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Journal Abstract Search

236 related items for PubMed ID: 11185741

  • 1. Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene.
    Akanuma J, Muraki K, Komaki H, Nonaka I, Goto Y.
    J Hum Genet; 2000; 45(6):337-41. PubMed ID: 11185741
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  • 3. Co-amplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations.
    Parfait B, Rustin P, Munnich A, Rötig A.
    Biochem Biophys Res Commun; 1998 Jun 09; 247(1):57-9. PubMed ID: 9636653
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  • 5. [Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].
    Zhang XA, Wu HC, Zhang BF, Yu W, Fan QS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb 09; 22(1):18-21. PubMed ID: 15696472
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  • 7. 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 Feb 09; 52(1):47-8. PubMed ID: 19015050
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  • 8. Multiple nuclear pseudogenes of mitochondrial DNA exist in the canine genome.
    Ishiguro N, Nakajima A, Horiuchi M, Shinagawa M.
    Mamm Genome; 2002 Jul 09; 13(7):365-72. PubMed ID: 12140679
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  • 10. Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms.
    Kato M, Nakamura M, Ichiba M, Tomiyasu A, Shimo H, Higuchi I, Ueno S, Sano A.
    Neurosci Res; 2011 Apr 09; 69(4):331-6. PubMed ID: 21185889
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  • 16. Nuclear pseudogenes of mitochondrial DNA as a variable part of the human genome.
    Yuan JD, Shi JX, Meng GX, An LG, Hu GX.
    Cell Res; 1999 Dec 09; 9(4):281-90. PubMed ID: 10628837
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  • 19. New genetics of mitochondrial DNA diseases.
    Poulton J.
    Br J Hosp Med; 1999 Dec 09; 55(11):712-6. PubMed ID: 8793140
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  • 20. The complete mitochondrial genome of Macaca thibetana and a novel nuclear mitochondrial pseudogene.
    Li D, Fan L, Zeng B, Yin H, Zou F, Wang H, Meng Y, King E, Yue B.
    Gene; 2009 Jan 15; 429(1-2):31-6. PubMed ID: 19013508
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