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Journal of Experimental Medicine, ISSN 0022-1007, 12/2006, Volume 203, Issue 13, pp. 2895 - 2906
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 11/2016, Volume 20, Issue 11, pp. 2064 - 2077
Journal Article
European Journal of Cancer, ISSN 0959-8049, 2013, Volume 49, Issue 13, pp. 2934 - 2948
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, pp. e57020 - e57020
Lung cancer (LC) with its different subtypes is generally known as a therapy resistant cancer with the highest morbidity rate worldwide. Therapy resistance of... 
EPITHELIAL-MESENCHYMAL TRANSITION | TRANSFORMATION | THERAPY | MULTIDISCIPLINARY SCIENCES | PANCREATIC-CANCER | GROWTH | HMGA2 | MICE | CARCINOMA | PROGRESSION | TUMOR-INITIATING CELLS | Adenocarcinoma - pathology | Adenocarcinoma of Lung | Cadherins - metabolism | Vimentin - metabolism | Carcinoma, Large Cell - pathology | Carcinoma, Squamous Cell - genetics | Carcinoma, Squamous Cell - metabolism | Carcinoma, Squamous Cell - pathology | Homeodomain Proteins - metabolism | Humans | Lung Neoplasms - metabolism | Gene Expression Regulation, Neoplastic | Lung Neoplasms - pathology | Antigens, CD - genetics | Antigens, CD - metabolism | Octamer Transcription Factor-3 - genetics | Small Cell Lung Carcinoma - metabolism | Adenocarcinoma - metabolism | Neoplastic Stem Cells - metabolism | Vimentin - genetics | Thy-1 Antigens - genetics | Hyaluronan Receptors - metabolism | Biomarkers, Tumor - metabolism | Neoplastic Stem Cells - pathology | Adenocarcinoma - genetics | Carcinoma, Large Cell - genetics | Cadherins - genetics | Lung Neoplasms - genetics | Carcinoma, Large Cell - metabolism | Nanog Homeobox Protein | Immunophenotyping | Small Cell Lung Carcinoma - genetics | Mice, SCID | Hyaluronan Receptors - genetics | Homeodomain Proteins - genetics | Thy-1 Antigens - metabolism | Small Cell Lung Carcinoma - pathology | Animals | Octamer Transcription Factor-3 - metabolism | Mice, Inbred NOD | Biomarkers, Tumor - genetics | Mice | Primary Cell Culture | Care and treatment | Analysis | Stem cells | Cancer cells | Physiological aspects | Research | Cancer | Adenocarcinoma | Vimentin | Cell culture | Therapy | Biotechnology | Thoracic surgery | Mesenchyme | Oct-4 protein | Lung | Lung cancer | Radiation | Population studies | Identification | Biology | mRNA | Metastasis | Cancer therapies | CD90 antigen | N-Cadherin | Immunology | CD44 antigen | Population | Medical research | Squamous cell carcinoma | Hematology | Cell division | Tumor cell lines | Gene expression | Cadherin | Spheroids | Morbidity | Medicine | Pathology | Medical prognosis | Pancreatic cancer | Cell lines | Irradiation | Prostate | Tumors | Index Medicus
Journal Article
Journal of Cell Science, ISSN 0021-9533, 03/2005, Volume 118, Issue 6, pp. 1267 - 1277
Nectins are Ca2+-independent immunoglobulin-like cell-cell adhesion molecules and comprise a family of four members. At the mossy fiber terminals of... 
Axon | Necl-1 | Glia | Myelin | Nectin | Schwann cell | myelin | TUMOR-SUPPRESSOR TSLC1 | ADHERENS JUNCTION | LOCALIZATION | PROTEIN | DEVELOPING MOUSE | AFADIN | glia | CELL BIOLOGY | LUNG-CANCER | EPITHELIAL-CELLS | GENE | axon | nectin | HUMAN HOMOLOG | Immunohistochemistry | Immunoglobulins - physiology | Cadherins - metabolism | Calcium - metabolism | Humans | Calcium - chemistry | Brain - metabolism | Immunoglobulins - metabolism | Tissue Distribution | Cell Adhesion Molecule-1 | Time Factors | Membrane Proteins - physiology | Antigens, Neoplasm - metabolism | Neurons - metabolism | Dimerization | Silver Staining | Schwann Cells - metabolism | Cell Adhesion | Cell Adhesion Molecules - metabolism | Plasmids - metabolism | Blotting, Western | Guanylate Kinases | Mice | Nucleoside-Phosphate Kinase - metabolism | Immunoprecipitation | Exons | Actins - metabolism | Cytoplasm - metabolism | Neoplasm Proteins - metabolism | Microscopy, Immunoelectron | Myelin Sheath - metabolism | Membrane Proteins - metabolism | Protein Structure, Tertiary | Cell Line | Gene Library | Cerebellum - metabolism | Electrophoresis, Polyacrylamide Gel | Axons - metabolism | Cell Communication | Nuclear Proteins - metabolism | Transcription Factors - metabolism | Hippocampus - metabolism | Two-Hybrid System Techniques | Animals | Presynaptic Terminals - metabolism | Protein Binding | Neuroglia - metabolism | Calcium-Calmodulin-Dependent Protein Kinases - metabolism | Microscopy, Fluorescence | Tumor Suppressor Proteins | Index Medicus
Journal Article
RNA, ISSN 1355-8382, 2012, Volume 18, Issue 7, pp. 1373 - 1384
The recruitment of ribosomes to eukaryotic cellular mRNAs requires the activity of two prototypic RNA helicases, eukaryotic initiation factor (eIF) 4AI and... 
Translation | eIF4AI | eIF4AII | DEAD-box RNA helicase | Hippuristanol | Translational control | RNA helicase | MAMMALIAN TRANSLATION | FACTOR EIF-4A | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | CROSS-LINKING | translational control | 5' END | EUKARYOTIC TRANSLATION INITIATION | MESSENGER-RNA | translation | hippuristanol | DEGRADATION | INHIBITS TRANSLATION | RNA HELICASE EIF4A | Transcription, Genetic - drug effects | Testis - metabolism | Humans | Fetus - metabolism | Male | Muscle, Skeletal - metabolism | Spleen - drug effects | Prostate - metabolism | Testis - drug effects | Brain - metabolism | Kidney - metabolism | Protein Isoforms - metabolism | Liver - drug effects | Muscle, Skeletal - drug effects | Myocardium - metabolism | Prostate - drug effects | Adult | Female | Ovary - drug effects | Lung - metabolism | Thymus Gland - metabolism | Ovary - metabolism | Sterols - pharmacology | Cell Line | Kidney - drug effects | Liver - metabolism | Pancreas - drug effects | Pancreas - metabolism | Thymus Gland - drug effects | Eukaryotic Initiation Factor-4A - antagonists & inhibitors | Brain - drug effects | Fetus - drug effects | Placenta - drug effects | Placenta - metabolism | Pregnancy | Transcription, Genetic - physiology | Spleen - metabolism | Lung - drug effects | Eukaryotic Initiation Factor-4A - metabolism | Index Medicus
Journal Article
Nature Cell Biology, ISSN 1465-7392, 08/2017, Volume 19, Issue 8, pp. 904 - 914
After influenza infection, lineage-negative epithelial progenitors (LNEPs) exhibit a binary response to reconstitute epithelial barriers: activating a... 
PROGENITOR CELLS | BREAST-CANCER | INDUCIBLE FACTOR-1-ALPHA | AIRWAY STEM-CELLS | ADULT LUNG | IN-VIVO | NOTCH | MICE | BETA-CATENIN | PULMONARY-FIBROSIS | CELL BIOLOGY | Cell Proliferation | Influenza, Human - pathology | Receptors, Notch - metabolism | Humans | Male | Gene Expression Profiling | Orthomyxoviridae Infections - genetics | SOXB1 Transcription Factors - metabolism | SOXB1 Transcription Factors - genetics | Time Factors | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Cell Transdifferentiation | Influenza, Human - virology | Single-Cell Analysis | Wnt Signaling Pathway | Disease Models, Animal | Hypoxia - virology | Tumor Suppressor Proteins - metabolism | Pulmonary Alveoli - pathology | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Orthomyxoviridae Infections - pathology | Epithelial Cells - pathology | Genotype | Mice, Transgenic | Cell Lineage | Phenotype | Hypoxia - pathology | Epithelial Cells - virology | Orthomyxoviridae Infections - virology | Cell Movement | Epithelial Cells - metabolism | Phosphoproteins - metabolism | Oxygen - metabolism | Hypoxia - metabolism | Pulmonary Alveoli - metabolism | Tumor Suppressor Proteins - genetics | Trans-Activators - genetics | Female | Influenza, Human - metabolism | Orthomyxoviridae Infections - metabolism | Cells, Cultured | Influenza A Virus, H1N1 Subtype - pathogenicity | Keratin-5 - genetics | Phosphoproteins - genetics | Transcription Factors - genetics | Transcription Factors - metabolism | Regeneration | Hypoxia - genetics | Animals | Influenza, Human - genetics | Keratin-5 - metabolism | Pulmonary Alveoli - virology | Trans-Activators - metabolism | Hypoxia-inducible factors | Cytokeratin | Respiratory function | Wnt protein | Transcription | Lung | Migration | Protein C | Surfactant protein C | Metaplasia | β-catenin | Signal transduction | Signaling | Clonal deletion | Lungs | Influenza | Fibrosis | Deletion | Hypoxia | Notch protein | Alveoli | Differentiation | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2003, Volume 278, Issue 44, pp. 42906 - 42912
Journal Article
Cell Metabolism, ISSN 1550-4131, 01/2015, Volume 21, Issue 1, pp. 81 - 94
Journal Article
Nature, ISSN 0028-0836, 05/2016, Volume 533, Issue 7604, pp. 493 - 498
Brain metastasis represents a substantial source of morbidity and mortality in various cancers, and is characterized by high resistance to chemotherapy. Here... 
CADHERIN SUPERFAMILY | LUNG | EXPRESSION ANALYSIS | CONNEXIN | BREAST-CANCER METASTASIS | MULTIDISCIPLINARY SCIENCES | GENES | CYTOSOLIC DNA | CLASSIFICATION | TUMOR-CELLS | RAT-BRAIN | Meclofenamic Acid - pharmacology | Meclofenamic Acid - therapeutic use | Nucleotides, Cyclic - metabolism | Gap Junctions - metabolism | Benzopyrans - therapeutic use | Cadherins - metabolism | Coculture Techniques | Humans | Brain Neoplasms - pathology | Drug Resistance, Neoplasm | Lung Neoplasms - pathology | NF-kappa B - metabolism | Brain Neoplasms - metabolism | Brain Neoplasms - secondary | STAT1 Transcription Factor - metabolism | Benzamides - therapeutic use | Female | Benzamides - pharmacology | Membrane Proteins - metabolism | Benzopyrans - pharmacology | Astrocytes - cytology | Astrocytes - drug effects | Interferon-alpha - metabolism | Connexin 43 - metabolism | Tumor Necrosis Factors - metabolism | Brain Neoplasms - drug therapy | Immunity, Innate | Xenograft Model Antitumor Assays | Animals | Breast Neoplasms - pathology | Paracrine Communication - drug effects | Cell Line, Tumor | Mice | Gap Junctions - drug effects | Astrocytes - metabolism | Astrocytes | Brain cancer | Physiological aspects | Metastasis | Observations | Adenylic acid | Health aspects | Proteins | Brain | Cytokines | Cells | Tumors | Cancer | Index Medicus
Journal Article
Molecular Carcinogenesis, ISSN 0899-1987, 10/2018, Volume 57, Issue 10, pp. 1342 - 1357
Ewing sarcoma (EWS) is a soft tissue and bone tumor that occurs primarily in adolescents and young adults. In most cases of EWS, the chimeric transcription... 
de novo serine‐glycine biosynthesis | Ewing sarcoma | metabolism | glutamine | ROS | de novo serine-glycine biosynthesis | BIOCHEMISTRY & MOLECULAR BIOLOGY | MULTICELLULAR TUMOR SPHEROIDS | PROLIFERATION | BREAST-CANCER | LUNG-CANCER | AMINO-ACID | ONCOLOGY | PROSTATE-CANCER | GROWTH | TRANSCRIPTIONAL TARGET | EXPRESSION | ONE-CARBON METABOLISM | Multifunctional Enzymes - genetics | Oncogene Proteins, Fusion - metabolism | Humans | Gene Expression Regulation, Neoplastic | Sarcoma, Ewing - pathology | Cell Survival - genetics | Glutamine - metabolism | Multienzyme Complexes - metabolism | Apoptosis - genetics | Serine - biosynthesis | Aminohydrolases - genetics | Multifunctional Enzymes - metabolism | Bone Neoplasms - pathology | Bone Neoplasms - metabolism | Proto-Oncogene Protein c-fli-1 - metabolism | HEK293 Cells | Minor Histocompatibility Antigens - genetics | Bone Neoplasms - genetics | Amino Acid Transport System ASC - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - metabolism | Sarcoma, Ewing - metabolism | Phosphoglycerate Dehydrogenase - metabolism | Proto-Oncogene Protein c-fli-1 - genetics | HCT116 Cells | RNA-Binding Protein EWS - genetics | Glycine - biosynthesis | Amino Acid Transport System ASC - metabolism | Multienzyme Complexes - genetics | RNA-Binding Protein EWS - metabolism | Phosphoglycerate Dehydrogenase - genetics | Formate-Tetrahydrofolate Ligase - metabolism | Minor Histocompatibility Antigens - metabolism | Oncogene Proteins, Fusion - genetics | Cell Line, Tumor | Formate-Tetrahydrofolate Ligase - genetics | Aminohydrolases - metabolism | Sarcoma, Ewing - genetics | Glucose metabolism | International trade | Enzymes | Sarcoma | Analysis | Amino acids | Carbon cycle (Biogeochemistry) | Adolescence | Reactive oxygen species | Serine | DNA damage | Biosynthesis | Bone tumors | Glycine | Ewing's sarcoma | Proteins | Transcription activation | Adolescents | Redox properties | Damage accumulation | Deoxyribonucleic acid--DNA | Cell survival | Young adults | Risk groups | Metabolism | Nutrient uptake | Gene expression | Survival | Carbon cycle | Gene silencing | Adults | Transporter | Tumors | Apoptosis | Glutamine | Index Medicus
Journal Article