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Journal Article
International Journal of Cancer, ISSN 0020-7136, 02/2005, Volume 113, Issue 5, pp. 752 - 760
The role of platelets in tumor progression and metastasis has been recognized but the mechanism of their action remains unclear. Five human lung cancer cell... 
lung cancer | platelet microvesicles | metastasis | matrix metalloproteinases | exosomes | Matrix metalloproteinases | Metastasis | Platelet microvesicles | Exosomes | Lung cancer | SURVIVAL | VESICLES | MEMBRANE-TYPE-1 MATRIX-METALLOPROTEINASE | ADHESION | IN-VITRO | ONCOLOGY | GROWTH | SURFACE | RHABDOMYOSARCOMA CELLS | GENERATION | ENDOTHELIAL MICROPARTICLES | Phosphorylation | Cell Proliferation | Humans | Lung Neoplasms - metabolism | Carcinoma, Lewis Lung - secondary | Lung Neoplasms - pathology | Metalloendopeptidases - metabolism | Vascular Endothelial Growth Factor A - metabolism | Carcinoma, Lewis Lung - blood supply | Cyclin D2 | Neovascularization, Pathologic - pathology | Mitogen-Activated Protein Kinase Kinases - metabolism | Matrix Metalloproteinase 9 - metabolism | Matrix Metalloproteinases, Membrane-Associated | Cyclins - metabolism | Neoplasm Invasiveness - pathology | Bone Marrow - metabolism | Platelet Membrane Glycoproteins - metabolism | Female | Interleukin-8 - metabolism | Tumor Cells, Cultured | Lung Neoplasms - blood supply | Matrix Metalloproteinase 14 | Endothelial Cells - metabolism | Mice, Inbred C57BL | Umbilical Veins | Carcinoma, Lewis Lung - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Cell Adhesion | Chemotaxis | Disease Progression | Hepatocyte Growth Factor - metabolism | Animals | Blood Platelets - metabolism | Endothelial Cells - cytology | Platelet Activation | Bone Marrow - pathology | Fibrinogen - metabolism | Mice | Neovascularization, Pathologic - metabolism
Journal Article
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 09/2011, Volume 194, Issue 5, pp. 705 - 720
DNA double-strand break (DSB) resection, which results in RPA-bound single-stranded DNA (ssDNA), is activated in S phase by Cdk2. RPA-ssDNA activates the... 
CYCLE CHECKPOINT CONTROL | DAMAGE RESPONSE | MRE11-RAD50-NBS1 COMPLEX | HOMOLOGOUS RECOMBINATION | RPA PHOSPHORYLATION | CELL-FREE-EXTRACTS | SACCHAROMYCES-CEREVISIAE | REPLICATION STRESS | DNA-END-RESECTION | WERNER-SYNDROME PROTEIN | CELL BIOLOGY | Protein Kinases - metabolism | Chromatin - metabolism | Meiosis - physiology | Nuclear Envelope - physiology | Antigens, Nuclear - metabolism | RecQ Helicases - metabolism | Humans | Werner Syndrome Helicase | DNA Repair - physiology | Endonucleases - metabolism | DNA Breaks, Double-Stranded | CDC2 Protein Kinase - metabolism | DNA-Binding Proteins - metabolism | MRE11 Homologue Protein | Cell Nucleus - metabolism | Protein Binding - drug effects | Phosphorylation - drug effects | Protein-Serine-Threonine Kinases - metabolism | Rad51 Recombinase - metabolism | Cyclin-Dependent Kinase 2 - metabolism | Tumor Suppressor Proteins - metabolism | CDC2 Protein Kinase - antagonists & inhibitors | DNA, Single-Stranded - metabolism | Xenopus laevis | Cell Cycle Proteins - metabolism | Replication Protein A - metabolism | Ataxia Telangiectasia Mutated Proteins | Xenopus Proteins - antagonists & inhibitors | Cell Division - physiology | DNA Helicases - metabolism | Animals | Cell-Free System | Ku Autoantigen | Mitosis - physiology | Cyclin-Dependent Kinase 2 - antagonists & inhibitors | S Phase - physiology | Checkpoint Kinase 1 | Xenopus Proteins - metabolism | Ovum | Protein Kinase Inhibitors - pharmacology | HeLa Cells | Histones - metabolism | Protein Binding - physiology
Journal Article
Nature Cell Biology, ISSN 1465-7392, 2014, Volume 16, Issue 6, pp. 538 - 549
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 08/2012, Volume 32, Issue 15, pp. 3121 - 3131
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
RNA-POLYMERASE-II | INDEPENDENT GROWTH | ANDROGEN RECEPTOR EXPRESSION | ACTIVATION | COACTIVATOR | LYSINE METHYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROSTATE-CANCER | GENE-EXPRESSION | H3 | PROGRESSION | CELL BIOLOGY | Tumor Necrosis Factor-alpha - metabolism | Chromatin - metabolism | Neoplasm Transplantation | Prostatic Neoplasms - metabolism | Vascular Endothelial Growth Factor A - biosynthesis | Cell Proliferation | Humans | Gene Expression Regulation, Neoplastic | Histones - biosynthesis | Male | NF-kappa B - metabolism | Transplantation, Heterologous | Vascular Endothelial Growth Factor A - metabolism | Histone-Lysine N-Methyltransferase - biosynthesis | Proto-Oncogene Proteins c-bcl-2 - metabolism | RNA Interference | Inhibitor of Apoptosis Proteins - metabolism | Acetylation | Interleukin-8 - metabolism | Interleukin-6 - metabolism | Repressor Proteins - metabolism | Autocrine Communication | Promoter Regions, Genetic | Prostatic Neoplasms - pathology | Inhibitor of Apoptosis Proteins - biosynthesis | Signal Transduction | Cell Survival | Interleukin-8 - biosynthesis | Survivin | Proto-Oncogene Proteins c-bcl-2 - biosynthesis | p300-CBP Transcription Factors - metabolism | Animals | Repressor Proteins - biosynthesis | Histone-Lysine N-Methyltransferase - metabolism | Cell Line, Tumor | Cyclin D - biosynthesis | Interleukin-6 - biosynthesis | Mice | Mice, Inbred BALB C | RNA, Small Interfering | Histones - metabolism | Cyclin D - metabolism
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2016, Volume 91, pp. 151 - 159
Abstract Wound healing is a physiological reparative response to injury and a well-orchestrated process that involves hemostasis, cellular migration,... 
Cardiovascular | Angiogenesis | MicroRNA | Wound healing | Diabetes | CYTOKINES | CARDIAC & CARDIOVASCULAR SYSTEMS | MOUSE | CLOSURE | DELAYS | MODEL | CELL BIOLOGY | ENDOTHELIAL-CELLS | GROWTH | MICE | MicroRNAs - antagonists & inhibitors | Humans | Diabetes Mellitus, Experimental - genetics | Oligonucleotides, Antisense - metabolism | Male | MicroRNAs - metabolism | Vascular Endothelial Growth Factor A - metabolism | Vascular Endothelial Growth Factor A - genetics | Dermis - drug effects | Neovascularization, Pathologic - pathology | Cyclin-Dependent Kinase Inhibitor p27 - metabolism | Wounds, Nonpenetrating - therapy | Mast Cells - metabolism | Smad1 Protein - genetics | Diabetes Mellitus, Experimental - metabolism | Wounds, Nonpenetrating - metabolism | Neovascularization, Pathologic - therapy | Fibroblasts - metabolism | Re-Epithelialization | Dermis - metabolism | Macrophages - pathology | Signal Transduction | Endothelial Cells - metabolism | Gene Expression Regulation | Glucose - pharmacology | Fibroblasts - pathology | Inhibitor of Differentiation Protein 1 - metabolism | Macrophages - metabolism | Animals | Oligonucleotides, Antisense - genetics | Mast Cells - pathology | Diabetes Mellitus, Experimental - pathology | Inhibitor of Differentiation Protein 1 - genetics | Smad1 Protein - metabolism | Dermis - pathology | Neovascularization, Pathologic - genetics | Mice | MicroRNAs - genetics | Neovascularization, Pathologic - metabolism | Wounds, Nonpenetrating - pathology | Endothelial Cells - pathology | Wounds, Nonpenetrating - genetics | Cell Movement | Cyclin-Dependent Kinase Inhibitor p27 - genetics | Endothelial Cells - drug effects | Type 2 diabetes | Care and treatment | Analysis | Physiological aspects | Glucose | Wounds and injuries | Dextrose | microRNA | wound healing | diabetes | angiogenesis
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 3/2008, Volume 180, Issue 5, pp. 915 - 929
Cyclin-dependent kinases (Cdks) fulfill key functions in many cellular processes, including cell cycle progression and cytoskeletal dynamics. A limited number... 
Growth cones | Phosphorylation | Neurites | HEK293 cells | Neurons | Microtubules | Cell cycle | Cell adhesion | Histones | Cyclins | NEURONAL MIGRATION | PROTEIN | NEURITE OUTGROWTH | GENE | PHOSPHORYLATION | TUBULIN DEACETYLASE | IN-VIVO | VERTEBRATE CELLS | CDK COMPLEXES | HISTONE DEACETYLASE | CELL BIOLOGY | Oncogene Proteins - genetics | Cyclin-Dependent Kinases - metabolism | Humans | Protein Processing, Post-Translational - genetics | Cyclin A - genetics | Cyclin E - genetics | Cell Movement - genetics | Cyclin-Dependent Kinase 5 - genetics | Cell Differentiation - genetics | Microtubules - metabolism | Sirtuin 2 | Microtubules - ultrastructure | Hippocampus - ultrastructure | Cyclin-Dependent Kinases - genetics | Sirtuins - genetics | Amino Acid Sequence | Cell Line | Cyclin-Dependent Kinase 2 - metabolism | Catalytic Domain | Hippocampus - embryology | Cyclin A - metabolism | Oncogene Proteins - metabolism | Cyclin-Dependent Kinase 2 - genetics | Nerve Tissue Proteins - genetics | Serine - metabolism | Cyclin-Dependent Kinase 5 - metabolism | Nerve Tissue Proteins - metabolism | Hippocampus - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Mice | Cyclin E - metabolism | HeLa Cells | Sirtuins - metabolism | Evaluation | Motility | Cell physiology | Research | Properties | Genetic regulation | Phosphotransferases | Cells
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 07/2013, Volume 98, Issue 7, pp. 2887 - 2896
Journal Article
Breast Cancer Research, ISSN 1465-5411, 08/2011, Volume 13, Issue 4, pp. R78 - R78
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 03/2012, Volume 287, Issue 13, pp. 10355 - 10367
Hepatic stellate cells (HSCs) undergo myofibroblastic activation in liver fibrosis and regeneration. This phenotypic switch is mechanistically similar to... 
PREF-1 | HETEROGENEITY | ACTIVATION | RAT HEPATOCYTES | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | EXPERIMENTAL MELANOMA METASTASIS | ADIPOCYTE DIFFERENTIATION | RECEPTOR | ADIPOGENESIS | EXPRESSION | Liver - pathology | Rats, Wistar | Coculture Techniques | Cyclin-Dependent Kinase 4 - genetics | Hepatic Stellate Cells - metabolism | Epithelial-Mesenchymal Transition - drug effects | Hepatocytes - pathology | Male | Cyclin A - genetics | Hepatocytes - metabolism | Epithelial-Mesenchymal Transition - genetics | Wnt Proteins - metabolism | Intercellular Signaling Peptides and Proteins - metabolism | Wnt Proteins - genetics | Liver Cirrhosis - metabolism | Epigenesis, Genetic - drug effects | Membrane Proteins - metabolism | Nuclear Proteins - genetics | Liver Cirrhosis - genetics | Hepatic Stellate Cells - pathology | PPAR gamma - genetics | Cell Line | Liver Regeneration | Mitogen-Activated Protein Kinase 3 - genetics | Membrane Proteins - genetics | Cyclin A - metabolism | Liver - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Rats | Nuclear Proteins - metabolism | Cyclin-Dependent Kinase 4 - metabolism | Chick Embryo | Nerve Tissue Proteins - genetics | PPAR gamma - biosynthesis | Antibodies - pharmacology | Nerve Tissue Proteins - metabolism | Proto-Oncogene Proteins c-akt | Animals | Wnt Signaling Pathway - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | Wnt Signaling Pathway - genetics | Epigenesis, Genetic - genetics | Chickens | Liver Cirrhosis - pathology | Cell Proliferation - drug effects | Mice | Cyclin D - genetics | Cyclin D - metabolism | Wnt Signaling | Regeneration | Partial Hepatectomy | Epigenetics | Pparγ | Peroxisome Proliferator-activated Receptor (PPAR) | Pref-1 | Cell Biology | Adipogenesis | Wnt10b
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 07/2010, Volume 122, Issue 2, pp. 337 - 346
Forkhead box M1 (FoxM1) transcription factor is known to play important role in human cancers which, in part, is mediated by its ability to modulate cell cycle... 
Matrix metalloproteinases | Migration | VEGF | uPA | FoxM1 | Invasion | Extra cellular matrix | GLIOMA-CELLS | PANCREATIC-CANCER | TRANSCRIPTION FACTOR FOXM1 | FACTOR-KAPPA-B | LUNG-CANCER | ONCOLOGY | LIVER-REGENERATION | PROSTATE-CANCER | FORKHEAD BOX M1 | EXPRESSION | ENDOTHELIAL GROWTH-FACTOR | Cell Proliferation | Humans | Extracellular Matrix - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Vascular Endothelial Growth Factor A - metabolism | Breast Neoplasms - metabolism | Matrix Metalloproteinase 9 - metabolism | Transfection | RNA Interference | Time Factors | Forkhead Transcription Factors - metabolism | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Female | Cyclin-Dependent Kinase 2 - metabolism | Matrix Metalloproteinase 2 - metabolism | Neoplasm Invasiveness | Down-Regulation | E2F1 Transcription Factor - metabolism | Urokinase-Type Plasminogen Activator - genetics | Forkhead Transcription Factors - genetics | Cyclin-Dependent Kinase Inhibitor p27 | Receptors, Urokinase Plasminogen Activator - metabolism | Breast Neoplasms - genetics | Urokinase-Type Plasminogen Activator - metabolism | Breast Neoplasms - pathology | Cell Line, Tumor | Forkhead Box Protein M1 | Cell Movement | Proteins | Breast cancer | Vascular endothelial growth factor | Cancer cells | Care and treatment | Cancer
Journal Article