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 *

118 related articles for article (PubMed ID: 8670185)

  • 1. Detection of DNA fragments encompassing the deletion junction of mitochondrial genome.
    Goto Y; Nishino I; Horai S; Nonaka I
    Biochem Biophys Res Commun; 1996 May; 222(2):215-9. PubMed ID: 8670185
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
    Moslemi AR; Melberg A; Holme E; Oldfors A
    Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.
    Bohlega S; Tanji K; Santorelli FM; Hirano M; al-Jishi A; DiMauro S
    Neurology; 1996 May; 46(5):1329-34. PubMed ID: 8628476
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection and quantification of mitochondrial DNA deletions.
    Soong NW; Arnheim N
    Methods Enzymol; 1996; 264():421-31. PubMed ID: 8965714
    [No Abstract]   [Full Text] [Related]  

  • 5. Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form.
    Poulton J; Deadman ME; Bindoff L; Morten K; Land J; Brown G
    Hum Mol Genet; 1993 Jan; 2(1):23-30. PubMed ID: 8490619
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
    Manfredi G; Vu T; Bonilla E; Schon EA; DiMauro S; Arnaudo E; Zhang L; Rowland LP; Hirano M
    Ann Neurol; 1997 Aug; 42(2):180-8. PubMed ID: 9266727
    [TBL] [Abstract][Full Text] [Related]  

  • 7. S1 nuclease hybrid analysis of mitochondrial DNA amplified by long-distance PCR: rapid screening for small-scale rearrangements.
    Lundin K; Wilichowski E; Ernst BP; Hanefeld F
    Nucleic Acids Res; 1997 Jun; 25(12):2535-6. PubMed ID: 9171111
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytoplasmic body and mitochondrial DNA deletion.
    Sahashi K; Ohno K; Tanaka M; Ibi T; Yamamoto T; Tashiro M; Sato W; Takahashi A; Ozawa T
    J Neurol Sci; 1990 Nov; 99(2-3):291-300. PubMed ID: 1964959
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Different tissue distribution of a mitochondrial DNA duplication and the corresponding deletion in a patient with a mild mitochondrial encephalomyopathy: deletion in muscle, duplication in blood.
    Houshmand M; Gardner A; Hällström T; Müntzing K; Oldfors A; Holme E
    Neuromuscul Disord; 2004 Mar; 14(3):195-201. PubMed ID: 15036329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.
    Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF
    Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fine mapping of randomly distributed multiple deletions of mitochondrial DNA in a case of chronic progressive external ophthalmoplegia.
    Ville-Ferlin T; Dumoulin R; Stepien G; Matha V; Bady B; Flocard F; Carrier H; Mathieu M; Mousson B
    Mol Cell Probes; 1995 Jun; 9(3):207-14. PubMed ID: 7477015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
    Johns DR; Rutledge SL; Stine OC; Hurko O
    Proc Natl Acad Sci U S A; 1989 Oct; 86(20):8059-62. PubMed ID: 2813377
    [TBL] [Abstract][Full Text] [Related]  

  • 13. AT-rich sequences flanking the 5'-end breakpoint of the 4977-bp deletion of human mitochondrial DNA are located between two bent-inducing DNA sequences that assume distorted structure in organello.
    Hou JH; Wei YH
    Mutat Res; 1998 Jul; 403(1-2):75-84. PubMed ID: 9726008
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA.
    Johns DR; Hurko O
    Genomics; 1989 Oct; 5(3):623-8. PubMed ID: 2533162
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of mitochondrial defects by laser fluorimetry.
    Kunz WS; Winkler K; Kuznetsov AV; Lins H; Kirches E; Wallesch CW
    Mol Cell Biochem; 1997 Sep; 174(1-2):97-100. PubMed ID: 9309672
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.
    Mita S; Rizzuto R; Moraes CT; Shanske S; Arnaudo E; Fabrizi GM; Koga Y; DiMauro S; Schon EA
    Nucleic Acids Res; 1990 Feb; 18(3):561-7. PubMed ID: 2308845
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.
    Mita S; Schmidt B; Schon EA; DiMauro S; Bonilla E
    Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9509-13. PubMed ID: 2556715
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel 7.4 kb mitochondrial deletion in a patient with congenital progressive external ophthalmoplegia, muscle weakness and mental retardation.
    Tabaku M; Legius E; Robberecht W; Sciot R; Fryns JP; Cassiman JJ; Matthijs G
    Genet Couns; 1999; 10(3):285-93. PubMed ID: 10546101
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.
    Shoffner JM; Lott MT; Voljavec AS; Soueidan SA; Costigan DA; Wallace DC
    Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR.
    Obermaier-Kusser B; Müller-Höcker J; Nelson I; Lestienne P; Enter C; Riedele T; Gerbitz KD
    Biochem Biophys Res Commun; 1990 Jun; 169(3):1007-15. PubMed ID: 1973036
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.