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Molecular Therapy, ISSN 1525-0016, 03/2017, Volume 25, Issue 3, pp. 715 - 727
MicroRNAs (miRNAs) are emerging as important regulators in osteoarthritis (OA) pathogenesis. In our study, a real-time PCR assay revealed that miR-483-5p was... 
antago-miR-483-5p | cartilage angiogenesis | chondrocyte | hypertrophy | osteoarthritis | tissue inhibitor of metalloproteinase 2 | matrilin 3 | MEDICINE, RESEARCH & EXPERIMENTAL | MICRORNAS | CARTILAGE | BETA | CHONDROCYTE HYPERTROPHY | IN-VITRO | GENE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | GROWTH-PLATE | EXPRESSION | CHONDROGENESIS | TRANSGENIC MICE | Humans | Middle Aged | Male | Tissue Inhibitor of Metalloproteinase-2 - genetics | Young Adult | RNA Interference | Cartilage, Articular - metabolism | Adult | Female | Osteoarthritis - pathology | Chondrocytes - metabolism | Disease Models, Animal | Gene Expression | Gene Expression Regulation | Osteoarthritis - metabolism | Antagomirs - administration & dosage | Matrilin Proteins - genetics | Osteoarthritis - genetics | Cartilage, Articular - pathology | Animals | Neovascularization, Pathologic - genetics | Aged | Mice | MicroRNAs - genetics | Antagomirs - genetics | Transcription factors | Meniscus | Pathogenesis | MiRNA | Transgenic mice | Homeostasis | Arthritis | Cartilage (articular) | Tissue inhibitor of metalloproteinase 2 | Cartilage matrix protein | Injection | Gene expression | Angiogenesis | Surgery | Doxycycline | Extracellular matrix | Metalloproteinase | Matrix protein | Osteoarthritis | Age | Hypertrophy | Cartilage diseases | Index Medicus | Original
Journal Article
Journal Article
Journal Article
Journal of Dermatological Science, ISSN 0923-1811, 07/2018, Volume 91, Issue 1, pp. 19 - 27
Ultraviolet (UV) radiation has been reported to influence epigenetic regulation by affecting the expression of genome regulators such as DNA methyltransferase... 
Ultraviolet irradiation | Tissue inhibitor of metalloproteinase | DNA methyltransferase 1 | HISTONE MODIFICATION | DNMT1 | METHYLATION | DEACETYLASE | INDUCTION | CANCER | DERMATOLOGY | MATRIX METALLOPROTEINASES | EPIGENETICS | GENE | DEGRADATION | Skin | Methyltransferases | Methylation | Analysis | DNA | Radiation | Index Medicus
Journal Article
Journal Article
Biochemical Journal, ISSN 0264-6021, 08/2010, Volume 430, Issue 1, pp. 79 - 86
The disintegrin and metalloprotease ADAM 12 has important functions in normal physiology as well as in diseases, such as cancer. Little is known about how ADAM... 
Tissue inhibitor of metalloproteinase (TIMP) | Therapeutic target | Tumour necrosis factor α-converting enzyme (TACE) | A disintegrin and metalloprotease 12 (ADAM12) | Ectodomain shedding | 1-MATRIX METALLOPROTEINASE | ectodomain shedding | CRYSTAL-STRUCTURE | MYOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | a disintegrin and metalloprotease 12 (ADAM12) | ESCHERICHIA-COLI | tissue inhibitor of metalloproteinase (TIMP) | CELL-SURFACE | therapeutic target | TERMINAL DOMAINS | tumour necrosis factor alpha-converting enzyme (TACE) | ALPHA-CONVERTING ENZYME | MELTRIN-ALPHA | EXPRESSION | EPITOPES | Protein Structure, Tertiary | Cell Line | Recombinant Proteins - antagonists & inhibitors | ADAM Proteins - antagonists & inhibitors | Humans | Epidermal Growth Factor - metabolism | Recombinant Proteins - genetics | Tissue Inhibitor of Metalloproteinase-2 - genetics | ADAM12 Protein | Heparin-binding EGF-like Growth Factor | Intercellular Signaling Peptides and Proteins - metabolism | Tissue Inhibitor of Metalloproteinase-2 - metabolism | ADAM Proteins - metabolism | Membrane Proteins - antagonists & inhibitors | Tissue Inhibitor of Metalloproteinase-3 - metabolism | Protein Engineering | Tissue Inhibitor of Metalloproteinase-2 - pharmacology | Protein Binding | Cell Membrane - metabolism | Membrane Proteins - metabolism | Catalysis | Kinetics | Mutation | Index Medicus | tumour necrosis factor α-converting enzyme (TACE)
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 10/2017, Volume 16, Issue 4, pp. 5464 - 5470
Human papillomavirus (HPV) infection alone is not sufficient for development of cervical cancer and further risk factors are involved, however, the underlying... 
MiR-20b | TIMP-2 | Migration | Cervical cancer | Invasion | HPV | MEDICINE, RESEARCH & EXPERIMENTAL | miR-20b | CELLS | INFECTIONS | MESENCHYMAL TRANSITION | cervical cancer | invasion | ONCOLOGY | DISEASE | migration | EXPRESSION | CARCINOMA | Papillomavirus Infections - complications | Humans | Gene Expression Regulation, Neoplastic | Uterine Cervical Neoplasms - pathology | Epithelial-Mesenchymal Transition - genetics | Tissue Inhibitor of Metalloproteinase-2 - genetics | DNA-Binding Proteins - metabolism | Tissue Inhibitor of Metalloproteinase-2 - metabolism | RNA Interference | Uterine Cervical Neoplasms - metabolism | Models, Biological | Cell Line, Tumor | Uterine Cervical Neoplasms - etiology | Female | Papillomavirus Infections - virology | MicroRNAs - genetics | HeLa Cells | 3' Untranslated Regions | Papillomaviridae - physiology | Genes, Reporter | Cell Movement | Oncogene Proteins, Viral - metabolism | Complications and side effects | Care and treatment | MicroRNA | Development and progression | Genetic aspects | Health aspects | Papillomavirus infections | Mesenchyme | Genes | MiRNA | mRNA | Metastasis | Tissue inhibitor of metalloproteinase 2 | Matrix metalloproteinase | Cervix | Risk factors | Metastases | Human papillomavirus | Plasmids | Fibroblasts | Hypoxia | Software | Metalloproteinase | Cervical carcinoma | Cell migration
Journal Article
Melanoma Research, ISSN 0960-8931, 2014, Volume 24, Issue 1, pp. 32 - 39
Journal Article