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Journal Abstract Search

221 related items for PubMed ID: 16916259

  • 1. Molecular analysis of mitochondrial DNA point mutations by polymerase chain reaction.
    Wong LJ, Cobb BR, Chen TJ.
    Methods Mol Biol; 2006; 336():135-43. PubMed ID: 16916259
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  • 2. Analysis of common mitochondrial DNA mutations by allele-specific oligonucleotide and Southern blot hybridization.
    Tang S, Halberg MC, Floyd KC, Wang J.
    Methods Mol Biol; 2012; 837():259-79. PubMed ID: 22215554
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  • 5. Real-time quantitative polymerase chain reaction analysis of mitochondrial DNA point mutation.
    Wong LJ, Bai RK.
    Methods Mol Biol; 2006; 335():187-200. PubMed ID: 16785629
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  • 6. Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.
    Genasetti A, Valentino ML, Carelli V, Vigetti D, Viola M, Karousou EG, Melzi d'Eril GV, De Luca G, Passi A, Pallotti F.
    J Mol Diagn; 2007 Sep; 9(4):538-45. PubMed ID: 17652639
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  • 7. A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy.
    Cassandrini D, Calevo MG, Tessa A, Manfredi G, Fattori F, Meschini MC, Carrozzo R, Tonoli E, Pedemonte M, Minetti C, Zara F, Santorelli FM, Bruno C.
    Biochem Biophys Res Commun; 2006 Apr 07; 342(2):387-93. PubMed ID: 16483543
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  • 9. Quantitative determination of heteroplasmy in Leber's hereditary optic neuropathy by single-strand conformation polymorphism.
    Mashima Y, Saga M, Hiida Y, Oguchi Y, Wakakura M, Kudoh J, Shimizu N.
    Invest Ophthalmol Vis Sci; 1995 Jul 07; 36(8):1714-20. PubMed ID: 7601652
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  • 10. Accurate detection and quantitation of heteroplasmic mitochondrial point mutations by pyrosequencing.
    White HE, Durston VJ, Seller A, Fratter C, Harvey JF, Cross NC.
    Genet Test; 2005 Jul 07; 9(3):190-9. PubMed ID: 16225398
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  • 11. Mitochondrial DNA mutations associated with neuromuscular diseases: analysis and diagnosis using the polymerase chain reaction.
    Wallace DC, Lott MT, Lezza AM, Seibel P, Voljavec AS, Shoffner JM.
    Pediatr Res; 1990 Nov 07; 28(5):525-8. PubMed ID: 2123980
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  • 12. Yield of mtDNA mutation analysis in 2,000 patients.
    Liang MH, Wong LJ.
    Am J Med Genet; 1998 Jun 05; 77(5):395-400. PubMed ID: 9632169
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  • 16. Quantification of mtDNA mutation heteroplasmy (ARMS qPCR).
    Venegas V, Halberg MC.
    Methods Mol Biol; 2012 Jun 05; 837():313-26. PubMed ID: 22215557
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  • 17. Time-resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy.
    Huoponen K, Juvonen V, Iitiä A, Dahlen P, Siitari H, Aula P, Nikoskelainen E, Savontaus ML.
    Hum Mutat; 1994 Jun 05; 3(1):29-36. PubMed ID: 8118464
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  • 18. Real-time detection and quantification of mitochondrial mutations with oligonucleotide primers containing locked nucleic acid.
    Strand H, Ingebretsen OC, Nilssen O.
    Clin Chim Acta; 2008 Apr 05; 390(1-2):126-33. PubMed ID: 18241671
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