190 related articles for article (PubMed ID: 9740668)
1. Mutational scanning of mitochondrial DNA by two-dimensional electrophoresis.
van Orsouw NJ; Zhang X; Wei JY; Johns DR; Vijg J
Genomics; 1998 Aug; 52(1):27-36. PubMed ID: 9740668
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
Seibel P; Flierl A; Kottlors M; Reichmann H
Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
[TBL] [Abstract][Full Text] [Related]
4. Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations.
Meierhofer D; Mayr JA; Ebner S; Sperl W; Kofler B
Mitochondrion; 2005 Aug; 5(4):282-96. PubMed ID: 16050991
[TBL] [Abstract][Full Text] [Related]
5. Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis.
Wong LJ; Chen TJ; Tan DJ
Electrophoresis; 2004 Aug; 25(15):2602-10. PubMed ID: 15300781
[TBL] [Abstract][Full Text] [Related]
6. Mutation screening using fluorescence multiplex denaturing gradient gel electrophoresis (FMD): detecting mutations in the BRCA1 gene.
Zhang S; Kuperstein G; Narod SA
Nat Protoc; 2006; 1(6):3101-10. PubMed ID: 17406573
[TBL] [Abstract][Full Text] [Related]
7. Surveyor Nuclease: a new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects.
Bannwarth S; Procaccio V; Paquis-Flucklinger V
Hum Mutat; 2005 Jun; 25(6):575-82. PubMed ID: 15880407
[TBL] [Abstract][Full Text] [Related]
8. Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene.
Laprise SL; Mak EK; Killoran KA; Layman LC; Gray MR
Hum Mutat; 1998; 12(6):393-402. PubMed ID: 9829908
[TBL] [Abstract][Full Text] [Related]
9. Two-dimensional gene scanning: exploring human genetic variability.
Vijg J; van Orsouw NJ
Electrophoresis; 1999 Jun; 20(6):1239-49. PubMed ID: 10380764
[TBL] [Abstract][Full Text] [Related]
10. Optimized PCR fragments for heteroduplex analysis of the whole human mitochondrial genome with denaturing HPLC.
Wulfert M; Tapprich C; Gattermann N
J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Feb; 831(1-2):236-47. PubMed ID: 16406745
[TBL] [Abstract][Full Text] [Related]
11. Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.
Biggin A; Henke R; Bennetts B; Thorburn DR; Christodoulou J
Mol Genet Metab; 2005 Jan; 84(1):61-74. PubMed ID: 15639196
[TBL] [Abstract][Full Text] [Related]
12. mtDNA point mutations are present at various levels of heteroplasmy in human oocytes.
Jacobs L; Gerards M; Chinnery P; Dumoulin J; de Coo I; Geraedts J; Smeets H
Mol Hum Reprod; 2007 Mar; 13(3):149-54. PubMed ID: 17259224
[TBL] [Abstract][Full Text] [Related]
13. A Standard Reference Material to determine the sensitivity of techniques for detecting low-frequency mutations, SNPs, and heteroplasmies in mitochondrial DNA.
Hancock DK; Tully LA; Levin BC
Genomics; 2005 Oct; 86(4):446-61. PubMed ID: 16024219
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive mutation analysis of TSC1 using two-dimensional DNA electrophoresis with DGGE.
Dabora SL; Sigalas I; Hall F; Eng C; Vijg J; Kwiatkowski DJ
Ann Hum Genet; 1998 Nov; 62(Pt 6):491-504. PubMed ID: 10363127
[TBL] [Abstract][Full Text] [Related]
15. Application of high-resolution melting for genotyping bovine mitochondrial DNA.
Zhou ZW; Yan JB; Li H; Ren ZR
Biotechnol Prog; 2011; 27(2):592-5. PubMed ID: 21448913
[TBL] [Abstract][Full Text] [Related]
16. Denaturing gradient gel electrophoresis (DGGE) increases resolution and informativity of Alu-directed inter-repeat PCR.
van Orsouw NJ; Li D; Vijg J
Mol Cell Probes; 1997 Apr; 11(2):95-101. PubMed ID: 9160323
[TBL] [Abstract][Full Text] [Related]
17. High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variants.
Larsen LA; Christiansen M; Vuust J; Andersen PS
Hum Mutat; 1999; 13(4):318-27. PubMed ID: 10220146
[TBL] [Abstract][Full Text] [Related]
18. [CSNP discovery by two-dimensional gene scanning (TDGS)].
Suh Y
Exp Mol Med; 2001 Apr; 33(1 Suppl):21-47. PubMed ID: 11708324
[TBL] [Abstract][Full Text] [Related]
19. Identifying sequence variants in the human mitochondrial genome using high-resolution melt (HRM) profiling.
Dobrowolski SF; Hendrickx AT; van den Bosch BJ; Smeets HJ; Gray J; Miller T; Sears M
Hum Mutat; 2009 Jun; 30(6):891-8. PubMed ID: 19370763
[TBL] [Abstract][Full Text] [Related]
20. Yield of mtDNA mutation analysis in 2,000 patients.
Liang MH; Wong LJ
Am J Med Genet; 1998 Jun; 77(5):395-400. PubMed ID: 9632169
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
