303 related articles for article (PubMed ID: 8582049)
1. Screening for mitochondrial DNA (mtDNA) point mutations using nonradioactive single strand conformation polymorphism (SSCP) analysis.
Jaksch M; Gerbitz KD; Kilger C
Clin Biochem; 1995 Oct; 28(5):503-9. PubMed ID: 8582049
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
Toyo-Oka Y; Wada C; Yamabe H; Inoue M; Ishigaki M; Matsuyama N; Ohnuki Y; Ichibe Y; Wakakura M; Ohtani H
Rinsho Byori; 1996 Jul; 44(7):676-80. PubMed ID: 8741498
[TBL] [Abstract][Full Text] [Related]
3. Diagnostic screening of mitochondrial DNA mutations in Australian adults 1990-2001.
Marotta R; Chin J; Quigley A; Katsabanis S; Kapsa R; Byrne E; Collins S
Intern Med J; 2004; 34(1-2):10-9. PubMed ID: 14748908
[TBL] [Abstract][Full Text] [Related]
4. 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; 9(3):190-9. PubMed ID: 16225398
[TBL] [Abstract][Full Text] [Related]
5. 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; 36(8):1714-20. PubMed ID: 7601652
[TBL] [Abstract][Full Text] [Related]
6. Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology.
Du W; Li W; Chen G; Cao H; Tang H; Tang X; Jin Q; Sun Z; Zhao H; Zhou W; He S; Lv Y; Zhao J; Zhang X
Biosens Bioelectron; 2009 Apr; 24(8):2371-6. PubMed ID: 19155171
[TBL] [Abstract][Full Text] [Related]
7. Defects of mitochondrial DNA.
Zeviani M; Antozzi C
Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953
[TBL] [Abstract][Full Text] [Related]
8. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
Mashima Y; Nagano M; Funayama T; Zhang Q; Egashira T; Kudho J; Shimizu N; Oguchi Y
Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
[TBL] [Abstract][Full Text] [Related]
9. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
Hofmann S; Bezold R; Jaksch M; Obermaier-Kusser B; Mertens S; Kaufhold P; Rabl W; Hecker W; Gerbitz KD
Genomics; 1997 Jan; 39(1):8-18. PubMed ID: 9027481
[TBL] [Abstract][Full Text] [Related]
10. Retinal manifestations in mitochondrial diseases associated with mitochondrial DNA mutation.
Isashiki Y; Nakagawa M; Ohba N; Kamimura K; Sakoda Y; Higuchi I; Izumo S; Osame M
Acta Ophthalmol Scand; 1998 Feb; 76(1):6-13. PubMed ID: 9541428
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
Sternberg D; Chatzoglou E; Laforêt P; Fayet G; Jardel C; Blondy P; Fardeau M; Amselem S; Eymard B; Lombès A
Brain; 2001 May; 124(Pt 5):984-94. PubMed ID: 11335700
[TBL] [Abstract][Full Text] [Related]
13. Detection of p53 mutations by single-strand conformation polymorphisms (SSCP) gel electrophoresis. A comparative study of radioactive and nonradioactive silver-stained SSCP analysis.
Bosari S; Marchetti A; Buttitta F; Graziani D; Borsani G; Loda M; Bevilacqua G; Coggi G
Diagn Mol Pathol; 1995 Dec; 4(4):249-55. PubMed ID: 8634780
[TBL] [Abstract][Full Text] [Related]
14. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in italian patients presenting with sporadic bilateral optic neuritis.
Sartore M; Grasso M; Piccolo G; Fasani R; Bergamaschi R; Malaspina A; Ceroni M; Kobayashi M; Semeraro A; Arbustini E
Biochem Mol Med; 1995 Oct; 56(1):45-51. PubMed ID: 8593537
[TBL] [Abstract][Full Text] [Related]
15. Point mutations of muscle mitochondrial DNA from patients with mitochondrial encephalomyopathies.
Song D; Zhang Y; Shi J; Lü Q; Chen J; Zhang H; Zhang W; Wang H; Cai Q
Chin Med J (Engl); 2001 Dec; 114(12):1273-5. PubMed ID: 11793851
[TBL] [Abstract][Full Text] [Related]
16. Nonradioactive characterization of low-level heteroplasmic mitochondrial DNA mutations by SSCP-PCR enrichment.
Sherratt EJ; Thomas AW; Gagg JW; Alcolado JC
Biotechniques; 1996 Mar; 20(3):430-2. PubMed ID: 8679202
[TBL] [Abstract][Full Text] [Related]
17. Screening of common point-mutations and discovery of new T14727C change in mitochondrial genome of Vietnamese encephalomyopathy patients.
Truong HT; Nguyen VA; Nguyen LV; Pham VA; Phan TN
Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(1):441-8. PubMed ID: 24708131
[TBL] [Abstract][Full Text] [Related]
18. Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA.
Suomalainen A; Ciafaloni E; Koga Y; Peltonen L; DiMauro S; Schon EA
J Neurol Sci; 1992 Sep; 111(2):222-6. PubMed ID: 1431990
[TBL] [Abstract][Full Text] [Related]
19. Detection of known thalassemia point mutations by snapback single-strand conformation polymorphism: the feasibility analysis.
Li W; Gao F; Tang W; Zhang X; Zhang H
Clin Biochem; 2006 Aug; 39(8):833-42. PubMed ID: 16820146
[TBL] [Abstract][Full Text] [Related]
20. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
Brown MD; Torroni A; Reckord CL; Wallace DC
Hum Mutat; 1995; 6(4):311-25. PubMed ID: 8680405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
