BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 17228326)

  • 1. Progranulin mutations in Dutch familial frontotemporal lobar degeneration.
    Bronner IF; Rizzu P; Seelaar H; van Mil SE; Anar B; Azmani A; Donker Kaat L; Rosso S; Heutink P; van Swieten JC
    Eur J Hum Genet; 2007 Mar; 15(3):369-74. PubMed ID: 17228326
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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;
    Hum Mutat; 2007 Sep; 28(9):846-55. PubMed ID: 17436289
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 28(4):416. PubMed ID: 17345602
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 66(2):142-51. PubMed ID: 17278999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update.
    Gijselinck I; Van Broeckhoven C; Cruts M
    Hum Mutat; 2008 Dec; 29(12):1373-86. PubMed ID: 18543312
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of progranulin function in frontotemporal lobar degeneration.
    Cruts M; Van Broeckhoven C
    Trends Genet; 2008 Apr; 24(4):186-94. PubMed ID: 18328591
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
    Sleegers K; Brouwers N; Van Damme P; Engelborghs S; Gijselinck I; van der Zee J; Peeters K; Mattheijssens M; Cruts M; Vandenberghe R; De Deyn PP; Robberecht W; Van Broeckhoven C
    Ann Neurol; 2009 May; 65(5):603-9. PubMed ID: 19288468
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.
    Rovelet-Lecrux A; Deramecourt V; Legallic S; Maurage CA; Le Ber I; Brice A; Lambert JC; Frébourg T; Hannequin D; Pasquier F; Campion D
    Neurobiol Dis; 2008 Jul; 31(1):41-5. PubMed ID: 18479928
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 60(3):314-22. PubMed ID: 16983685
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 442(7105):920-4. PubMed ID: 16862115
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.
    Ghidoni R; Benussi L; Glionna M; Franzoni M; Binetti G
    Neurology; 2008 Oct; 71(16):1235-9. PubMed ID: 18768919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease.
    Brouwers N; Sleegers K; Engelborghs S; Maurer-Stroh S; Gijselinck I; van der Zee J; Pickut BA; Van den Broeck M; Mattheijssens M; Peeters K; Schymkowitz J; Rousseau F; Martin JJ; Cruts M; De Deyn PP; Van Broeckhoven C
    Neurology; 2008 Aug; 71(9):656-64. PubMed ID: 18565828
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 64(10):1436-46. PubMed ID: 17923627
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 33(3):379-85. PubMed ID: 19101631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.
    Behrens MI; Mukherjee O; Tu PH; Liscic RM; Grinberg LT; Carter D; Paulsmeyer K; Taylor-Reinwald L; Gitcho M; Norton JB; Chakraverty S; Goate AM; Morris JC; Cairns NJ
    Alzheimer Dis Assoc Disord; 2007; 21(1):1-7. PubMed ID: 17334266
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progranulin genetic variability contributes to amyotrophic lateral sclerosis.
    Sleegers K; Brouwers N; Maurer-Stroh S; van Es MA; Van Damme P; van Vught PW; van der Zee J; Serneels S; De Pooter T; Van den Broeck M; Cruts M; Schymkowitz J; De Jonghe P; Rousseau F; van den Berg LH; Robberecht W; Van Broeckhoven C
    Neurology; 2008 Jul; 71(4):253-9. PubMed ID: 18184915
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration.
    Borroni B; Bonvicini C; Galimberti D; Tremolizzo L; Papetti A; Archetti S; Turla M; Alberici A; Agosti C; Premi E; Appollonio I; Rainero I; Ferrarese C; Gennarelli M; Scarpini E; Padovani A
    Neurobiol Aging; 2011 Mar; 32(3):555.e1-8. PubMed ID: 20947212
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.
    Skoglund L; Brundin R; Olofsson T; Kalimo H; Ingvast S; Blom ES; Giedraitis V; Ingelsson M; Lannfelt L; Basun H; Glaser A
    Neurogenetics; 2009 Feb; 10(1):27-34. PubMed ID: 18855025
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 29(1):53-8. PubMed ID: 18157829
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
    Gass J; Cannon A; Mackenzie IR; Boeve B; Baker M; Adamson J; Crook R; Melquist S; Kuntz K; Petersen R; Josephs K; Pickering-Brown SM; Graff-Radford N; Uitti R; Dickson D; Wszolek Z; Gonzalez J; Beach TG; Bigio E; Johnson N; Weintraub S; Mesulam M; White CL; Woodruff B; Caselli R; Hsiung GY; Feldman H; Knopman D; Hutton M; Rademakers R
    Hum Mol Genet; 2006 Oct; 15(20):2988-3001. PubMed ID: 16950801
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.