- 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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- 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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- Control of Mitochondrial Dynamics by Fas-induced Caspase-8 Activation in Hippocampal Neurons
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Cho HM, Sun W
- KMID: 2165558
- Exp Neurobiol.
- 2015 Sep;24(3):219-225.
- doi: 10.5607/en.2015.24.3.219
Cells undergo apoptosis mainly via two pathways-the mitochondrial pathway and the cytosolic pathway. It has been well documented that activation of the mitochondrial pathway promotes mitochondrial fragmentation and inhibition of... -
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- Genetics of Mitochondrial Myopathies
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Shin JH, Kim DS
- KMID: 2055574
- J Genet Med.
- 2013 Jun;10(1):20-26.
- doi: 10.5734/JGM.2013.10.1.20
Mitochondrion is an intracellular organelle with its own genome. Its function in cellular metabolism is indispensable that mitochondrial dysfunction gives rise to multisystemic failure. The manifestation is most prominent with... -
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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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- 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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- 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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- 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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- MitGEN: Single Nucleotide Polymorphism DB Browser for Human Mitochondrial Genome
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Park HS, Lee SU
- KMID: 2053082
- Genomics Inform.
- 2004 Sep;2(3):147-148.
Recently completed mitochondrial genome databses from public resources provide us with a better understanding of individual mitochondrial genomes for population genomics. By determining the substitution rate of the genomic sequences,... -
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- Vascular Hyperemia and Crossed Cerebellar Diaschisis in MELAS Patient Presented as Stroke-Like Episode and Seizure
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Kim DW, Choi KH, Oh HJ, Kang M, Kim C, Choi HC, Sohn JH
- KMID: 2184752
- J Korean Neurol Assoc.
- 2013 Aug;31(3):183-185.
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is one of the mitochondrial disorders that can present as a stroke-like episode or seizure. Although the pathophysiology of MELAS remains inconclusive,... -
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- Mitochondrial Disorders
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Chae JH
- KMID: 2137157
- J Korean Child Neurol Soc.
- 2001 May;9(1):13-24.
No abstract available. -
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- Mitochondrial Disorders
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Woo YJ
- KMID: 1517104
- J Korean Pediatr Soc.
- 2003 Jul;46(Suppl 2):S340-S351.
No abstract available. -
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- Mitochondrial Dynamics in the Heart as a Novel Therapeutic Target for Cardioprotection
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Hwang SJ, Kim W
- KMID: 2048813
- Chonnam Med J.
- 2013 Dec;49(3):101-107.
- doi: 10.4068/cmj.2013.49.3.101
Traditionally, mitochondria have been regarded solely as energy generators for cells; however, accumulating data have demonstrated that these complex organelles play a variety of roles within the cardiomyocyte that extend... -
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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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- Mitochondrial Gene Therapy
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Ko KS
- KMID: 1523006
- J Korean Diabetes Assoc.
- 2007 May;31(3):187-192.
- doi: 10.4093/jkda.2007.31.3.187
Mitochondrial dysfunction contributes to a large variety of human disorders, ranging from neurodegenerative and neuromuscular diseases, obesity, and diabetes to ischemia-reperfusion injury and cancer. Increasing pharmacological efforts toward therapeutic interventions... -
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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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- 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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- Anesthetic Management of a Patient with Mitochondrial Myopathy Undergoing Orthopedic Surgery
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Koo BS, Kim MJ, Lee MS
- KMID: 2317698
- Soonchunhyang Med Sci.
- 2013 Jun;19(1):38-41.
Mitochondria myopathies consist of large heterogeneous groups of disorders resulting from primary dysfunction of the mitochondrial respiratory chain and causing muscle disease. These disorders involve the multiple organ system and... -
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- Mitochondrial Mechanisms in Diabetic Cardiomyopathy
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Gollmer J, Zirlik A, Bugger H
- KMID: 2470953
- Diabetes Metab J.
- 2020 Feb;44(1):33-53.
- doi: 10.4093/dmj.2019.0185
Mitochondrial medicine is increasingly discussed as a promising therapeutic approach, given that mitochondrial defects are thought to contribute to many prevalent diseases and their complications. In individuals with diabetes mellitus... -
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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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