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Clinical & Experimental Ophthalmology, ISSN 1442-6404, 11/2008, Volume 36, Issue 8, pp. 717 - 720
Background:  To perform a comprehensive serum growth factor analysis in dry eye syndrome patients and to compare this with matched controls. Methods... 
growth factor | anterior segment | autologous serum | dry eye syndrome | Dry eye syndrome | Autologous serum | Anterior segment | Growth factor | DROPS | MAINTENANCE | DISEASE | OPHTHALMOLOGY | EYEDROPS | Fibroblast Growth Factor 7 - blood | Proto-Oncogene Proteins c-sis | Humans | Middle Aged | Vascular Endothelial Growth Factor A - blood | Brain-Derived Neurotrophic Factor - blood | Insulin-Like Growth Factor I - analysis | Fibroblast Growth Factor 2 - blood | Case-Control Studies | Epidermal Growth Factor - blood | Intercellular Signaling Peptides and Proteins - blood | Nerve Growth Factor - blood | Hepatocyte Growth Factor - blood | Dry Eye Syndromes - blood | Platelet-Derived Growth Factor - analysis | Aged, 80 and over | Ophthalmic Solutions | Female | Transforming Growth Factor beta2 - blood | Aged | Transforming Growth Factor beta1 - blood | Dry Eye Syndromes - etiology | Nerve Growth Factor, blood | Platelet-Derived Growth Factor, analysis | Intercellular Signaling Peptides and Proteins, blood | Transforming Growth Factor beta1, blood | Transforming Growth Factor beta2, blood | Dry Eye Syndromes, etiology | Fibroblast Growth Factor 7, blood | Brain-Derived Neurotrophic Factor, blood | Insulin-Like Growth Factor I, analysis | Fibroblast Growth Factor 2, blood | Hepatocyte Growth Factor, blood | Vascular Endothelial Growth Factor A, blood | Epidermal Growth Factor, blood | Dry Eye Syndromes, blood | Peptides | Analysis | Eye diseases | Nerve growth factor | Ophthalmology | Growth factors | Vascular endothelial growth factor
Journal Article
Nature (London), ISSN 1476-4687, 2018, Volume 562, Issue 7725, pp. 128 - 132
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 1, p. e52419
Intratracheal transplantation of human umbilical cord blood (UCB)-derived mesenchymal stem cells (MSCs... 
NADPH OXIDASE COMPLEX | RETINOIC ACID | MULTIDISCIPLINARY SCIENCES | ALVEOLARIZATION | INFANTS | GROWTH | Lung Injury - pathology | Body Weight | Lung Injury - surgery | Humans | NADPH Oxidases - metabolism | Vascular Endothelial Growth Factor A - metabolism | Mesenchymal Stromal Cells - cytology | Time Factors | Hyperoxia - complications | Lung Injury - metabolism | Female | Cell Membrane - metabolism | Animals, Newborn | Cytokines - metabolism | Gene Expression Regulation | Rats | Survival Rate | Fetal Blood - cytology | Rats, Sprague-Dawley | Hepatocyte Growth Factor - metabolism | Mesenchymal Stem Cell Transplantation - methods | Pregnancy | Collagen - metabolism | Animals | Cytosol - metabolism | Lung Injury - complications | Peroxidase - metabolism | Infants (Newborn) | Transplantation | Health aspects | Lung diseases | Enzyme-linked immunosorbent assay | Stem cells | Neonates | Pediatrics | Oxidative stress | Biomedical research | Mesenchyme | Syngeneic grafts | RANTES | Interleukin | Lung transplantation | Adhesion tests | Macrophages | Experiments | Blood | Interleukin 6 | Newborn babies | Cord blood | Rodents | Cell adhesion | Attenuation | Tumor necrosis factor-TNF | L-selectin | Peroxidase | Bioindicators | Metalloproteinase | Alveoli | Vascular endothelial growth factor | Growth factors | Injuries | Medical research | Cytokines | Intercellular adhesion molecule 1 | Pulmonary arteries | Hepatocyte growth factor | Inflammation | Medicine | Protein arrays | Hyperoxia | Collagen | Umbilical cord | Laboratory animals | Apoptosis
Journal Article
Diabetes (New York, N.Y.), ISSN 0012-1797, 05/2013, Volume 62, Issue 5, pp. 1453 - 1463
.... Notably, GcgR activation also raised hepatic expression and circulating levels of fibroblast growth factor 21 (FGF21... 
PPAR-ALPHA | BODY-WEIGHT | METABOLISM | FIBROBLAST-GROWTH-FACTOR-21 | PHARMACOLOGY | INCREASES ENERGY-EXPENDITURE | ENDOCRINOLOGY & METABOLISM | DEGRADATION | MICE | INSULIN SENSITIVITY | FGF21 | Obesity - drug therapy | Humans | Peptides - pharmacokinetics | Fibroblast Growth Factors - genetics | Male | Fibroblast Growth Factors - secretion | Obesity - blood | Anti-Obesity Agents - therapeutic use | Glucagon - agonists | Fibroblast Growth Factors - metabolism | Anti-Obesity Agents - pharmacokinetics | Peptides - chemical synthesis | Hepatocytes - secretion | Hypoglycemic Agents - therapeutic use | Receptors, Glucagon - agonists | Receptors, Glucagon - genetics | Hypoglycemic Agents - pharmacokinetics | Peptides - physiology | Rats | Hypoglycemic Agents - pharmacology | Mice, Knockout | Cross-Over Studies | Anti-Obesity Agents - chemical synthesis | Mice | Anti-Obesity Agents - pharmacology | Hepatocytes - pathology | Diabetes Mellitus, Type 2 - metabolism | Hepatocytes - metabolism | Molecular Targeted Therapy | Mice, Mutant Strains | HEK293 Cells | Adult | Female | Hepatocytes - drug effects | Recombinant Proteins - metabolism | Double-Blind Method | Cells, Cultured | Insulin Resistance | Receptors, Glucagon - metabolism | Recombinant Proteins - agonists | Glucagon - pharmacology | Obesity - metabolism | Diabetes Mellitus, Type 2 - blood | Animals | Fibroblast Growth Factors - blood | Hypoglycemic Agents - chemical synthesis | Glucagon - metabolism | Diabetes Mellitus, Type 2 - drug therapy | Peptides - therapeutic use | Physiological aspects | Fibroblast growth factors | Research | Glucagon | Analysis | Original Research
Journal Article
PloS one, ISSN 1932-6203, 06/2015, Volume 10, Issue 6, p. e0128952
... there is currently no therapy available. In the present work we analyzed a set of thirty different plasma cytokines, chemokines and growth factors present in circulation of 129 MS patients with different clinical forms... 
CHEMOKINE RECEPTOR EXPRESSION | APPEARING WHITE-MATTER | FACTOR-SCATTER FACTOR | MULTIDISCIPLINARY SCIENCES | HEPATOCYTE GROWTH-FACTOR | C-MET | BETA-CHEMOKINES | CENTRAL-NERVOUS-SYSTEM | CEREBROSPINAL-FLUID | UP-REGULATION | T-CELLS | Predictive Value of Tests | Diagnosis, Differential | Multiple Sclerosis, Relapsing-Remitting - blood | Humans | Middle Aged | Multiple Sclerosis, Chronic Progressive - blood | Multiple Sclerosis, Relapsing-Remitting - diagnosis | Biomarkers - blood | Case-Control Studies | Epidermal Growth Factor - blood | Multiple Sclerosis, Chronic Progressive - diagnosis | Hepatocyte Growth Factor - blood | Adult | Female | ROC Curve | Chemokine CCL4 - blood | Chemokine CCL11 - blood | Cohort Studies | Multiple sclerosis | Care and treatment | Physiological aspects | Genetic aspects | Research | Diagnosis | Biological markers | Nuclear magnetic resonance--NMR | Pathogenesis | Carbon tetrachloride | Eotaxin | Cell adhesion & migration | Angiogenesis | Immunology | Epidermal growth factor | Lymphocytes | Bioindicators | Growth factors | Public health | Cytokines | Blood & organ donations | Therapeutic applications | Histology | Regression analysis | CCL4 protein | Patients | Trauma | Neurology | Neurological complications | Biomarkers | Interferon | Chemokines | Epidermal Growth Factor/blood | Multiple Sclerosis, Relapsing-Remitting/diagnosis | Multiple Sclerosis, Relapsing-Remitting/blood | Chemokine CCL11/blood | Hepatocyte Growth Factor/blood | Life Sciences | Chemokine CCL4/blood | Biomarkers/blood | Multiple Sclerosis, Chronic Progressive/blood | Multiple Sclerosis, Chronic Progressive/diagnosis | Nuclear magnetic resonance | NMR
Journal Article
Internal medicine (Tokyo, 1992), ISSN 0918-2918, 2017, Volume 56, Issue 5, pp. 473 - 480
...), and GH supplementation has been shown to improve the histology of NAFLD. The aim of the present study was to clarify the relationship between the histological severity of NAFLD and production of the GH/insulin-like growth factor 1 (IGF-1) axis... 
nonalcoholic fatty liver disease (NAFLD) | growth hormone (GH) | insulin-like growth factor 1 (IGF-1) | insulin-like growth factor-binding protein 3 (IGFBP-3) | Growth hormone (GH) | Nonalcoholic fatty liver disease (NAFLD) | Insulin-like growth factor 1 (IGF-1) | Insulin-like growth factor-binding protein 3 (IGFBP-3) | HORMONE DEFICIENCY | RAT HEPATOCYTES | SERUM | FACTOR-I | INSULIN | FACTOR-BINDING-PROTEINS | MEDICINE, GENERAL & INTERNAL | HEPATITIS | REPLACEMENT THERAPY | ACID-LABILE SUBUNIT | SCORING SYSTEM | Non-alcoholic Fatty Liver Disease - pathology | Hepatitis C, Chronic - pathology | Liver - pathology | Age Factors | Humans | Middle Aged | Insulin-Like Growth Factor Binding Protein 3 - blood | Male | Young Adult | Non-alcoholic Fatty Liver Disease - blood | Aged, 80 and over | Adult | Female | Retrospective Studies | Severity of Illness Index | Liver Cirrhosis - blood | Hepatitis C, Chronic - blood | Disease Progression | Biopsy | Adolescent | Sex Factors | Liver Cirrhosis - pathology | Human Growth Hormone - blood | Aged | Insulin-Like Growth Factor I - metabolism | Insulin-like growth factor I | Liver | Viruses | Insulin-like growth factors | Hepatitis | Fatty liver | Insulin-like growth factor-binding protein 3 | Supplementation | Physical growth | Growth factors | Age | Liver diseases | Statistical analysis | Sex differences | Histology | Insulin | Steatosis | Serum levels | Cirrhosis | Fibrosis | Growth hormones | Hepatitis C virus | Hepatitis C | Growth hormone | Original
Journal Article
Journal of hematology and oncology, ISSN 1756-8722, 2019, Volume 12, Issue 1, pp. 4 - 10
...), but no validated biomarkers are available for the prediction of a clinical outcome. We aimed to establish whether pretreatment blood and bone marrow plasma concentrations of major cytokines and angiogenic factors (CAFs... 
Response rate | Angiogenic factors | Overall survival | Progression-free survival | Multiple myeloma | LENALIDOMIDE PLUS DEXAMETHASONE | THALIDOMIDE | CANCER | RENAL-CELL CARCINOMA | CHEMOTHERAPY | BORTEZOMIB-MELPHALAN-PREDNISONE | STAGING SYSTEM | PLASMA | ONCOLOGY | SERUM-LEVELS | HEMATOLOGY | ELDERLY-PATIENTS | Prognosis | Follow-Up Studies | Humans | Middle Aged | Vascular Endothelial Growth Factor A - blood | Becaplermin - blood | Logistic Models | Male | Fibroblast Growth Factor 2 - blood | Biomarkers, Tumor - blood | Multiple Myeloma - drug therapy | Hepatocyte Growth Factor - blood | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Progression-Free Survival | Aged, 80 and over | Female | ROC Curve | Aged | Bone Marrow | Multiple Myeloma - blood | Enzymes | Platelet-derived growth factor | Endothelial growth factors | Tumor necrosis factor | Clinical trials | Drug therapy | Drug approval | Enzyme-linked immunosorbent assay | Plasma | Lung cancer | Metastasis | Tissue inhibitor of metalloproteinase 2 | Tissue inhibitor of metalloproteinase 1 | Cancer therapies | Blood | Angiogenesis | Bone marrow | Diagnosis | Vascular endothelial growth factor | Interleukin 8 | Fibroblast growth factor 2 | Cytokines | Risk groups | Tumor necrosis factor-α | Gene expression | Patients | Medical prognosis | Kidney cancer | Biomarkers | Plasma levels
Journal Article
PloS one, ISSN 1932-6203, 2015, Volume 10, Issue 5, p. e0127518
.... We previously reported that growth differentiation factor 15 (GDF15) was significantly induced in HCV-infected hepatocytes... 
ACTIVATED GENE NAG-1 | MIC-1 | MULTIDISCIPLINARY SCIENCES | MACROPHAGE INHIBITORY CYTOKINE-1 | DISEASE SEVERITY | TGF-BETA SUPERFAMILY | HEPATITIS-C | EXPRESSION | ALPHA-FETOPROTEIN | CELL-DEATH | P53 | Immunohistochemistry | alpha-Fetoproteins | Humans | Middle Aged | Hepatitis B - virology | Male | Hepatitis B - blood | Case-Control Studies | Hepatitis B - complications | Liver Neoplasms - blood | Liver Neoplasms - etiology | Hepatitis C - blood | Sensitivity and Specificity | Adult | Female | Hepatitis C - complications | Liver Neoplasms - pathology | Carcinoma, Hepatocellular - etiology | Retrospective Studies | Carcinoma, Hepatocellular - blood | Liver Cirrhosis - etiology | Enzyme-Linked Immunosorbent Assay | Carcinoma, Hepatocellular - diagnosis | Liver Cirrhosis - blood | Growth Differentiation Factor 15 - blood | Liver Neoplasms - diagnosis | Carcinoma, Hepatocellular - pathology | Hepatitis C - virology | Biomarkers | Liver Cirrhosis - pathology | Aged | Neoplasm Staging | Hepatitis | Tuberculosis | Growth | Mortality | Hepatoma | Hepatitis C virus | Health aspects | Liver cirrhosis | Laboratories | Liver | Viruses | Hepatocellular carcinoma | Biology | Kinases | Medical diagnosis | Liver cancer | Hepatology | Physiology | Heart failure | Pathogens | Liver diseases | Cytokines | Melanoma | Breast cancer | Gene expression | α-Fetoprotein | Patients | Carriers | Cirrhosis | Sensitivity | Hospitals | Hepatocytes | Medical prognosis | Diagnostic systems | Diabetes | Differentiation
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 1999, Volume 96, Issue 12, pp. 7088 - 7092
Journal Article