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Plant Physiology, ISSN 0032-0889, 11/2015, Volume 169, Issue 3, pp. 2048 - 2063
Journal Article
Journal of Biomechanics, ISSN 0021-9290, 2011, Volume 45, Issue 5, pp. 824 - 831
Abstract The elastic modulus of bioengineered materials has a strong influence on the phenotype of many cells including cardiomyocytes. On polyacrylamide (PAA)... 
Physical Medicine and Rehabilitation | Elastic modulus | Cardiac myocyte | Hyaluronic acid | Sarcomere | Mechanosensing | MERLIN | MATRIX | ENGINEERING, BIOMEDICAL | PHENOTYPE | BIOPHYSICS | GROWTH | SUBSTRATE STIFFNESS | CELL | CD44 | Biocompatible Materials - metabolism | Fibroblasts - physiology | Actins - metabolism | Extracellular Matrix - metabolism | Cell Culture Techniques - methods | Integrins - metabolism | Bioengineering - methods | Acrylic Resins - metabolism | Extracellular Matrix - physiology | Hydrogels - metabolism | Sarcomeres - physiology | Extracellular Matrix Proteins - metabolism | Fibroblasts - metabolism | Collagen Type I - metabolism | Receptor Cross-Talk | Tissue Engineering - methods | Myocytes, Cardiac - cytology | Sarcomeres - metabolism | Rats | Biomechanical Phenomena - physiology | Rats, Sprague-Dawley | Fibronectins - metabolism | Animals | Myocytes, Cardiac - physiology | Hyaluronic Acid - metabolism | Fibrinogen - metabolism | Myocytes, Cardiac - metabolism | Elastic Modulus - physiology | Fibroblasts - cytology | Gelatin - metabolism | Actins - physiology | Polyacrylamide | Integrins | Proteins | Genotype & phenotype | Heart attacks | Hydrogels | Rodents | Stem cells | Surface chemistry | Cardiomyocytes | Ligands | Molecular weight | mechanosensing | elastic modulus | cardiac myocyte | sarcomere | hyaluronic acid
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2009, Volume 106, Issue 30, pp. 12530 - 12535
Diffuse infiltration of glioma cells into normal brain tissue is considered to be a main reason for the unfavorable outcomes of patients with malignant... 
Glioma | Cell death | Toll like receptors | Parenchyma | Mice | Gelatins | Endothelial cells | Cells | Microglia | Tumors | Brain tumor | Metalloprotease | Invasion | Toll-like receptor | ACTIVATION | MULTIDISCIPLINARY SCIENCES | brain tumor | METALLOPROTEASE-2 | BRAIN-TUMORS | INVASIVENESS | IN-VITRO | TOLL-LIKE RECEPTOR-4 | INHIBITION | invasion | GENE | toll-like receptor | metalloprotease | UP-REGULATION | GLIOBLASTOMA CELLS | Immunohistochemistry | Microglia - metabolism | Humans | Brain Neoplasms - pathology | Gene Expression Regulation, Neoplastic | Male | Green Fluorescent Proteins - genetics | Brain Neoplasms - metabolism | Glioma - metabolism | Glioma - genetics | Glioma - pathology | Gelatinases - metabolism | Microglia - pathology | Female | p38 Mitogen-Activated Protein Kinases - metabolism | Toll-Like Receptors - metabolism | Green Fluorescent Proteins - metabolism | Signal Transduction | Mice, Inbred C57BL | Myeloid Differentiation Factor 88 - genetics | Brain Neoplasms - genetics | Tumor Burden | Matrix Metalloproteinase 14 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Enzyme Precursors - metabolism | Animals | Matrix Metalloproteinase 14 - genetics | Cell Line, Tumor | Myeloid Differentiation Factor 88 - metabolism | Complications and side effects | Development and progression | Gliomas | Brain tumors | Biological Sciences
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e69354
In previous research, we found alpha-enolase to be inversely correlated with progression-free and overall survival in lung cancer patients and detected... 
SYSTEM | AUTOANTIBODIES | LUNG-CANCER | PROTEIN | MECHANISM | UROKINASE PLASMINOGEN-ACTIVATOR | AUTOIMMUNITY | MULTIDISCIPLINARY SCIENCES | PANCREATIC-CANCER | RECEPTOR | IDENTIFICATION | Neoplasms - metabolism | Tumor Suppressor Proteins - antagonists & inhibitors | Lung Neoplasms - mortality | Humans | Lung Neoplasms - metabolism | Bone Neoplasms - secondary | Extracellular Matrix - metabolism | Lung Neoplasms - pathology | Male | Phosphopyruvate Hydratase - metabolism | Plasminogen - metabolism | DNA-Binding Proteins - metabolism | Neoplasm Metastasis | Biomarkers, Tumor - metabolism | Cell Membrane - metabolism | Bone Neoplasms - drug therapy | Biomarkers, Tumor - antagonists & inhibitors | Tumor Suppressor Proteins - metabolism | DNA-Binding Proteins - antagonists & inhibitors | Antibodies, Monoclonal - pharmacology | Neoplasms - mortality | Phosphopyruvate Hydratase - antagonists & inhibitors | Receptors, Urokinase Plasminogen Activator - metabolism | Xenograft Model Antitumor Assays | Animals | Urokinase-Type Plasminogen Activator - metabolism | Antibodies, Monoclonal - administration & dosage | Cell Line, Tumor | Protein Binding | Mice | Immunocompromised Host | Neoplasms - pathology | Cell Movement | Lung cancer | Metastasis | Matrix metalloproteinase | Adoptive transfer | Metastases | Degradation | Proteins | Urokinase | Gelatin | Medical laboratories | Extracellular matrix | Metalloproteinase | Pharmaceutical sciences | Phosphopyruvate hydratase | Medical research | Enzymes | Breast cancer | U-Plasminogen activator | Medicine | Studies | Plasmids | Rheumatoid arthritis | Pharmacy | Collagen | Laboratory animals | Prostate | Cancer
Journal Article
STEM CELLS Translational Medicine, ISSN 2157-6564, 02/2016, Volume 5, Issue 2, pp. 206 - 217
A microparticle‐based growth factor delivery system was engineered to drive endochondral ossification within human bone marrow‐derived mesenchymal stem cell... 
Growth factor delivery | Adult human bone marrow | High-density culture | Bone | Tissue regeneration | Mesenchymal stem cells | REGENERATION | OSTEOGENIC DIFFERENTIATION | CHONDROGENIC DIFFERENTIATION | ADULT HUMAN | CULTURE | CARTILAGE | CELL & TISSUE ENGINEERING | GELATIN MICROSPHERES | GENERATION | MORPHOGENETIC PROTEINS | STROMAL CELLS | Bone Morphogenetic Protein 2 - pharmacology | Osteopontin - genetics | Chondrogenesis - drug effects | Calcium - metabolism | Chondrogenesis - genetics | Humans | Transforming Growth Factor beta1 - metabolism | Alkaline Phosphatase - metabolism | Osteocalcin - genetics | Osteopontin - metabolism | Collagen Type II - metabolism | Mesenchymal Stromal Cells - cytology | Collagen Type I - genetics | Bone Morphogenetic Protein 2 - metabolism | Drug Compounding | Bone Marrow Cells - drug effects | Gelatin - chemistry | Osteogenesis - genetics | Transforming Growth Factor beta1 - pharmacology | Biomarkers - metabolism | Calcification, Physiologic - genetics | Mesenchymal Stromal Cells - drug effects | Gene Expression | Alkaline Phosphatase - genetics | Collagen Type I - metabolism | Tissue Engineering - methods | Calcification, Physiologic - drug effects | Bone Marrow Cells - cytology | Glycosaminoglycans - metabolism | Osteocalcin - metabolism | Osteogenesis - drug effects | Mesenchymal Stromal Cells - metabolism | Durapatite - chemistry | Collagen Type II - genetics | Cell Aggregation | Primary Cell Culture | Delayed-Action Preparations | Bone Marrow Cells - metabolism | Alkaline phosphatase | Data analysis | Mesenchyme | Tissue engineering | Hydroxyapatite | Bone healing | Microparticles | Ossification | Angiogenesis | Fractures | Mineralization | Stem cells | Bone marrow | Nutrients | Chondrogenesis | Growth factors | Vascular endothelial growth factor | Bone (endochondral) | Tissue Engineering and Regenerative Medicine
Journal Article
Molecular Neurobiology, ISSN 0893-7648, 2018, Volume 56, Issue 6, pp. 4566 - 4581
The role of astrocytes is becoming increasingly important to understanding how glioblastoma (GBM) tumor cells diffusely invade the brain. Yet, little is known... 
Astrocytes | MYC | Extracellular vesicles | Glioblastoma stem-like cells | Podosome formation | Senescence-associated secretory phenotype | TP53 | GLIOMA-CELLS | SECRETORY PHENOTYPE | RNA | MICROVESICLES | INVASION IN-VIVO | BLOOD-BRAIN-BARRIER | NEUROSCIENCES | STATISTICAL-MODEL | GROWTH | FIBRONECTIN | EXPRESSION | Extracellular Vesicles - ultrastructure | Humans | Middle Aged | Male | Brain Neoplasms - metabolism | Extracellular Vesicles - metabolism | Podosomes - metabolism | Protein Isoforms - metabolism | Neoplastic Stem Cells - metabolism | Cellular Senescence | Proteolysis | Neoplastic Stem Cells - pathology | Glioblastoma - metabolism | Cell Differentiation | Signal Transduction | Nanoparticles - ultrastructure | Tumor Suppressor Protein p53 - metabolism | Proto-Oncogene Proteins c-myc - metabolism | Particle Size | Phenotype | Cell Line, Tumor | Aged | Gelatin - metabolism | Proteome - metabolism | Astrocytes - metabolism | Development and progression | Genetic aspects | Analysis | Brain tumors | Fluorescence microscopy | Phenotypes | Senescence | Intercellular signalling | Tumor cells | p53 Protein | Glioblastoma | Fluorescence | Mass spectroscopy | Inflammation | Myc protein | Proteins | Genotype & phenotype | Signal transduction | Gelatin | Stem cells | Proteomics | Glioblastoma cells | Inhibition | Bioinformatics | Mass spectrometry | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 5, p. e20164
Background: Diosgenin, a steroidal saponin obtained from fenugreek (Trigonella foenum graecum), was found to exert anti-carcinogenic properties, such as... 
APOPTOSIS | SIGNALING PATHWAYS | ACTIVATION | METASTASIS | ANGIOGENESIS | COLORECTAL-CANCER | KINASE | BIOLOGY | CYCLE ARREST | OSTEOSARCOMA CELLS | PROGRESSION | Prostatic Neoplasms - metabolism | Humans | Immunoblotting | JNK Mitogen-Activated Protein Kinases - metabolism | Male | NF-kappa B - metabolism | Vascular Endothelial Growth Factor A - metabolism | Vascular Endothelial Growth Factor A - genetics | Tissue Inhibitor of Metalloproteinase-2 - genetics | Tissue Inhibitor of Metalloproteinase-2 - metabolism | Matrix Metalloproteinase 9 - metabolism | Matrix Metalloproteinase 7 - metabolism | Basigin - genetics | Matrix Metalloproteinase 9 - genetics | Polymerase Chain Reaction | JNK Mitogen-Activated Protein Kinases - genetics | Phosphatidylinositol 3-Kinase - metabolism | Diosgenin - pharmacology | Matrix Metalloproteinase 2 - metabolism | Cell Movement - drug effects | Matrix Metalloproteinase 2 - genetics | Matrix Metalloproteinase 7 - genetics | NF-kappa B - genetics | Phosphatidylinositol 3-Kinase - genetics | Basigin - metabolism | Cell Line, Tumor | Progesterone | Metastasis | Vascular endothelial growth factor | Health aspects | Prostate cancer | Apoptosis | Transcription factors | Boyden chamber | Matrix metalloproteinases | Leukocyte migration | AKT protein | Assaying | Metastases | Proteins | Angiogenesis | Cell growth | Gelatin | Inhibition | Enzymes | NF-κB protein | Medical technology | Wound healing | Gene expression | 1-Phosphatidylinositol 3-kinase | Pharmacy | Cell migration | Cell proliferation | Biotechnology | Tissue inhibitor of metalloproteinases | Phosphorylation | Colorectal cancer | Science | mRNA | Matrix metalloproteinase | Kinases | Cell adhesion & migration | Carcinogens | Cell cycle | Fenugreek | Metalloproteinase | Tumor cells | Extracellular signal-regulated kinase | c-Jun protein | Breast cancer | Endothelial cells | Gelatinase B | Gelatinase A | Signaling | Collagen | Prostate | Tumors | Cancer
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, p. e42714
The hormone, relaxin, inhibits aberrant myofibroblast differentiation and collagen deposition by disrupting the TGF-beta 1/Smad2 axis, via its cognate... 
RENAL FIBROSIS | LUNG FIBROSIS | COLLAGEN | MULTIDISCIPLINARY SCIENCES | GROWTH | INTERSTITIAL FIBROSIS | TISSUE INHIBITORS | SMOOTH-MUSCLE-CELLS | NITRIC-OXIDE PATHWAY | HORMONE RELAXIN | FIBROBLASTS | Relaxin - metabolism | Matrix Metalloproteinases - genetics | Receptors, G-Protein-Coupled - metabolism | Humans | Male | Receptors, Peptide - genetics | Matrix Metalloproteinase 9 - metabolism | Relaxin - genetics | Matrix Metalloproteinase 9 - genetics | Fibroblasts - metabolism | Cell Line | Matrix Metalloproteinase 2 - metabolism | Matrix Metalloproteinase 13 - genetics | Cells, Cultured | Rats | Kidney - cytology | Signal Transduction - genetics | Extracellular Signal-Regulated MAP Kinases | Rats, Sprague-Dawley | Matrix Metalloproteinase 13 - metabolism | Mice, Knockout | Matrix Metalloproteinase 2 - genetics | Animals | Cyclic GMP - metabolism | Nitric Oxide Synthase Type I - metabolism | Signal Transduction - physiology | Fibroblasts - cytology | Mice | Nitric Oxide Synthase Type I - genetics | Receptors, G-Protein-Coupled - genetics | Matrix Metalloproteinases - metabolism | Nitric Oxide - metabolism | Receptors, Peptide - metabolism | Physiological aspects | Genetic aspects | Research | Transforming growth factors | Metalloenzymes | Nitric oxide | Neurosciences | Phosphorylation | Matrix metalloproteinases | Guanosine | Smooth muscle | Genomes | Arthritis | Biochemistry | Matrix metalloproteinase | Guanylate cyclase | Western blotting | Signal transduction | Arginine | Gelatin | Rodents | Cyclic GMP | Fibroblasts | Metalloproteinase | Interstitial collagenase | Kidneys | Extracellular signal-regulated kinase | Collagenase 3 | Nitric-oxide synthase | Gelatinase B | NG-Nitroarginine methyl ester | Gelatinase A | Signaling | Inhibitors | Human performance | Collagen | Isoforms | Fibrosis | Skin | Aberration | Molecular biology | Ornithine
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