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106 related items for PubMed ID: 11553688

  • 21. Study of methylation levels of parkin gene promoter in Parkinson's disease patients.
    Cai M, Tian J, Zhao GH, Luo W, Zhang BR.
    Int J Neurosci; 2011 Sep; 121(9):497-502. PubMed ID: 21663383
    [Abstract] [Full Text] [Related]

  • 22. Early-onset Parkinson's disease associated with a new parkin mutation in a Spanish family.
    Alvarez V, Guisasola LM, Moreira VG, Lahoz CH, Coto E.
    Neurosci Lett; 2001 Nov 02; 313(1-2):108-10. PubMed ID: 11684352
    [Abstract] [Full Text] [Related]

  • 23. Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease.
    Chung KK, Zhang Y, Lim KL, Tanaka Y, Huang H, Gao J, Ross CA, Dawson VL, Dawson TM.
    Nat Med; 2001 Oct 02; 7(10):1144-50. PubMed ID: 11590439
    [Abstract] [Full Text] [Related]

  • 24. Parkin is linked to the ubiquitin pathway.
    Tanaka K, Suzuki T, Chiba T, Shimura H, Hattori N, Mizuno Y.
    J Mol Med (Berl); 2001 Sep 02; 79(9):482-94. PubMed ID: 11692161
    [Abstract] [Full Text] [Related]

  • 25. Genetics of Parkinson's disease.
    Gasser T.
    Clin Genet; 1998 Oct 02; 54(4):259-65. PubMed ID: 9831335
    [Abstract] [Full Text] [Related]

  • 26. Parkin mutations and susceptibility alleles in late-onset Parkinson's disease.
    Oliveira SA, Scott WK, Martin ER, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Ondo WG, Allen FH, Scott BL, Goetz CG, Small GW, Mastaglia F, Stajich JM, Zhang F, Booze MW, Winn MP, Middleton LT, Haines JL, Pericak-Vance MA, Vance JM.
    Ann Neurol; 2003 May 02; 53(5):624-9. PubMed ID: 12730996
    [Abstract] [Full Text] [Related]

  • 27. Characterization of the 5' flanking region of the rat D(3) dopamine receptor gene.
    D'Souza UM, Wang W, Gao DQ, Kanda S, Lee G, Junn E, Hwang CK, Jose PA, Mouradian MM.
    J Neurochem; 2001 Mar 02; 76(6):1736-44. PubMed ID: 11259491
    [Abstract] [Full Text] [Related]

  • 28. [Parkin gene: its mutations and function].
    Hattori N.
    Rinsho Shinkeigaku; 2002 Nov 02; 42(11):1077-81. PubMed ID: 12784670
    [Abstract] [Full Text] [Related]

  • 29. Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.
    Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y.
    Biochem Biophys Res Commun; 1998 Aug 28; 249(3):754-8. PubMed ID: 9731209
    [Abstract] [Full Text] [Related]

  • 30. A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism.
    Muñoz E, Pastor P, Martí MJ, Oliva R, Tolosa E.
    Neurosci Lett; 2000 Jul 28; 289(1):66-8. PubMed ID: 10899410
    [Abstract] [Full Text] [Related]

  • 31. Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.
    Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C.
    Ann Neurol; 2005 Sep 28; 58(3):411-22. PubMed ID: 16130111
    [Abstract] [Full Text] [Related]

  • 32. Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease.
    da Costa CA, Sunyach C, Giaime E, West A, Corti O, Brice A, Safe S, Abou-Sleiman PM, Wood NW, Takahashi H, Goldberg MS, Shen J, Checler F.
    Nat Cell Biol; 2009 Nov 28; 11(11):1370-5. PubMed ID: 19801972
    [Abstract] [Full Text] [Related]

  • 33. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N.
    Rinsho Shinkeigaku; 2004 Nov 28; 44(4-5):241-62. PubMed ID: 15287506
    [Abstract] [Full Text] [Related]

  • 34. Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin's effect on neuronal survival.
    Muqit MM, Davidson SM, Payne Smith MD, MacCormac LP, Kahns S, Jensen PH, Wood NW, Latchman DS.
    Hum Mol Genet; 2004 Jan 01; 13(1):117-35. PubMed ID: 14645198
    [Abstract] [Full Text] [Related]

  • 35. Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.
    Lesage S, Magali P, Lohmann E, Lacomblez L, Teive H, Janin S, Cousin PY, Dürr A, Brice A, French Parkinson Disease Genetics Study Group.
    Hum Mutat; 2007 Jan 01; 28(1):27-32. PubMed ID: 17068781
    [Abstract] [Full Text] [Related]

  • 36. Characterization of the 5'-flanking promoter region of the rat somatostatin receptor subtype 3 gene.
    Glos M, Kreienkamp HJ, Hausmann H, Richter D.
    FEBS Lett; 1998 Nov 27; 440(1-2):33-7. PubMed ID: 9862419
    [Abstract] [Full Text] [Related]

  • 37. A multidisciplinary study of patients with early-onset PD with and without parkin mutations.
    Lohmann E, Thobois S, Lesage S, Broussolle E, du Montcel ST, Ribeiro MJ, Remy P, Pelissolo A, Dubois B, Mallet L, Pollak P, Agid Y, Brice A, French Parkinson's Disease Genetics Study Group.
    Neurology; 2009 Jan 13; 72(2):110-6. PubMed ID: 18987353
    [Abstract] [Full Text] [Related]

  • 38. Genetics of Parkinsonism: a review.
    Vaughan JR, Davis MB, Wood NW.
    Ann Hum Genet; 2001 Mar 13; 65(Pt 2):111-26. PubMed ID: 11427172
    [Abstract] [Full Text] [Related]

  • 39. Loss of locus coeruleus neurons and reduced startle in parkin null mice.
    Von Coelln R, Thomas B, Savitt JM, Lim KL, Sasaki M, Hess EJ, Dawson VL, Dawson TM.
    Proc Natl Acad Sci U S A; 2004 Jul 20; 101(29):10744-9. PubMed ID: 15249681
    [Abstract] [Full Text] [Related]

  • 40. Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.
    Kim JS, Lee KS, Kim YI, Lee KH, Kim HT.
    Yonsei Med J; 2003 Apr 30; 44(2):336-9. PubMed ID: 12728478
    [Abstract] [Full Text] [Related]

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