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 *

127 related articles for article (PubMed ID: 9507371)

  • 1. The polymerase chain reaction in the study of mitochondrial genetics.
    Kapsa R; Siregar N; Quigley A; Ojaimi J; Katsabanis S; Sue C; Byrne E
    J Biochem Biophys Methods; 1997 Dec; 36(1):31-50. PubMed ID: 9507371
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detection and quantification of point mutations in mitochondrial DNA by PCR.
    Yoneda M; Tanno Y; Tsuji S; Attardi G
    Methods Enzymol; 1996; 264():432-41. PubMed ID: 8965716
    [No Abstract]   [Full Text] [Related]  

  • 3. Update in molecular genetics: mitochondrial energy transduction disorders.
    Marzuki S; Sudoyo H; Lertrit P
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():155-61. PubMed ID: 8629096
    [No Abstract]   [Full Text] [Related]  

  • 4. 74th ENMC international workshop: mitochondrial diseases 19-20 november 1999, Naarden, the netherlands.
    Poulton J; Turnbull DM
    Neuromuscul Disord; 2000 Aug; 10(6):460-2. PubMed ID: 10899455
    [No Abstract]   [Full Text] [Related]  

  • 5. Mitochondrial diseases.
    Nonaka I
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P; Flierl A; Kottlors M; Reichmann H
    Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rapid and noninvasive screening of patients with mitochondrial myopathy.
    Kotsimbos N; Jean-Francois MJ; Huizing M; Kapsa RM; Lertrit P; Siregar NC; Marzuki S; Sue C; Byrne E
    Hum Mutat; 1994; 4(2):132-5. PubMed ID: 7981717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome.
    Mancuso M; Vives-Bauza C; Filosto M; Marti R; Solano A; Montoya J; Gamez J; DiMauro S; Andreu AL
    J Med Genet; 2004 Jun; 41(6):e73. PubMed ID: 15173239
    [No Abstract]   [Full Text] [Related]  

  • 10. Screening for the two most frequent mutations in Leber's hereditary optic neuropathy by duplex PCR based on allele-specific amplification.
    Nørby S
    Hum Mutat; 1993; 2(4):309-13. PubMed ID: 8401538
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transmission of the human mitochondrial genome.
    Howell N; Chinnery PF; Ghosh SS; Fahy E; Turnbull DM
    Hum Reprod; 2000 Jul; 15 Suppl 2():235-45. PubMed ID: 11041529
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy.
    Mashima Y; Hiida Y; Oguchi Y; Kudoh J; Shimizu N
    Hum Genet; 1993 Aug; 92(1):101-2. PubMed ID: 8103501
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis of quantitative mitochondrial DNA defects by rapidly prepared whole mitochondrial DNA probe.
    Seyrantepe V; Topaloglu H
    Diagn Mol Pathol; 2000 Jun; 9(2):81-3. PubMed ID: 10850543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuro-ophthalmology of mitochondrial diseases.
    Riordan-Eva P
    Curr Opin Ophthalmol; 2000 Dec; 11(6):408-12. PubMed ID: 11141634
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Accumulation of somatic nucleotide substitutions in mitochondrial DNA associated with the 3243 A-to-G tRNA(leu)(UUR) mutation in encephalomyopathy and cardiomyopathy.
    Kovalenko SA; Tanaka M; Yoneda M; Iakovlev AF; Ozawa T
    Biochem Biophys Res Commun; 1996 May; 222(2):201-7. PubMed ID: 8670183
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial disorders in muscle.
    Schon EA
    Curr Opin Neurol Neurosurg; 1993 Feb; 6(1):19-26. PubMed ID: 8428062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. False-positive diagnosis of a single, large-scale mitochondrial DNA deletion by Southern blot analysis: the role of neutral polymorphisms.
    Deschauer M; Krasnianski A; Zierz S; Taylor RW
    Genet Test; 2004; 8(4):395-9. PubMed ID: 15684869
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ischaemic colitis due to mitochondrial cytopathy.
    Hess J; Burkhard P; Morris M; Lalioti M; Myers P; Hadengue A
    Lancet; 1995 Jul; 346(8968):189-90. PubMed ID: 7603260
    [No Abstract]   [Full Text] [Related]  

  • 19. The other human genome: mitochondrial DNA and disease.
    Johns DR
    Nat Med; 1996 Oct; 2(10):1065-8. PubMed ID: 8837595
    [No Abstract]   [Full Text] [Related]  

  • 20. Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(exo-) DNA polymerase and RFLP analysis.
    Jacobi FK; Meyer J; Pusch CM; Wissinger B
    Mutat Res; 2001 Jul; 478(1-2):141-51. PubMed ID: 11406178
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.