Browsing by Keyword : Extracellular Matrix Proteins
Showing results 1 to 16 of 16
| Pub Year | | Title | AJOU Author(s) |
| 2015 | | AKT-independent Reelin signaling requires interactions of heterotrimeric Go and Src. | 김성수, 서해영, 이영돈, 최정미 |
| 2005 | | Amelioration of pancreatic fibrosis in mice with defective TGF-beta signaling. | 김욱환, 김진홍, 여말희, 유병무, 조성원, 최준혁, 함기백 |
| 2017 | | Anti-fibrogenic effect of PPAR-gamma agonists in human intestinal myofibroblasts | 신성재, 이광재, 이기명 |
| 2003 | | Bone morphogenetic protein-2 facilitates expression of chondrogenic, not osteogenic, phenotype of human intervertebral disc cells. | 한경진 |
| 2012 | | Chip-based cartilage oligomeric matrix protein detection in serum and synovial fluid for osteoarthritis diagnosis | 민병현 |
| 2016 | | Comparative Gene Expression Analysis of the Coronal Pulp and Apical Pulp Complex in Human Immature Teeth | 김승혜 |
| 2019 | | Disentangling the genetics of lean mass | 조남한 |
| 2012 | | Evaluation of a pretreatment method for two-dimensional gel electrophoresis of synovial fluid using cartilage oligomeric matrix protein as a marker | 민병현 |
| 2009 | | Expression of Disabled 1 suppresses astroglial differentiation in neural stem cells. | 서해영, 이영돈 |
| 2006 | | Low-intensity ultrasound stimulates the viability and matrix gene expression of human articular chondrocytes in alginate bead culture. | 민병현 |
| 2007 | | Mechanotransduction pathways of low-intensity ultrasound in C-28/I2 human chondrocyte cell line. | 민병현, 최병현 |
| 2011 | | Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes. | 김옥화 |
| 2005 | | Tissue-engineered cartilage using fibrin/hyaluronan composite gel and its in vivo implantation. | 민병현, 배기수 |
| 2003 | | Transforming growth factor-beta-inducible gene-h3 (beta(ig)-h3) promotes cell adhesion of human astrocytoma cells in vitro: implication of alpha6beta4 integrin. | 손성향 |
| 2003 | | Urokinase receptor deficiency accelerates renal fibrosis in obstructive nephropathy. | 김흥수 |
| 2014 | | Whole-exome sequencing identifies a novel genotype-phenotype correlation in the entactin domain of the known deafness gene TECTA. | 정주용 |
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