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Showing results 140 to 156 of 156

Pub YearTitleAJOU Author(s)
2010The 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
2014The effect of perinatal anxiety on bronchiolitis is influenced by polymorphisms in ROS-related genes.장형윤
2008The effect of the ApoE genotype on the association between head circumference and cognition.홍창형
2019The Liver X Receptor Is Upregulated in Monocyte-Derived Macrophages and Modulates Inflammatory Cytokines Based on LXRalpha Polymorphism김현아, 서창희, 정주양
2003The origin of cells that repopulate patellar tendons used for reconstructing anterior cruciate ligaments in man.민병현
2006The spectrum of NF1 mutations in Korean patients with neurofibromatosis type 1.김현주, 박상진, 정선용
2005Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.김대중, 이관우
2012Transgenic mice expressing yellow fluorescent protein under control of the human tyrosine hydroxylase promoter이명애
2010Type 2 Diabetes Genetic Association Database manually curated for the study design and odds ratio.진현석
2015Underlying Mechanisms and Management of Refractory Gastroesophageal Reflux Disease이광재
2003Urokinase receptor deficiency accelerates renal fibrosis in obstructive nephropathy.김흥수
2003Urokinase receptor modulates cellular and angiogenic responses in obstructive nephropathy.김흥수
2008VanB phenotype-vanA genotype Enterococcus faecium with heterogeneous expression of teicoplanin resistance.박일중, 이위교
2006Which gene is a dominant predictor of response during FOLFOX chemotherapy for the treatment of metastatic colorectal cancer, the MTHFR or XRCC1 gene?김영배, 서광욱
2011Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).김옥화
2014Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA.정주용
2011Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.김옥화
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