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Molecular characterization of Plasmodium juxtanucleare in Thai native fowls based on partial cytochrome C oxidase subunit I gene

Pohuang T, Junnu S

Avian malaria is one of the most important general blood parasites of poultry in Southeast Asia. Plasmodium (P.) juxtanucleare causes avian malaria in wild and domestic fowl. This study aimed...
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Blood transcriptome resources of chinstrap (Pygoscelis antarcticus) and gentoo (Pygoscelis papua) penguins from the South Shetland Islands, Antarctica

Kim BM, Jeong J, Jo E, Ahn DH, Kim JH, Rhee JS, Park H

The chinstrap (Pygoscelis antarcticus) and gentoo (P. papua) penguins are distributed throughout Antarctica and the sub-Antarctic islands. In this study, high-quality de novo assemblies of blood transcriptomes from these penguins...
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The First Genetically Confirmed McLeod Syndrome in Korea

Park KW, Jeong S, Seo EJ, Lee CS

McLeod syndrome is a rare X-linked multisystem disorder which forms the core of neuroacanthocytosis syndrome. Neurological symptoms characterized by chorea, seizure, cognitive impairment, and psychosis mostly develop around the 5-6th...
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Planarians: an In Vivo Model for Regenerative Medicine

Karami A, Tebyanian , Goodarzi V, Shiri S

The emergence of regenerative medicine has raised the hope of treating an extraordinary range of disease and serious injuries. Understanding the processes of cell proliferation, differentiation and pattern formation in...
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Mitochondrial DNA 4977bp Deletion Mutation in Peripheral Blood Reflects Atrial Remodeling in Patients with Non-Valvular Atrial Fibrillation

Lee JS, Ko YG, Shin KJ, Kim SK, Park JH, Hwang KC, Pak HN

PURPOSE: Recently, mitochondrial DNA 4977bp deletion (mtDNA4977-mut), a somatic mutation related to oxidative stress, has been shown to be associated with atrial fibrillation (AF). We hypothesized that patient age, as...
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MicroRNA Analysis during Cultured Odontoblast Differentiation

Park MG, Lee MH, Yu SK, Park E, Kim S, Lee SA, Moon YH, Kim HJ, Kim CS, Kim DK

  • KMID: 1436490
  • Int J Oral Biol.
  • 2012 Sep;37(3):146-152.
MicroRNAs (miRNAs, miRs) are about 21-25 nucleotides in length and regulate mRNA translation by base pairing to partially complementary sites, predominantly in the 3'-untranslated region (3'-UTR) of the target mRNA....
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Isolation and Cloning of an ABC Transporter-Like Gene of Haemophilus parasuis and Its Use in a New Diagnostic PCR

Kim H, Cho Y, Shin S, Kang S, Kwon OB, Hahn TW

The aim of this study was to identify a new gene of Haemophilus parasuis that could be used to develop a polymerase chain reaction (PCR) test for this porcine pathogen....
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The Association among the Genetic Polymorphism of Dopamine D4 Receptor, Temperament and Alcohol Drinking Behavior in Young Korean Adults

Nam YW, Lee SI, Shin CJ, Son JW, Kim SK

  • KMID: 2299909
  • Korean J Biol Psychiatry.
  • 2011 May;18(2):101-108.
OBJECTIVES: The aim of this study is to explore the association among DRD4 polymorphism, temperament and alcohol drinking behavior of Koreans in their early adulthood. METHOD: Participants were 172 healthy Korean...
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Molecular Cloning and Characterization of the Estrogen Receptor from the Slender Bitterling (Acheilognathus yamatsutae)

Kim JG, Kim HR, Park YJ, Chung KH, Oh SM

  • KMID: 2380155
  • Environ Health Toxicol.
  • 2011 ;26(1):e2011005.
OBJECTIVES: In order to identify the possibility of slender bitterling (SB) (Acheilognathus yamatsutae) being used as a test species for estrogenic endocrine disrupting chemicals (EEDCs), we carried out the cloning...
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Genetic Variation in the Immunoregulatory Gene of Adenovirus Type 3

Choi EH, Kim HS, Lee HJ

  • KMID: 2278925
  • Korean J Pediatr Infect Dis.
  • 2009 Dec;16(2):199-204.
PURPOSE: Various proteins encoded in the early region 3 (E3) of adenoviruses protect cells from being killed by cytotoxic T cells and death-inducing cytokines. We sought to find out whether...
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Somatic Mutational Analysis of MEN1 and Phenotypic Correlation in Sporadic Parathyroid Tumors

Chae YS, Kim HJ, Kim SW, Chang MC

PURPOSE: MEN1 gene mutation causes multiple endocrine neoplasia type 1. It also suggests that somatic MEN1 gene mutation plays a role in sporadic endocrine tumor. In this study, we examined...
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Understanding of single nucleotide polymorphism of human genome

Oh JH, Yoon BW

  • KMID: 2190178
  • J Korean Assoc Oral Maxillofac Surg.
  • 2008 Aug;34(4):450-455.
A Single Nucleotide Polymorphism (SNP) is a small genetic change or variation that can occur within a DNA sequence. It's the difference of one base at specific base pair position....
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Association Study Between Dopamine Transporter Gene 40 bp VNTR and Antipsychotics-Induced Restless Legs Syndrome

Kang SG, Lee HJ, Choi JE, Kim L, Jung IK

  • KMID: 2317460
  • Sleep Med Psychophysiol.
  • 2008 Jun;15(1):39-43.
OBJECTIVES: The pathophysiology of restless legs syndrome (RLS) is not obvious, but many promising theories involve dopaminergic deficiency and genetic causes. The RLS is presumed to occur more frequently among...
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Relationship between PTC Genotype and Taste Phenotype in Normal Volunteers

Ye MK, Shin TH

  • KMID: 2276971
  • Korean J Otorhinolaryngol-Head Neck Surg.
  • 2008 Dec;51(12):1124-1128.
BACKGROUND AND OBJECTIVES: The ability to taste the bitter compounds phenylthiocarbamide is a classic inherited trait in humans. This trait has also been shown to correlate with a number of...
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Comparison of PCR-RFLP and Real-Time PCR for Allelotyping of Single Nucleotide Polymorphisms of RRM1, a Lung Cancer Suppressor Gene

Jeong JY, Kim MR, Son JG, Jung JP, Oh IJ, Kim KS, Kim YC

  • KMID: 2318944
  • Tuberc Respir Dis.
  • 2007 May;62(5):406-416.
BACKGROUND: Single nucleotide polymorphisms (SNPs), which consist of a substitution of a single nucleotide pair, are the most abundant form of genetic variations occurring with a frequency of approximately 1...
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Polymorphism Study of Susceptibility Genes Related to Sporadic Alzheimer's Disease

Choi YS, Lee KS, Park YG, Kim SH

  • KMID: 2338467
  • J Korean Geriatr Soc.
  • 2006 Jun;10(2):115-124.
Background: We investigated whether any single nucleotide polymorphism of the 7 candidate susceptibility genes is associated with sporadic Alzheimer's disease (AD). Methods: Genomic DNA from brain tissues of registered cases of...
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Comparative Genomics of T-complex protein 10 like in Humans and Chimpanzees

Kim IC, Kim DS, Kim DW, Choi SH, Choi HH, Chae SH, Park HS

  • KMID: 1572634
  • Genomics Inform.
  • 2005 Jun;3(2):61-65.
Comparing 231 genes on chimpanzee chromosome 22 with their orthologous on human chromosome 21, we have found that 15 orthologs have indels within their coding sequences. It was rather surprising...
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Factor V Leiden mutation in Korean women with pregnancy-induced hypertension

Cho YK, Ko JK, Lee CM, Choi H, Kim BR, Lee HK

  • KMID: 2272563
  • Korean J Obstet Gynecol.
  • 2005 Apr;48(4):857-866.
OBJECTIVE: The purposes of this study was to evaluate the frequency of Leiden mutation (missense mutation in the factor V gene at exon 10, 1691 CGA to CAA) in Korean...
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Mutation Analysis in X-linked Recessive Congenital Immunodeficiency Syndromes

Baek HJ, Choi SH, Sohn KR, Kook H, Kim SJ, Song ES, Han DK, Hwang TJ

  • KMID: 2172339
  • Chonnam Med J.
  • 2005 Apr;41(1):48-61.
In patients and their families who had relevant clinical findings and compatible immunologic data suggestive of X-linked congenital immunodeficiency syndromes, the authors tried to identify the genetic abnormalities employing the...
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Analysis of EBV in Extranodal NK/T Cell Lymphoma

Cho MS, Woo SY

OBJECTIVES: Epstein-Barr virus(EBV) is associated with development of various types of lymphoma, especially NK/T cell lymphoma. Recently, its subtypes and LMP-1, major oncoprotein of EBV, have been studied. We investigated...
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