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Journal of the National Cancer Institute, ISSN 0027-8874, 04/2011, Volume 103, Issue 8, pp. 645 - 661
Background Ionizing radiation (IR) is effectively used in cancer therapy. However, in subsets of patients, a few radioresistant cancer cells survive and cause... 
STEM-CELLS | IN-VITRO | ONCOLOGY | TYROSINE KINASE | HGF | CELL INVASION | RECEPTOR | EPITHELIAL-MESENCHYMAL TRANSITIONS | NF-KAPPA-B | SCATTER-FACTOR | PROTOONCOGENE | Humans | Neoplasm Invasiveness - prevention & control | Radiation Tolerance | Receptors, Growth Factor - antagonists & inhibitors | NF-kappa B - metabolism | RNA, Messenger - metabolism | NF-kappa B - radiation effects | Receptors, Growth Factor - genetics | Proto-Oncogene Proteins c-met - radiation effects | Signal Transduction - radiation effects | Protein-Serine-Threonine Kinases - metabolism | Radiation, Ionizing | Tumor Suppressor Proteins - metabolism | DNA-Binding Proteins - radiation effects | Proto-Oncogene Proteins c-met - antagonists & inhibitors | Cell Cycle Proteins - metabolism | Cell Cycle Proteins - radiation effects | Receptors, Growth Factor - radiation effects | Proto-Oncogene Proteins c-met - drug effects | Ataxia Telangiectasia Mutated Proteins | Phosphorylation - radiation effects | Cell Line, Tumor | Mice | RNA, Small Interfering | Tumor Suppressor Proteins - radiation effects | Receptors, Growth Factor - metabolism | Neoplasms - metabolism | Proto-Oncogene Proteins c-met - metabolism | Apoptosis - radiation effects | Up-Regulation - radiation effects | Transcription, Genetic - radiation effects | Transplantation, Heterologous | Sulfones - pharmacology | DNA-Binding Proteins - metabolism | Chromatin Immunoprecipitation | Protein-Serine-Threonine Kinases - radiation effects | Tumor Suppressor Proteins - genetics | Polymerase Chain Reaction | Cell Cycle Proteins - genetics | Indoles - pharmacology | Neoplasms - radiotherapy | Gene Expression Regulation, Neoplastic - drug effects | In Situ Nick-End Labeling | Enzyme-Linked Immunosorbent Assay | Radiation-Sensitizing Agents - pharmacology | Gene Silencing | Protein-Serine-Threonine Kinases - genetics | DNA-Binding Proteins - genetics | Cell Survival - radiation effects | Cell Movement - radiation effects | Proto-Oncogene Proteins c-met - genetics | Blotting, Northern | Animals | NF-kappa B - genetics | Protein Kinase Inhibitors - pharmacology | Neoplasms - pathology | Receptors, Growth Factor - drug effects | DNA Damage - radiation effects | Mitogen-Activated Protein Kinases - metabolism | Ionizing radiation | Physiological aspects | Genetic aspects | Cancer invasiveness | Research | Gene expression | Radiotherapy | Health aspects | Oncology | Radiation therapy | Kinases | Index Medicus
Journal Article
Cell, ISSN 0092-8674, 10/2000, Volume 103, Issue 3, pp. 501 - 510
The Listeria monocytogenes surface protein InIB promotes bacterial entry into mammalian cells. Here, we identify a cellular surface receptor required for... 
Proto-Oncogene Proteins c-met - metabolism | Epithelial Cells - drug effects | Humans | Cell Aggregation - drug effects | Membrane Proteins - pharmacology | Phosphoproteins - metabolism | Kidney | Phosphotyrosine - metabolism | Dose-Response Relationship, Drug | Endocytosis | Proto-Oncogene Proteins c-cbl | Gene Deletion | Listeria monocytogenes - metabolism | Cytoskeletal Proteins - metabolism | Membrane Proteins - metabolism | Listeria monocytogenes - physiology | Phosphorylation - drug effects | Epithelial Cells - cytology | Protein Structure, Tertiary | Proto-Oncogene Proteins - metabolism | Cell Line | Signal Transduction | Membrane Proteins - genetics | Bacterial Proteins - genetics | Precipitin Tests | Proto-Oncogene Proteins c-met - genetics | Ubiquitin-Protein Ligases | Adaptor Proteins, Signal Transducing | Bacterial Proteins - pharmacology | Animals | Hepatocytes | Epithelial Cells - microbiology | Epithelial Cells - enzymology | Listeria monocytogenes - genetics | Protein Binding | Avian Proteins | Bacterial Proteins - metabolism | Ligands | Kinetics | Proto-Oncogene Proteins c-met - chemistry | Cell receptors | Foodborne diseases | Physiological aspects | Listeria monocytogenes | Listeriosis | Protein tyrosine kinase | Research | Permeability | Cytochemistry | Mammals | Cells | InIB protein | Met protein | Index Medicus
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 6/2000, Volume 149, Issue 7, pp. 1419 - 1432
Journal Article
CELL DEATH & DISEASE, ISSN 2041-4889, 12/2017, Volume 8, Issue 12, pp. 1 - 13
Multiple target inhibition has gained considerable interest in combating drug resistance in glioblastoma, however, understanding the molecular mechanisms of... 
CELL BIOLOGY | Phosphorylation | Hepatocyte growth factor | Transforming growth factor | Glioblastoma | Extracellular signal-regulated kinase | MAP kinase | AKT protein | Gene expression | Drug resistance | Kinases | 1-Phosphatidylinositol 3-kinase | c-Met protein | Signal transduction | Molecular modelling | Glioma cells | Stem cells | Growth factors | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 08/2012, Volume 44, Issue 8, pp. 852 - 860
Human non-small cell lung cancers (NSCLCs) with activating mutations in EGFR frequently respond to treatment with EGFRtargeted tyrosine kinase inhibitors... 
GEFITINIB | RECEPTOR TYROSINE KINASES | MET AMPLIFICATION | GROWTH | GENETICS & HEREDITY | ACQUIRED-RESISTANCE | MUTATIONS | NF-KAPPA-B | TUMORS | MUTANT EGFR | ERLOTINIB | Erlotinib Hydrochloride | Proto-Oncogene Proteins c-met - metabolism | Lung Neoplasms - drug therapy | Receptor, Epidermal Growth Factor - genetics | Humans | Lung Neoplasms - metabolism | Middle Aged | Lung Neoplasms - pathology | Male | Intercellular Signaling Peptides and Proteins - metabolism | Epithelial-Mesenchymal Transition | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Adult | Female | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Proto-Oncogene Proteins - metabolism | Proto-Oncogene Proteins - antagonists & inhibitors | Signal Transduction | Carcinoma, Non-Small-Cell Lung - genetics | Carcinoma, Non-Small-Cell Lung - metabolism | Intercellular Signaling Peptides and Proteins - genetics | Proto-Oncogene Proteins - genetics | Receptor Protein-Tyrosine Kinases - metabolism | Proto-Oncogene Proteins c-met - genetics | Xenograft Model Antitumor Assays | Drug Resistance, Neoplasm - genetics | Animals | Receptor Protein-Tyrosine Kinases - genetics | Cell Line, Tumor | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Aged | Protein Kinase Inhibitors - pharmacology | Carcinoma, Non-Small-Cell Lung - drug therapy | Enzyme Activation | Mutation | Quinazolines - pharmacology | Erlotinib | Physiological aspects | Genetic aspects | Research | Lung cancer, Non-small cell | Drug therapy | Health aspects | Protein kinases | Studies | Medical research | Rodents | Lung cancer | Genomics | Kinases | Gene expression | Acquisitions & mergers | Tumors | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2012, Volume 7, Issue 7, pp. e40967 - e40967
MicroRNAs (miRNAs) are endogenous small non-coding RNAs that play central roles in diverse pathological processes. In this study, we investigated the effect of... 
METASTASIS | MULTIDISCIPLINARY SCIENCES | C-MET | LINEAGE SURVIVAL | GENE-EXPRESSION | PROGNOSTIC MARKER | PROLIFERATION | MALIGNANT-MELANOMA | TRANSCRIPTION FACTOR | MASTER REGULATOR | MELANOCYTES | Cyclin D2 - genetics | Humans | Gene Expression Regulation, Neoplastic | 3' Untranslated Regions - genetics | Male | Proto-Oncogene Proteins c-akt - genetics | Tumor Suppressor Protein p53 - genetics | MAP Kinase Signaling System - genetics | Melanoma - genetics | Mitogen-Activated Protein Kinase 1 - genetics | Female | Uveal Neoplasms - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Genes, Tumor Suppressor | Microphthalmia-Associated Transcription Factor - biosynthesis | Melanoma - metabolism | Uveal Neoplasms - genetics | Uveal Neoplasms - pathology | Mitogen-Activated Protein Kinase 3 - genetics | Down-Regulation | Tumor Suppressor Protein p53 - metabolism | MicroRNAs - biosynthesis | Melanoma - pathology | Proto-Oncogene Proteins c-bcl-2 - biosynthesis | RNA, Neoplasm - biosynthesis | Mitogen-Activated Protein Kinase 3 - metabolism | Cell Line, Tumor | RNA, Neoplasm - genetics | MicroRNAs - genetics | Cyclin D2 - biosynthesis | Microphthalmia-Associated Transcription Factor - genetics | Proto-Oncogene Proteins c-bcl-2 - genetics | Mitogen-Activated Protein Kinase 1 - metabolism | MicroRNA | Analysis | Melanoma | Research | Tumor proteins | Tumors | Apoptosis | Transcription factors | Target recognition | Leukocyte migration | Laboratories | p53 Protein | Science | AKT protein | Metastasis | D2 protein | Cyclin D2 | Skin cancer | c-Met protein | Transfection | Cell cycle | Tumorigenesis | Bioinformatics | Microphthalmia-associated transcription factor | Invasiveness | MiRNA | Extracellular signal-regulated kinase | Optometry | Gene expression | Ribonucleic acid--RNA | Hospitals | MicroRNAs | Tumor suppressor genes | Mutation | Cell migration | Index Medicus | RNA | Ribonucleic acid
Journal Article
Journal of Molecular Biology, ISSN 0022-2836, 2010, Volume 395, Issue 3, pp. 522 - 532
The surface protein InlB mediates bacterial invasion into host cells by activating the human receptor tyrosine kinase Met. So far, it is unknown how InlB or... 
crystal structure | protein–protein interaction | protein engineering | internalin | signal transduction | protein-protein interaction | HOST-CELL INVASION | SCATTER FACTOR | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEPATOCYTE GROWTH-FACTOR | PATHOGEN LISTERIA-MONOCYTOGENES | FACTOR/SCATTER FACTOR | SIGNAL-TRANSDUCTION | STRUCTURAL BASIS | LIVER-REGENERATION | MOLECULAR-CLONING | Humans | Protein Multimerization | Bacterial Proteins - chemistry | Crystallography, X-Ray | Proto-Oncogene Proteins - chemistry | Proto-Oncogene Proteins - agonists | Membrane Proteins - metabolism | Listeria monocytogenes - physiology | Proto-Oncogene Proteins - metabolism | Recombinant Proteins - metabolism | Mutagenesis, Site-Directed | Membrane Proteins - genetics | Proto-Oncogene Proteins c-met | Bacterial Proteins - genetics | Models, Molecular | Recombinant Proteins - chemistry | Recombinant Proteins - genetics | Receptors, Growth Factor - chemistry | Static Electricity | Receptors, Growth Factor - agonists | Listeria monocytogenes - pathogenicity | Membrane Proteins - chemistry | Listeria monocytogenes - genetics | Protein Binding | Bacterial Proteins - metabolism | Ligands | Enzyme Activation | Receptors, Growth Factor - metabolism | Tyrosine | Follicle-stimulating hormone | Proteoglycans | Crystals | Peptide hormones | Sulfates | Polyethylene glycol | Glutathione transferase | Physiological aspects | Phenols | Structure | Growth factors | Integrins | Glutathione | Index Medicus
Journal Article
Prostate, ISSN 0270-4137, 2009, Volume 69, Issue 15, pp. 1683 - 1693
BACKGROUND: According to the cancer stem cell hypothesis, tumor growth is sustained by a subpopulation of cancer stem/progenitor-like cells. Self-renewal and... 
Cancer stem/progenitor-like cells | Self-renewal | PSCA | Prostaspheres | CD49f | PROGENITOR CELLS | POPULATION | PROSPECTIVE IDENTIFICATION | prostaspheres | self-renewal | TUMOR-INITIATING CELLS | MURINE | EPITHELIAL STEM-CELLS | ENDOCRINOLOGY & METABOLISM | UROLOGY & NEPHROLOGY | cancer stem/progenitor-like cells | DIFFERENTIATION | PROGRESSION | CD133 | Immunohistochemistry | Prostatic Neoplasms - metabolism | Nestin | Proto-Oncogene Proteins c-met - biosynthesis | Antigens, CD - biosynthesis | Humans | Membrane Glycoproteins - biosynthesis | GPI-Linked Proteins | Octamer Transcription Factor-3 - biosynthesis | Cell Growth Processes - physiology | Intercellular Signaling Peptides and Proteins - biosynthesis | Male | Gene Expression Profiling | Proto-Oncogene Proteins - biosynthesis | Antigens, CD - genetics | Octamer Transcription Factor-3 - genetics | RNA, Messenger - biosynthesis | Prostatic Neoplasms - genetics | Neoplastic Stem Cells - metabolism | Serrate-Jagged Proteins | Intermediate Filament Proteins - genetics | Nerve Tissue Proteins - biosynthesis | Neoplastic Stem Cells - pathology | Retrospective Studies | Neoplasm Proteins - genetics | Jagged-1 Protein | Prostatic Neoplasms - pathology | Antigens, Neoplasm | Calcium-Binding Proteins - biosynthesis | Homeodomain Proteins - biosynthesis | Nanog Homeobox Protein | Keratin-14 - biosynthesis | Membrane Proteins - genetics | Neoplasm Proteins - biosynthesis | RNA, Messenger - genetics | Intercellular Signaling Peptides and Proteins - genetics | Intermediate Filament Proteins - biosynthesis | Proto-Oncogene Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Keratin-14 - genetics | Nerve Tissue Proteins - genetics | Homeodomain Proteins - genetics | Membrane Glycoproteins - genetics | Proto-Oncogene Proteins c-met - genetics | Membrane Proteins - biosynthesis | Clone Cells - pathology | Calcium-Binding Proteins - genetics | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2014, Volume 9, Issue 2, pp. e83957 - e83957
Purpose: Nearly all primary uveal melanoma (UM) that metastasize involve the liver. Hepatocyte growth factor (HGF) is proposed to be an important... 
SURVIVAL | GNAQ | HGF | MULTIDISCIPLINARY SCIENCES | C-MET | MUTATIONS | FACTOR RECEPTOR | EXPRESSION | CANCER | LINES | Proto-Oncogene Proteins c-met - metabolism | Apoptosis - drug effects | Humans | Mitogen-Activated Protein Kinase 3 - antagonists & inhibitors | Gene Expression Regulation, Neoplastic | Hepatocyte Growth Factor - antagonists & inhibitors | Mitogen-Activated Protein Kinase 1 - genetics | Hepatocyte Growth Factor - genetics | Benzocycloheptenes - pharmacology | GTP-Binding Protein alpha Subunits - metabolism | Mitogen-Activated Protein Kinase 3 - genetics | Signal Transduction | Proto-Oncogene Proteins c-met - antagonists & inhibitors | Mitogen-Activated Protein Kinase 1 - antagonists & inhibitors | GTP-Binding Protein alpha Subunits - genetics | Sulfonamides - pharmacology | Hepatocyte Growth Factor - metabolism | Proto-Oncogene Proteins c-met - genetics | Cell Movement - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | GTP-Binding Protein alpha Subunits, Gq-G11 | Cell Line, Tumor | Benzimidazoles - pharmacology | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Mutation | Cell Cycle - drug effects | Mitogen-Activated Protein Kinase 1 - metabolism | Proteins | Metastasis | RNA | Growth | Melanoma | Cell proliferation | Phosphorylation | Laboratories | Downstream effects | Liver | Oncology | Biology | Cancer therapies | Metastases | c-Met protein | Cell growth | Rodents | Inhibition | MET protein | Growth factors | Deoxyribonucleic acid--DNA | Medical research | Immunoglobulins | Hepatocyte growth factor | Mortality | Extracellular signal-regulated kinase | Gene expression | DNA fingerprints | Cell lines | Cell migration | Apoptosis | Tumors | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 2018, Volume 36, Issue 9, pp. 911 - 919
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, pp. e0177871 - e0177871
Baculoviral IAP repeat containing 6 (BIRC6) is a member of the inhibitors of apoptosis proteins (IAPs), a family of functionally and structurally related... 
CANCER-CELLS | SURVIVIN | MULTIDISCIPLINARY SCIENCES | PROTEIN-KINASE CK2 | BCR-ABL | MYELOGENOUS LEUKEMIA | ACQUIRED-RESISTANCE | INHIBITORS | IDENTIFICATION | APOPTOSIS PROTEIN | CHRONIC MYELOID-LEUKEMIA | Cyclin-Dependent Kinase 9 - genetics | Inhibitor of Apoptosis Proteins - genetics | Humans | Myeloid Cell Leukemia Sequence 1 Protein - metabolism | Imatinib Mesylate - toxicity | Myeloid Cell Leukemia Sequence 1 Protein - genetics | Antineoplastic Agents - toxicity | Drug Resistance, Neoplasm - genetics | src-Family Kinases - metabolism | Cell Line, Tumor | Cyclin-Dependent Kinase 9 - metabolism | Inhibitor of Apoptosis Proteins - metabolism | src-Family Kinases - genetics | Apoptosis | Care and treatment | RNA | Analysis | Patient outcomes | Research | Chronic myeloid leukemia | Drug resistance | Health aspects | Cytochrome | Regulations | Bcl-2 protein | Liver | Radiation | Biochemistry | Cancer therapies | Anticancer properties | Proteins | Casein | Bone marrow | Diagnosis | Inhibition | Damage | Chromosomes | Assembly | Deoxyribonucleic acid--DNA | BAK protein | Substrates | Quenching | Amplification | Inhibitors | Stem cells | Affinity | Mutation | Aberration | Apollon | Binding sites | BCR protein | Residues | Phosphorylation | Leukemia | Amino acids | Transplantation | Identification | Activation | Malignancy | Kinases | DNA repair | c-Met protein | Cascades | Cell cycle | Age | Myeloid leukemia | Caspase | Abl protein | Pharmacology | Dentistry | C-Terminus | Medicine | Protein kinase | Proteomics | Bcl protein | BIM protein | Cancer | Index Medicus | Deoxyribonucleic acid | DNA
Journal Article