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아주대학교 의학문헌정보센터
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Showing results 101 to 117 of 117
Pub Year
Title
Author(s)
2014
Simultaneous determination of metoprolol and its metabolites, α-hydroxymetoprolol and O-desmethylmetoprolol, in human plasma by liquid chromatography with tandem mass spectrometry: Application to the pharmacokinetics of metoprolol associated with CYP2D6 genotypes.
조두연
2003
Sources of polycyclic aromatic hydrocarbon exposure in non-occupationally exposed Koreans.
장재연
2005
Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.
정윤석
2004
Subcellular localization and transcriptional repressor activity of HBx on p21(WAF1/Cip1) promoter is regulated by ERK-mediated phosphorylation.
최경숙
2010
The common exon 3 polymorphism of the growth hormone receptor gene and the effect of growth hormone therapy on growth in Korean patients with Turner syndrome.
고정민
2014
The effect of perinatal anxiety on bronchiolitis is influenced by polymorphisms in ROS-related genes.
장형윤
2019
The Liver X Receptor Is Upregulated in Monocyte-Derived Macrophages and Modulates Inflammatory Cytokines Based on LXRalpha Polymorphism
김현아
,
서창희
,
정주양
2003
The origin of cells that repopulate patellar tendons used for reconstructing anterior cruciate ligaments in man.
민병현
2005
Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.
김대중
,
이관우
2012
Transgenic mice expressing yellow fluorescent protein under control of the human tyrosine hydroxylase promoter
이명애
2010
Type 2 Diabetes Genetic Association Database manually curated for the study design and odds ratio.
진현석
2015
Underlying Mechanisms and Management of Refractory Gastroesophageal Reflux Disease
이광재
2003
Urokinase receptor deficiency accelerates renal fibrosis in obstructive nephropathy.
김흥수
2003
Urokinase receptor modulates cellular and angiogenic responses in obstructive nephropathy.
김흥수
2011
Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).
김옥화
2014
Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA.
정주용
2011
Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.
김옥화
1
2
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