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    Results: 1 to 20 of 36

    1.

    Tau isoform regulation is region- and cell-specific in mouse brain.

    McMillan P, Korvatska E, Poorkaj P, Evstafjeva Z, Robinson L, Greenup L, Leverenz J, Schellenberg GD, D'Souza I.

    J Comp Neurol. 2008 Dec 20;511(6):788-803.PMID: 18925637 [PubMed - indexed for MEDLINE]Related articles

    2.

    Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.

    Kay DM, Moran D, Moses L, Poorkaj P, Zabetian CP, Nutt J, Factor SA, Yu CE, Montimurro JS, Keefe RG, Schellenberg GD, Payami H.

    Ann Neurol. 2007 Jan;61(1):47-54.PMID: 17187375 [PubMed - indexed for MEDLINE]Related articles

    3.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.

    Poorkaj P, Moses L, Montimurro JS, Nutt JG, Schellenberg GD, Payami H.

    BMC Neurol. 2005 Feb 22;5(1):4.PMID: 15725358 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.

    Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H.

    Am J Med Genet A. 2004 Aug 15;129A(1):44-50. Erratum in: Am J Med Genet A. 2005 Nov 15;139(1):56. PMID: 15266615 [PubMed - indexed for MEDLINE]Related articles

    6.

    Familial dementia with lewy bodies: a clinical and neuropathological study of 2 families.

    Tsuang DW, Dalan AM, Eugenio CJ, Poorkaj P, Limprasert P, La Spada AR, Steinbart EJ, Bird TD, Leverenz JB.

    Arch Neurol. 2002 Oct;59(10):1622-30.PMID: 12374501 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.

    Poorkaj P, Muma NA, Zhukareva V, Cochran EJ, Shannon KM, Hurtig H, Koller WC, Bird TD, Trojanowski JQ, Lee VM, Schellenberg GD.

    Ann Neurol. 2002 Oct;52(4):511-6.PMID: 12325083 [PubMed - indexed for MEDLINE]Related articles

    8.

    TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of Guam.

    Poorkaj P, Tsuang D, Wijsman E, Steinbart E, Garruto RM, Craig UK, Chapman NH, Anderson L, Bird TD, Plato CC, Perl DP, Weiderholt W, Galasko D, Schellenberg GD.

    Arch Neurol. 2001 Nov;58(11):1871-8.PMID: 11708997 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia.

    Steinbart EJ, Smith CO, Poorkaj P, Bird TD.

    Arch Neurol. 2001 Nov;58(11):1828-31.PMID: 11708991 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    A genomic sequence analysis of the mouse and human microtubule-associated protein tau.

    Poorkaj P, Kas A, D'Souza I, Zhou Y, Pham Q, Stone M, Olson MV, Schellenberg GD.

    Mamm Genome. 2001 Sep;12(9):700-12.PMID: 11641718 [PubMed - indexed for MEDLINE]Related articles

    11.

    Identification and characterization of the Drosophila tau homolog.

    Heidary G, Fortini ME.

    Mech Dev. 2001 Oct;108(1-2):171-8.PMID: 11578871 [PubMed - indexed for MEDLINE]Related articles

    12.

    Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia.

    Poorkaj P, Grossman M, Steinbart E, Payami H, Sadovnick A, Nochlin D, Tabira T, Trojanowski JQ, Borson S, Galasko D, Reich S, Quinn B, Schellenberg G, Bird TD.

    Arch Neurol. 2001 Mar;58(3):383-7.PMID: 11255441 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    The genetics of Alzheimer's disease.

    Schellenberg GD, D'Souza I, Poorkaj P.

    Curr Psychiatry Rep. 2000 Apr;2(2):158-64. Review.PMID: 11122949 [PubMed - indexed for MEDLINE]Related articles

    14.

    Single-step conversion of P1 and P1 artificial chromosome clones into yeast artificial chromosomes.

    Poorkaj P, Peterson KR, Schellenberg GD.

    Genomics. 2000 Aug 15;68(1):106-10.PMID: 10950935 [PubMed - indexed for MEDLINE]Related articles

    15.

    A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)

    Yasuda M, Takamatsu J, D'Souza I, Crowther RA, Kawamata T, Hasegawa M, Hasegawa H, Spillantini MG, Tanimukai S, Poorkaj P, Varani L, Varani G, Iwatsubo T, Goedert M, Schellenberg DG, Tanaka C.

    Ann Neurol. 2000 Apr;47(4):422-9.PMID: 10762152 [PubMed - indexed for MEDLINE]Related articles

    16.

    Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions.

    Kertesz A, Kawarai T, Rogaeva E, St George-Hyslop P, Poorkaj P, Bird TD, Munoz DG.

    Neurology. 2000 Feb 22;54(4):818-27.PMID: 10690970 [PubMed - indexed for MEDLINE]Related articles

    17.

    A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

    Yasuda M, Kawamata T, Komure O, Kuno S, D'Souza I, Poorkaj P, Kawai J, Tanimukai S, Yamamoto Y, Hasegawa H, Sasahara M, Hazama F, Schellenberg GD, Tanaka C.

    Neurology. 1999 Sep 11;53(4):864-8.PMID: 10489057 [PubMed - indexed for MEDLINE]Related articles

    18.

    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.

    J Biol Chem. 1999 May 21;274(21):15134-43.PMID: 10329720 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements.

    D'Souza I, Poorkaj P, Hong M, Nochlin D, Lee VM, Bird TD, Schellenberg GD.

    Proc Natl Acad Sci U S A. 1999 May 11;96(10):5598-603.PMID: 10318930 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

    Bird TD, Nochlin D, Poorkaj P, Cherrier M, Kaye J, Payami H, Peskind E, Lampe TH, Nemens E, Boyer PJ, Schellenberg GD.

    Brain. 1999 Apr;122 ( Pt 4):741-56. Erratum in: Brain 1999 Jul;122(Pt 7):1398. PMID: 10219785 [PubMed - indexed for MEDLINE]Related articlesFree article

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