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Journal Article
EMBO Molecular Medicine, ISSN 1757-4676, 10/2014, Volume 6, Issue 10, pp. 1279 - 1293
Epithelial‐mesenchymal transition ( EMT ) is a reversible and dynamic process hypothesized to be co‐opted by carcinoma during invasion and metastasis. Yet,... 
drug response | microarray | gene expression signature | epithelial‐mesenchymal transition | prognosis | Drug response | Epithelial-mesenchymal transition | Prognosis | Microarray | Gene expression signature | MOLECULAR SUBTYPES | MEDICINE, RESEARCH & EXPERIMENTAL | GENE-EXPRESSION SIGNATURE | STEM-CELLS | GENOMIC ANALYSES | OVARIAN-CANCER | NEGATIVE BREAST-CANCER | CLINICAL-RELEVANCE | MICRORNA CONTROL | CLAUDIN-LOW | epithelial-mesenchymal transition | SIGNATURE PREDICTS RESISTANCE | Lung Neoplasms - drug therapy | Oligonucleotide Array Sequence Analysis | Colorectal Neoplasms - genetics | Humans | Epithelial-Mesenchymal Transition - drug effects | Antineoplastic Agents - therapeutic use | Epithelial-Mesenchymal Transition - genetics | Ovarian Neoplasms - genetics | Urinary Bladder Neoplasms - genetics | Neoplasms - genetics | Colorectal Neoplasms - drug therapy | Female | Gene Expression Regulation, Neoplastic - drug effects | Ovarian Neoplasms - drug therapy | Lung Neoplasms - genetics | Stomach Neoplasms - genetics | Treatment Outcome | Transcriptome - drug effects | Transcriptome - genetics | Stomach Neoplasms - drug therapy | Urinary Bladder Neoplasms - drug therapy | Breast Neoplasms - drug therapy | Neoplasms - drug therapy | Disease-Free Survival | Breast Neoplasms - genetics | Cell Line, Tumor | Cancer patients | Chemotherapy | Patient outcomes | Stem cells | Development and progression | Drug therapy | Gene expression | Ovarian cancer | Cancer | Medical research | Breast cancer | Tumors | Mesenchyme | Colorectal carcinoma | Genomes | Metastasis | Kinases | Cancer therapies | Metastases | Breast carcinoma | Genotype & phenotype | Cell lines | Paclitaxel | Breast | Software | Index Medicus
Journal Article
Science, ISSN 0036-8075, 12/2008, Volume 322, Issue 5908, pp. 1695 - 1699
Enhancer of zeste homolog 2 (EZH2) is a mammalian histone methyltransferase that contributes to the epigenetic silencing of target genes and regulates the... 
Cell growth | MicroRNA | Epithelial cells | Genomics | Stem cells | Cell lines | Small interfering RNA | Reports | Prostate cancer | Cancer | Tumors | MOUSE DEVELOPMENT | DEVELOPMENTAL REGULATORS | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | IN-VIVO | H3 LYSINE-27 METHYLATION | ZESTE HOMOLOG-2 | ENHANCER | TARGETS | POLYCOMB | EXPRESSION | Neoplasms - metabolism | Prostatic Neoplasms - metabolism | RNA, Small Interfering - genetics | Epigenesis, Genetic | Humans | Gene Expression Regulation, Neoplastic | Stomach Neoplasms - metabolism | Male | MicroRNAs - metabolism | Breast Neoplasms - metabolism | DNA-Binding Proteins - metabolism | Neoplasm Metastasis | Prostatic Neoplasms - genetics | Neoplasms - genetics | Female | Lysine - metabolism | 3' Untranslated Regions | Stomach Neoplasms - genetics | Promoter Regions, Genetic | Prostatic Neoplasms - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Disease Progression | Enhancer of Zeste Homolog 2 Protein | Transcription Factors - metabolism | Polycomb Repressive Complex 2 | Algorithms | Breast Neoplasms - genetics | Cell Line, Tumor | MicroRNAs - genetics | Histones - metabolism | Genome, Human | Methylation | Methyltransferases | RNA | Physiological aspects | Genetic aspects | Research | Health aspects | Oncology | Gene expression | Ribonucleic acid--RNA | Index Medicus
Journal Article
Carcinogenesis, ISSN 0143-3334, 12/2014, Volume 35, Issue 12, pp. 2731 - 2739
Journal Article
Journal of Clinical Oncology, ISSN 0732-183X, 02/2016, Volume 34, Issue 5, pp. 443 - 451
Journal Article
Scientific Reports, ISSN 2045-2322, 08/2014, Volume 4, Issue 1, pp. 6088 - 6088
Some long noncoding RNAs (lncRNAs) play important roles in the regulation of gene expression by acting as competing endogenous RNAs (ceRNAs). However, the... 
MESSENGER-RNAS | DATABASE | GENE | ANNOTATION | MULTIDISCIPLINARY SCIENCES | IN-VIVO | MICRORNA TARGETS | CERNA HYPOTHESIS | NETWORKS | IDENTIFICATION | EXPRESSION | Oligonucleotide Array Sequence Analysis | Carcinoma, Squamous Cell - genetics | Humans | Male | Gene Expression Profiling | Leukemia, Lymphocytic, Chronic, B-Cell - genetics | Ovarian Neoplasms - genetics | Retinoblastoma Protein - biosynthesis | Squamous Cell Carcinoma of Head and Neck | Prostatic Neoplasms - genetics | RNA Interference | Cell Transformation, Neoplastic - genetics | Female | Gene Expression Regulation, Neoplastic - genetics | Stomach Neoplasms - genetics | Pituitary Neoplasms - genetics | RNA, Long Noncoding - genetics | Thyroid Cancer, Papillary | Thyroid Neoplasms - genetics | Algorithms | Carcinoma, Papillary | Retinoblastoma Protein - genetics | Cell Line, Tumor | Carcinoma - genetics | Head and Neck Neoplasms - genetics | MicroRNAs - genetics | RNA, Small Interfering | Post-transcription | Transcription | Gene regulation | Regulatory sequences | Stomach cancer | Ovarian cancer | Neck | Gastric cancer | Thyroid | Squamous cell carcinoma | Chronic lymphatic leukemia | MiRNA | Pituitary (anterior) | Runx1 protein | siRNA | Lymphatic leukemia | Gene expression | DNA microarrays | Pituitary | Interleukin 10 | Head and neck cancer | Prostate | Prostate cancer | PTEN protein | Papillary thyroid carcinoma | Tumors | Index Medicus
Journal Article
Annals of Surgical Oncology, ISSN 1068-9265, 12/2015, Volume 22, Issue S3, pp. 915 - 922
A recent study reported that long non-coding RNA activated by TGF-β (lncRNA-ATB) induced epithelial–mesenchymal transition (EMT) through the transforming... 
Oncology | Medicine & Public Health | Surgical Oncology | Surgery | SURGERY | INVASION | NETWORK | METASTASIS | ZEB1 | ONCOLOGY | CELL-PROLIFERATION | EPITHELIAL-MESENCHYMAL TRANSITIONS | MIR-200 FAMILY | PROMOTES | EXPRESSION | CARCINOMA | Cell Proliferation | Prognosis | Follow-Up Studies | Carcinoma, Signet Ring Cell - metabolism | Homeodomain Proteins - metabolism | Humans | Stomach Neoplasms - metabolism | Male | Stomach Neoplasms - pathology | Carcinoma, Signet Ring Cell - genetics | Immunoenzyme Techniques | Adenocarcinoma - metabolism | Biomarkers, Tumor - metabolism | Female | Adenocarcinoma - genetics | Tumor Cells, Cultured | Liver Neoplasms - secondary | Real-Time Polymerase Chain Reaction | Peritoneal Neoplasms - secondary | Stomach Neoplasms - genetics | Liver Neoplasms - genetics | Neoplasm Invasiveness | RNA, Messenger - genetics | Survival Rate | Adenocarcinoma, Mucinous - secondary | Lymphatic Metastasis | RNA, Long Noncoding - genetics | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Adenocarcinoma - secondary | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Transforming Growth Factor beta - genetics | Carcinoma, Signet Ring Cell - secondary | Peritoneal Neoplasms - genetics | Peritoneal Neoplasms - metabolism | Adenocarcinoma, Mucinous - metabolism | Liver Neoplasms - metabolism | Aged | Biomarkers, Tumor - genetics | MicroRNAs - genetics | Adenocarcinoma, Mucinous - genetics | Neoplasm Staging | Transforming Growth Factor beta - metabolism | Apoptosis | Zinc Finger E-box-Binding Homeobox 1 | Index Medicus
Journal Article
by Kim, Jihun and Bowlby, Reanne and Mungall, Andrew J and Robertson, A. Gordon and Odze, Robert D and Cherniack, Andrew D and Shih, Juliann and Pedamallu, Chandra Sekhar and Cibulskis, Carrie and Dunford, Andrew and Meier, Samuel R and Kim, Jaegil and Raphael, J and Wu, Hsin-Ta and Wong, Alexandra M and Willis, Joseph E and Bass, Adam J and Derks, Sarah and Garman, Katherine and McCall, Shannon J and Wiznerowicz, MacIej and Pantazi, Angeliki and Parfenov, Michael and Thorsson, Vésteinn and Shmulevich, Ilya and Dhankani, Varsha and Miller, Michael and Sakai, Ku Leuven Ryo and Wang, Kenneth and Schultz, Nikolaus and Shen, Ronglai and Arora, Arshi and Weinhold, Nils and Sánchez-Vega, Francisco and Kelsen, David P and Zhang, Julia and Felau, Ina and Demchok, John and Rabkin, Charles S and Camargo, M. Constanza and Zenklusen, Jean Claude and Bowen, Jay and Leraas, Kristen and Lichtenberg, Tara M and Curtis, Christina and Seoane, Jose A and Ojesina, Akinyemi I and Beer, David G and Gulley, Margaret L and Pennathur, Arjun and Luketich, James D and Zhou, Zhongren and Weisenberger, Daniel J and Akbani, Rehan and Lee, Ju-Seog and Liu, Wenbin and Mills, Gordon B and Zhang, Wei and Reid, Brian J and Hinoue, Toshinori and Laird, Peter W and Shen, Hui and Piazuelo, M. Blanca and Schneider, Barbara G and McLellan, Michael and Taylor-Weiner, Amaro and Lawrence, Michael and Cibulskis, Kristian and Stewart, Chip and Getz, Gad and Lander, Eric and Gabriel, Stacey B and DIng, Li and McLellan, Michael D and Miller, Christopher A and Appelbaum, Elizabeth L and Cordes, Matthew G and Fronick, Catrina C and Fulton, Lucinda A and Mardis, Elaine R and Wilson, Richard K and Schmidt, Heather K and Fulton, Robert S and Ally, Adrian and Balasundaram, Miruna and Carlsen, Rebecca and Chuah, Eric and Dhalla, Noreen and Holt, Robert A and Jones, Steven J. M and Kasaian, Katayoon and Brooks, Denise and Li, Haiyan I and Ma, Yussanne and Marra, Marco A and Mayo, Michael and Moore, Richard A and Mungall, Karen L and Schein, Jacqueline E and Sipahimalani, Payal and ... and Canc Genome Atlas Res Network and Data Coordination Center: CSRA Inc and Duke University and Ribeirão Preto Medical School and Israelitisches Krankenhaus Hamburg and Project Team: National Institutes of Health and Tissue Source Sites: Analytic Biologic Services and Nationwide Children’s Hospital and Greater Poland Cancer Centre and Brown University and University of Michigan and Mayo Clinic and Broad Institute and Keimyung University School of Medicine and Asan Medical Center and Barretos Cancer Hospital and University of Alabama and Indiana University School of Medicine and Invidumed and National Cancer Center Goyang and Yonsei University College of Medicine and Vanderbilt University and University of North Carolina at Chapel Hill and Cureline and Cancer Genome Atlas Research Network and Institute of Oncology of Moldova and University of Pittsburgh School of Medicine and University of Pittsburgh and Genome Characterization Centers: BC Cancer Agency and Analysis Working Group: Asan University and University of Texas MD Anderson Cancer Center and Case Western Reserve University and National Cancer Institute and Genome Data Analysis Centers: Broad Institute and St. Joseph’s Hospital &Medical Center and University of Southern California and Institute for Systems Biology and Ontario Tumour Bank and University of Washington and University of Rochester and Harvard Medical School and KU Leuven and Genome Sequencing Center: Broad Institute and Brigham and Women’s Hospital and Memorial Sloan Kettering Cancer Center and Disease Working Group: Duke University and Erasmus University and Christiana Care Health System and University of Kansas Medical Center and Research Institute at Nationwide Children’s Hospital and International Genomics Consortium and Tayside Tissue Bank and Peter MacCallum Cancer Centre and Pusan National University Medical School and Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University and BioreclamationIVT and Dana-Farber Cancer Institute and University of Southern California Epigenome Center and Stanford University and BC Cancer Agency and Chonnam National University Medical School and St. Petersburg Academic University and University of North Carolina and University of Dundee and Van Andel Research Institute and Washington University in St. Louis and Emory University and Washington University and University of California Santa Cruz and Biospecimen Core Resource: International Genomics Consortium and Asterand Bioscience and Botkin Municipal Clinic and The Cancer Genome Atlas Research Network
Nature: international weekly journal of science, ISSN 0028-0836, 01/2017, Volume 541, Issue 7636, pp. 169 - 174
Journal Article