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Hypertension, ISSN 0194-911X, 10/2009, Volume 54, Issue 4, pp. 877 - 884
Journal Article
Oncogene, ISSN 0950-9232, 12/2010, Volume 29, Issue 49, pp. 6485 - 6498
Transforming growth factor-beta (TGF-beta) and epidermal growth factor (EGF) have critical roles in regulating the metastasis of aggressive breast cancers, yet... 
FAK | breast cancer | TGF-b | invasion | metastasis | EGFR | ACTIVATION | MAMMARY-CARCINOMA CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | TUMOR | FACTOR RECEPTOR INHIBITION | PROLIFERATION | LINES | CELL BIOLOGY | TGF-beta | ONCOLOGY | GENETICS & HEREDITY | GENE-EXPRESSION | FOCAL ADHESION KINASE | Animal models | Aggressive behavior | Epidermal growth factor receptors | Epithelial cells | Invasiveness | MAP kinase | Breast cancer | Transforming growth factor- beta | Metastases | E- double prime Cadherin | Epidermal growth factor | Veins | Mammary gland | Focal adhesion kinase | spheroids | Tumors | Cadherins - metabolism | Humans | Mammary Neoplasms, Experimental - metabolism | Breast Neoplasms - metabolism | Receptor, Epidermal Growth Factor - metabolism | Epithelial-Mesenchymal Transition | Mammary Neoplasms, Experimental - pathology | Female | Indoles - pharmacology | p38 Mitogen-Activated Protein Kinases - metabolism | Carcinoma - secondary | Mammary Neoplasms, Experimental - drug therapy | Carcinoma - drug therapy | Focal Adhesion Protein-Tyrosine Kinases - metabolism | Epidermal Growth Factor - metabolism | Sulfonamides - pharmacology | Breast Neoplasms - drug therapy | Transforming Growth Factor beta - pharmacology | Animals | Receptors, Transforming Growth Factor beta - metabolism | Breast Neoplasms - pathology | Cell Line, Tumor | Mice | Carcinoma - metabolism | Epidermal Growth Factor - pharmacology | Transforming Growth Factor beta - metabolism | RNA, Small Interfering - metabolism | Index Medicus
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 508, Issue 1, pp. 118 - 122
Treatment of BRAF(V600E) mutant melanoma by small molecule drugs that target the BRAF or MEK kinases can be effective, but resistance develops invariably(1,2).... 
GROWTH-FACTOR RECEPTOR | BRAF INHIBITOR | RAF INHIBITION | CELLS | MULTIDISCIPLINARY SCIENCES | IMPROVED SURVIVAL | DIFFERENTIATION | C-JUN | CANCER | EXPRESSION | EGFR | Cell Proliferation | Humans | Gene Expression Regulation, Neoplastic | Cell Aging | Drug Resistance, Neoplasm | Flow Cytometry | Mitogen-Activated Protein Kinase Kinases | SOX10 protein, human | SOXE Transcription Factors | Female | Indoles | Proto-Oncogene Proteins B-raf | Transforming Growth Factor beta | Gene Library | Signal Transduction | Melanoma | Receptor, Platelet-Derived Growth Factor beta | Antineoplastic Agents | vemurafenib | BRAF protein, human | Receptor Protein-Tyrosine Kinases | Index Medicus | Protein Kinase Inhibitors | Animals | Sulfonamides | Mice | RNA, Small Interfering | Receptor, Epidermal Growth Factor | Genes | Kinases | Drug resistance | Proteins | Rodents | PLX4032 | Patients | Biopsy | Mutation | Tumors | Receptor, Epidermal Growth Factor - genetics | Receptor Protein-Tyrosine Kinases - biosynthesis | Cellular Senescence - drug effects | Melanoma - enzymology | Antineoplastic Agents - administration & dosage | Receptor, Platelet-Derived Growth Factor beta - genetics | Indoles - administration & dosage | Mitogen-Activated Protein Kinase Kinases - metabolism | Receptor, Epidermal Growth Factor - metabolism | Melanoma - genetics | Indoles - pharmacology | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | SOXE Transcription Factors - deficiency | Proto-Oncogene Proteins B-raf - metabolism | Receptor, Platelet-Derived Growth Factor beta - metabolism | Receptor, Epidermal Growth Factor - biosynthesis | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | Melanoma - pathology | Receptor Protein-Tyrosine Kinases - metabolism | Sulfonamides - pharmacology | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Protein Kinase Inhibitors - administration & dosage | Transforming Growth Factor beta - pharmacology | Drug Resistance, Neoplasm - genetics | Receptor Protein-Tyrosine Kinases - genetics | Signal Transduction - drug effects | Proto-Oncogene Proteins B-raf - genetics | Melanoma - drug therapy | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Transforming Growth Factor beta - metabolism | Receptor, Platelet-Derived Growth Factor beta - biosynthesis | Sulfonamides - administration & dosage | Drug Resistance, Neoplasm - drug effects | SOXE Transcription Factors - genetics
Journal Article
Hepatology, ISSN 0270-9139, 12/2012, Volume 56, Issue 6, pp. 2255 - 2267
Liver cirrhosis is a predominant risk factor for hepatocellular carcinoma (HCC). However, the mechanism underlying the progression from cirrhosis to HCC... 
PROGENITOR CELLS | HEPATOCELLULAR-CARCINOMA | STEM-CELLS | HEPATOCYTES | TGF-BETA | EPIGENETIC REGULATION | PTEN | SELF-RENEWAL | TUMORIGENICITY | GASTROENTEROLOGY & HEPATOLOGY | EXPRESSION | Antigens, Differentiation | MIRN216 microRNA, rat | Peptides | Rats, Wistar | Cell Adhesion Molecules | Humans | Liver | Male | AC133 antigen | Pten protein, rat | Proteins | Liver cancer | Pluripotent Stem Cells | PTEN Phosphohydrolase | Hepatology | Diethylnitrosamine | Antigens, Thy-1 | Liver Neoplasms, Experimental | Transforming Growth Factor beta | oval cell marker OV-6 | Antigens, Neoplasm | Tumor Markers, Biological | Mice, Inbred C57BL | Rats | Stat3 protein, rat | Glycoproteins | Neoplastic Stem Cells | Mice, SCID | Proto-Oncogene Proteins c-akt | Animals | Cell Transformation, Neoplastic | MicroRNAs | mTOR protein, rat | Mice, Inbred NOD | Mice | STAT3 Transcription Factor | TOR Serine-Threonine Kinases | Liver cirrhosis | EPCAM protein, human | Antigens, CD | TOR Serine-Threonine Kinases - metabolism | Glycoproteins - metabolism | Liver Neoplasms, Experimental - chemically induced | MicroRNAs - metabolism | Proto-Oncogene Proteins c-akt - genetics | Antigens, CD - metabolism | Epithelial Cell Adhesion Molecule | Pluripotent Stem Cells - pathology | Liver Neoplasms, Experimental - metabolism | Peptides - metabolism | Neoplastic Stem Cells - metabolism | Liver Cirrhosis - metabolism | Antigens, Neoplasm - metabolism | Biomarkers, Tumor - metabolism | Antigens, Differentiation - metabolism | Liver Neoplasms, Experimental - pathology | Proto-Oncogene Proteins c-akt - metabolism | STAT3 Transcription Factor - metabolism | Liver - metabolism | PTEN Phosphohydrolase - metabolism | AC133 Antigen | Cell Adhesion Molecules - metabolism | Cell Transformation, Neoplastic - metabolism | Pluripotent Stem Cells - metabolism | Thy-1 Antigens - metabolism | Transforming Growth Factor beta - pharmacology | Pluripotent Stem Cells - drug effects | Liver Cirrhosis - pathology | Cell Transformation, Neoplastic - pathology | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
Journal Article
Cancer Cell, ISSN 1535-6108, 05/2014, Volume 25, Issue 5, pp. 666 - 681
Journal Article
NATURE MEDICINE, ISSN 1078-8956, 02/2015, Volume 21, Issue 2, pp. 150 - 158
Journal Article
Nature Immunology, ISSN 1529-2908, 12/2008, Volume 9, Issue 12, pp. 1347 - 1355
Journal Article
NATURE MEDICINE, ISSN 1078-8956, 03/2012, Volume 18, Issue 3, pp. 429 - U192
In advanced cancer, including glioblastoma, the transforming growth factor beta (TGF-beta) pathway acts as an oncogenic factor and is considered to be a... 
MEDICINE, RESEARCH & EXPERIMENTAL | SMURF2 | GLIOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SMAD7 | CELL BIOLOGY | GROWTH-FACTOR-BETA | PATHWAY | GENETICS | BIOLOGY | DEGRADATION | TARGETS | E3 UBIQUITIN LIGASE | Enzymes | Signal transduction | Animal models | Prognosis | RNA-mediated interference | peptidase | Glioblastoma | Tumorigenesis | Transforming growth factor- beta | Ubiquitin-protein ligase | Ovarian cancer | Ubiquitin | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Humans | Gene Expression Regulation, Neoplastic | Brain Neoplasms - metabolism | Glioblastoma - genetics | RNA Interference | Cell Transformation, Neoplastic - genetics | Smad2 Protein - genetics | HEK293 Cells | Glioblastoma - metabolism | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Smad7 Protein - metabolism | Endopeptidases - metabolism | Signal Transduction | Protein-Serine-Threonine Kinases - genetics | Smad2 Protein - metabolism | Ubiquitin-Protein Ligases - metabolism | Brain Neoplasms - genetics | Cell Transformation, Neoplastic - metabolism | Ubiquitin-Specific Proteases | Magnetic Resonance Imaging | Animals | Endopeptidases - genetics | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Cell Line, Tumor | Mice | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
Nature Medicine, ISSN 1078-8956, 08/2013, Volume 19, Issue 8, pp. 1047 - 1053
Myofibroblasts are associated with organ fibrosis, but their precise origin and functional role remain unknown. We used multiple genetically engineered mice to... 
MEDICINE, RESEARCH & EXPERIMENTAL | CELLS | ANGIOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | IDENTIFICATION | FIBROBLASTS | CELL BIOLOGY | ADHESION | TO-MESENCHYMAL TRANSITION | DIFFERENTIATION | RENAL INTERSTITIAL FIBROSIS | PULMONARY-FIBROSIS | PERICYTES | Cell Proliferation | Protein-Serine-Threonine Kinases | Male | Kidney | Mesenchymal Stromal Cells | Rodents | Epithelial-Mesenchymal Transition | Female | Cell Differentiation | Antigens | alpha-smooth muscle actin, mouse | Proteoglycans | Signal Transduction | Receptor, Platelet-Derived Growth Factor beta | Actins | chondroitin sulfate proteoglycan 4 | Pathology | transforming growth factor-beta type II receptor | Animals | Bone Marrow Cells | Cellular biology | Fibrosis | Pericytes | Receptors, Transforming Growth Factor beta | Genetic engineering | Mice | Kidney diseases | Myofibroblasts | Myofibroblasts - pathology | Kidney - pathology | Kidney Diseases - pathology | Pericytes - metabolism | Actins - metabolism | Bone Marrow Cells - pathology | Mesenchymal Stromal Cells - metabolism | Proteoglycans - metabolism | Antigens - metabolism | Myofibroblasts - metabolism | Kidney - metabolism | Receptors, Transforming Growth Factor beta - metabolism | Protein-Serine-Threonine Kinases - metabolism | Kidney Diseases - metabolism | Receptor, Platelet-Derived Growth Factor beta - metabolism | Fibroblasts | Physiological aspects | Development and progression | Genetic aspects | Research | Index Medicus
Journal Article