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Nature, ISSN 0028-0836, 2014, Volume 508, Issue 1, pp. 118 - 122
Treatment of BRAF(V600E) mutant melanoma by small molecule drugs that target the BRAF or MEK kinases can be effective, but resistance develops invariably(1,2).... 
GROWTH-FACTOR RECEPTOR | BRAF INHIBITOR | RAF INHIBITION | CELLS | MULTIDISCIPLINARY SCIENCES | IMPROVED SURVIVAL | DIFFERENTIATION | C-JUN | CANCER | EXPRESSION | EGFR | Cell Proliferation | Humans | Gene Expression Regulation, Neoplastic | Cell Aging | Drug Resistance, Neoplasm | Flow Cytometry | Mitogen-Activated Protein Kinase Kinases | SOX10 protein, human | SOXE Transcription Factors | Female | Indoles | Proto-Oncogene Proteins B-raf | Transforming Growth Factor beta | Gene Library | Signal Transduction | Melanoma | Receptor, Platelet-Derived Growth Factor beta | Antineoplastic Agents | vemurafenib | BRAF protein, human | Receptor Protein-Tyrosine Kinases | Index Medicus | Protein Kinase Inhibitors | Animals | Sulfonamides | Mice | RNA, Small Interfering | Receptor, Epidermal Growth Factor | Genes | Kinases | Drug resistance | Proteins | Rodents | PLX4032 | Patients | Biopsy | Mutation | Tumors | 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
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 505, Issue 7482, pp. 212 - 217
Non-small-cell lung cancer (NSCLC) is the most prevalent histological cancer subtype worldwide(1). As the majority of patients present with invasive,... 
TRANSFORMATION | MESSENGER-RNAS | OVEREXPRESSION | TGF-BETA | GENE | ADENOCARCINOMA | MULTIDISCIPLINARY SCIENCES | LET-7 | INHIBITOR | BINDING | EXPRESSION DATA | Cell Proliferation | RNA Isoforms | betaglycan | Carcinoma, Non-Small-Cell Lung | Humans | Gene Expression Regulation, Neoplastic | Lung Neoplasms | Neoplasm Metastasis | Transcription, Genetic | HMGA2 Protein | mirnlet7 microRNA, mouse | Transforming Growth Factor beta | Disease Models, Animal | Binding, Competitive | Proteoglycans | Neoplasm Invasiveness | Disease Progression | Index Medicus | EIF2C2 protein, human | Animals | MicroRNAs | Argonaute Proteins | Cell Line, Tumor | Receptors, Transforming Growth Factor beta | Mice | Transplants & implants | Lung cancer | Genomes | Proteins | Tumorigenesis | Hypothesis testing | Gene expression | Survival analysis | Hypotheses | Mutation | Tumors | Adenocarcinoma | Transformation | non-coding RNA | RNA | Invasiveness | Data processing | Transforming growth factor- beta | Argonaute 2 protein | Carcinogenesis | Metastases | Algorithms | miRNA | Oncogenes | Receptors, Transforming Growth Factor beta - genetics | Lung Neoplasms - pathology | MicroRNAs - metabolism | Proteoglycans - deficiency | RNA Isoforms - metabolism | HMGA2 Protein - genetics | Gene Expression Regulation, Neoplastic - genetics | Carcinoma, Non-Small-Cell Lung - pathology | Lung Neoplasms - genetics | Argonaute Proteins - metabolism | RNA Isoforms - genetics | Carcinoma, Non-Small-Cell Lung - genetics | Proteoglycans - biosynthesis | Neoplasm Metastasis - genetics | Receptors, Transforming Growth Factor beta - biosynthesis | Binding, Competitive - genetics | MicroRNAs - genetics | Transcription, Genetic - genetics | Neoplasm Invasiveness - genetics | Transforming Growth Factor beta - metabolism | Proteoglycans - genetics | Receptors, Transforming Growth Factor beta - deficiency | RNA sequencing | Gene targeting | Development and progression | Genetic aspects | Genetic transcription | Lung cancer, Non-small cell | Identification and classification | Methods
Journal Article
by Burk, Robert D and Chen, Zigui and Saller, Charles and Tarvin, Katherine and Carvalho, Andre L and Scapulatempo-Neto, Cristovam and Silveira, Henrique C and Fregnani, José H and Creighton, Chad J and Anderson, Matthew L and Castro, Patricia and Wang, Sophia S and Yau, Christina and Benz, Christopher and Gordon Robertson, A and Mungall, Karen and Lim, Lynette and Bowlby, Reanne and Sadeghi, Sara and Brooks, Denise and Sipahimalani, Payal and Mar, Richard and Ally, Adrian and Clarke, Amanda and Mungall, Andrew J and Tam, Angela and Lee, Darlene and Chuah, Eric and Schein, Jacqueline E and Tse, Kane and Kasaian, Katayoon and Ma, Yussanne and Marra, Marco A and Mayo, Michael and Balasundaram, Miruna and Thiessen, Nina and Dhalla, Noreen and Carlsen, Rebecca and Moore, Richard A and Holt, Robert A and Jones, Steven J. M and Wong, Tina and Pantazi, Angeliki and Parfenov, Michael and Kucherlapati, Raju and Hadjipanayis, Angela and Seidman, Jonathan and Kucherlapati, Melanie and Ren, Xiaojia and Xu, Andrew W and Yang, Lixing and Park, Peter J and Lee, Semin and Rabeno, Brenda and Huelsenbeck-Dill, Lori and Borowsky, Mark and Cadungog, Mark and Iacocca, Mary and Petrelli, Nicholas and Swanson, Patricia and Ojesina, Akinyemi I and Ojesina, Akinyemi I and Ojesina, Akinyemi I and Le, Xuan and Sandusky, George and Adebamowo, Sally N and Akeredolu, Teniola and Adebamowo, Clement and Reynolds, Sheila M and Shmulevich, Ilya and Shelton, Candace and Crain, Daniel and Mallery, David and Curley, Erin and Gardner, Johanna and Penny, Robert and Morris, Scott and Shelton, Troy and Liu, Jia and Lolla, Laxmi and Chudamani, Sudha and Wu, Ye and Birrer, Michael and McLellan, Michael D and Bailey, Matthew H and Miller, Christopher A and Wyczalkowski, Matthew A and Fulton, Robert S and Fronick, Catrina C and Lu, Charles and Mardis, Elaine R and Appelbaum, Elizabeth L and Schmidt, Heather K and Fulton, Lucinda A and Cordes, Matthew G and Li, Tiandao and Ding, Li and Wilson, Richard K and Rader, Janet S and Behmaram, Behnaz and ... and Canc Genome Atlas Res Network and Eli &Edythe L. Broad Institute of Massachusetts Institute of Technology &Harvard University and Research Institute at Nationwide Children's Hospital and University of Alabama at Birmingham and McDonnell Genome Institute at Washington University and Washington University in St Louis and University of Wisconsin School of Medicine &Public Health and National Hospital, Abuja, Nigeria and Baylor College of Medicine and Barretos Cancer Hospital and Indiana University School of Medicine and Ontario Tumour Bank, The Ottawa Hospital and Massachusetts General Hospital and University of New Mexico Health Sciences Center and National Institute on Deafness &Other Communication Disorders and University of North Carolina at Chapel Hill and Buck Institute for Research on Aging and Cancer Genome Atlas Research Network and Medical College of Wisconsin and University of Abuja Teaching Hospital and University of Oklahoma Health Sciences Center and Institute of Human Virology and St Joseph's Candler Health System and University of Pittsburgh and University of Texas MD Anderson Cancer Center and National Cancer Institute and Montefiore Medical Center and University of Southern California and Institute for Systems Biology and University of Washington and Analytical Biological Services and Harvard Medical School and National Human Genome Research Institute and Memorial Sloan Kettering Cancer Center and Medical University of South Carolina and Ontario Tumour Bank, London Health Sciences Centre and SRA International and University of Kansas Medical Center and University of Lausanne and ILSbio, LLC and University of Bergen and University of California, Irvine and Canada's Michael Smith Genome Sciences Centre and International Genomics Consortium and Oregon Health &Science University and NantOmics and Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University and University of São Paulo, Ribeir ão Preto Medical School and HudsonAlpha Institute for Biotechnology and Albert Einstein College of Medicine and Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center and National Institute of Environmental Health Sciences and Van Andel Research Institute and Ontario Tumour Bank, Ontario Institute for Cancer Research and University of California Santa Cruz and Beckman Research Institute of City of Hope and Leidos Biomedical and Helen F. Graham Cancer Center &Research Institute at Christiana Care Health Services and The Cancer Genome Atlas Research Network
Nature, ISSN 0028-0836, 03/2017, Volume 543, Issue 7645, pp. 378 - 384
Cervical cancer remains one of the leading causes of cancer-related deaths worldwide. Here we report the extensive molecular characterization of 228 primary... 
TRANSCRIPTION FACTORS | BREAST-CANCER | TO-MESENCHYMAL TRANSITION | ACCURATE | DNA METHYLATION | RNA-SEQ | MULTIDISCIPLINARY SCIENCES | 14-3-3-SIGMA | RESISTANCE | EXPRESSION | SIGNATURE | Adenocarcinoma | Keratins | Proto-Oncogene Proteins p21(ras) | Uterine Cervical Neoplasms | Caspase 8 | Genomics | Humans | Protein-Serine-Threonine Kinases | PDCD1LG2 protein, human | Molecular Targeted Therapy | KRAS protein, human | Phosphatidylinositol 3-Kinases | Human papillomavirus 16 | Mitogen-Activated Protein Kinase Kinases | APOBEC-1 Deaminase | PTEN Phosphohydrolase | ARID1A protein, human | BCAR4 non-coding RNA, human | ERBB3 protein, human | Female | PTEN protein, human | Signal Transduction | B7-H1 Antigen | Programmed Cell Death 1 Ligand 2 Protein | Virus Integration | Nuclear Proteins | Index Medicus | Carcinoma, Squamous Cell | CASP8 protein, human | transforming growth factor-beta type II receptor | CD274 protein, human | RNA, Long Noncoding | Proteomics | HLA-A Antigens | Receptors, Transforming Growth Factor beta | Transcription Factors | Mutation | Receptor, ErbB-3 | Human papillomavirus | Gynecology | Molecular biology | Cancer therapies | Cervical cancer | Tumors | Receptors, Transforming Growth Factor beta - genetics | Proto-Oncogene Proteins p21(ras) - genetics | Carcinoma, Squamous Cell - genetics | APOBEC-1 Deaminase - genetics | Phosphatidylinositol 3-Kinases - metabolism | Caspase 8 - genetics | Mitogen-Activated Protein Kinase Kinases - metabolism | Human papillomavirus 16 - isolation & purification | Adenocarcinoma - genetics | Nuclear Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | PTEN Phosphohydrolase - genetics | Programmed Cell Death 1 Ligand 2 Protein - genetics | Protein-Serine-Threonine Kinases - genetics | Uterine Cervical Neoplasms - drug therapy | RNA, Long Noncoding - genetics | Receptor, ErbB-3 - genetics | Transcription Factors - genetics | Uterine Cervical Neoplasms - genetics | B7-H1 Antigen - genetics | Receptors, Transforming Growth Factor beta - metabolism | HLA-A Antigens - genetics | Keratins - genetics | Human papillomavirus 16 - genetics | Uterine Cervical Neoplasms - classification | Causes of | Care and treatment | Genetic aspects | Gene mutations | Health aspects
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 10/2010, Volume 207, Issue 11, pp. 2331 - 2341
Foxp3-expressing regulatory T (T reg) cells have been implicated in parasite-driven inhibition of host immunity during chronic infection. We addressed whether... 
B-CELLS | MEDICINE, RESEARCH & EXPERIMENTAL | TH2 RESPONSES | PROTECTIVE IMMUNITY | TRANSCRIPTION FACTOR FOXP3 | IN-VIVO | AIRWAY INFLAMMATION | NEMATODE INFECTION | POLYGYRUS INFECTION | IMMUNOLOGY | ORAL ANTIGEN | AUTOIMMUNE-DISEASE | Receptors, Transforming Growth Factor beta - genetics | Strongylida Infections - metabolism | Receptors, Transforming Growth Factor beta - immunology | Smad3 Protein - immunology | Nematospiroides dubius - metabolism | Th2 Cells - immunology | T-Lymphocytes, Regulatory - immunology | Th1 Cells - metabolism | Host-Parasite Interactions - genetics | Phosphorylation - genetics | Smad2 Protein - genetics | Dioxoles - pharmacology | Phosphorylation - immunology | Protein-Serine-Threonine Kinases - metabolism | Smad2 Protein - metabolism | Mice, Transgenic | Signal Transduction - genetics | Antigens, Helminth - immunology | Receptors, Transforming Growth Factor beta - antagonists & inhibitors | Signal Transduction - drug effects | Mice | Mice, Inbred BALB C | Chronic Disease | Forkhead Transcription Factors - immunology | T-Lymphocytes, Regulatory - metabolism | Antigens, Helminth - metabolism | Strongylida Infections - genetics | Smad3 Protein - metabolism | Th1 Cells - immunology | Nematospiroides dubius - immunology | Signal Transduction - immunology | Smad3 Protein - genetics | Strongylida Infections - immunology | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Benzamides - pharmacology | Transforming Growth Factor beta - immunology | Forkhead Transcription Factors - biosynthesis | Gene Expression Regulation - genetics | Gene Expression Regulation - immunology | Protein-Serine-Threonine Kinases - genetics | Host-Parasite Interactions - immunology | Forkhead Transcription Factors - genetics | Th2 Cells - metabolism | Gene Expression Regulation - drug effects | Host-Parasite Interactions - drug effects | Smad2 Protein - immunology | Animals | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Protein-Serine-Threonine Kinases - immunology | Cell Proliferation - drug effects | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
NATURE MEDICINE, ISSN 1078-8956, 03/2012, Volume 18, Issue 3, pp. 429 - U192
In advanced cancer, including glioblastoma, the transforming growth factor beta (TGF-beta) pathway acts as an oncogenic factor and is considered to be a... 
MEDICINE, RESEARCH & EXPERIMENTAL | SMURF2 | GLIOMA | BIOCHEMISTRY & MOLECULAR BIOLOGY | SMAD7 | CELL BIOLOGY | GROWTH-FACTOR-BETA | PATHWAY | GENETICS | BIOLOGY | DEGRADATION | TARGETS | E3 UBIQUITIN LIGASE | Enzymes | Signal transduction | Animal models | Prognosis | RNA-mediated interference | peptidase | Glioblastoma | Tumorigenesis | Transforming growth factor- beta | Ubiquitin-protein ligase | Ovarian cancer | Ubiquitin | Phosphorylation | Receptors, Transforming Growth Factor beta - genetics | Humans | Gene Expression Regulation, Neoplastic | Brain Neoplasms - metabolism | Glioblastoma - genetics | RNA Interference | Cell Transformation, Neoplastic - genetics | Smad2 Protein - genetics | HEK293 Cells | Glioblastoma - metabolism | Protein-Serine-Threonine Kinases - metabolism | Disease Models, Animal | Smad7 Protein - metabolism | Endopeptidases - metabolism | Signal Transduction | Protein-Serine-Threonine Kinases - genetics | Smad2 Protein - metabolism | Ubiquitin-Protein Ligases - metabolism | Brain Neoplasms - genetics | Cell Transformation, Neoplastic - metabolism | Ubiquitin-Specific Proteases | Magnetic Resonance Imaging | Animals | Endopeptidases - genetics | Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - metabolism | Cell Line, Tumor | Mice | Transforming Growth Factor beta - metabolism | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2013, Volume 288, Issue 42, pp. 30708 - 30719
Journal Article
Immunity, ISSN 1074-7613, 10/2013, Volume 39, Issue 4, pp. 687 - 696
Tissue-resident memory T (Trm) cells represent a population of memory CD8 Tcells that can act as first responders to local infection. The mechanisms regulating... 
INTESTINAL EPITHELIUM | TGF-BETA | NONLYMPHOID TISSUE | DENDRITIC CELLS | LYMPHOID ORGANS | RM CELLS | IN-VIVO | PERSISTENT VIRAL-INFECTION | E-CADHERIN | IMMUNOLOGY | INTRAEPITHELIAL LYMPHOCYTES | Spleen | Memory cells | Immunological memory | Cytokines | CD8 antigen | Effector cells | Cytotoxicity | Lymphocytes T | Transforming growth factor- beta | Infection | CD69 antigen | Intestine | Differentiation | Digestive tract | Cell migration | Integrins | Lymphocytic choriomeningitis virus - immunology | Spleen - virology | Antigens, CD - immunology | CD8-Positive T-Lymphocytes - pathology | Spleen - immunology | Humans | Lectins, C-Type - immunology | Integrins - genetics | Adoptive Transfer | Lectins, C-Type - genetics | Lymphocytic Choriomeningitis - immunology | Antigens, CD - genetics | Intestines - immunology | Signal Transduction - immunology | Intestines - virology | Spleen - pathology | Lymphocytic Choriomeningitis - genetics | Transforming Growth Factor beta - immunology | Lymphocytic Choriomeningitis - virology | Intestines - pathology | Antigens, Differentiation, T-Lymphocyte - immunology | Lymphocytic Choriomeningitis - pathology | Integrins - immunology | Gene Expression Regulation | Mice, Transgenic | Animals | Transforming Growth Factor beta - genetics | CD8-Positive T-Lymphocytes - virology | Antigens, Differentiation, T-Lymphocyte - genetics | Immunologic Memory | Integrin alpha1 - genetics | Integrin alpha1 - immunology | Mice | CD8-Positive T-Lymphocytes - immunology | Cell Movement | Index Medicus
Journal Article
Nature Immunology, ISSN 1529-2908, 12/2013, Volume 14, Issue 12, pp. 1294 - 1301
Tissue-resident memory T cells (TRM cells) provide superior protection against infection in extralymphoid tissues. Here we found that CD103(+)CD8(+) TRM cells... 
MIGRATION | EFFECTOR | INTESTINAL EPITHELIUM | NONLYMPHOID TISSUE | RM CELLS | PERIPHERAL-TISSUES | DIFFERENTIATION | IMMUNOLOGY | LYMPHOCYTE EGRESS | CD103 EXPRESSION | CUTTING EDGE | Oligonucleotide Array Sequence Analysis | Protein-Serine-Threonine Kinases | Transcriptome | Antigens, Differentiation, T-Lymphocyte | CD8-Positive T-Lymphocytes | Herpes Simplex | CD69 antigen | Flow Cytometry | Interleukin-15 | Cell Differentiation | Signal Transduction | Lectins, C-Type | Mice, Inbred C57BL | Mice, Transgenic | Mice, Inbred Strains | Reverse Transcriptase Polymerase Chain Reaction | Herpesvirus 1, Human | Mice, Knockout | Host-Pathogen Interactions | transforming growth factor-beta type II receptor | Animals | Receptors, Immunologic | Immunologic Memory | Receptors, Transforming Growth Factor beta | Mice | Skin | Klrg1 protein, mouse | alpha E integrins | Integrin alpha Chains | Antigens, CD | Receptors, Transforming Growth Factor beta - genetics | Receptors, Transforming Growth Factor beta - immunology | Skin - metabolism | Antigens, CD - genetics | Antigens, CD - metabolism | Host-Pathogen Interactions - immunology | Lectins, C-Type - metabolism | Herpesvirus 1, Human - physiology | Integrin alpha Chains - immunology | CD8-Positive T-Lymphocytes - metabolism | Protein-Serine-Threonine Kinases - metabolism | Antigens, Differentiation, T-Lymphocyte - metabolism | Signal Transduction - genetics | Herpes Simplex - immunology | Cell Differentiation - immunology | Herpes Simplex - virology | Interleukin-15 - metabolism | CD8-Positive T-Lymphocytes - immunology | Receptors, Immunologic - genetics | Antigens, CD - immunology | Lectins, C-Type - immunology | Transcriptome - immunology | Lectins, C-Type - genetics | Interleukin-15 - immunology | Cell Differentiation - genetics | Signal Transduction - immunology | Herpesvirus 1, Human - immunology | Receptors, Immunologic - immunology | Skin - virology | Immunologic Memory - immunology | Skin - immunology | Antigens, Differentiation, T-Lymphocyte - immunology | Protein-Serine-Threonine Kinases - genetics | Integrin alpha Chains - metabolism | Transcriptome - genetics | Interleukin-15 - genetics | Receptors, Transforming Growth Factor beta - metabolism | CD8-Positive T-Lymphocytes - virology | Antigens, Differentiation, T-Lymphocyte - genetics | Protein-Serine-Threonine Kinases - immunology | Integrin alpha Chains - genetics | Receptors, Immunologic - metabolism | 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 | Prognosis | RNA-directed DNA polymerase | non-coding RNA | biomarkers | Hepatocellular carcinoma | Transforming growth factor- beta 1 | Transforming growth factor- beta | Guanylate cyclase | Multivariate analysis | Metastases | Polymerase chain reaction | CDH1 protein | Glyceraldehyde-3-phosphate dehydrogenase | Gastric cancer | Cell Proliferation | 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