Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.
about
The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspringChip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patients.Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutationMitochondrial disease in autism spectrum disorder patients: a cohort analysisSingle-molecule LATE-PCR analysis of human mitochondrial genomic sequence variationsBiomarker Validation for Aging: Lessons from mtDNA Heteroplasmy Analyses in Early Cancer Detection.The in-depth evaluation of suspected mitochondrial diseaseMultiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants.Quantitative genotyping of single nucleotide polymorphism by single-molecule multi-color fluorescence resonance energy transfer.Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutationDefective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.Micro-processing events in mRNAs identified by DHPLC analysis.Mitochondrial DNA mutations in head and neck cancer are infrequent and lack prognostic utility.The use of denaturing high-performance liquid chromatography (DHPLC) for the analysis of genetic variations: impact for diagnostics and pharmacogenetics.A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides?Separating human DNA mixtures using denaturing high-performance liquid chromatography.Rapid screening mitochondrial DNA mutation by using denaturing high-performance liquid chromatography.Pitfalls in the denaturing high-performance liquid chromatography analysis of mitochondrial DNA mutationMutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.Mitochondrial DNA deletion and sarcopenia.Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution.Comparing methods of detection and quantitation of RNA editing of rat glycine receptor alpha3.DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis.Rapid denaturing high-performance liquid chromatography (DHPLC) for mutation scanning of the transforming growth factor beta3 gene using a novel proof-reading polymerase.Detection of low levels of the mitochondrial tRNALeu(UUR) 3243A>G mutation in blood derived from patients with diabetes.Mitochondrial DNA analysis by multiplex denaturing high-performance liquid chromatography and selective sequencing in pediatric patients with cardiomyopathy.DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.Spontaneous DNA-DNA interaction of homologous duplexes and factors affecting the result of heteroduplex formation.Genotyping mitochondrial DNA single nucleotide polymorphisms by PCR ligase detection reactions.
P2860
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P2860
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Mutation analysis of the entir ...... ormance liquid chromatography.
@en
Mutation analysis of the entir ...... ormance liquid chromatography.
@nl
type
label
Mutation analysis of the entir ...... ormance liquid chromatography.
@en
Mutation analysis of the entir ...... ormance liquid chromatography.
@nl
prefLabel
Mutation analysis of the entir ...... ormance liquid chromatography.
@en
Mutation analysis of the entir ...... ormance liquid chromatography.
@nl
P2093
P2860
P356
P1476
Mutation analysis of the entir ...... ormance liquid chromatography.
@en
P2093
Nijland JG
Scholte HR
de Die-Smulders CE
de Visser M
van Den Bogaard R
van Den Bosch BJ
P2860
P356
10.1093/NAR/28.20.E89
P407
P577
2000-10-01T00:00:00Z