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1. Full Text WIF1 re-expression in glioblastoma inhibits migration through attenuation of non-canonical WNT signaling by downregulating the lncRNA MALAT1
by Vassallo, I and Zinn, P and Lai, M and Rajakannu, P and Hamou, M.-F and Hegi, M.E
Oncogene, ISSN 0950-9232, 01/2016, Volume 35, Issue 1, pp. 12 - 21
Biochemistry & Molecular Biology | Oncology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Humans | Brain Neoplasms - pathology | Gene Expression Regulation, Neoplastic | Wnt-5a Protein | Wnt Proteins - metabolism | Brain Neoplasms - metabolism | Cell Movement - physiology | Heterografts | Wnt Proteins - genetics | Glioblastoma - genetics | Glioblastoma - metabolism | Wnt Signaling Pathway | Proto-Oncogene Proteins - metabolism | Signal Transduction | Down-Regulation | Cell Proliferation - physiology | Brain Neoplasms - genetics | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | RNA, Long Noncoding - genetics | Animals | Repressor Proteins - biosynthesis | Mice, Nude | Glioblastoma - pathology | Adaptor Proteins, Signal Transducing - genetics | Cell Line, Tumor | Adaptor Proteins, Signal Transducing - biosynthesis | Mice | RNA, Long Noncoding - metabolism | Cellular proteins | Development and progression | Genetic aspects | Cellular signal transduction | Genetic regulation | Glioblastoma multiforme | Health aspects | Ribonucleic acid--RNA | Brain cancer | Cell adhesion & migration | Index Medicus
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2. Full Text In vitro propagation and characterization of neoplastic stem/progenitor-like cells from human prostate cancer tissue
by Guzman-Ramirez, N and Voller, M.C.W and Wetterwald, A and Germann, M and Cross, N.A and Rentsch, C.A and Schalken, J.A and Thalmann, G.N and Cecchini, M.G
The Prostate, ISSN 0270-4137, 2009, Volume 69, Issue 15, pp. 1683 - 1693
self‐renewal | PSCA | prostaspheres | cancer stem/progenitor‐like cells | CD49f | Cancer stem/progenitor-like cells | Self-renewal | Prostaspheres | Endocrinology & Metabolism | Life Sciences & Biomedicine | Urology & Nephrology | Science & Technology | 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
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3. Full Text Helios marks strongly autoreactive CD4+ T cells in two major waves of thymic deletion distinguished by induction of PD-1 or NF-κB
by Daley, Stephen R and Hu, Daniel Y and Goodnow, Christopher C
The Journal of experimental medicine, ISSN 0022-1007, 02/2013, Volume 210, Issue 2, pp. 269 - 285
Immunology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Autoimmunity | Cell Proliferation | NF-kappa B - immunology | Proto-Oncogene Proteins c-rel - metabolism | Proto-Oncogene Proteins - biosynthesis | Proto-Oncogene Proteins c-rel - immunology | CARD Signaling Adaptor Proteins - genetics | CD4-Positive T-Lymphocytes - immunology | Membrane Proteins - deficiency | CARD Signaling Adaptor Proteins - metabolism | Bcl-2-Like Protein 11 | Receptors, CCR7 - metabolism | Apoptosis Regulatory Proteins - deficiency | Programmed Cell Death 1 Receptor - biosynthesis | Proto-Oncogene Proteins - immunology | Apoptosis Regulatory Proteins - genetics | Transcription Factors - immunology | Apoptosis Regulatory Proteins - biosynthesis | CARD Signaling Adaptor Proteins - immunology | Apoptosis Regulatory Proteins - immunology | DNA-Binding Proteins - immunology | Lymphocyte Activation | Membrane Proteins - genetics | CD4-Positive T-Lymphocytes - cytology | Mice, Inbred C57BL | CD4-Positive T-Lymphocytes - metabolism | Self Tolerance | Membrane Proteins - immunology | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Transcription Factors - biosynthesis | Proto-Oncogene Proteins - deficiency | Clonal Deletion - immunology | Mice, Knockout | Membrane Proteins - biosynthesis | Animals | Apoptosis - immunology | Proto-Oncogene Proteins c-rel - genetics | NF-kappa B - biosynthesis | Mice | Mutation | Programmed Cell Death 1 Receptor - immunology | DNA-Binding Proteins - biosynthesis | Index Medicus | 309
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4. Full Text Down-regulation of micro-RNA-1 (miR-1) in lung cancer: Suppression of tumorigenic property of lung cancer cells and their sensitization to doxorubicin-induced apoptosis by miR-1
by Nasser, Mohd W and Datta, Jharna and Nuovo, Gerard and Kutay, Huban and Motiwala, Tasneem and Majumder, Sarmila and Wang, Bo and Suster, Saul and Jacob, Samson T and Ghoshal, Kalpana
The Journal of biological chemistry, ISSN 0021-9258, 11/2008, Volume 283, Issue 48, pp. 33394 - 33405
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Lung Neoplasms - drug therapy | Histone Deacetylases - biosynthesis | Antibiotics, Antineoplastic - pharmacology | Caspase 7 - biosynthesis | Apoptosis - drug effects | Humans | Lung Neoplasms - metabolism | Apoptosis - genetics | MicroRNAs - metabolism | Proto-Oncogene Proteins - biosynthesis | RNA, Neoplasm - metabolism | Receptors, Growth Factor - genetics | Caspase 3 - genetics | Caspase 3 - biosynthesis | Gene Expression Regulation, Neoplastic - drug effects | Gene Expression Regulation, Neoplastic - genetics | Lung Neoplasms - genetics | Forkhead Transcription Factors - biosynthesis | Histone Deacetylases - genetics | Caspase 7 - genetics | Cell Survival | Proto-Oncogene Proteins c-met | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | Poly(ADP-ribose) Polymerases - biosynthesis | Down-Regulation - drug effects | Forkhead Transcription Factors - genetics | Proto-Oncogene Proteins c-bcl-2 - biosynthesis | Down-Regulation - genetics | Animals | Poly(ADP-ribose) Polymerases - genetics | Repressor Proteins - biosynthesis | Mice, Nude | Myeloid Cell Leukemia Sequence 1 Protein | Receptors, Growth Factor - biosynthesis | Cell Line, Tumor | Proto-Oncogene Proteins c-pim-1 - genetics | RNA, Neoplasm - genetics | Mice | MicroRNAs - genetics | Poly (ADP-Ribose) Polymerase-1 | Proto-Oncogene Proteins c-bcl-2 - genetics | Proto-Oncogene Proteins c-pim-1 - biosynthesis | Doxorubicin - pharmacology | Cell Movement | Index Medicus | RNA-Mediated Regulation and Noncoding Rnas
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5. Full Text Reversible and adaptive resistance to BRAF(V600E) inhibition in melanoma
by Sun, Chong and Wang, Liqin and Huang, Sidong and Heynen, Guus J J E and Prahallad, Anirudh and Robert, Caroline and Haanen, John and Blank, Christian and Wesseling, Jelle and Willems, Stefan M and Zecchin, Davide and Hobor, Sebastijan and Bajpe, Prashanth K and Lieftink, Cor and Mateus, Christina and Vagner, Stephan and Grernrum, Wipawadee and Hofland, Ingrid and Schlicker, Aneas and Wessels, Lodewyk F A and Beijersbergen, Roderick L and Bardelli, Alberto and Di Nicolantonio, Federica and Eggermont, Alexander M M and Bernards, Rene
Nature (London), ISSN 0028-0836, 04/2014, Volume 508, Issue 7494, pp. 118 - 22
Antineoplastic Agents/administration & dosage | Transforming Growth Factor beta/metabolism | Humans | Mitogen-Activated Protein Kinase Kinases/antagonists & inhibitors | Indoles/administration & dosage | Flow Cytometry | Receptor, Platelet-Derived Growth Factor beta/biosynthesis | Proto-Oncogene Proteins B-raf/antagonists & inhibitors | ErbB Receptors/biosynthesis | Melanoma/drug therapy | Female | Cell Proliferation/drug effects | Sulfonamides/administration & dosage | Gene Library | Cellular Senescence/drug effects | Receptor Protein-Tyrosine Kinases/biosynthesis | Drug Resistance, Neoplasm/drug effects | Gene Expression Regulation, Neoplastic/drug effects | SOXE Transcription Factors/deficiency | Signal Transduction/drug effects | Protein Kinase Inhibitors/administration & dosage | Vemurafenib | Animals | Mice | RNA, Small Interfering | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Receptor, Epidermal Growth Factor - genetics | Receptor Protein-Tyrosine Kinases - biosynthesis | Cellular Senescence - drug effects | Melanoma - enzymology | Antineoplastic Agents - administration & dosage | Receptor, Platelet-Derived Growth Factor beta - genetics | Indoles - administration & dosage | Mitogen-Activated Protein Kinase Kinases - metabolism | Receptor, Epidermal Growth Factor - metabolism | Melanoma - genetics | Indoles - pharmacology | Antineoplastic Agents - pharmacology | Gene Expression Regulation, Neoplastic - drug effects | SOXE Transcription Factors - deficiency | Proto-Oncogene Proteins B-raf - metabolism | Receptor, Platelet-Derived Growth Factor beta - metabolism | Receptor, Epidermal Growth Factor - biosynthesis | Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors | Melanoma - pathology | Receptor Protein-Tyrosine Kinases - metabolism | Sulfonamides - pharmacology | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Protein Kinase Inhibitors - administration & dosage | Transforming Growth Factor beta - pharmacology | Drug Resistance, Neoplasm - genetics | Receptor Protein-Tyrosine Kinases - genetics | Signal Transduction - drug effects | Proto-Oncogene Proteins B-raf - genetics | Melanoma - drug therapy | Cell Proliferation - drug effects | Protein Kinase Inhibitors - pharmacology | Transforming Growth Factor beta - metabolism | Receptor, Platelet-Derived Growth Factor beta - biosynthesis | Sulfonamides - administration & dosage | Drug Resistance, Neoplasm - drug effects | SOXE Transcription Factors - genetics | Proteins | Biopsy | Rodents | Genes | Melanoma | Mutation | Kinases | Drug resistance | Patients | Tumors | Index Medicus
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6. Full Text Akt3-mediated resistance to apoptosis in B-RAF-targeted melanoma cells
by Shao, Yongping and Aplin, Andrew E
Cancer research (Chicago, Ill.), ISSN 0008-5472, 08/2010, Volume 70, Issue 16, pp. 6670 - 6681
Life Sciences & Biomedicine | Oncology | Science & Technology | Tumors of the skin and soft tissue. Premalignant lesions | Dermatology | Pharmacology. Drug treatments | Biological and medical sciences | Medical sciences | Antineoplastic agents | Tumors | Humans | Proto-Oncogene Proteins - biosynthesis | Proto-Oncogene Proteins c-akt - genetics | Bcl-2-Like Protein 11 | Melanoma - genetics | Apoptosis Regulatory Proteins - genetics | Indoles - pharmacology | Proto-Oncogene Proteins c-akt - metabolism | Proto-Oncogene Proteins B-raf - metabolism | Apoptosis Regulatory Proteins - biosynthesis | Melanoma - metabolism | Proto-Oncogene Proteins B-raf - deficiency | Membrane Proteins - genetics | Proto-Oncogene Proteins - genetics | Melanoma - pathology | Sulfonamides - pharmacology | Proto-Oncogene Proteins c-bcl-2 - biosynthesis | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Proto-Oncogene Proteins c-akt - biosynthesis | Up-Regulation - drug effects | Membrane Proteins - biosynthesis | Proto-Oncogene Proteins B-raf - genetics | Myeloid Cell Leukemia Sequence 1 Protein | Adaptor Proteins, Signal Transducing - genetics | Cell Line, Tumor | Adaptor Proteins, Signal Transducing - biosynthesis | Apoptosis - physiology | Index Medicus | Mcl-1 | Anoikis | apoptosis | Bmf | B-RAF | Bim-EL
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7. Full Text MDM4 is a key therapeutic target in cutaneous melanoma
by Gembarska, Agnieszka and Luciani, Flavie and Fedele, Clare and Russell, Elisabeth A and Dewaele, Michael and Villar, Stéphanie and Zwolinska, Aleksana and Haupt, Sue and de Lange, Job and Yip, Dana and Goydos, James and Haigh, Jody J and Haupt, Ygal and Larue, Lionel and Jochemsen, Aart and Shi, Hubing and Moriceau, Gatien and Lo, Roger S and Ghanem, Ghanem and Shackleton, Mark and Bernal, Federico and Marine, Jean-Christophe
Nature medicine, ISSN 1078-8956, 2012, Volume 18, Issue 8, pp. 1239 - 1247
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Up-Regulation | Proto-Oncogene Proteins c-mdm2 - genetics | Tumor Suppressor Protein p53 - antagonists & inhibitors | Apoptosis - drug effects | Humans | Neoplasm Proteins - physiology | Gene Expression Regulation, Neoplastic | Recombinant Fusion Proteins - physiology | Skin Neoplasms - chemistry | Male | Melanocytes - metabolism | Neoplasm Proteins - antagonists & inhibitors | Cell Line, Tumor - transplantation | Proto-Oncogene Proteins - biosynthesis | Tumor Suppressor Protein p53 - physiology | Cell-Penetrating Peptides - pharmacology | Nuclear Proteins - biosynthesis | Female | Antineoplastic Agents - pharmacology | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Cell Line, Tumor - metabolism | Melanoma - chemistry | Proto-Oncogene Proteins c-mdm2 - biosynthesis | Proto-Oncogene Proteins - antagonists & inhibitors | Tumor Stem Cell Assay | Membrane Proteins - genetics | Neoplasm Proteins - biosynthesis | Melanoma, Experimental - etiology | Mice, Inbred C57BL | Mice, Transgenic | Proto-Oncogene Proteins - genetics | Melanoma - pathology | Melanoma - secondary | Proto-Oncogene Proteins B-raf - antagonists & inhibitors | Xenograft Model Antitumor Assays | Animals | Melanoma, Experimental - genetics | GTP Phosphohydrolases - genetics | Keratinocytes - metabolism | Mice, Nude | Nuclear Proteins - antagonists & inhibitors | Proto-Oncogene Proteins - physiology | Signal Transduction - physiology | Mice | Nuclear Proteins - physiology | Drug Resistance, Neoplasm - physiology | Drug Resistance, Neoplasm - drug effects | Care and treatment | Gene mutations | Melanoma | Diagnosis | Research | Gene expression | Identification and classification | Skin cancer | Proteins | Cell growth | Mutation | Cell cycle | Index Medicus
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8. Full Text Acquisition of epithelial-mesenchymal transition phenotype of gemcitabine-resistant pancreatic cancer cells is linked with activation of the notch signaling pathway
by Wang, Zhiwei and Li, Yiwei and Kong, Dejuan and Banerjee, Sanjeev and Ahmad, Aamir and Azmi, Asfar Sohail and Ali, Shadan and Abbruzzese, James L and Gallick, Gary E and Sarkarr, Fazlul H
Cancer research (Chicago, Ill.), ISSN 0008-5472, 03/2009, Volume 69, Issue 6, pp. 2400 - 2407
Life Sciences & Biomedicine | Oncology | Science & Technology | Gastroenterology. Liver. Pancreas. Abdomen | Liver. Biliary tract. Portal circulation. Exocrine pancreas | Pharmacology. Drug treatments | Biological and medical sciences | Medical sciences | Antineoplastic agents | Tumors | RNA, Small Interfering - genetics | Pancreatic Neoplasms - metabolism | Receptors, Notch - metabolism | Humans | Deoxycytidine - pharmacology | Drug Resistance, Neoplasm | Intercellular Signaling Peptides and Proteins - biosynthesis | NF-kappa B - metabolism | Receptor, Notch2 - genetics | Receptors, Notch - genetics | Proto-Oncogene Proteins - biosynthesis | Cell Movement - physiology | Pancreatic Neoplasms - drug therapy | Intercellular Signaling Peptides and Proteins - metabolism | Transfection | Receptors, Notch - biosynthesis | Serrate-Jagged Proteins | Antimetabolites, Antineoplastic - pharmacology | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Proto-Oncogene Proteins - metabolism | Calcium-Binding Proteins - biosynthesis | Signal Transduction | Membrane Proteins - genetics | Down-Regulation | Pancreatic Neoplasms - pathology | Intercellular Signaling Peptides and Proteins - genetics | Receptor, Notch2 - metabolism | Epithelial Cells - pathology | Pancreatic Neoplasms - genetics | Proto-Oncogene Proteins - genetics | Membrane Proteins - biosynthesis | Phenotype | Receptor, Notch2 - biosynthesis | Mesoderm - pathology | RNA, Messenger | Deoxycytidine - analogs & derivatives | Receptor, Notch4 | Calcium-Binding Proteins - genetics | Index Medicus
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9. Full Text The Bmi-1 polycomb protein antagonizes the (-)-epigallocatechin-3-gallate-dependent suppression of skin cancer cell survival
by Balasubramanian, Sivaprakasam and Adhikary, Gautam and Eckert, Richard L
Carcinogenesis (New York), ISSN 0143-3334, 03/2010, Volume 31, Issue 3, pp. 496 - 503
Life Sciences & Biomedicine | Oncology | Science & Technology | Tumors of the skin and soft tissue. Premalignant lesions | Biological and medical sciences | Carcinogenesis, carcinogens and anticarcinogens | Medical sciences | Dermatology | Tumors | Apoptosis - drug effects | DNA Replication - drug effects | Carcinoma, Squamous Cell - pathology | Cell Count | Humans | Neoplasm Proteins - physiology | Recombinant Fusion Proteins - physiology | Anticarcinogenic Agents - antagonists & inhibitors | Culture Media, Serum-Free | Cell Line, Tumor - drug effects | Cell Line, Transformed - drug effects | Proto-Oncogene Proteins - biosynthesis | Gene Knockdown Techniques | Repressor Proteins - physiology | Nuclear Proteins - biosynthesis | Cell Cycle Proteins - genetics | Epigenesis, Genetic - drug effects | Catechin - pharmacology | Neoplasm Proteins - genetics | Nuclear Proteins - genetics | Anticarcinogenic Agents - pharmacology | Cell Line, Transformed - cytology | Skin Neoplasms - pathology | DNA-Binding Proteins - physiology | Transcription Factors - physiology | Neoplasm Proteins - biosynthesis | Catechin - antagonists & inhibitors | Repressor Proteins - genetics | Proto-Oncogene Proteins - genetics | Transcription Factors - biosynthesis | Cell Cycle Proteins - biosynthesis | Keratinocytes - cytology | Polycomb-Group Proteins | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Enhancer of Zeste Homolog 2 Protein | Polycomb Repressive Complex 2 | Polycomb Repressive Complex 1 | Repressor Proteins - biosynthesis | Genetic Vectors - pharmacology | Keratinocytes - drug effects | Cell Line, Tumor - cytology | Proto-Oncogene Proteins - physiology | Catechin - analogs & derivatives | Nuclear Proteins - physiology | Cell Cycle Proteins - physiology | DNA-Binding Proteins - biosynthesis | Index Medicus | Cancer Prevention
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