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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,...
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Genetic Background of Congenital Hearing Loss

Oh SH, Song JJ

  • KMID: 2244888
  • J Genet Med.
  • 2009 Jun;6(1):8-24.
Understanding the genetic background of hearing loss is important since almost 50% of the cases of profound hearing loss are caused by genetic factors. Until now, more than 150 causative...
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Mitochondrial Gene Therapy

Ko KS

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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The Frequency of Mitochondrial Gene Point Mutations in Korean Non-syndromic Sensorineural Hearing Loss

Jeong HS, Lim MJ, Chang SO, Kim CS, Oh SH

  • KMID: 2276112
  • Korean J Otolaryngol-Head Neck Surg.
  • 2004 Mar;47(3):206-211.
BACKGROUND AND OBJECTIVES: Mitochondrial point mutations have been shown to be responsible for syndromic and non-syndromic hearing impairment. Among these mitochondrial point mutations, 1555 A-->G, 3243 A-->G, and 7445 A-->G...
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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...
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Mitochondrial DNA Content and the MTND4 Gene Expression in Leber's Hereditary Optic Neuropathy

Seong MW, Kim JY, Ko HS, Hwang JM, Park SS

  • KMID: 2143217
  • Korean J Lab Med.
  • 2004 Dec;24(6):439-445.
BACKGROUND: Leber's hereditary optic neuropathy (LHON) is characterized by acute or subacute bilateral visual loss, primarily caused by a mitochondrial DNA (mtDNA) point mutation. However the pathogenic mechanism of visual...
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The quantitative analysis the number of mitochondrial DNA copy using real-time PCR and mitochondrial tRNA mutation analysis at position 3243 in Korean gestational diabetes mellitus

Chang SW, Lee SH, Jun HS, Kwack KB, Cho SW, Jeong HJ, Ahn SY, Kim YL, Kim SH, Park LS, Cho JH, Yoon TK

  • KMID: 2272577
  • Korean J Obstet Gynecol.
  • 2005 Apr;48(4):978-986.
OBJECTIVE: Mitochondrial gene mutations may play a role in the development of gestational diabetes mellitus. This study has assisted to confirm the relationship between the mitochondrial DNA copy number and...
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The Correlation of Plasma Homocysteine and Mitochondrial DNA Content in Peripheral Blood in Healthy Women

Lim S, Shin WS, Park KS, Kim SY, Lee JH, Yim MJ, Song JH, Lee HK

  • KMID: 2199618
  • J Korean Soc Endocrinol.
  • 2000 Jun;15(2):248-261.
BACKGROUND: Hyperhomocysteinemia is an independent risk factor for cardiovascular diseases. Previous reports showed that homocysteine damages mitochondrial gene expression, function and structure. In recent years, homocysteine and mitochondrial DNA (mtDNA)...
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Familial Hearing Loss Associated with mtDNA A1555G Mutation in Korea: 1 Pedigree

Oh SH, Chang SO, Park HJ, Kim DY, Jeon SJ, Lim MJ, Cheong HI, Park HW, Byun SW

  • KMID: 1977713
  • Korean J Otolaryngol-Head Neck Surg.
  • 1999 Nov;42(11):1353-1358.
BACKGROUND AND OBJECTIVES: Familial aminoglycoside-induced deafness has been described in a number of Chinese and Japanese pedigrees. Recently, the familial aminoglycoside-induced ototoxicity is proved to be associated with a mutation...
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Prevalence of Hymenolepis nana and H. diminuta from Brown Rats (Rattus norvegicus) in Heilongjiang Province, China

Yang D, Zhao W, Zhang Y, Liu A

Hymenolepis nana and Hymenolepis diminuta are globally widespread zoonotic cestodes. Rodents are the main reservoir host of these cestodes. Brown rats (Rattus norvegicus) are the best known and most common...
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Devrease of Mitochondrial DNA Content in Non-Insulin Dependent Diabetic Rats

Song JH, Yim SH, Han BG, Lee HK, Kim YM, Park KS, Suzuki S

  • KMID: 2177908
  • J Korean Diabetes Assoc.
  • 2000 Apr;24(2):202-215.
BACKGROUND: Although genetic disorder in diabetes mellitus (DM) is not well understood, it has been suggested that the maternally inherited mitochondrial DNA which does not follow the Mendel's laws is...
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Asian Ethnic Group Classification Model Using Data Mining

Kim YG, Lee JH, Cho S, Kim MY, Lee SD, Ha EH, Ahn JJ

In addition to identifying genetic differences between target populations, it is also important to determine the impact of genetic differences with regard to the respective target populations. In recent years,...
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Effects of chronic alcohol and excessive iron intake on mitochondrial DNA damage in the rat liver

Park JE, Lee JR, Chung J

PURPOSE: In this study, we investigated the effects of chronic alcohol and excessive iron intake on mitochondrial DNA (mtDNA) damage and the progression of alcoholic liver injury in rats. METHODS: Twenty-four...
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Leber's Hereditary Optic Neuropathy in a Patient Diagnosed With Normal Tension Glaucoma: A Case Report

Lee S, Choi J, Jang JW, Kim DM, Kim SJ

PURPOSE: Leber's hereditary optic neuropathy (LHON) is caused by point mutations in mitochondrial DNA. The authors report a case of a middle-aged man with genetically confirmed LHON, combined with bilateral...
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Molecular Detection of Spirometra decipiens in the United States

Jeon HK, Park H, Lee D, Choe S, Sohn WM, Eom KS

The genus Spirometra belongs to the family Diphyllobothriidae and order Pseudophyllidea, and includes intestinal parasites of cats and dogs. In this study, a plerocercoid labeled as Spirometra mansonoides from the...
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Familial Dilated Cardiomyopathy

Oh BH, Kim KI, Rhee MY, Chae IH, Kim HS, Sohn DW, Lee MM, Park YB, Choi YS, Lee YW

Dilated cardiomyopathy is a primary myocardial disease characterized by ventricular dilatation and impaired ventricular contractility. It is not a rare disease and the age-adjusted prevalence in the United States is...
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First Record of Paramphistomes Fischoederius cobboldi and Paramphistomum epiclitum Detected in Bovine Rumen from a Local Market of Savannakhet Province, Lao PDR

Sanguankiat S, Sato MO, Sato M, Maipanich , Yoonuan T, Pongvongsa T, Boupha B, Chigusa Y, Moji K, Waikagul J

In the present study, we report on the occurrence of paramphistomes, Fischoederius cobboldi and Paramphistomum epiclitum, in Lao PDR with the basis of molecular data. Parasite materials were collected from...
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