- Failure to Support Associations of Neurotrophin-3(NT-3) Gene Polymorphism in Korean Schizophrenic Patients
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Lee YS
- KMID: 2202985
- J Korean Soc Biol Psychiatry.
- 1997 Nov;4(2):234-236.
Though initial report from Japan showed positive association of schizophrenia with dinucleotide repeat polymorphism in the NT-3 gene, subsequent studies showed mixed results. Therefore we conducted a replication study with... -
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- Understanding of single nucleotide polymorphism of human genome
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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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- Cloning and Sequencing Analysis of the Gene Encoding the 66-kDa Protein in Borrelia hermsii
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Kook YH, Park KH, Lee SH, Kim JH
- KMID: 2099295
- J Korean Soc Microbiol.
- 1998 Oct;33(5):463-473.
The gene encoding the 66 kilodalton (kDa) protein of Borrelia hermsii HS1 was cloned and sequenced. Chromosomal DNA was prepared from purified B. hermsii and used in construction of genomic... -
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- The First Genetically Confirmed McLeod Syndrome in Korea
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Park KW, Jeong S, Seo EJ, Lee CS
- KMID: 2379308
- J Korean Neurol Assoc.
- 2017 May;35(2):85-88.
- doi: 10.17340/jkna.2017.2.4
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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- Characterization of Cyclic AMP Response Element (CRE) in the Promoter of the Rat Thyrotropin Releasing Hormone (TRH) Gene
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Jung WW, Yang IM, Seo KS, Jung SW
- KMID: 2461510
- J Korean Soc Endocrinol.
- 1994 Sep;9(3):190-199.
We investigated whether the two variant elements of CRE(TGcCGTCA[5'CRE], TGACcTCA[3'CRE]) in the 5'flanking region of the rat TRH gene, which are different from the CRE consensus sequence(5'-TGACGTCA-3') by one base... -
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- DNAse I hypersensitive sites of lung specific transcription factor gene
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Lee YC
- KMID: 2160239
- Tuberc Respir Dis.
- 2000 Jun;48(6):879-886.
- doi: 10.4046/trd.2000.48.6.879
BACKGROUND: Thyroid Transcription Factor-1(TTF-1) acts as a tissue specific transcription factor in the regulation of lung specific gene expression and as morphogenic protein during lung organogenesis. Currently, there is very... -
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- MicroRNA Analysis during Cultured Odontoblast Differentiation
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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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- Analysis of EBV in Extranodal NK/T Cell Lymphoma
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Cho MS, Woo SY
- KMID: 1964090
- Ewha Med J.
- 2004 Sep;27(2):87-91.
- doi: 10.12771/emj.2004.27.2.87
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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- Cloning and Nucleotide Sequence of the aroA Gene from Shigella sonnei KNIH104S
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Park YC, Shin HJ, Hong SG, Hwang SY, Park GD, Ju YR, Lee KJ, Kim YC
- KMID: 1943458
- J Korean Soc Microbiol.
- 1997 Apr;32(2):151-160.
Shigella sonnei is important causes of human enteric infections. S. sonnei KNIH104S was isolated from patient of shigellosis in Korea and previously reported. We cloned 5.2-kb KpnI fragment containing the... -
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- Mutations of the NF1 gene in Korean Neurofibromatosis type 1 patients
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Park KC, Choi HO, Han WS, Hwang JH, Kim KH, Chung JH, Eun HC
- KMID: 2163872
- Ann Dermatol.
- 2001 Jun;13(2):102-105.
- doi: 10.5021/ad.2001.13.2.102
BACKGROUND: Neurofibromatosis type 1 (NF1) is one of the most common inherited disorders and is characterized by abnormalities in multiple tissues derived from the neural crest. OBJECTIVES: We analyzed the presence... -
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- Expression of p58 in Fetal Thymocytes and Fetal Liver Lymphocytes
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Kim JD, Choi IH, Shin JS, Kim SJ, Kwon DH, Park HW, Shin EC
- KMID: 2083010
- Korean J Immunol.
- 1998 Mar;20(1):17-24.
Bipotent progenitors for T and natural killer (NK) lymphocytes are thought to exist among early precursor thymocytes or liver lymphocytes. The identification of such a progenitor population or mature NK... -
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- Detection of Penicillin-resistant Streptococcus pneumoniae by Polymerase Chain Reaction
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Lim SY, Bae SI, Lee CH, Kim KD
- KMID: 2031018
- Korean J Clin Pathol.
- 1999 Oct;19(5):516-512.
BACKGROUND: Resistance to penicillin of Streptococcus pneumoniae in clinical isolates has occurred by the development of altered penicillin-binding proteins (PBPs) that have greatly decreased affinity for antibiotics and has been... -
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- Isolation and Cloning of an ABC Transporter-Like Gene of Haemophilus parasuis and Its Use in a New Diagnostic PCR
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Kim H, Cho Y, Shin S, Kang S, Kwon OB, Hahn TW
- KMID: 2168667
- J Bacteriol Virol.
- 2012 Dec;42(4):321-329.
- doi: 10.4167/jbv.2012.42.4.321
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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- Identification of Mycobacterium tuberculosis in Pleural Effusion by Polymerase Chain Reaction(PCR)
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Kim ST, Gang CW
- KMID: 2128548
- Tuberc Respir Dis.
- 1995 Oct;42(5):695-702.
- doi: 10.4046/trd.1995.42.5.695
BACKGROUND: Since polymerase chain reaction(PCR) was devised by Saiki in 1985, it has been used extensively in various fields of molecular biology. Clinically, PCR is especially useful in situation when... -
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- Follicle stimulating hormone receptor gene mutation in Korean women with premature ovarian failure and normal karyotype
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Choi YM, Kim SH, Kim JK, Moon SY, Lee JY, Lee GW
- KMID: 2261940
- Korean J Obstet Gynecol.
- 2000 May;43(5):836-841.
OBJECTIVE: To determine whether the follicle stimulating hormone(FSH) receptor gene mutation (C566T point mutation) is present in Korean women with premature ovarian failure and normal karyotype. METHODS: Genomic deoxyribonucleic acid(DNA) obtained... -
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- DNA - based Prenatal Diagnosis of Epidermolytic Palmoplantar Keratoderma
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Yang SH, Roh CR, Lee JH, Chung JH, Moon ZS, Yang JM, Kim SW
- KMID: 2261255
- Korean J Obstet Gynecol.
- 1999 Jan;42(1):19-24.
OBJECTIVE: The purpose of this investigation was to establish the prenatal diagnosis for identifying the risk for epidermolytic palmoplantar keratoderma(EPPK) of a fetus by sequence analysis of fetal genomic DNA... -
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- Molecular characterization of Plasmodium juxtanucleare in Thai native fowls based on partial cytochrome C oxidase subunit I gene
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Pohuang T, Junnu S
- KMID: 2451640
- Korean J Vet Res.
- 2019 Jun;59(2):69-74.
- doi: 10.14405/kjvr.2019.59.2.69
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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- Detection of Chlamydia trachomatis by the Polymerase Chain Reaction in the Cervice of Women with Genital Tract Infecion
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Chun SH
- KMID: 2261202
- Korean J Obstet Gynecol.
- 1998 Dec;41(12):2932-2936.
OBJECTIVE: To evaluate the diagnostic value of polymerase chain reaction (PCR) as opposed to Enzyme immunoassay (EIA) of Chlamydia trachomatis in cervices of women with genital tract infection. METHODS: Sixty... -
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- Prevalence of Zidovudine Resistant Human Immunodeficiency Virus Type 1 in Zidovudine-naive Patients
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Kim NJ, Choi ES, Kim ES, Lee DH, Choe YJ, Bang JH, Oh MD, Choe KW
- KMID: 1599898
- Korean J Infect Dis.
- 2001 Feb;33(1):40-45.
BACKGROUD: Drug resistant virus has been seen with all effective antiretroviral drugs in current practice. The isolation of resistant virus from subjects is associated with more rapid clinical outcome. The... -
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- Association between Attention Deficit Hyperactivity Disorder and Dopamine Transporter Gene(DAT1) Polymorphism in Korean
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Shin DW, Noh KS, Oh KS, Lee MS
- KMID: 2340728
- J Korean Neuropsychiatr Assoc.
- 2002 Jul;41(4):612-618.
OBJECTIVES: Study results of association between dopamine transporter gene(DAT1) and attention deficit hyperactivity disorder(ADHD) were not conclusive. Distribution of DAT1 polymorphism is variable according to ethnicity. Ethnic differences in the... -
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