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Oncogene, ISSN 1476-5594, 2010, Volume 29, Issue 49, pp. 6485 - 6498
Journal Article
Journal of cellular and molecular medicine, ISSN 1582-1838, 2013, Volume 17, Issue 1, pp. 30 - 54
.... Particularly, the sustained stimulation of epidermal growth factor receptor (EGFR), insulin‐like growth factor‐1 receptor (IGF‐1R), stem cell factor (SCF) receptor KIT, transforming growth factor... 
Hypoxia‐inducible factors | Targeted therapies | Cancer‐initiating cells | Hypoxia | Cancer progression | Metabolic pathways | Cancer stem/progenitor cells | Metastasis‐initiating cells | Metastases | Hypoxia-inducible factors | Cancer-initiating cells | Metastasis-initiating cells | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICALLY RELEVANT SUBTYPES | PANCREATIC-CANCER | Cancer stem | progenitor cells | CHRONIC MYELOID-LEUKEMIA | INHIBITS TUMOR-GROWTH | CELL BIOLOGY | EPITHELIAL-MESENCHYMAL TRANSITION | BREAST-CANCER | PROSTATE-CANCER | GENE-EXPRESSION | FATTY-ACID SYNTHASE | ENDOTHELIAL GROWTH-FACTOR | Neoplasms - metabolism | Hypoxia - drug therapy | Neoplastic Stem Cells - drug effects | Humans | Gene Expression Regulation, Neoplastic | Molecular Targeted Therapy | Hypoxia - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Neoplasm Metastasis | Basic Helix-Loop-Helix Transcription Factors - metabolism | Neoplasms - genetics | Neoplastic Stem Cells - metabolism | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Neoplastic Stem Cells - pathology | Antineoplastic Agents - pharmacology | Basic Helix-Loop-Helix Transcription Factors - genetics | Signal Transduction | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Intercellular Signaling Peptides and Proteins - genetics | Transcription Factors - genetics | Neoplasms - drug therapy | Transcription Factors - metabolism | Hypoxia - genetics | Hypoxia - pathology | Cell Transformation, Neoplastic - drug effects | Neoplasms - pathology | Apoptosis | Prevention | Glucose metabolism | Physiological aspects | Development and progression | Genetic transcription | Metastasis | Transforming growth factors | Vascular endothelial growth factor | Cancer | Energy metabolism | Transcription factors | Mesenchyme | AKT protein | Insulin-like growth factors | Kinases | Autophagy | Cancer therapies | Neoplasms | Proteins | Homing | Angiogenesis | Signal transduction | Receptors | Epidermal growth factor | Bone marrow | Tumor necrosis factor-TNF | miRNA | Growth factors | Deprivation | Cell survival | Cytokines | Epidermal growth factor receptors | Breast cancer | Rapamycin | Metabolism | Gene expression | Cell differentiation | Insulin | CXCR4 protein | 1-Phosphatidylinositol 3-kinase | Signaling | Pancreatic cancer | Stem cells | Glycolysis | Regulation | Prostate | Cell migration | Tumors | Reviews
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 1, p. e54001
... of extracellular matrix (ECM) proteins [1], [2]. It has been demonstrated that transforming growth factor-beta1 (TGF-beta1) is the most important growth factor in inducing... 
GROWTH-FACTOR-BETA | SOLID TUMORS | OBSTRUCTIVE NEPHROPATHY | MULTIDISCIPLINARY SCIENCES | CARDIAC-HYPERTROPHY | INTERSTITIAL FIBROSIS | INJURY | ANGIOTENSIN-II | CHRONIC KIDNEY-DISEASE | FACTOR RECEPTOR | MOLECULAR-MECHANISMS | Kidney - pathology | Transforming Growth Factor beta1 - metabolism | Actins - metabolism | Smad3 Protein - metabolism | Ureteral Obstruction - metabolism | Leukocytes - immunology | Kidney - metabolism | Receptor, Epidermal Growth Factor - metabolism | Benzamides - therapeutic use | Benzamides - pharmacology | Phosphorylation - drug effects | Ureteral Obstruction - drug therapy | Protein-Serine-Threonine Kinases - metabolism | Transforming Growth Factor beta1 - biosynthesis | Fibroblasts - metabolism | Pyridines - therapeutic use | Collagen Type I - metabolism | Kidney - drug effects | Histone Deacetylases - metabolism | Fibroblasts - pathology | Fibronectins - metabolism | Ureteral Obstruction - immunology | Gene Expression Regulation - drug effects | Acetylation - drug effects | Animals | Receptors, Transforming Growth Factor beta - metabolism | Signal Transduction - drug effects | Cell Cycle Checkpoints - drug effects | Fibroblasts - drug effects | Ureteral Obstruction - pathology | Fibrosis | Histone Deacetylase Inhibitors - pharmacology | Leukocytes - drug effects | Cell Proliferation - drug effects | Histone Deacetylase Inhibitors - therapeutic use | Mice | Pyridines - pharmacology | Histones - metabolism | Fibronectins | Muscle proteins | Growth factors | Collagen | Analysis | Drugs | Histone deacetylase | Phosphorylation | Smad protein | Animal models | Collagen (type I) | Nephrology | Transcription | Syngeneic grafts | Transforming growth factor-b | Smooth muscle | Activation | Kinases | Fibronectin | Medical schools | Epidermal growth factor | Actin | Rodents | Cell cycle | Fibroblasts | Ureter | Inhibition | Kidneys | Transforming growth factor-b1 | Epidermal growth factor receptors | Pulmonary arteries | Fibrils | Muscles | Medicine | Signaling | Hospitals | Kidney diseases | Cancer
Journal Article
Placenta, ISSN 0143-4004, 2014, Volume 36, Issue 3, pp. 270 - 278
Abstract Introduction The epidermal growth factor (EGF) signaling system regulates trophoblast differentiation, and its disruption could contribute to perinatal disease... 
Internal Medicine | Obstetrics and Gynecology | Epidermal growth factors | Preeclampsia | Placenta | TROPHOBLAST CELLS | APOPTOSIS | OXIDATIVE STRESS | CYTOTROPHOBLASTS | EGF | HUMAN-PLACENTA | DEVELOPMENTAL BIOLOGY | FACTOR RECEPTOR | OBSTETRICS & GYNECOLOGY | WOMEN | RETARDATION | REPRODUCTIVE BIOLOGY | ENDOMETRIAL | Receptor, Epidermal Growth Factor - genetics | Humans | Trophoblasts - pathology | Young Adult | Receptor, Epidermal Growth Factor - metabolism | Protein Isoforms - metabolism | Protein Isoforms - chemistry | Transforming Growth Factor alpha - blood | Epidermal Growth Factor - chemistry | Heparin-binding EGF-like Growth Factor - blood | Peptide Fragments - blood | Adult | Female | Pre-Eclampsia - metabolism | Transforming Growth Factor alpha - metabolism | Peptide Fragments - metabolism | Trophoblasts - metabolism | Placentation | Down-Regulation | Epidermal Growth Factor - metabolism | Chorionic Villi - metabolism | Pre-Eclampsia - pathology | Epidermal Growth Factor - blood | Receptor, Epidermal Growth Factor - chemistry | Heparin-binding EGF-like Growth Factor - metabolism | Placenta - metabolism | Pregnancy | Chorionic Villi - pathology | Pre-Eclampsia - blood | Placenta - pathology | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Cell Line, Transformed | Apoptosis | Cohort Studies | Protein Isoforms - genetics | Physiological aspects | Medical colleges | Epidermal growth factor | Cells | placenta | epidermal growth factors | preeclampsia
Journal Article
Nature communications, ISSN 2041-1723, 2011, Volume 2, Issue 1, p. 229
The fibroblast growth factor receptor 2-IIIb (FGFR2b) and the vascular endothelial growth factor receptor 2 (VEGFR2... 
FACTOR-RECEPTOR | LIGANDS | HB-EGF | MULTIDISCIPLINARY SCIENCES | ECTODOMAIN | KINASE | TACE | ALPHA-CONVERTING-ENZYME | MICE | POTENTIAL ROLE | KERATINOCYTE MIGRATION | ADAM17 Protein | Receptor, Epidermal Growth Factor - genetics | Phosphorylation | Cell Proliferation | Receptor, Fibroblast Growth Factor, Type 2 - metabolism | Humans | Transcriptional Activation | Phosphatidylinositol 3-Kinases - metabolism | Vascular Endothelial Growth Factor Receptor-2 - genetics | Intercellular Signaling Peptides and Proteins - metabolism | Fibroblast Growth Factor 7 - metabolism | Receptor, Epidermal Growth Factor - metabolism | Transfection | Mitogen-Activated Protein Kinase 1 - genetics | src-Family Kinases - metabolism | Female | Fetus | p38 Mitogen-Activated Protein Kinases - metabolism | Endothelial Cells - physiology | Cell Line | Gene Expression | Mitogen-Activated Protein Kinase 3 - genetics | Signal Transduction | Epidermal Growth Factor - genetics | Intercellular Signaling Peptides and Proteins - genetics | Vascular Endothelial Growth Factor Receptor-2 - metabolism | p38 Mitogen-Activated Protein Kinases - genetics | Epidermal Growth Factor - metabolism | Mice, Transgenic | Keratinocytes - cytology | Fibroblast Growth Factor 7 - genetics | Phosphatidylinositol 3-Kinases - genetics | Heparin-binding EGF-like Growth Factor | ADAM Proteins - metabolism | Animals | Mitogen-Activated Protein Kinase 3 - metabolism | Endothelial Cells - cytology | Mice | ADAM Proteins - genetics | src-Family Kinases - genetics | Fetal Blood | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Cell Movement | Keratinocytes - physiology | Mitogen-Activated Protein Kinase 1 - metabolism
Journal Article
Traffic (Copenhagen, Denmark), ISSN 1600-0854, 2009, Volume 10, Issue 8, pp. 1115 - 1127
...). It is well established that whereas EGF binding leads to lysosomal degradation of EGFR, transforming growth factor (TGF)‐α... 
amphiregulin | betacellulin | epiregulin | transforming growth factor‐α | epidermal growth factor receptor | heparin‐binding EGF‐like growth factor | endocytic trafficking | epidermal growth factor | Epidermal growth factor | Betacellulin | Heparin-binding EGF-like growth factor | Transforming growth factor-α | Endocytic trafficking | Epiregulin | Amphiregulin | Epidermal growth factor receptor | heparin-binding EGF-like growth factor | transforming growth factor-alpha | CBL | FACTOR-ALPHA | CELL BIOLOGY | UBIQUITINATION | CETUXIMAB | INTERNALIZATION | COLORECTAL-CANCER | EPIDERMAL-GROWTH-FACTOR | ERBB RECEPTORS | Cell Line | Receptor, Epidermal Growth Factor - genetics | Phosphorylation | Proto-Oncogene Proteins c-cbl - metabolism | Vesicular Transport Proteins - metabolism | Humans | Glycoproteins - metabolism | Epidermal Growth Factor - metabolism | Protein Transport - physiology | Endocytosis - physiology | Heparin-binding EGF-like Growth Factor | Intercellular Signaling Peptides and Proteins - metabolism | Receptor, Epidermal Growth Factor - metabolism | Ubiquitination | Animals | EGF Family of Proteins | Ligands | Lysosomal-Associated Membrane Protein 1 - metabolism | Signal Transduction - physiology | Transforming Growth Factor alpha - metabolism | Hydrogen-Ion Concentration | Ubiquitin | Universities and colleges | Transforming growth factors | Ligases | transforming growth factor-α | Original
Journal Article