BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 9708539)

  • 1. Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease.
    Gu M; Cooper JM; Taanman JW; Schapira AH
    Ann Neurol; 1998 Aug; 44(2):177-86. PubMed ID: 9708539
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA in focal dystonia: a cybrid analysis.
    Tabrizi SJ; Cooper JM; Schapira AH
    Ann Neurol; 1998 Aug; 44(2):258-61. PubMed ID: 9708550
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytoplasmic transfer of platelet mtDNA from elderly patients with Parkinson's disease to mtDNA-less HeLa cells restores complete mitochondrial respiratory function.
    Aomi Y; Chen CS; Nakada K; Ito S; Isobe K; Murakami H; Kuno SY; Tawata M; Matsuoka R; Mizusawa H; Hayashi JI
    Biochem Biophys Res Commun; 2001 Jan; 280(1):265-73. PubMed ID: 11162509
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biochemical analysis of cybrids expressing mitochondrial DNA from Contursi kindred Parkinson's subjects.
    Swerdlow RH; Parks JK; Cassarino DS; Binder DR; Bennett JP; Di Iorio G; Golbe LI; Parker WD
    Exp Neurol; 2001 Jun; 169(2):479-85. PubMed ID: 11358461
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Abnormal mitochondrial morphology in sporadic Parkinson's and Alzheimer's disease cybrid cell lines.
    Trimmer PA; Swerdlow RH; Parks JK; Keeney P; Bennett JP; Miller SW; Davis RE; Parker WD
    Exp Neurol; 2000 Mar; 162(1):37-50. PubMed ID: 10716887
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease.
    Sandy MS; Langston JW; Smith MT; Di Monte DA
    Mov Disord; 1993; 8(1):74-82. PubMed ID: 8419811
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Absence of the mitochondrial A7237T mutation in Parkinson's disease.
    Lücking CB; Kösel S; Mehraein P; Graeber MB
    Biochem Biophys Res Commun; 1995 Jun; 211(2):700-4. PubMed ID: 7794285
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family.
    Swerdlow RH; Parks JK; Davis JN; Cassarino DS; Trimmer PA; Currie LJ; Dougherty J; Bridges WS; Bennett JP; Wooten GF; Parker WD
    Ann Neurol; 1998 Dec; 44(6):873-81. PubMed ID: 9851431
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial complex I, II/III, and IV activities in familial and sporadic Parkinson's disease.
    Hanagasi HA; Ayribas D; Baysal K; Emre M
    Int J Neurosci; 2005 Apr; 115(4):479-93. PubMed ID: 15809215
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisal.
    Schapira AH
    Mov Disord; 1994 Mar; 9(2):125-38. PubMed ID: 8196673
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondria in the etiology and pathogenesis of Parkinson's disease.
    Schapira AH; Gu M; Taanman JW; Tabrizi SJ; Seaton T; Cleeter M; Cooper JM
    Ann Neurol; 1998 Sep; 44(3 Suppl 1):S89-98. PubMed ID: 9749579
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sequence analysis of the entire mitochondrial genome in Parkinson's disease.
    Vives-Bauza C; Andreu AL; Manfredi G; Beal MF; Janetzky B; Gruenewald TH; Lin MT
    Biochem Biophys Res Commun; 2002 Feb; 290(5):1593-601. PubMed ID: 11820805
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of cybrid cell lines containing mtDNA from Huntington's disease patients.
    Swerdlow RH; Parks JK; Cassarino DS; Shilling AT; Bennett JP; Harrison MB; Parker WD
    Biochem Biophys Res Commun; 1999 Aug; 261(3):701-4. PubMed ID: 10441489
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial respiratory chain function in multiple system atrophy.
    Gu M; Gash MT; Cooper JM; Wenning GK; Daniel SE; Quinn NP; Marsden CD; Schapira AH
    Mov Disord; 1997 May; 12(3):418-22. PubMed ID: 9159739
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Origin and functional consequences of the complex I defect in Parkinson's disease.
    Swerdlow RH; Parks JK; Miller SW; Tuttle JB; Trimmer PA; Sheehan JP; Bennett JP; Davis RE; Parker WD
    Ann Neurol; 1996 Oct; 40(4):663-71. PubMed ID: 8871587
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction.
    Kösel S; Egensperger R; Schnopp NM; Graeber MB
    Mov Disord; 1997 Sep; 12(5):639-45. PubMed ID: 9380043
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Role of mitochondria in Parkinson disease.
    Kösel S; Hofhaus G; Maassen A; Vieregge P; Graeber MB
    Biol Chem; 1999; 380(7-8):865-70. PubMed ID: 10494835
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial function in Parkinson's disease cybrids containing an nt2 neuron-like nuclear background.
    Esteves AR; Domingues AF; Ferreira IL; Januário C; Swerdlow RH; Oliveira CR; Cardoso SM
    Mitochondrion; 2008 Jun; 8(3):219-28. PubMed ID: 18495557
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
    Huerta C; Castro MG; Coto E; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; Martínez C; Lahoz CH; Alvarez V
    J Neurol Sci; 2005 Sep; 236(1-2):49-54. PubMed ID: 15975594
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.
    Smigrodzki R; Parks J; Parker WD
    Neurobiol Aging; 2004; 25(10):1273-81. PubMed ID: 15465623
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.