- Analysis of Nuclear Mitochondrial DNA Segments of Nine Plant Species: Size, Distribution, and Insertion Loci
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Ko YJ, Kim S
- KMID: 2353660
- Genomics Inform.
- 2016 Sep;14(3):90-95.
- doi: 10.5808/GI.2016.14.3.90
Nuclear mitochondrial DNA segment (Numt) insertion describes a well-known phenomenon of mitochondrial DNA transfer into a eukaryotic nuclear genome. However, it has not been well understood, especially in plants. Numt... -
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- Analysis of Mitochondrial DNA in Patients with Essential Tremor
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Lee U, Yoo YM, Yoo CJ
- KMID: 1546446
- J Korean Neurosurg Soc.
- 2000 Feb;29(2):188-195.
No abstract available. -
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- Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
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Finsterer
- KMID: 2431641
- Yonsei Med J.
- 2019 Feb;60(2):230-231.
- doi: 10.3349/ymj.2019.60.2.230
No abstract available. -
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- Mitochondrial DNA A3243G mutation in noise-induced sensorineural hearing loss
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Shin DH, Baek WK, Chung IS
- KMID: 2028111
- Korean J Occup Environ Med.
- 2000 Sep;12(3):319-326.
OBJECTIVES: A different sequence change, in the mitochondrial tRNA gene, has been proposed as a candidate mutation in the sensorineurnal hearing loss. The purpose of current study is to... -
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- The Author Reply: Mitochondrial Ophthalmoplegia Is Not Only due to mtDNA Deletions
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Lee YM
- KMID: 2431642
- Yonsei Med J.
- 2019 Feb;60(2):232-233.
- doi: 10.3349/ymj.2019.60.2.232
No abstract available. -
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- Mechanisms of Uniparental Mitochondrial DNA Inheritance in Cryptococcus neoformans
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Gyawali R, Lin X
- KMID: 2312648
- Mycobiology.
- 2011 Dec;39(4):235-242.
In contrast to the nuclear genome, the mitochondrial genome does not follow Mendelian laws of inheritance. The nuclear genome of meiotic progeny comes from the recombination of both parental genomes,... -
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- The Analysis of Mitochondrial DNA in the Patients with Essential Tremor and Parkinson's Disease
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Kim RS, Yoo CJ, Lee SG, Kim WK, Han KS, Kim YB, Park CW, Lee U
- KMID: 1548080
- J Korean Neurosurg Soc.
- 2000 Nov;29(11):1415-1420.
No abstract available. -
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- A Case of Leber's Hereditary Optic Nouropathy Showing 11778 Point Mutation of Mitochondrial DNA
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Jung YS, Park SK, Lee SY, Hah JS, Park MY, Lee SJ, Lee J
- KMID: 1969409
- Yeungnam Univ J Med.
- 1999 Jun;16(1):114-118.
- doi: 10.12701/yujm.1999.16.1.114
Leber's hereditary optic neuropathy(LHON) is an optic nerve disease that causes blindness and is associated with maternally inherited mitochondrial DNA(mt DNA) mutations. The most common mitochondrial DNA mutation among LHON... -
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- MELAS Syndrome Confirmed by Mitochondrial DNA Analysis in Siblings
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Rah YG, Chae SA, Lim IS, Lee DK, Yoo BH, Ko TS, Yoo HW
- KMID: 1946343
- J Korean Pediatr Soc.
- 1999 Mar;42(3):412-418.
MELAS(mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) syndrome is a major subgroup of mitochondrial myopathy. Recent advances in molecular genetics revealed specific mutations in mitochondrial DNA which cause MELAS.... -
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- The role of mitochondrial DNA mutation on neurodegenerative diseases
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Cha MY, Kim DK, Mook-Jung
- KMID: 2155415
- Exp Mol Med.
- 2015 Mar;47(3):e150.
- doi: 10.1038/emm.2014.122
Many researchers have reported that oxidative damage to mitochondrial DNA (mtDNA) is increased in several age-related disorders. Damage to mitochondrial constituents and mtDNA can generate additional mitochondrial dysfunction that may... -
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- A Case of Early Onset MELAS Patient with Wolff-Parkinson-White Syndrome
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Kim JA, Ahn JM, Lee YM, Kang HC, Lee JS, Kim HD
- KMID: 2329491
- J Korean Child Neurol Soc.
- 2011 Dec;19(3):266-271.
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is one of the classic mitochondrial diseases characterized by symptoms of repeated episodes of hemiparesis with mitochondrial DNA mutation. We report... -
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- The Analysis of Mitochondrial DNA in the Failing and Normal Hearts
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Choi HS, Kim HS, Oh BH, Lee MM, Choe SC, Hong SK, Sohn DW, Park YB, Choi YS, Seo JD, Lee YW
- KMID: 2251563
- Korean J Med.
- 1997 Sep;53(3):404-413.
OBJECTIVE: The aim of this study is to analyze the mitochondrial DNA in failing and normal hearts. METHODS: Genomic DNA was extracted from 18 failing and 4 normal hearts. The DNA... -
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- Relationship between Mitochondrial DNA Point Mutation and Noise-induced Sensorineural Hearing Loss
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Park SH, Kim TW, Lee MY, Bae JH, Shin DH
- KMID: 1589163
- Korean J Aerosp Environ Med.
- 2005 Dec;15(3):93-99.
BACKGROUND: A different sequence change in the mitochondrial 12S rRNA gene has been proposed as a candidate mutation in the sensorineural hearing loss. The purpose of this study was to... -
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- A Mitochondrial Mutation in Leber's Hereditary Optic Neuropathy
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Hwang JM, Park HW
- KMID: 2205183
- J Korean Ophthalmol Soc.
- 1995 Dec;36(12):2218-2224.
Leber's hereditary optic neuropathy is caused by a single nucleotide change in the mitochondrial deoxynucleic acid(mtDNA). We identified a single guanine to adenine transition mutation in the mitochondrial DNA at... -
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- A Two Cases of MELAS in Siblings
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Yeon YY, Choi BJ, Kim YH, Kim JW, Park SS, Ji JG, Whang KT
- KMID: 2329217
- J Korean Child Neurol Soc.
- 1997 Oct;5(1):138-146.
MELAS is the condition associated with mutant mtDNA that most closely mimics thrombotic cerebrovascular disease. It is characterized by mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes. These children develop short... -
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- Analysis of Five Coding Region Polymorphism in Mitochondrial DNA
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Zhang YJ, Park JC, Zheng ZJ, Lin HY, Kim SY, Choi YT, Lee JB
- KMID: 1849283
- Korean J Leg Med.
- 2003 Oct;27(2):56-61.
For evaluation of the five coding region (CR) polymorphism in mitochondrial DNA (mtDNA); we had performed PCR and direct sequencing in 599 unrelated Korean who showed the identical DNA type... -
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- Unusual mtDNA sequencing results from ancient DNA
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Seo SB, Choung CM, Zhang A, Jang BS, Yoo SH, Lee SD
- KMID: 2082684
- Korean J Leg Med.
- 2007 May;31(1):36-40.
Sequence analysis of human mitochondrial DNA(mtDNA) is being used widely to characterize individual identification, particularly when there is insufficient nuclear DNA in samples for typing. Hair shafts, bones, teeth and other... -
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- Whole Mitochondrial Genome Sequence of an Indian Plasmodium falciparum Field Isolate
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Tyagi S, Pande V, Das A
- KMID: 1715680
- Korean J Parasitol.
- 2014 Feb;52(1):99-103.
- doi: 10.3347/kjp.2014.52.1.99
Mitochondrial genome sequence of malaria parasites has served as a potential marker for inferring evolutionary history of the Plasmodium genus. In Plasmodium falciparum, the mitochondrial genome sequences from around the... -
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- Statistical Evaluation of Lineage Markers in Individual Identification
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Lee HJ, Lee SD, Lee SH, Park SJ, Jeong SJ, Lee JW
- KMID: 1849352
- Korean J Leg Med.
- 2014 May;38(2):39-47.
- doi: 10.7580/kjlm.2014.38.2.39
Mitochondrial DNA (mt DNA) and the non-recombining region of the Y chromosome are passed down, unaltered, from generation to generation, matrilineally and patrilineally, respectively. Therefore, the Y-chromosome DNA and mtDNA... -
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- Back to the Ends: Chromosomal DNA
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Lee MH, Suh D
- KMID: 2322080
- J Korean Soc Pediatr Nephrol.
- 2008 Apr;12(1):1-10.
Nucleic scids transfer the genetic information for serving a central biological purpose. The nucleic acids are polymers of nucleotides and they are mainly ribonucleic acid(RNA) and deoxyribonucleic acid(DNA). The nucleotides... -
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