.

Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.

Ezquerra M, Pastor P, Gaig C, Vidal-Taboada JM, Cruchaga C, Muñoz E, Martí MJ, Valldeoriola F, Aguilar M, Calopa M, Hernandez-Vara J, Tolosa E.

Neurobiol Aging. 2011 Mar;32(3):547.e11-6. doi: 10.1016/j.neurobiolaging.2009.09.011. Epub 2009 Oct 29.

PMID:
19879020
3.

The structure of the tau haplotype in controls and in progressive supranuclear palsy.

Pittman AM, Myers AJ, Duckworth J, Bryden L, Hanson M, Abou-Sleiman P, Wood NW, Hardy J, Lees A, de Silva R.

Hum Mol Genet. 2004 Jun 15;13(12):1267-74. Epub 2004 Apr 28.

PMID:
15115761
4.

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy.

Pastor P, Ezquerra M, Perez JC, Chakraverty S, Norton J, Racette BA, McKeel D, Perlmutter JS, Tolosa E, Goate AM.

Ann Neurol. 2004 Aug;56(2):249-58.

PMID:
15293277
5.

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.

Cruchaga C, Vidal-Taboada JM, Ezquerra M, Lorenzo E, Martinez-Lage P, Blazquez M, Tolosa E; Iberian Atypical Parkinsonism Study Group Researchers, Pastor P.

Neurobiol Dis. 2009 Feb;33(2):164-70. doi: 10.1016/j.nbd.2008.09.027. Epub 2008 Nov 1.

PMID:
19022385
6.

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.

Rademakers R, Melquist S, Cruts M, Theuns J, Del-Favero J, Poorkaj P, Baker M, Sleegers K, Crook R, De Pooter T, Bel Kacem S, Adamson J, Van den Bossche D, Van den Broeck M, Gass J, Corsmit E, De Rijk P, Thomas N, Engelborghs S, Heckman M, Litvan I, Crook J, De Deyn PP, Dickson D, Schellenberg GD, Van Broeckhoven C, Hutton ML.

Hum Mol Genet. 2005 Nov 1;14(21):3281-92. Epub 2005 Sep 29.

PMID:
16195395
7.

Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease.

Vandrovcova J, Pittman AM, Malzer E, Abou-Sleiman PM, Lees AJ, Wood NW, de Silva R.

Neurobiol Aging. 2009 Sep;30(9):1477-82. Epub 2007 Dec 26.

PMID:
18162161
8.

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.

Houlden H, Baker M, Morris HR, MacDonald N, Pickering-Brown S, Adamson J, Lees AJ, Rossor MN, Quinn NP, Kertesz A, Khan MN, Hardy J, Lantos PL, St George-Hyslop P, Munoz DG, Mann D, Lang AE, Bergeron C, Bigio EH, Litvan I, Bhatia KP, Dickson D, Wood NW, Hutton M.

Neurology. 2001 Jun 26;56(12):1702-6.

PMID:
11425937
9.

Haplotype-specific expression of exon 10 at the human MAPT locus.

Caffrey TM, Joachim C, Paracchini S, Esiri MM, Wade-Martins R.

Hum Mol Genet. 2006 Dec 15;15(24):3529-37. Epub 2006 Nov 3.

PMID:
17085483
10.

H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers.

Canu E, Boccardi M, Ghidoni R, Benussi L, Testa C, Pievani M, Bonetti M, Binetti G, Frisoni GB.

Eur J Hum Genet. 2009 Mar;17(3):287-94. doi: 10.1038/ejhg.2008.185. Epub 2008 Oct 15.

11.

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

Oliveira SA, Scott WK, Zhang F, Stajich JM, Fujiwara K, Hauser M, Scott BL, Pericak-Vance MA, Vance JM, Martin ER.

Neurogenetics. 2004 Sep;5(3):147-55. Epub 2004 Jun 8.

PMID:
15459824
12.

Functional MAPT haplotypes: bridging the gap between genotype and neuropathology.

Caffrey TM, Wade-Martins R.

Neurobiol Dis. 2007 Jul;27(1):1-10. Epub 2007 May 5. Review.

13.

An association study of common variation at the MAPT locus with late-onset Alzheimer's disease.

Abraham R, Sims R, Carroll L, Hollingworth P, O'Donovan MC, Williams J, Owen MJ.

Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1152-5. doi: 10.1002/ajmg.b.30951.

PMID:
19308965
14.

Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders.

Webb A, Miller B, Bonasera S, Boxer A, Karydas A, Wilhelmsen KC.

Arch Neurol. 2008 Nov;65(11):1473-8. doi: 10.1001/archneur.65.11.1473.

15.

Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.

Scaravilli T, Tolosa E, Ferrer I.

Mov Disord. 2005 Aug;20 Suppl 12:S21-8.

PMID:
16092076
16.

Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders.

Lai MC, Bechy AL, Denk F, Collins E, Gavriliouk M, Zaugg JB, Ryan BJ, Wade-Martins R, Caffrey TM.

Mol Neurodegener. 2017 Oct 30;12(1):79. doi: 10.1186/s13024-017-0224-6.

17.

Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.

Yokoyama JS, Karch CM, Fan CC, Bonham LW, Kouri N, Ross OA, Rademakers R, Kim J, Wang Y, Höglinger GU, Müller U, Ferrari R, Hardy J; International FTD-Genomics Consortium (IFGC), Momeni P, Sugrue LP, Hess CP, James Barkovich A, Boxer AL, Seeley WW, Rabinovici GD, Rosen HJ, Miller BL, Schmansky NJ, Fischl B, Hyman BT, Dickson DW, Schellenberg GD, Andreassen OA, Dale AM, Desikan RS.

Acta Neuropathol. 2017 May;133(5):825-837. doi: 10.1007/s00401-017-1693-y. Epub 2017 Mar 7.

18.

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.

de Silva R, Weiler M, Morris HR, Martin ER, Wood NW, Lees AJ.

Neurosci Lett. 2001 Oct 5;311(3):145-8.

PMID:
11578815
19.

Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner.

de Jong S, Chepelev I, Janson E, Strengman E, van den Berg LH, Veldink JH, Ophoff RA.

BMC Genomics. 2012 Sep 6;13:458. doi: 10.1186/1471-2164-13-458.

20.

The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.

Camuzat A, Romana M, Dürr A, Feingold J, Brice A, Ruberg M, Lannuzel A.

Mov Disord. 2008 Dec 15;23(16):2384-91. doi: 10.1002/mds.22297.

PMID:
18785640

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