Výsledky vyhledávání - Parvoneh Poorkaj

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  1. 1
    Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

    Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements Autor Ian D’Souza, Parvoneh Poorkaj, Ming Hong, David Nochlin, Virginia M.‐Y. Lee, Thomas D. Bird, Gerard D. Schellenberg

    Vydáno 1999
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  2. 2
    Tau isoform regulation is region‐ and cell‐specific in mouse brain

    Tau isoform regulation is region‐ and cell‐specific in mouse brain Autor Pamela J. McMillan, Elena Korvatska, Parvoneh Poorkaj, Zana Evstafjeva, Linda C. Robinson, Lynne Greenup, James B. Leverenz, Gerard D. Schellenberg, Ian D’Souza

    Vydáno 2008
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  3. 3
    Familial prion disease with alzheimer disease‐like tau pathology and clinical phenotype

    Familial prion disease with alzheimer disease‐like tau pathology and clinical phenotype Autor Suman Jayadev, David Nochlin, Parvoneh Poorkaj, Ellen J. Steinbart, James A. Mastrianni, Thomas J. Montine, Bernardino Ghetti, Gerard D. Schellenberg, Thomas D. Bird, James B. Leverenz

    Vydáno 2011
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  4. 4
    A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

    A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L) Autor Thomas D. Bird, David Nochlin, Parvoneh Poorkaj, Monique Cherrier, Jeffrey Kaye, Haydeh Payami, Elaine R. Peskind, Thomas H. Lampe, Ellen Nemens, Philip J. Boyer, Daniela Berg

    Vydáno 1999
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  5. 5
    Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

    Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development Autor Michael A. Crackower, Stephen W. Scherer, Johanna M. Rommens, Chi Chung Hui, Parvoneh Poorkaj, Sylvia Soder, Jan Maarten Cobben, Louanne Hudgins, James P. Evans, Lap Chee Tsui

    Vydáno 1996
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  6. 6
    Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

    Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17 Autor Lorraine N. Clark, Parvoneh Poorkaj, Zbigniew K. Wszołek, Daniel H. Geschwind, Ziad Nasreddine, Bruce L. Miller, Diane Li, Haydeh Payami, Fre Awert, Katerina Markopoulou, Athena Andreadis, Ian D’Souza, Virginia M.‐Y. Lee, Lee Reed, John Q. Trojanowski, Victoria Zhukareva, Thomas D. Bird, Gerard D. Schellenberg, Kirk C. Wilhelmsen

    Vydáno 1998
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  7. 7
    High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

    High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy Autor Rosa Rademakers, Stacey Melquist, Marc Cruts, Jessie Theuns, Jurgen Del‐Favero, Parvoneh Poorkaj, Matt Baker, Kristel Sleegers, Richard Crook, Tim De Pooter, Samira Bel Kacem, Jennifer Adamson, Dirk Van den Bossche, Marleen Van den Broeck, Jennifer Gass, Ellen Corsmit, Peter De Rijk, Natalie Thomas, Sebastiaan Engelborghs, Michael G. Heckman, Irene Litvan, Julia E. Crook, Peter Paul De Deyn, Dennis W. Dickson, Gerard D. Schellenberg, Christine Van Broeckhoven, Michael Hutton

    Vydáno 2005
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