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Oncogene, ISSN 0950-9232, 06/2007, Volume 26, Issue 27, pp. 3909 - 3919
KIT or alpha-platelet-derived growth factor receptor (alpha-PDGFR) activating mutations are the pathogenic mechanisms that characterize gastrointestinal... 
Kit mutations | Tyrosine kinases | GIST | Morphological change | SURVIVAL | morphological change | CELL-ADHESION MOLECULE | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-KIT | RECEPTOR | tyrosine kinases | IDENTIFICATION | CELL BIOLOGY | MICROENVIRONMENT | ONCOLOGY | GROWTH | GENETICS & HEREDITY | MUTATIONS | INHIBITOR | Gene Expression Regulation, Enzymologic - drug effects | Oncogene Proteins - genetics | Taxoids - pharmacology | Oligonucleotide Array Sequence Analysis | Humans | Antineoplastic Agents - therapeutic use | Green Fluorescent Proteins - genetics | Proto-Oncogene Proteins c-kit - metabolism | Recombinant Fusion Proteins - metabolism | Pyrimidines - chemistry | Protein Kinase Inhibitors - chemistry | Gastrointestinal Stromal Tumors - pathology | Proto-Oncogene Proteins c-kit - genetics | Antineoplastic Agents - pharmacology | Proto-Oncogene Proteins | Gene Expression Regulation, Neoplastic - drug effects | Phosphorylation - drug effects | Gastrointestinal Stromal Tumors - genetics | Protein Structure, Tertiary | Cell Survival - drug effects | Green Fluorescent Proteins - metabolism | Oncogene Proteins - chemistry | Oncogene Proteins - metabolism | Models, Molecular | Piperazines - therapeutic use | Pyrimidines - pharmacology | Receptor Protein-Tyrosine Kinases - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Imatinib Mesylate | Piperazines - pharmacology | Blotting, Western | Cell Shape - drug effects | Drug Synergism | Drug Resistance, Neoplasm - genetics | Receptor Protein-Tyrosine Kinases - genetics | Gastrointestinal Stromal Tumors - drug therapy | Pyrimidines - therapeutic use | Cell Line, Tumor | Recombinant Fusion Proteins - genetics | Protein Kinase Inhibitors - pharmacology | Benzamides | Mutation | Proto-Oncogene Proteins c-kit - chemistry | Receptor Protein-Tyrosine Kinases - chemistry | Control | Gastrointestinal tumors | Protein tyrosine kinase | Genetic aspects | Research | Gene expression | Health aspects | Gastroenterology | Oncology | Kinases | Drug resistance | Tumors | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2012, Volume 7, Issue 5, pp. e37776 - e37776
The KIT-inhibitor imatinib mesylate (IM) has greatly improved the treatment of metastatic gastrointestinal stromal tumors (GIST). IM exhibits strong... 
APOPTOSIS | ACTIVATION | HEAT-SHOCK-PROTEIN-90 | INHIBITION | MULTIDISCIPLINARY SCIENCES | IN-VIVO | MDM2 | GENE AMPLIFICATION | C-KIT | MUTATIONS | IMATINIB MESYLATE | Phosphorylation | Gastrointestinal Neoplasms - genetics | Apoptosis - drug effects | Gastrointestinal Neoplasms - drug therapy | Humans | Caspase 3 - metabolism | Antineoplastic Agents - therapeutic use | Proto-Oncogene Proteins c-kit - metabolism | Proto-Oncogene Proteins c-kit - antagonists & inhibitors | Tumor Suppressor Protein p53 - genetics | DNA-Binding Proteins - metabolism | Protein Binding - drug effects | Tumor Suppressor Proteins - genetics | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Transcription, Genetic | Antineoplastic Agents - pharmacology | Nuclear Proteins - genetics | Gastrointestinal Stromal Tumors - genetics | Proto-Oncogene Proteins c-mdm2 - antagonists & inhibitors | Gastrointestinal Neoplasms - metabolism | Tumor Suppressor Proteins - metabolism | Tumor Suppressor Protein p53 - metabolism | Nuclear Proteins - metabolism | Imidazoles - pharmacology | Pyrimidines - pharmacology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Imatinib Mesylate | Piperazines - pharmacology | Sequence Analysis, DNA | Transcription Factors - metabolism | Heterogeneous-Nuclear Ribonucleoprotein K - metabolism | Tumor Protein p73 | Signal Transduction - drug effects | Gastrointestinal Stromal Tumors - drug therapy | Protein Kinase Inhibitors - therapeutic use | Cell Line, Tumor | Gastrointestinal Stromal Tumors - metabolism | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Benzamides | Mutation | Cell Cycle - drug effects | Care and treatment | Analysis | Drug therapy, Combination | Metastasis | Tumor proteins | Health aspects | Apoptosis | Drugs | Biotechnology | p53 Protein | Cytotoxicity | Oncology | Activation | Bone surgery | Medical schools | Metastases | Signal transduction | Modulation | Cell cycle | Remission | Medical research | MDM2 protein | Imatinib | Heat shock proteins | Exploration | Pathology | Gene amplification | Inhibitors | Cell lines | Stem cells | Cancer | Tumors | Index Medicus
Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 02/2004, Volume 24, Issue 4, pp. 1439 - 1452
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
TRANSCRIPTION FACTOR SCL | HEMATOPOIETIC-CELLS | LOOP-HELIX PROTEINS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROTEIN-PROTEIN INTERACTION | C-KIT EXPRESSION | T-CELL LEUKEMIA | ZINC-FINGER PROTEIN | GENE-EXPRESSION | ACTIVITY IN-VIVO | RED-BLOOD-CELLS | CELL BIOLOGY | Transcription Factors - chemistry | Molecular Sequence Data | Sp1 Transcription Factor - metabolism | Proto-Oncogene Proteins - chemistry | Promoter Regions, Genetic - genetics | DNA-Binding Proteins - metabolism | GATA1 Transcription Factor | Metalloproteins - metabolism | Base Sequence | TCF Transcription Factors | Electrophoretic Mobility Shift Assay | Binding Sites | T-Cell Acute Lymphocytic Leukemia Protein 1 | Basic Helix-Loop-Helix Transcription Factors | Protein Structure, Tertiary | Proto-Oncogene Proteins - metabolism | Cell Line | LIM Domain Proteins | Response Elements | Gene Expression Regulation | Transcription Factor 7-Like 1 Protein | Glycophorin - genetics | Hematopoietic Stem Cells - metabolism | Reverse Transcriptase Polymerase Chain Reaction | DNA-Binding Proteins - chemistry | Macromolecular Substances | Transcription Factors - metabolism | Adaptor Proteins, Signal Transducing | Animals | Protein Binding | Erythroid-Specific DNA-Binding Factors | Mice | Glycophorin A | SCL protein | E47 protein | TAL1 protein | GPA gene | Ldb1 protein | FOG protein | LMO2 protein | Index Medicus | Transcriptional Regulation
Journal Article
Journal Article
Journal of Proteome Research, ISSN 1535-3893, 11/2015, Volume 14, Issue 11, pp. 4704 - 4713
Disease and death caused by bacterial infections are global health problems. Effective bacterial strategies are required to promote survival and proliferation... 
in vivo biotinylation | affinity proteomics | Streptoccous pyogenes | mass spectrometry | scFv antibody fragments | selected reaction monitoring | virulence factors | PROTEOME | COMPLEXES | BIOCHEMICAL RESEARCH METHODS | IGG | GROUP-A STREPTOCOCCI | PYOGENES | GENERATION | ABSOLUTE QUANTIFICATION | FIBRINOGEN | Antibody Specificity | Epitope Mapping | Virulence Factors - genetics | Humans | Antigens, Bacterial - immunology | Bacterial Proteins - chemistry | Molecular Sequence Data | Suppressor Factors, Immunologic - genetics | Virulence Factors - immunology | Peptide Library | Antigens, Bacterial - genetics | Lymphokines - genetics | Single-Chain Antibodies - genetics | Immunoglobulin G - immunology | Suppressor Factors, Immunologic - immunology | Chromatography, Liquid | Carrier Proteins - chemistry | Bacterial Proteins - immunology | Binding Sites | Streptococcus pyogenes - chemistry | Tandem Mass Spectrometry - methods | Bacterial Outer Membrane Proteins - genetics | Carrier Proteins - immunology | Amino Acid Sequence | Gene Expression | Antigens, Bacterial - chemistry | Bacterial Outer Membrane Proteins - immunology | DNA-Binding Proteins - immunology | Streptococcus pyogenes - immunology | Immunoglobulin G - chemistry | Bacterial Proteins - genetics | Bacterial Outer Membrane Proteins - chemistry | Recombinant Proteins - chemistry | Antibody Affinity | Recombinant Proteins - genetics | Virulence Factors - chemistry | Suppressor Factors, Immunologic - chemistry | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Lymphokines - chemistry | Carrier Proteins - genetics | Immunoglobulin G - genetics | Recombinant Proteins - immunology | Reagent Kits, Diagnostic | Lymphokines - immunology | Protein Binding | Single-Chain Antibodies - chemistry | Single-Chain Antibodies - immunology | Index Medicus | unclassified drug | Article | selected reaction monitoring mass spectrometry | single chain fragment variable antibody | antibody affinity | antigen binding | surface protein h | phage display | Biochemistry and Molecular Biology | protein targeting | Streptococcus pyogenes | Natural Sciences | priority journal | Biological Sciences | immunoglobulin G | biotinylation | surface protein m1 | in vivo study | liquid chromatography | bacterial strain | protein binding | bacterial virulence | Naturvetenskap | Biokemi och molekylärbiologi | Biologiska vetenskaper | membrane protein | nonhuman | wild type
Journal Article
Scientific Reports, ISSN 2045-2322, 08/2014, Volume 4, Issue 1, pp. 6127 - 6127
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 09/2007, Volume 102, Issue 6, pp. 1749 - 1757
Imatinib, a protein tyrosine kinase inhibitor, may prevent the growth of glioblastoma cells. Unfortunately, its brain distribution is restricted by... 
CGP74588 | mouse | p‐glycoprotein | imatinib | blood–brain barrier | breast cancer resistance protein | Imatinib | Blood-brain barrier | Mouse | Breast cancer resistance protein | p-glycoproteinz | blood-brain barrier | CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | p-glycoprotein | C-KIT | DRUG-RESISTANCE | DEFICIENT MICE | GF120918 | NEUROSCIENCES | REVERSAL | IN-VITRO | PHARMACOKINETICS | TYROSINE KINASE INHIBITOR | MULTIDRUG-RESISTANCE | Male | Piperazines - metabolism | Cyclosporins - pharmacology | Pyrimidines - metabolism | Quinolines - pharmacology | Antineoplastic Agents - metabolism | Brain - metabolism | Dose-Response Relationship, Drug | Brain - blood supply | ATP Binding Cassette Transporter, Subfamily B, Member 1 | ATP-Binding Cassette Transporters - genetics | Biological Transport, Active - physiology | ATP-Binding Cassette Transporters - metabolism | Dibenzocycloheptenes - pharmacology | ATP Binding Cassette Transporter, Subfamily B - genetics | Piperazines - pharmacokinetics | Immunosuppressive Agents - pharmacology | ATP Binding Cassette Transporter, Subfamily G, Member 2 | Tetrahydroisoquinolines - pharmacology | Biological Transport, Active - drug effects | Enzyme Inhibitors - pharmacology | Blood-Brain Barrier - drug effects | Imatinib Mesylate | ATP Binding Cassette Transporter, Subfamily B - metabolism | Blood-Brain Barrier - metabolism | Mice, Knockout | Brain - drug effects | Animals | ATP Binding Cassette Transporter, Subfamily B - antagonists & inhibitors | Acridines - pharmacology | Pyrimidines - pharmacokinetics | Mice | Benzamides | ATP-Binding Cassette Transporters - antagonists & inhibitors | Physiological aspects | Breast cancer | Proteins | Neurosciences | Inhibitor drugs | Rodents | Biochemistry | Glycoproteins | Index Medicus
Journal Article
Blood, ISSN 0006-4971, 12/2000, Volume 96, Issue 12, pp. 3907 - 3914
Somatic mutations of the receptor tyrosine kinase Flt3 consisting of internal tandem duplications (ITD) occur in 20% of patients with acute myeloid leukemia.... 
INTERNAL TANDEM DUPLICATION | STEM-CELLS | HEMATOPOIETIC PROGENITOR CELLS | HUMAN BONE-MARROW | CONSTITUTIVE ACTIVATION | C-KIT | MURINE FLT3 | GROWTH-FACTOR | HEMATOLOGY | RECEPTOR TYROSINE KINASE | HUMAN HOMOLOG | Clone Cells - cytology | Recombinant Fusion Proteins - pharmacology | Apoptosis - drug effects | Apoptosis - radiation effects | DNA Replication - drug effects | Humans | Leukemia, Myeloid - genetics | Myeloid Cells - physiology | Protein-Serine-Threonine Kinases | fms-Like Tyrosine Kinase 3 | ras Proteins - metabolism | Recombinant Fusion Proteins - metabolism | Trans-Activators - physiology | DNA-Binding Proteins - metabolism | Neoplasms, Experimental - pathology | Mitogen-Activated Protein Kinase Kinases - metabolism | Transfection | Milk Proteins | Female | Myeloid Cells - drug effects | Neoplasms, Experimental - mortality | Tumor Cells, Cultured | Tandem Repeat Sequences - genetics | ras Proteins - physiology | Proto-Oncogene Proteins - metabolism | Proto-Oncogene Proteins - pharmacology | Acute Disease | DNA-Binding Proteins - physiology | Receptor Protein-Tyrosine Kinases - pharmacology | Proto-Oncogene Proteins - genetics | Receptor Protein-Tyrosine Kinases - metabolism | Cell Division - drug effects | Mice, Inbred C3H | Proto-Oncogene Proteins c-akt | Animals | STAT5 Transcription Factor | Receptor Protein-Tyrosine Kinases - genetics | Signal Transduction - drug effects | Leukemia, Myeloid - physiopathology | Recombinant Fusion Proteins - genetics | Trans-Activators - metabolism | Mice | Cell Transformation, Neoplastic - drug effects | Mutation | Index Medicus | Abridged Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2013, Volume 8, Issue 2, pp. e55481 - e55481
AML1-ETO fusion protein (AE) is generated by t(8;21)(q22;q22) chromosomal translocation, which is one of the most frequently observed structural abnormalities... 
AML1-ETO | PATHWAYS | MONOCYTIC LEUKEMIA | MULTIDISCIPLINARY SCIENCES | G1/S TRANSITION | AML1/ETO | TRANSCRIPTION | KINASE | FUSION PROTEIN | CBP/P300 | ACUTE MYELOID-LEUKEMIA | Oncogene Proteins, Fusion - metabolism | p300-CBP Transcription Factors - antagonists & inhibitors | Apoptosis - drug effects | Humans | Leukemia, Myeloid, Acute - metabolism | Proto-Oncogene Proteins c-kit - metabolism | Proto-Oncogene Proteins c-bcl-2 - metabolism | p300-CBP Transcription Factors - genetics | Leukemia, Myeloid, Acute - drug therapy | Female | Proto-Oncogene Proteins c-kit - genetics | Hematopoietic Stem Cells - drug effects | Core Binding Factor Alpha 2 Subunit - metabolism | Leukemia, Myeloid, Acute - pathology | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Gene Expression Regulation, Leukemic - drug effects | Hematopoietic Stem Cells - metabolism | RUNX1 Translocation Partner 1 Protein | Granulocyte Colony-Stimulating Factor - pharmacology | p300-CBP Transcription Factors - metabolism | Acetylation - drug effects | Animals | Histones - genetics | Signal Transduction - drug effects | Cell Cycle Checkpoints - drug effects | Oncogene Proteins, Fusion - genetics | Hematopoietic Stem Cells - cytology | Cell Line, Tumor | Cell Proliferation - drug effects | Mice | Histones - metabolism | Core Binding Factor Alpha 2 Subunit - genetics | Proto-Oncogene Proteins c-bcl-2 - genetics | Leukemia, Myeloid, Acute - genetics | Physiological aspects | Genetic aspects | Research | Transferases | Cell proliferation | Transcription | Bcl-2 protein | Leukemia | Event-related potentials | Kinases | Proteins | Cell growth | Allografts | Granulocyte colony-stimulating factor | Peripheral blood | Cell cycle | Colony-stimulating factor | Inhibition | Acetylation | Fusion protein | G1 phase | Translocation | Hematology | Colonies | Myeloid leukemia | Abnormalities | Melanoma | Gene expression | Histone acetyltransferase | c-Kit protein | Patients | AML1 protein | Inhibitors | Cell lines | Stem cells | Leukemogenesis | Leukocytes (granulocytic) | Laboratory animals | Acute myeloid leukemia | Prostate cancer | Histone H3 | Apoptosis | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2017, Volume 12, Issue 8, pp. e0182935 - e0182935
Allergy to peanuts has become a common and severe problem, especially in westernized countries. In this study, we evaluated the target and epitope specificity... 
ATOPIC-DERMATITIS | CRYSTAL-STRUCTURE | FOOD ALLERGY | MULTIDISCIPLINARY SCIENCES | IGE-BINDING EPITOPES | MAJOR PEANUT ALLERGEN | SANDWICH ELISA | 11S GLOBULIN | PREVALENCE | MUTATIONAL ANALYSIS | EXPRESSION | Arachis - chemistry | Epitope Mapping | Epitopes - analysis | Antibodies, Monoclonal - biosynthesis | Humans | Protein Multimerization | Alanine - chemistry | Antigens, Plant - chemistry | Enzyme-Linked Immunosorbent Assay - standards | Epitopes - immunology | Peanut Hypersensitivity - diagnosis | Alanine - genetics | Allergens - immunology | Plant Proteins - chemistry | Seed Storage Proteins - immunology | Allergens - chemistry | Antibodies, Monoclonal - chemistry | Amino Acid Sequence | Gene Expression | Protein Structure, Secondary | Alanine - immunology | Models, Molecular | Recombinant Proteins - chemistry | Antigens, Plant - immunology | Plant Proteins - immunology | Recombinant Proteins - genetics | Antibodies, Monoclonal - isolation & purification | Peanut Hypersensitivity - immunology | Antigens, Plant - genetics | Plant Proteins - genetics | Seed Storage Proteins - chemistry | Animals | Recombinant Proteins - immunology | Reagent Kits, Diagnostic | Arachis - immunology | Protein Array Analysis | Seed Storage Proteins - genetics | Epitopes - chemistry | Mice | Amino Acid Substitution | Monoclonal antibodies | Usage | Identification and classification | Enzyme-linked immunosorbent assay | Antigenic determinants | Testing | Allergens | Health sciences | Nuts | Target recognition | Peptides | Amino acids | Immunoblotting | Proteins | Life sciences | Isoelectric focusing | Inhibition | Recombinant | Binding | Food allergies | Alanine | Peanuts | Cloning | Hypersensitivity | Mass spectroscopy | Liquid chromatography | Epitopes | Ara h 3 antigen | Diagnostic systems | Mass spectrometry | Index Medicus
Journal Article
Journal Article