These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 15022188)

  • 1. Autosomal recessive juvenile parkinsonism Cys212Tyr mutation in parkin renders lymphocytes susceptible to dopamine- and iron-mediated apoptosis.
    Jimenez Del Rio M; Moreno S; Garcia-Ospina G; Buritica O; Uribe CS; Lopera F; Velez-Pardo C
    Mov Disord; 2004 Mar; 19(3):324-30. PubMed ID: 15022188
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism.
    Illarioshkin SN; Periquet M; Rawal N; Lücking CB; Zagorovskaya TB; Slominsky PA; Miloserdova OV; Markova ED; Limborska SA; Ivanova-Smolenskaya IA; Brice A
    Mov Disord; 2003 Aug; 18(8):914-9. PubMed ID: 12889082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.
    Muñoz E; Tolosa E; Pastor P; Martí MJ; Valldeoriola F; Campdelacreu J; Oliva R
    J Neurol Neurosurg Psychiatry; 2002 Nov; 73(5):582-4. PubMed ID: 12397156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonism.
    Chen H; Huang X; Yuan L; Xia H; Xu H; Yang Y; Zheng W; Deng H
    Neurosci Lett; 2016 Jun; 624():100-4. PubMed ID: 27177722
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Autosomal recessive juvenile parkinsonism.
    Saito M; Maruyama M; Ikeuchi K; Kondo H; Ishikawa A; Yuasa T; Tsuji S
    Brain Dev; 2000 Sep; 22 Suppl 1():S115-7. PubMed ID: 10984671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.
    Shimizu N; Asakawa S; Minoshima S; Kitada T; Hattori N; Matsumine H; Yokochi M; Yamamura Y; Mizuno Y
    J Neural Transm Suppl; 2000; (58):19-30. PubMed ID: 11128608
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism.
    Kuroda Y; Mitsui T; Akaike M; Azuma H; Matsumoto T
    J Neurol Neurosurg Psychiatry; 2001 Aug; 71(2):231-4. PubMed ID: 11459900
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diagnostic considerations in juvenile parkinsonism.
    Paviour DC; Surtees RA; Lees AJ
    Mov Disord; 2004 Feb; 19(2):123-35. PubMed ID: 14978667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year period.
    Clarimon J; Johnson J; Djaldetti R; Hernandez D; Hattori N; Sroka H; Barhom Y; Singleton A
    Mov Disord; 2005 Jul; 20(7):887-90. PubMed ID: 15852366
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. [Genotype and phenotype analyses of three families with autosomal recessive juvenile parkinsonism].
    Guo JF; Tang BS; Zhang YH; Liu HJ; Yan XX; Chen T; Shen L; Jiang H; Xia K; Cai F; Pan Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb; 23(1):70-3. PubMed ID: 16456791
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Effect of overexpression of wild-type or mutant parkin on the cellular response induced by toxic insults.
    Hyun DH; Lee M; Halliwell B; Jenner P
    J Neurosci Res; 2005 Oct; 82(2):232-44. PubMed ID: 16130151
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
    Gouider-Khouja N; Larnaout A; Amouri R; Sfar S; Belal S; Ben Hamida C; Ben Hamida M; Hattori N; Mizuno Y; Hentati F
    Parkinsonism Relat Disord; 2003 Jun; 9(5):247-51. PubMed ID: 12781588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of compound heterozygous deletions in the parkin gene of fibroblasts in patients with autosomal recessive hereditary parkinsonism (PARK2).
    Nakaso K; Adachi Y; Yasui K; Sakuma K; Nakashima K
    Neurosci Lett; 2006 May; 400(1-2):44-7. PubMed ID: 16517073
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.
    Nisipeanu P; Inzelberg R; Blumen SC; Carasso RL; Hattori N; Matsumine H; Mizuno Y
    Neurology; 1999 Oct; 53(7):1602-4. PubMed ID: 10534280
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of eighteen deletion breakpoints in the parkin gene.
    Asakawa S; Hattori N; Shimizu A; Shimizu Y; Minoshima S; Mizuno Y; Shimizu N
    Biochem Biophys Res Commun; 2009 Nov; 389(1):181-6. PubMed ID: 19715670
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Autosomal recessive juvenile parkinsonism: its pathogenesis is involved in the ubiquitin-proteasome pathway].
    Hattori N; Shimura H; Kubo S; Suzuki T; Tanaka K; Mizuno Y
    Rinsho Shinkeigaku; 2000 Dec; 40(12):1293-6. PubMed ID: 11464483
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 79(9):482-94. PubMed ID: 11692161
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reduction in endogenous parkin levels renders glial cells sensitive to both caspase-dependent and caspase-independent cell death.
    MacCormac LP; Muqit MM; Faulkes DJ; Wood NW; Latchman DS
    Eur J Neurosci; 2004 Oct; 20(8):2038-48. PubMed ID: 15450083
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygous partial genomic triplication of the parkin gene in early-onset parkinsonism.
    Mata IF; Alvarez V; Coto E; Blazquez M; Guisasola LM; Salvador C; Kachergus JM; Lincoln SJ; Farrer M
    Neurosci Lett; 2005 Jun; 380(3):257-9. PubMed ID: 15862897
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.