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Journal Abstract Search

1039 related items for PubMed ID: 16862115

  • 1. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
    Cruts M, Gijselinck I, van der Zee J, Engelborghs S, Wils H, Pirici D, Rademakers R, Vandenberghe R, Dermaut B, Martin JJ, van Duijn C, Peeters K, Sciot R, Santens P, De Pooter T, Mattheijssens M, Van den Broeck M, Cuijt I, Vennekens K, De Deyn PP, Kumar-Singh S, Van Broeckhoven C.
    Nature; 2006 Aug 24; 442(7105):920-4. PubMed ID: 16862115
    [Abstract] [Full Text] [Related]

  • 2. Progranulin mutations in ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
    Cruts M, Kumar-Singh S, Van Broeckhoven C.
    Curr Alzheimer Res; 2006 Dec 24; 3(5):485-91. PubMed ID: 17168647
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  • 3. Progranulin null mutations in both sporadic and familial frontotemporal dementia.
    Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A, French Research Network on FTD/FTD-MND.
    Hum Mutat; 2007 Sep 24; 28(9):846-55. PubMed ID: 17436289
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  • 4. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
    Baker M, Mackenzie IR, Pickering-Brown SM, Gass J, Rademakers R, Lindholm C, Snowden J, Adamson J, Sadovnick AD, Rollinson S, Cannon A, Dwosh E, Neary D, Melquist S, Richardson A, Dickson D, Berger Z, Eriksen J, Robinson T, Zehr C, Dickey CA, Crook R, McGowan E, Mann D, Boeve B, Feldman H, Hutton M.
    Nature; 2006 Aug 24; 442(7105):916-9. PubMed ID: 16862116
    [Abstract] [Full Text] [Related]

  • 5. Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.
    Brouwers N, Nuytemans K, van der Zee J, Gijselinck I, Engelborghs S, Theuns J, Kumar-Singh S, Pickut BA, Pals P, Dermaut B, Bogaerts V, De Pooter T, Serneels S, Van den Broeck M, Cuijt I, Mattheijssens M, Peeters K, Sciot R, Martin JJ, Cras P, Santens P, Vandenberghe R, De Deyn PP, Cruts M, Van Broeckhoven C, Sleegers K.
    Arch Neurol; 2007 Oct 24; 64(10):1436-46. PubMed ID: 17923627
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  • 6. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
    Cruts M, Rademakers R, Gijselinck I, van der Zee J, Dermaut B, de Pooter T, de Rijk P, Del-Favero J, van Broeckhoven C.
    Hum Mol Genet; 2005 Jul 01; 14(13):1753-62. PubMed ID: 15888485
    [Abstract] [Full Text] [Related]

  • 7. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
    van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Sleegers K, Hannequin D, Dermaut B, Schymkowitz J, Campion D, Santens P, Martin JJ, Lacomblez L, De Pooter T, Peeters K, Mattheijssens M, Vercelletto M, Van den Broeck M, Cruts M, De Deyn PP, Rousseau F, Brice A, Van Broeckhoven C.
    Hum Mutat; 2007 Apr 01; 28(4):416. PubMed ID: 17345602
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  • 8. [Clinical, pathological, and genetic characteristics of frontotemporal dementia and parkinsonism linked to chromosome 17 with mutations in the MAPT and PGRN].
    Tsuboi Y.
    Brain Nerve; 2009 Nov 01; 61(11):1285-91. PubMed ID: 19938685
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  • 9. Progranulin locus deletion in frontotemporal dementia.
    Gijselinck I, van der Zee J, Engelborghs S, Goossens D, Peeters K, Mattheijssens M, Corsmit E, Del-Favero J, De Deyn PP, Van Broeckhoven C, Cruts M.
    Hum Mutat; 2008 Jan 01; 29(1):53-8. PubMed ID: 18157829
    [Abstract] [Full Text] [Related]

  • 10. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations.
    Josephs KA, Ahmed Z, Katsuse O, Parisi JF, Boeve BF, Knopman DS, Petersen RC, Davies P, Duara R, Graff-Radford NR, Uitti RJ, Rademakers R, Adamson J, Baker M, Hutton ML, Dickson DW.
    J Neuropathol Exp Neurol; 2007 Feb 01; 66(2):142-51. PubMed ID: 17278999
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  • 13. Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.
    Benussi L, Ghidoni R, Pegoiani E, Moretti DV, Zanetti O, Binetti G.
    Neurobiol Dis; 2009 Mar 01; 33(3):379-85. PubMed ID: 19101631
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  • 15. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.
    Rademakers R, Cruts M, Dermaut B, Sleegers K, Rosso SM, Van den Broeck M, Backhovens H, van Swieten J, van Duijn CM, Van Broeckhoven C.
    Mol Psychiatry; 2002 Mar 01; 7(10):1064-74. PubMed ID: 12476321
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  • 16. HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin.
    Mukherjee O, Pastor P, Cairns NJ, Chakraverty S, Kauwe JS, Shears S, Behrens MI, Budde J, Hinrichs AL, Norton J, Levitch D, Taylor-Reinwald L, Gitcho M, Tu PH, Tenenholz Grinberg L, Liscic RM, Armendariz J, Morris JC, Goate AM.
    Ann Neurol; 2006 Sep 01; 60(3):314-22. PubMed ID: 16983685
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  • 18. Loss of progranulin function in frontotemporal lobar degeneration.
    Cruts M, Van Broeckhoven C.
    Trends Genet; 2008 Apr 01; 24(4):186-94. PubMed ID: 18328591
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