Identification of a Mitochondrial DNA Mutation in Paraffin-Embedded Muscle Tissues |
김상호
(대구대학교 사범대학 생물교육전공)
유석호 (한국과학기술원 의과학연구센터) |
1 |
A new point mutation at nucleotide pair 3219 of the mitochondrial tRNA Leu (UUR) gene in A patient with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
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DOI ScienceOn |
2 |
Use of neuropathological tissue for molecular genetic studies: parameters affecting DNA extraction and polymerase chain reaction
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DOI ScienceOn |
3 |
A new mtDNA mutation associated with mitochondrial myopathy, encephalopthy, lactic acidosis and stroke-like episodes (MELAS)
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DOI ScienceOn |
4 |
Mitochondrial genetics and disease
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5 |
Removel of inhibitor (s) of the polymerase chain reaction from formalin fixed, paraffin wax embedded tissues
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DOI |
6 |
Mitochondrial DNA mutations in the pathogenesis of human disease
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DOI ScienceOn |
7 |
A mutation in the tRNA Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encepalomyopathies
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DOI ScienceOn |
8 |
Characterization of a Mitochondrial DNA Deletion in Patients with Mitochondrial Myopathy
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과학기술학회마을 |
9 |
DNA extraction from paraffin-embedded tissues using a salting-out procedure: a reliable method for PCR amplification of archival material
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10 |
DNA genotyping of unbuffered formalin fixed paraffin embedded tissues
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DOI ScienceOn |
11 |
An Efficient Method for the Assessment of DNA Quality of Archival Microdissected Specimens
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DOI ScienceOn |
12 |
Sequence and organization of the human mitochondrial genome
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DOI ScienceOn |
13 |
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA Leu (UUR) mutation associated with mitochondrial myopathy, enceph-alopathy, lactic acidosis and stroke-like episodes
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14 |
A spin cartridge system for DNA extraction from paraffin wax embedded tissues
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DOI ScienceOn |
15 |
Evaluation of extraction methods from paraffin wax embedded tissues for PCR amplification of human and viral DNA
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16 |
Identification of large deletion of mitochondrial DNA in Kearns-Sayre Syndrome (KSS)
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과학기술학회마을 |
17 |
Quantitative analysis of mitochondrial DNA deletion in pareffin embedded muscle tissues from patients with KSS and CPEO
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DOI ScienceOn |
18 |
Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS
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DOI ScienceOn |