Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

26 results
Display

Analysis of Nuclear Mitochondrial DNA Segments of Nine Plant Species: Size, Distribution, and Insertion Loci

Ko YJ, Kim S

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
MitGEN: Single Nucleotide Polymorphism DB Browser for Human Mitochondrial Genome

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,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genetics of Mitochondrial Myopathies

Shin JH, Kim DS

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Whole Mitochondrial Genome Sequence of an Indian Plasmodium falciparum Field Isolate

Tyagi S, Pande V, Das A

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mechanisms of Uniparental Mitochondrial DNA Inheritance in Cryptococcus neoformans

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,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Sequence of the Mitochondrial Genome of Spirometra ranarum: Comparison with S. erinaceieuropaei and S. decipiens

Jeon HK, Park H, Lee D, Choe S, Kang Y, Bia MM, Lee SH, Eom KS

This study was undertaken to determine the complete mitochondrial DNA sequence and structure of the mitochondrial genome of Spirometra ranarum, and to compare it with those of S. erinaceieuropaei and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Re-engineering the mitochondrial genomes in mammalian cells

Yoon YG, Koob MD, Yoo YH

Mitochondria are subcellular organelles composed of two discrete membranes in the cytoplasm of eukaryotic cells. They have long been recognized as the generators of energy for the cell and also...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mitochondrial DNA A3243G mutation in noise-induced sensorineural hearing loss

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Mitochondrial Genome of Anoplocephala magna Solidifying the Species

Guo A

The 2 species of the genus Anoplocephala (Anoplocephalidae), A. perfoliata and A. magna, are among the most important equine cestode parasites. However, there is little information about their differences at...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Leigh Syndrome with Typical MRI and MRS Findings

Kang JW, Kim JC, Cho PZ, Cho JH, Kim SM, Sunwoo IN

  • KMID: 2137952
  • J Korean Neurol Assoc.
  • 2004 Oct;22(5):545-547.
Leigh syndrome (LS) is a genetically and clinically heterogeneous disorder caused by metabolic defects affecting lactate/pyruvate metabolism. The consequence of the metabolic defects are decreased amounts of APT and basic...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Mitochondrial Genome of the Chagas Disease Vector, Triatoma rubrofasciata

Dong L, Ma X, Wang M, Zhu D, Feng Y, Zhang Y, Wang J

Triatoma rubrofasciata is a wide-spread vector of Chagas disease in Americas. In this study, we completed the mitochondrial genome sequencing of T. rubrofasciata. The total length of T. rubrofasciata mitochondrial...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Mitochondrial Genome Sequences of Spirometra erinaceieuropaei and S. decipiens (Cestoidea: Diphyllobothriidae)

Eom KS, Park H, Lee D, Choe S, Kim KH, Jeon HK

The present study was performed to compare the mitochondrial genomes between 2 Spirometra tapeworms, Spirometra erinaceieuropaei and Spirometra decipiens (Cestoidea: Diphyllobothriidae), which larval stages are important etiological agents of sparganosis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Mitochondrial Genome of Echinostoma hortense (Digenea: Echinostomatidae)

Liu ZX, Zhang Y, Liu YT, Chang QC, Su X, Fu X, Yue DM, Gao Y, Wang CR

Echinostoma hortense (Digenea: Echinostomatidae) is one of the intestinal flukes with medical importance in humans. However, the mitochondrial (mt) genome of this fluke has not been known yet. The present...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Mitochondrial Genome of a Tongue Worm Armillifer agkistrodontis

Li J, He FN, Zheng HX, Zhang RX, Ren YJ, Hu W

Armillifer agkistrodontis (Ichthyostraca: Pantastomida) is a parasitic pathogen, only reported in China, which can cause a zoonotic disease, pentastomiasis. A complete mitochondrial (mt) genome was 16,521 bp comprising 13 protein-coding...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Back to the Ends: Chromosomal DNA

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Congenital Orbital Fibrosis: Molecular Genetic Analysis by Whole-Exome and Mitochondrial Genome Sequencing

Ko J, Lee HJ, Lee JS, Yoon JS

A 3-year-old girl presented with congenital orbital fibrosis. We performed molecular genetic analysis by whole exome and mitochondrial genome sequencing. No pathologic mutation was identified in the present case. To...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Relationship between Mitochondrial DNA Point Mutation and Noise-induced Sensorineural Hearing Loss

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...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Sequence Analysis of Mitochondrial Genome of Toxascaris leonina from a South China Tiger

Li K, Yang F, Abdullahi , Song M, Shi X, Wang M, Fu Y, Pan W, Shan F, Chen W, Li G

Toxascaris leonina is a common parasitic nematode of wild mammals and has significant impacts on the protection of rare wild animals. To analyze population genetic characteristics of T. leonina from...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Complete Mitochondrial Genome of Haplorchis taichui and Comparative Analysis with Other Trematodes

Lee D, Choe S, Park H, Jeon HK, Chai JY, Sohn WM, Yong TS, Min DY, Rim HJ, Eom KS

Mitochondrial genomes have been extensively studied for phylogenetic purposes and to investigate intra- and interspecific genetic variations. In recent years, numerous groups have undertaken sequencing of platyhelminth mitochondrial genomes. Haplorchis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Screening of the A11084G Polymorphism and Scanning of a Mitochondrial Genome SNP in Korean Migraineurs

Kang L, Lee ST, Im W, Kim SC, Hun KS, Kim BK, Kim M

BACKGROUND AND PURPOSE: Migraine is a genetically heterogeneous disorder that is frequently associated with a familial history, and mitochondrial dysfunction has been suggested to be associated with its pathogenesis. We...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2025 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr