Showing results 1 to 60 of 102
|A glutamate to lysine mutation at the end of 2B rod domain of keratin 2e gene in ichthyosis bullosa of Siemens.
|A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene
|A new autoantigen reactive with prediabetic nonobese diabetic mice sera.
|강엽, 김현만, 윤지원, 최경숙
|A pseudoknot improves selection efficiency in ribosome display.
|A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A.
|A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V
|A synonymous variation in protease-activated receptor-2 is associated with atopy in Korean children.
|A Tat-grafted anti-nucleic acid antibody acquires nuclear-localization property and a preference for TAR RNA
|A visible phagemid system for the estimation of Cre-mediated recombination efficiency.
|권명희, 김경민, 김형일, 박선, 신호준, 이명신
|Activated cAMP-response element-binding protein regulates neuronal expression of presenilin-1.
|An interstitial, apparently-balanced chromosomal insertion in the etiology of Langer-Giedion syndrome in an Asian family.
|Analysis of spacer regions derived from intramolecular recombination between heterologous loxP sites.
|권명희, 박선, 신호준, 이광
|Association between variable number tandem repeats within the 3' flanking region of the interleukin-6 gene and systemic lupus erythematosus in Korean patients.
|김승현, 김현아, 서창희
|Association of polymorphism in microRNA 604 with susceptibility to persistent hepatitis B virus infection and development of hepatocellular carcinoma.
|B-RafV600E inhibits sodium iodide symporter expression via regulation of DNA methyltransferase 1.
|김장희, 박태준, 소의영, 이정훈, 최용원, 최용준
|Blockade of PKC epsilon activation attenuates phorbol ester-induced increase of alpha-secretase-derived secreted form of amyloid precursor protein.
|김승업, 묵인희, 정민환, 하만준, 허균
|Characterization and gene cloning of monoclonal antibody specific for the hepatitis B virus X protein.
|김형일, 박선, 신호준, 윤정구, 조혜성
|Characterization of human SMARCE1r high-mobility-group protein.
|Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency
|Cloning and characterization of the promoter region of the Wilson disease gene.
|Colorimetric microwell plate hybridization assay for detection of amplified Mycobacterium tuberculosis DNA from sputum samples.
|Complete sequence of a gene encoding KAR3-related kinesin-like protein in Candida albicans.
|Cross-species hybridization of microarrays for studying tumor transcriptome of brain metastasis
|Direct activation of TGF-beta1 transcription by androgen and androgen receptor complex in Huh7 human hepatoma cells and its tumor in nude mice.
|Distribution of insertion sequences associated with Tn1546-like elements among Enterococcus faecium isolates from patients in Korea.
|E1a activation of insulin receptor gene expression is mediated by Sp1-binding sites.
|Effect of genetic polymorphism of ALOX15 on aspirin-exacerbated respiratory disease
|Effective therapeutic approach for head and neck cancer by an engineered minibody targeting the EGFR receptor.
|강호철, 박동선, 조혜성
|Effects of suppressing intrarenal angiotensinogen on renal transforming growth factor-beta1 expression in acute ureteral obstruction.
|김욱환, 김흥수, 신규태, 임현이
|Emerging invasive liver abscess caused by K1 serotype Klebsiella pneumoniae in Korea.
|Evidence that the 5'-end cap structure is essential for encapsidation of hepatitis B virus pregenomic RNA.
|Expression of beta-defensins in human middle ear cholesteatoma.
|문성균, 박기현, 정연훈, 최호석
|Expression of p50 C-terminal Src kinase (Csk) in mouse testis.
|Expression of rat BTG(3) gene, Rbtg3, is regulated by redox changes.
|Expression of the nicotinic acetylcholine receptor subunit, alpha9, in the guinea pig cochlea.
|Expression of tyrosine hydroxylase is epigenetically regulated in neural stem cells.
|Factor VNew Brunswick: Ala221-to-Val substitution results in reduced cofactor activity.
|First identified Korean family with Sotos syndrome caused by a novel intragenic mutation in NSD1.
|Five novel mutations of GALNS in Korean patients with mucopolysaccharidosis IVA.
|Genetic polymorphism of interferon-gamma, interferon-gamma receptor, and interferon regulatory factor-1 genes in patients with hepatitis B virus infection.
|김진홍, 여말희, 왕희정, 정재연, 조성원, 함기백
|Genome-Wide Analysis Identifies NURR1-Controlled Network of New Synapse Formation and Cell Cycle Arrest in Human Neural Stem Cells
|GSK3 inactivation is involved in mitochondrial complex IV defect in transforming growth factor (TGF) β1-induced senescence
|Heavy and light chain variable single domains of an anti-DNA binding antibody hydrolyze both double- and single-stranded DNAs without sequence specificity.
|Heavy chain dominance in the binding of DNA by a lupus mouse monoclonal autoantibody.
|Hepatitis B virus X protein modulates peroxisome proliferator-activated receptor gamma through protein-protein interaction.
|Heterozygosity for an exon 12 splicing mutation and a W234G missense mutation in an American child with chronic tyrosinemia type 1.
|High glucose enhances IL-1beta-induced cyclooxygenase-2 expression in rat vascular smooth muscle cells.
|문창현, 백은주, 이수환
|Human act and AR1 sequences differentially regulate murine and human D1A dopamine receptor promoters.
|Human endogenous retrovirus with a high genomic sequence homology with IDDMK(1,2)22 is not specific for Type I (insulin-dependent) diabetic patients but ubiquitous.
|Identification of a novel HLA-B*55 variant (B*5513) from a Korean family.
|Identification of a novel insertion sequence in vanB2-containing Enterococcus faecium.
|Identification of a rare homozygous c.790C>T variation in the TFB2M gene in Korean patients with autism spectrum disorder
|김정현, 박찬배, 이영수, 임신영, 정선용
|Identification of FAM13A gene associated with the ratio of FEV1 to FVC in Korean population by genome-wide association studies including gene-environment interactions.
|Identification of the human homologue of mouse KIF4, a kinesin superfamily motor protein.
|Identification of three novel mutations and a high frequency of the Arg778Leu mutation in Korean patients with Wilson disease.
|In situ detection of hepatitis C virus RNA in liver tissue using a digoxigenin-labeled probe created during a polymerase chain reaction.
|Induction of growth inhibition of 293 cells by downregulation of the cyclin E and cyclin-dependent kinase 4 proteins due to overexpression of TIS21.
|백운기, 이명숙, 임인경
|Inhibition of BETA2/NeuroD by Id2.
|Inhibition of the 3-hydroxy-3-methylglutaryl-coenzyme A reductase pathway induces p53-independent transcriptional regulation of p21(WAF1/CIP1) in human prostate carcinoma cells.
|Interleukin 3 (IL3) polymorphisms associated with decreased risk of asthma and atopy.