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 *

106 related articles for article (PubMed ID: 7894476)

  • 1. Mitochondrial DNA: does more lead to less?
    Poulton J; Holt IJ
    Nat Genet; 1994 Dec; 8(4):313-5. PubMed ID: 7894476
    [No Abstract]   [Full Text] [Related]  

  • 2. Mitochondrial genetics and human disease.
    Grossman LI; Shoubridge EA
    Bioessays; 1996 Dec; 18(12):983-91. PubMed ID: 8976155
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pathogenicity of homoplasmic mitochondrial DNA mutation and nuclear gene involvement.
    Odawara M; Maki H; Yamada N
    J Med Genet; 1999 Dec; 36(12):934-5. PubMed ID: 10636741
    [No Abstract]   [Full Text] [Related]  

  • 4. New genetics of mitochondrial DNA diseases.
    Poulton J
    Br J Hosp Med; 1996 Jun 5-18; 55(11):712-6. PubMed ID: 8793140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotypes from patients indicate no paternal mitochondrial DNA contribution.
    Taylor RW; McDonnell MT; Blakely EL; Chinnery PF; Taylor GA; Howell N; Zeviani M; Briem E; Carrara F; Turnbull DM
    Ann Neurol; 2003 Oct; 54(4):521-4. PubMed ID: 14520666
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies.
    Brockington M; Sweeney MG; Hammans SR; Morgan-Hughes JA; Harding AE
    Nat Genet; 1993 May; 4(1):67-71. PubMed ID: 8513327
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homoplasmic mitochondrial DNA diseases as the paradigm to understand the tissue specificity and variable clinical severity of mitochondrial disorders.
    Fischel-Ghodsian N
    Mol Genet Metab; 2000; 71(1-2):93-9. PubMed ID: 11001802
    [No Abstract]   [Full Text] [Related]  

  • 8. [Molecular genetics of mitochondrial cytopathologies].
    Arenas J; Campos Y; Martín MA
    Neurologia; 1995 Dec; 10 Suppl 1():44-9. PubMed ID: 8838558
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes].
    Inoue K; Nakada K; Hayashi J; Isobe K
    Tanpakushitsu Kakusan Koso; 2001 Jun; 46(7):829-37. PubMed ID: 11431926
    [No Abstract]   [Full Text] [Related]  

  • 10. Complete mitochondrial DNA sequence analysis in a family with early-onset dystonia and optic atrophy.
    Brown MD; Hosseini S; Steiner I; Wallace DC; Korn-Lubetzki I
    Mov Disord; 2004 Feb; 19(2):235-7. PubMed ID: 14978686
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Mitochondrial cardiomyopathies: a new entity in cardiology research and diagnosis].
    Bernucci P; D'Amati G; Casali C; De Biase L; Autore C; Fedele F; Gallo P
    G Ital Cardiol; 1996 Sep; 26(9):1031-7. PubMed ID: 9036041
    [No Abstract]   [Full Text] [Related]  

  • 12. [Mutations of the mitochondrial genome and its clinical expression in cardiology].
    Barrera-Ramírez CF; Barragán-Campos HM; Sánchez-Guerrero J
    Gac Med Mex; 2000; 136(6):585-94. PubMed ID: 11131860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA and disease.
    Odawara M; Yamashita K
    N Engl J Med; 1996 Jan; 334(4):270-1. PubMed ID: 8532014
    [No Abstract]   [Full Text] [Related]  

  • 14. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
    Filosto M; Mancuso M; Vives-Bauza C; Vilà MR; Shanske S; Hirano M; Andreu AL; DiMauro S
    Ann Neurol; 2003 Oct; 54(4):524-6. PubMed ID: 14520667
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A; Moslemi AR; Palm O; Raininko R; Stålberg E; Oldfors A
    Eur J Med Genet; 2009; 52(1):47-8. PubMed ID: 19015050
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA, human evolution and the cancer genotype.
    Rew DA
    Eur J Surg Oncol; 2001 Mar; 27(2):209-11. PubMed ID: 11289761
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence?
    Melberg A; Nennesmo I; Moslemi AR; Kollberg G; Luoma P; Suomalainen A; Holme E; Oldfors A
    Acta Neuropathol; 2005 Sep; 110(3):315-6. PubMed ID: 15981013
    [No Abstract]   [Full Text] [Related]  

  • 18. Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion.
    Tulinius M; Moslemi AR; Darin N; Holme E; Oldfors A
    Neuromuscul Disord; 2005 Jun; 15(6):412-5. PubMed ID: 15907288
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA and disease.
    Hammans SR
    Essays Biochem; 1994; 28():99-112. PubMed ID: 7925322
    [No Abstract]   [Full Text] [Related]  

  • 20. Mitochondrial Genetics. A clever way to model defects...
    Alfred J
    Nat Rev Genet; 2000 Nov; 1(2):84-5. PubMed ID: 11253658
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.