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Journal of Cellular Biochemistry, ISSN 0730-2312, 08/2017, Volume 118, Issue 8, pp. 2409 - 2419
The protein kinases ERK1/2 and JNK1/2 function as signal transducers connecting activated TRPM3 channels with AP‐1‐regulated gene transcription, while a... 
CALCINEURIN | c‐JUN | PREGNENOLONE SULFATE | JNK | TRPM3 | ERK | c-JUN | CA2+ IONS | PHOSPHATASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HUMAN KERATINOCYTES | CELL BIOLOGY | DESIGNER RECEPTORS | STIMULATED INSULINOMA CELLS | PANCREATIC BETA-CELLS | EGR-1 | CHANNELS | EXPRESSION | GENE-TRANSCRIPTION | RNA, Small Interfering - genetics | Transcription Factor AP-1 - genetics | Humans | JNK Mitogen-Activated Protein Kinases - metabolism | Extracellular Signal-Regulated MAP Kinases - metabolism | Extracellular Signal-Regulated MAP Kinases - genetics | Transcription Factor AP-1 - metabolism | Blotting, Western | Calcineurin - genetics | HEK293 Cells | Pregnenolone - pharmacology | TRPM Cation Channels - genetics | Lentivirus - genetics | TRPM Cation Channels - metabolism | JNK Mitogen-Activated Protein Kinases - genetics | Phosphorylation - drug effects | Calcineurin - metabolism | Phosphatases | Progesterone | Sulfates | Protein kinases | Calmodulin | Phosphorylation | Regulators | Transcription factors | Calcineurin | Stimulation | Activation | Biochemistry | Kinases | Phosphatase | Channels | Calcium influx | Pregnenolone | MAP kinase phosphatase | Proteins | Transient receptor potential proteins | Calcium-binding protein | Transcription activation | Attenuation | c-Fos protein | Calcium (intracellular) | Activator protein 1 | Extracellular signal-regulated kinase | c-Jun protein | MAP kinase | Ions | Pharmacology | Pregnenolone sulfate | Protein kinase | Terminal protein | Ca2+/calmodulin-dependent protein phosphatase | Protein phosphatase | Cations | Sulfate | Intracellular | Index Medicus
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 12/2017, Volume 232, Issue 12, pp. 3496 - 3509
Angiotensin‐II‐induced intracellular calcium release depletes the endoplasmic reticulum store, resulting in the activation of the stromal interaction molecule... 
Egr‐1 | Orai‐1 | CREB | STIM‐1 | angiotensin‐II | Egr-1 | angiotensin-II | Orai-1 | STIM-1 | CA2+ ENTRY | PHYSIOLOGY | ELEMENT-BINDING PROTEIN | NEOINTIMA FORMATION | KINASE-II | CELL BIOLOGY | SIGNAL-TRANSDUCTION | FIBROBLAST GROWTH FACTOR-2 | OPERATED CALCIUM-ENTRY | INOSITOL TRISPHOSPHATE RECEPTOR | INTERACTION MOLECULE-1 STIM1 | UP-REGULATION | Up-Regulation | Phosphorylation | Muscle, Smooth, Vascular - metabolism | Extracellular Signal-Regulated MAP Kinases - metabolism | Stromal Interaction Molecule 1 - genetics | Dose-Response Relationship, Drug | Transfection | RNA Interference | Time Factors | Inositol 1,4,5-Trisphosphate Receptors - metabolism | Early Growth Response Protein 1 - genetics | Inositol 1,4,5-Trisphosphate Receptors - antagonists & inhibitors | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - metabolism | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - metabolism | Muscle, Smooth, Vascular - drug effects | ORAI1 Protein - metabolism | Cell Line | Angiotensin II - pharmacology | Calmodulin - metabolism | ORAI1 Protein - genetics | Rats | Calcium Channel Blockers - pharmacology | Calcium-Calmodulin-Dependent Protein Kinase Type 2 - antagonists & inhibitors | Stromal Interaction Molecule 1 - metabolism | Animals | Calcium Signaling - drug effects | Cyclic AMP Response Element-Binding Protein - metabolism | Protein Kinase Inhibitors - pharmacology | Calmodulin - antagonists & inhibitors | Early Growth Response Protein 1 - metabolism | Calcium-binding proteins | Angiotensin | Phosphates | Calcium | Peptides | Pathogenesis | Hyperplasia | STIM1 protein | Smooth muscle | Activation | mRNA | Calcium signalling | Vascular diseases | Vasoactive agents | Calcium-binding protein | Atherosclerosis | Angiotensin II | Calmodulin | Inositol 1,4,5-trisphosphate receptors | Calcium (intracellular) | EGR-1 protein | RNA-mediated interference | Extracellular signal-regulated kinase | siRNA | Cyclic AMP response element-binding protein | Gene expression | Depletion | Ribonucleic acids | Arteriosclerosis | Ca2+/calmodulin-dependent protein kinase II | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, pp. e63425 - e63425
Although the effects of sanguinarine, a benzophenanthridine alkaloid, on the inhibition of some kinds of cancer cell growth have been established, the... 
CARCINOMA-CELLS | ACTIVATION | DEPOLARIZATION | MITOCHONDRIAL PATHWAY | MULTIDISCIPLINARY SCIENCES | ROS | PTEN | EGR-1 TRANSCRIPTION | DEATH | KAPPA-B | EXPRESSION | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Humans | Cell Survival - genetics | Apoptosis - genetics | JNK Mitogen-Activated Protein Kinases - metabolism | BH3 Interacting Domain Death Agonist Protein - genetics | Caspases - metabolism | Isoquinolines - pharmacology | Urinary Bladder Neoplasms - genetics | Early Growth Response Protein 1 - genetics | Antineoplastic Agents - pharmacology | JNK Mitogen-Activated Protein Kinases - genetics | Urinary Bladder Neoplasms - metabolism | BH3 Interacting Domain Death Agonist Protein - metabolism | bcl-2-Associated X Protein - genetics | Cell Survival - drug effects | Caspases - genetics | bcl-2-Associated X Protein - metabolism | Up-Regulation - genetics | Urinary Bladder Neoplasms - drug therapy | Down-Regulation - drug effects | Benzophenanthridines - pharmacology | X-Linked Inhibitor of Apoptosis Protein - genetics | Up-Regulation - drug effects | X-Linked Inhibitor of Apoptosis Protein - metabolism | Cell Line, Tumor | Early Growth Response Protein 1 - metabolism | Proteins | Prevention | Cysteine | Care and treatment | Growth | Genes | Cancer cells | Free radicals (Chemistry) | Bladder cancer | Apoptosis | Cancer | Oxidative stress | Reactive oxygen species | Deregulation | Transcription factors | Bax protein | Bladder | Acetylcysteine | XIAP protein | Activation | Biochemistry | Kinases | Cancer therapies | Anticancer properties | Mitochondria | Cell growth | Urinary bladder | Physiology | Interception | Inhibition | Pretreatment | Oxygen | Free radicals | EGR-1 protein | c-Jun protein | siRNA | Tumor cell lines | Metabolism | Gene expression | Sanguinarine | Medicine | Studies | Ribonucleic acids | Cell lines | Tumors | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2011, Volume 6, Issue 10, pp. e25676 - e25676
Background: Human early growth response-1 (EGR1) is a member of the zing-finger family of transcription factors induced by a range of molecular and... 
APOPTOSIS | ACTIVATION | PHOSPHORYLATION | GROWTH | BIOLOGY | GENE-EXPRESSION | A EGR-1 | INDUCTION | DIFFERENTIATION | CELL-SURVIVAL | TRANSCRIPTION FACTOR | Cell Line | Transcription, Genetic - drug effects | Humans | Early Growth Response Protein 1 - chemistry | Enzyme Activation - drug effects | Sumoylation - drug effects | Gene Expression Regulation - drug effects | Proteolysis - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | Time Factors | Ubiquitin-Conjugating Enzymes - metabolism | Protein Stability - drug effects | Early Growth Response Protein 1 - genetics | SUMO-1 Protein - metabolism | Epidermal Growth Factor - pharmacology | Proteasome Endopeptidase Complex - metabolism | Early Growth Response Protein 1 - metabolism | Mitogen-Activated Protein Kinase 1 - metabolism | Ubiquitin | Ionizing radiation | Epidermal growth factor | RNA | Analysis | Genetic transcription | DNA binding proteins | Phosphorylation | Transcription factors | AKT protein | Proteins | SUMO protein | Ubiquitination | Cell growth | Transfection | Post-translation | Forkhead protein | Acetylation | Biodegradation | Stability | Epidermal growth factor receptors | EGR-1 protein | Extracellular signal-regulated kinase | Gene expression | Environmental effects | 1-Phosphatidylinositol 3-kinase | Overexpression | Human behavior | Cancer | Stimuli | Apoptosis | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2016, Volume 11, Issue 6, pp. e0156994 - e0156994
Background Fibulin-5 is an extracellular matrix glycoprotein that plays critical roles in vasculogenesis and embryonic development. Deletion of Fibulin-5 in... 
EXTRACELLULAR-MATRIX PROTEINS | ANGIOGENESIS | MECHANISM | TIE2 | PATHWAY | ROLES | MULTIDISCIPLINARY SCIENCES | IN-VIVO | ALPHA-5-BETA-1 | EXPRESSION | Cricetulus | Gene Expression - drug effects | Human Umbilical Vein Endothelial Cells - metabolism | Humans | Immunoblotting | Angiopoietin-1 - metabolism | Early Growth Response Protein 1 - genetics | HEK293 Cells | Receptor, TIE-2 - metabolism | Extracellular Matrix Proteins - metabolism | Angiopoietin-1 - pharmacology | CHO Cells | Recombinant Proteins - metabolism | Cell Survival - drug effects | Cricetinae | Human Umbilical Vein Endothelial Cells - drug effects | Signal Transduction | Extracellular Matrix Proteins - genetics | Cells, Cultured | Extracellular Matrix Proteins - pharmacology | Recombinant Proteins - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Receptor, TIE-2 - genetics | Angiopoietin-1 - genetics | Animals | Inhibitor of Differentiation Protein 1 - genetics | Protein Binding | Mutation | Kruppel-Like Transcription Factors - genetics | Transcription factors | Phosphorylation | Id1 protein | Laboratories | Toxicity | Angiopoietin | Cytotoxicity | AKT protein | Kinases | Caspase-3 | Cell surface | Cell adhesion & migration | Proteins | Angiogenesis | Signal transduction | Embryogenesis | Cell growth | Clonal deletion | Penicillin | Deletion | Extracellular matrix | Deoxyribonucleic acid--DNA | Kruppel protein | Recombinant | Binding | Deprivation | Proteoglycans | Cell survival | EGR-1 protein | Incubation | Research & development--R&D | Glycoprotein | Extracellular signal-regulated kinase | Caspase | Gene expression | Endothelial cells | Embryonic growth stage | Medicine | Signaling | Inhibitors | Respiratory diseases | Skin | Lung Kruppel-like factor | Heparin | Angiogenesis inhibitors | Viability | Integrins | Index Medicus | Research & development | R&D | Deoxyribonucleic acid | DNA
Journal Article
Blood, ISSN 0006-4971, 09/2011, Volume 118, Issue 9, pp. 2622 - 2631
Most antiangiogenic therapies currently being evaluated in clinical trials target the vascular endothelial growth factor pathway; however, the tumor... 
CELL LUNG-CANCER | FACTOR-BINDING PROTEIN-3 | C-FOS SRE | PROSTATE-CANCER | FACTOR-I-ALPHA | TERNARY COMPLEX FACTORS | FARNESYLTRANSFERASE INHIBITOR SCH66336 | QUATERNARY COMPLEX | HEMATOLOGY | EGR-1 EXPRESSION | ENDOTHELIAL GROWTH-FACTOR | Lung Neoplasms - drug therapy | Transcription, Genetic - drug effects | Recombinant Fusion Proteins - pharmacology | Cells, Cultured - cytology | Humans | Neoplasm Proteins - antagonists & inhibitors | Insulin-Like Growth Factor Binding Protein 3 - pharmacology | Promoter Regions, Genetic - drug effects | Insulin-Like Growth Factor Binding Protein 3 - metabolism | Neoplasm Proteins - genetics | Carcinoma - drug therapy | Cells, Cultured - drug effects | Specific Pathogen-Free Organisms | Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors | Head and Neck Neoplasms - drug therapy | Angiogenesis Inhibitors - pharmacology | Chick Embryo | Head and Neck Neoplasms - pathology | Head and Neck Neoplasms - blood supply | Mitogen-Activated Protein Kinase 3 - metabolism | Mice, Nude | Neovascularization, Pathologic - drug therapy | Cell Line, Tumor | Carcinoma - blood supply | Mice | Mitogen-Activated Protein Kinase 1 - metabolism | Mitogen-Activated Protein Kinase 3 - antagonists & inhibitors | Recombinant Fusion Proteins - therapeutic use | Lung Neoplasms - pathology | Neoplasm Proteins - metabolism | ets-Domain Protein Elk-1 - metabolism | Early Growth Response Protein 1 - genetics | Angiogenesis Inhibitors - therapeutic use | Female | Gene Expression Regulation, Neoplastic - drug effects | Carcinoma - pathology | Lung Neoplasms - blood supply | Carcinoma, Non-Small-Cell Lung - pathology | Carcinoma, Non-Small-Cell Lung - blood supply | Neoplasm Proteins - biosynthesis | Insulin-Like Growth Factor Binding Protein 3 - therapeutic use | Enzyme Activation - drug effects | Xenograft Model Antitumor Assays | Angiogenesis Inhibitors - metabolism | Animals | Endothelial Cells - cytology | Carcinoma, Non-Small-Cell Lung - drug therapy | Early Growth Response Protein 1 - metabolism | Endothelial Cells - drug effects | Index Medicus | Abridged Index Medicus | Vascular Biology
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 1, pp. e16301 - e16301
Journal Article
Scientific reports, ISSN 2045-2322, 10/2015, Volume 5, Issue 1, pp. 15212 - 15212
Journal Article
PLoS Pathogens, ISSN 1553-7366, 09/2010, Volume 6, Issue 9, pp. e1001103 - e1001103
Apoptosis in HIV-1-infected CD4+ primary T cells is triggered by the alteration of the PI3K and p53 pathways, which converge on the FOXO3a transcriptional... 
P300 | MICROBIOLOGY | PROTEIN PHOSPHATASE 2A | HUMAN-IMMUNODEFICIENCY-VIRUS | P-TEFB | VIROLOGY | PROSTATE-CANCER | CREB-BINDING-PROTEIN | LONG-TERMINAL REPEAT | TYPE-1 TAT | FOXO3A | T-CELLS | PARASITOLOGY | Protein Subunits | HIV-1 - pathogenicity | Phosphorylation | Luciferases - metabolism | Oligonucleotide Array Sequence Analysis | Humans | Transcriptional Activation | Gene Expression Profiling | CD4-Positive T-Lymphocytes - pathology | Promoter Regions, Genetic - genetics | Proto-Oncogene Proteins c-akt - genetics | Flow Cytometry | Chromatin Immunoprecipitation | HIV Infections - pathology | Forkhead Transcription Factors - metabolism | Forkhead Transcription Factors - antagonists & inhibitors | CD4-Positive T-Lymphocytes - virology | Proto-Oncogene Proteins c-akt - metabolism | Biomarkers - metabolism | PTEN Phosphohydrolase - genetics | Protein Phosphatase 2 - antagonists & inhibitors | Signal Transduction | tat Gene Products, Human Immunodeficiency Virus - genetics | HIV Infections - virology | RNA, Messenger - genetics | RNA, Small Interfering - pharmacology | CD4-Positive T-Lymphocytes - metabolism | Protein Phosphatase 2 - genetics | PTEN Phosphohydrolase - metabolism | Forkhead Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Fluorescent Antibody Technique | Protein Phosphatase 2 - metabolism | Apoptosis | HIV Infections - metabolism | tat Gene Products, Human Immunodeficiency Virus - metabolism | Phosphatases | Promoters (Genetics) | CD4 lymphocytes | Physiological aspects | Genetic aspects | Genetic transcription | Properties | Index Medicus | Proteins | Enzymes | Biomedical research | Lymphocytes | Ligands | RNA polymerase | Kinases | Experiments
Journal Article
Journal of Molecular and Cellular Cardiology, ISSN 0022-2828, 2014, Volume 72, Issue 100, pp. 9 - 19
Abstract Aims Cyclic AMP inhibits vascular smooth muscle cell (VSMC) proliferation which is important in the aetiology of numerous vascular diseases. The... 
Cardiovascular | Serum response factor | Early growth response gene 1 | 3′-5′-Cyclic adenosine monophosphate | Exchange protein activated by cAMP | Zif268 | 3'-5'-Cyclic adenosine monophosphate | MIGRATION | CARDIAC & CARDIOVASCULAR SYSTEMS | RNA | RAT | TRANSCRIPTION | NEOINTIMA FORMATION | PROLIFERATION | EARLY GROWTH | TARGETING EGR-1 | CELL BIOLOGY | IN-VITRO | 3 '-5 '-Cyclic adenosine monophosphate | Serum Response Factor - genetics | Human Umbilical Vein Endothelial Cells - metabolism | Muscle, Smooth, Vascular - metabolism | Male | ets-Domain Protein Elk-1 - genetics | Cyclic AMP-Dependent Protein Kinases - genetics | Guanine Nucleotide Exchange Factors - metabolism | ets-Domain Protein Elk-1 - metabolism | Human Umbilical Vein Endothelial Cells - cytology | Early Growth Response Protein 1 - genetics | Epoprostenol - pharmacology | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Muscle, Smooth, Vascular - drug effects | Cyclic AMP-Dependent Protein Kinases - metabolism | Guanine Nucleotide Exchange Factors - genetics | Human Umbilical Vein Endothelial Cells - drug effects | Signal Transduction | Colforsin - pharmacology | Serum Response Factor - metabolism | Gene Expression Regulation | Rats | Adenosine - pharmacology | Muscle, Smooth, Vascular - cytology | Organ Specificity | Rats, Sprague-Dawley | Cyclic AMP - pharmacology | Cyclic AMP Response Element-Binding Protein - genetics | Epoprostenol - analogs & derivatives | Animals | Aminopyridines - pharmacology | Cyclic AMP Response Element-Binding Protein - metabolism | Protein Binding | Early Growth Response Protein 1 - antagonists & inhibitors | Cell Proliferation - drug effects | Primary Cell Culture | Early Growth Response Protein 1 - metabolism | rac1 GTP-Binding Protein - metabolism | rac1 GTP-Binding Protein - genetics | Smooth muscle | Analysis | Index Medicus | Original
Journal Article