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 *

119 related articles for article (PubMed ID: 2041210)

  • 1. [Myoglobinuria caused by multiple deletions of mitochondrial DNA].
    Tanaka M; Ohno K; Sahashi K; Ibi T; Tashiro M; Ino H; Takahashi A; Ozawa T
    Rinsho Byori; 1991 Feb; 39(2):133-9. PubMed ID: 2041210
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA deletions in inherited recurrent myoglobinuria.
    Ohno K; Tanaka M; Sahashi K; Ibi T; Sato W; Yamamoto T; Takahashi A; Ozawa T
    Ann Neurol; 1991 Apr; 29(4):364-9. PubMed ID: 1929207
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Age-dependent respiratory function decline and DNA deletions in human muscle mitochondria.
    Hsieh RH; Hou JH; Hsu HS; Wei YH
    Biochem Mol Biol Int; 1994 Apr; 32(6):1009-22. PubMed ID: 8061617
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of platelet mitochondrial DNA deletions in Kearns-Sayre syndrome.
    Ota Y; Tanaka M; Sato W; Ohno K; Yamamoto T; Maehara M; Negoro T; Watanabe K; Awaya S; Ozawa T
    Invest Ophthalmol Vis Sci; 1991 Sep; 32(10):2667-75. PubMed ID: 1894466
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Multiple deletions of the mitochondrial DNA in polymyalgia rheumatica.
    Reynier P; Pellissier JF; Harle JR; Malthiéry Y
    Biochem Biophys Res Commun; 1994 Nov; 205(1):375-80. PubMed ID: 7999051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia.
    Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T
    Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Widespread tissue distribution of multiple mitochondrial DNA deletions in familial mitochondrial myopathy.
    Kawashima S; Ohta S; Kagawa Y; Yoshida M; Nishizawa M
    Muscle Nerve; 1994 Jul; 17(7):741-6. PubMed ID: 8008000
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial abnormalities in inclusion-body myositis.
    Oldfors A; Moslemi AR; Jonasson L; Ohlsson M; Kollberg G; Lindberg C
    Neurology; 2006 Jan; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].
    Laforêt P; Eymard B; Danan C; Chevallay M; Rouche A; Frachon P; Fardeau M; Lombès A
    Rev Neurol (Paris); 1997 Feb; 153(1):51-8. PubMed ID: 9296156
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.
    Moslemi AR; Lindberg C; Oldfors A
    Hum Mutat; 1997; 10(5):381-6. PubMed ID: 9375854
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multiple skeletal muscle mitochondrial DNA deletions in patients with unilateral peripheral arterial disease.
    Brass EP; Wang H; Hiatt WR
    Vasc Med; 2000; 5(4):225-30. PubMed ID: 11213234
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria.
    Keightley JA; Hoffbuhr KC; Burton MD; Salas VM; Johnston WS; Penn AM; Buist NR; Kennaway NG
    Nat Genet; 1996 Apr; 12(4):410-6. PubMed ID: 8630495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.
    Santorelli FM; Sciacco M; Tanji K; Shanske S; Vu TH; Golzi V; Griggs RC; Mendell JR; Hays AP; Bertorini TE; Pestronk A; Bonilla E; DiMauro S
    Ann Neurol; 1996 Jun; 39(6):789-95. PubMed ID: 8651651
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy.
    Sahashi K; Tanaka M; Tashiro M; Ohno K; Ibi T; Takahashi A; Ozawa T
    Gerontology; 1992; 38(1-2):18-29. PubMed ID: 1319380
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
    Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
    Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome.
    Ohno K; Tanaka M; Ino H; Suzuki H; Tashiro M; Ibi T; Sahashi K; Takahashi A; Ozawa T
    Biochim Biophys Acta; 1991 Aug; 1090(1):9-16. PubMed ID: 1832017
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.
    Suomalainen A; Majander A; Haltia M; Somer H; Lönnqvist J; Savontaus ML; Peltonen L
    J Clin Invest; 1992 Jul; 90(1):61-6. PubMed ID: 1634620
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multiple deletions of mtDNA remove the light strand origin of replication.
    Bank C; Soulimane T; Schröder JM; Buse G; Zanssen S
    Biochem Biophys Res Commun; 2000 Dec; 279(2):595-601. PubMed ID: 11118331
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation.
    Emmanuele V; Sotiriou E; Shirazi M; Tanji K; Haller RG; Heinicke K; Bosch PE; Hirano M; DiMauro S
    J Neurol Sci; 2011 Apr; 303(1-2):39-42. PubMed ID: 21324494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.