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Journal Article
Molecular Oncology, ISSN 1574-7891, 08/2017, Volume 11, Issue 8, pp. 1065 - 1077
Panitumumab is a monoclonal antibody developed against the human epidermal growth factor receptor (EGFR). TAS‐102 is a novel chemotherapeutic agent containing... 
TAS‐102 | colorectal cancer | panitumumab | phosphorylation | trifluridine | EGFR | TAS-102 | TARGETED THERAPY | CELLS | THYMIDYLATE SYNTHASE | ANTITUMOR-ACTIVITY | METASTATIC COLORECTAL-CANCER | GROWTH-FACTOR RECEPTOR | INHIBITION | ONCOLOGY | DNA | ORAL CHEMOTHERAPEUTIC-AGENT | GASTROINTESTINAL MALIGNANCIES | Trifluridine - pharmacology | Antibodies, Monoclonal - pharmacology | Colonic Neoplasms - drug therapy | Humans | Colonic Neoplasms - metabolism | Antineoplastic Combined Chemotherapy Protocols - pharmacology | Uracil - pharmacology | Receptor, Epidermal Growth Factor - metabolism | Colonic Neoplasms - pathology | Cell Line, Tumor | Receptor, Epidermal Growth Factor - antagonists & inhibitors | Drug Combinations | Drug Screening Assays, Antitumor | Uracil - analogs & derivatives | Cell culture | Phosphorylation | Dehydrogenases | Transcription | DNA damage | Serine | Colorectal carcinoma | Colorectal cancer | Cytotoxicity | AKT protein | Metastasis | Kinases | Cancer therapies | Metastases | Proteins | Cell growth | Colon cancer | Epidermal growth factor | Xenografts | Tumor necrosis factor-TNF | Growth factors | Protein-tyrosine kinase | Deoxyribonucleic acid--DNA | Tyrosine | Immunoglobulins | Threonine | Epidermal growth factor receptors | Stat3 protein | Extracellular signal-regulated kinase | Chemotherapy | Monoclonal antibodies | Ligands | Scientific imaging | Mutation | Frontotemporal dementia | Mass spectrometry
Journal Article
Journal Article
Journal Article
Journal Article
Tuberculosis, ISSN 1472-9792, 09/2018, Volume 112, pp. 98 - 109
The search for compounds with biological activity for many diseases is turning increasingly to drug repurposing. In this study, we have focused on the European... 
Antimalarial | Tuberculosis | Mycobacterium tuberculosis | Repurposing | Gyrase | Pyronaridine | Topoisomerase | RNA polymerase | NALIDIXIC-ACID | VITRO | SMALL MOLECULES | CONNECTIVITY MAP | MICROBIOLOGY | FUNCTIONAL-CHARACTERIZATION | DRUG-RESISTANCE | IMMUNOLOGY | DNA TOPOISOMERASE-I | KILL MYCOBACTERIUM-TUBERCULOSIS | EFFLUX PUMP | INHIBITION | RESPIRATORY SYSTEM | Antitubercular Agents - chemistry | DNA-Directed RNA Polymerases - antagonists & inhibitors | Humans | Bacterial Proteins - chemistry | Drug Resistance, Bacterial | Structure-Activity Relationship | Mycobacterium tuberculosis - drug effects | Microbial Sensitivity Tests | DNA-Directed RNA Polymerases - chemistry | Drug Therapy, Combination | Binding Sites | Bacterial Proteins - antagonists & inhibitors | Naphthyridines - chemistry | Antitubercular Agents - pharmacology | THP-1 Cells | Drug Repositioning | Antibiotics, Antitubercular - pharmacology | Antimalarials - pharmacology | Drug Synergism | Mycobacterium tuberculosis - enzymology | Antimalarials - chemistry | Protein Binding | Bacterial Proteins - metabolism | Protein Conformation | Molecular Docking Simulation | Rifampin - pharmacology | DNA-Directed RNA Polymerases - metabolism | Naphthyridines - pharmacology | Mycobacterium tuberculosis - growth & development | RNA | Drug approval | Rifampin | Analysis
Journal Article
mSphere, ISSN 2379-5042, 11/2016, Volume 1, Issue 6, p. e00191-16
The use of amphotericin B (AmB) in conjunction with 5-fluorocytosine (5-FC) is known to be the optimal therapy for treating cryptococcosis, but the mechanism... 
Amphotericin B | Pyrimidine biosynthesis | Cell wall integrity | PRACTICE GUIDELINES | MICROBIOLOGY | amphotericin B | COMBINATION | VIRULENCE | pyrimidine biosynthesis | MENINGITIS | IN-VITRO | FLUCYTOSINE | CANDIDA-ALBICANS | ANTIFUNGAL AGENTS | cell wall integrity | TIME-KILL | HUMAN DIHYDROOROTATE DEHYDROGENASE | Cell walls
Journal Article
Journal Article
Journal of Translational Medicine, ISSN 1479-5876, 04/2011, Volume 9, Issue 1, pp. 39 - 39
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 2008, Volume 372, Issue 1, pp. 266 - 271
Tolerance of human pathogenic fungi to antifungal drugs is an emerging medical problem. We show how strains of the causative agent of human aspergillosis,... 
Antifungal chemotherapy | Aspergillus fumigatus | MAPK | Chemosensitization | Combination therapy | Natural compounds | natural compounds | ACTIVATED PROTEIN-KINASE | MEMBRANE | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIFUNGAL ACTIVITY | CALCOFLUOR WHITE | chemosensitization | SACCHAROMYCES-CEREVISIAE | MUTANTS | CELL-WALL | BIOPHYSICS | PATHWAY | CHITIN | combination therapy | MODULATION | antifungal chemotherapy | Aspergillus fumigatus - drug effects | Fluconazole - pharmacology | Mitogen-Activated Protein Kinase Kinases - genetics | Oxidative Stress | Saccharomyces cerevisiae - genetics | Humans | Saccharomyces cerevisiae - drug effects | Ketoconazole - pharmacology | Catechols - isolation & purification | Microbial Sensitivity Tests | Cell Wall - drug effects | Benzaldehydes - isolation & purification | Gene Deletion | Catechols - pharmacology | Cell Membrane - drug effects | Antifungal Agents - pharmacology | Drug Resistance, Fungal - drug effects | Amphotericin B - pharmacology | Benzaldehydes - pharmacology | Thymol - isolation & purification | Drug Resistance, Fungal - genetics | Saccharomyces cerevisiae Proteins - genetics | Aspergillus fumigatus - genetics | Antifungal Agents - isolation & purification | Thymol - pharmacology | Aspergillosis - microbiology | Mitogen-Activated Protein Kinases - genetics | Sorbitol - pharmacology | Protein kinases | Antifungal agents
Journal Article