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PLoS ONE, ISSN 1932-6203, 06/2017, Volume 12, Issue 6, pp. e0179610 - e0179610
Objective To assess the prognostic roles of BAP1, PBRM1, pS6, PTEN, TGase2, PD-L1, CA9, PSMA, and Ki-67 tissue biomarkers in localized renal cell carcinoma... 
SURVIVAL | MORTALITY | CARBONIC-ANHYDRASE-IX | PROTEIN | MULTIDISCIPLINARY SCIENCES | CANCER INCIDENCE | METASTASES | OUTCOMES | KI67 | EXPRESSION | TUMORS | Immunohistochemistry | Prognosis | Tissue Array Analysis | Humans | Middle Aged | Ki-67 Antigen - metabolism | Male | Kidney Neoplasms - metabolism | Porphyrins - metabolism | Neoplasm Recurrence, Local - mortality | Neoplasm Recurrence, Local - pathology | Glutamate Carboxypeptidase II - metabolism | Neoplasm Grading | Antigens, Neoplasm - metabolism | Antigens, Surface - metabolism | Biomarkers, Tumor - metabolism | Ubiquitin Thiolesterase - metabolism | Adult | Female | Carbonic Anhydrase IX - metabolism | Retrospective Studies | Tumor Suppressor Proteins - metabolism | Neoplasm Recurrence, Local - metabolism | Carcinoma, Renal Cell - pathology | PTEN Phosphohydrolase - metabolism | Nuclear Proteins - metabolism | Survival Rate | Kidney Neoplasms - mortality | Transcription Factors - metabolism | Carcinoma, Renal Cell - metabolism | Carcinoma, Renal Cell - mortality | Disease-Free Survival | B7-H1 Antigen - metabolism | Transglutaminases - metabolism | Sulfonamides - metabolism | Kidney Neoplasms - pathology | Aged | Neoplasm Staging | GTP-Binding Proteins - metabolism | Genetic aspects | Carcinoma, Renal cell | Research | Biological markers | Biometrics | Slopes | Metastasis | Kinases | Epidemiology | Cancer therapies | Urology | Proteins | Nephrectomy | Quality | Bioindicators | Growth factors | Age | Antigens | Markers | Hazards | Patients | Survival | Disease prevention | Hospitals | Medical prognosis | PD-L1 protein | Biomarkers | Death | Mutation | Diabetes | Prostate cancer | PTEN protein | Clear cell-type renal cell carcinoma | Cancer | Kidney transplantation | Tumors | Index Medicus
Journal Article
Nature Cell Biology, ISSN 1465-7392, 09/2010, Volume 12, Issue 9, pp. 863 - 875
Accumulation of unwanted/misfolded proteins in aggregates has been observed in airways of patients with cystic fibrosis (CF), a life-threatening genetic... 
APOPTOSIS | UNFOLDED PROTEIN RESPONSE | BECLIN 1 | DOWN-REGULATION | ENDOPLASMIC-RETICULUM | MICE | GENE-TRANSFER | TISSUE TRANSGLUTAMINASE | NEURODEGENERATIVE DISEASES | CELL-DEATH | CELL BIOLOGY | Reactive Oxygen Species - metabolism | Respiratory Mucosa - drug effects | Sequestosome-1 Protein | Humans | Transglutaminases - genetics | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Autophagy - drug effects | Young Adult | Cystamine - therapeutic use | Inflammation - metabolism | Autophagy - genetics | Nasal Polyps - metabolism | Mice, Inbred CFTR | Respiratory Mucosa - cytology | Cystic Fibrosis - metabolism | Membrane Proteins - genetics | Mice, Transgenic | Protein Transport - genetics | Apoptosis Regulatory Proteins - metabolism | Reactive Oxygen Species - antagonists & inhibitors | Models, Biological | Cystic Fibrosis - genetics | Transglutaminases - metabolism | Adolescent | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Mice | GTP-Binding Proteins | Cystic Fibrosis - drug therapy | Protein Binding - physiology | Microtubule-Associated Proteins - metabolism | Phosphatidylinositol 3-Kinases - metabolism | Salicylates - pharmacology | Epithelial Sodium Channels - genetics | Apoptosis Regulatory Proteins - genetics | Adult | Cystamine - pharmacology | Membrane Proteins - metabolism | Acetylcysteine - therapeutic use | Beclin-1 | Cystic Fibrosis Transmembrane Conductance Regulator - antagonists & inhibitors | Cell Line | Small Ubiquitin-Related Modifier Proteins - metabolism | Heat-Shock Proteins - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Antioxidants - pharmacology | Mice, Inbred Strains | Nasal Polyps - drug therapy | Antioxidants - therapeutic use | Animals | Acetylcysteine - pharmacology | Adaptor Proteins, Signal Transducing - genetics | Respiratory Mucosa - metabolism | Adaptor Proteins, Signal Transducing - metabolism | Organometallic Compounds - pharmacology | Complications and side effects | Active oxygen | Gene mutations | Lung diseases | Physiological aspects | Cystic fibrosis | Genetic aspects | Research | Health aspects | Risk factors | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 8, pp. 2640 - 2649
Transglutaminase 2 (TG2) is a ubiquitously expressed, intracellular as well as extracellular protein with multiple modes of post-translational regulation,... 
SELECTIVE-INHIBITION | HUMAN THIOREDOXIN-1 | ACTIVE-SITE | THROMBUS FORMATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ISOMERASE | THIOL-DISULFIDE EXCHANGE | EXTRACELLULAR-MATRIX | QUIESCIN-SULFHYDRYL OXIDASE | TISSUE TRANSGLUTAMINASE | CELIAC-DISEASE | Enzymes, Immobilized - metabolism | Oxidants - pharmacology | Human Umbilical Vein Endothelial Cells - metabolism | Membrane Glycoproteins - metabolism | Glutathione - metabolism | Protein Disulfide-Isomerases - metabolism | GTP-Binding Proteins - antagonists & inhibitors | Humans | Membrane Glycoproteins - chemistry | Oxidants - metabolism | Extracellular Matrix - metabolism | Transglutaminases - genetics | Protein Disulfide-Isomerases - antagonists & inhibitors | Protein Transport - drug effects | GTP-Binding Proteins - genetics | Thioredoxins - genetics | Oxidoreductases Acting on Sulfur Group Donors - chemistry | Protein Processing, Post-Translational - drug effects | RNA Interference | Biocatalysis - drug effects | Human Umbilical Vein Endothelial Cells - cytology | Thioredoxins - metabolism | Peptide Fragments - genetics | Transglutaminases - antagonists & inhibitors | Transglutaminases - chemistry | Allosteric Regulation - drug effects | Oxidoreductases Acting on Sulfur Group Donors - metabolism | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | GTP-Binding Proteins - chemistry | Oxidation-Reduction | Extracellular Matrix - drug effects | Cells, Cultured | Hydrogen Peroxide - pharmacology | Recombinant Proteins - chemistry | Membrane Glycoproteins - genetics | Extracellular Matrix - enzymology | Peptide Fragments - chemistry | Protein Disulfide-Isomerases - genetics | Human Umbilical Vein Endothelial Cells - enzymology | Cystine - metabolism | Transglutaminases - metabolism | Oxidoreductases Acting on Sulfur Group Donors - genetics | Enzymes, Immobilized - antagonists & inhibitors | GTP-Binding Proteins - metabolism | Index Medicus | Editors' Picks | post-translational modification (PTM) | PDIA3 | transglutaminase | thioredoxin | disulfide | oxidation-reduction (redox) | ERp57 | redox switch | celiac disease | transglutaminase 2 | protein disulfide isomerase family A member 3
Journal Article
Cellular Signalling, ISSN 0898-6568, 06/2013, Volume 25, Issue 6, pp. 1514 - 1525
Journal Article
International Journal of Cancer, ISSN 0020-7136, 05/2009, Volume 124, Issue 9, pp. 2060 - 2070
Ovarian cancer cells are present in malignant ascites both as individual cells and as multicellular spheroid aggregates. Although spheroid formation affords... 
Spheroid | 3D culture | Myofibroblast | Contraction | Invasion | SURFACE EPITHELIUM | myofibroblast | PERITONEAL | TUMOR-CELLS | E-CADHERIN | PLASMINOGEN-ACTIVATOR RECEPTOR | IN-VITRO | invasion | ONCOLOGY | contraction | MULTICELLULAR SPHEROIDS | EXTRACELLULAR-MATRIX | GROWTH-FACTOR | spheroids | CARCINOMA | Cell Proliferation | Humans | Transforming Growth Factor beta1 - metabolism | Ovarian Neoplasms - pathology | Spheroids, Cellular - pathology | Extracellular Matrix - metabolism | Transglutaminases - genetics | GTP-Binding Proteins - genetics | Female | Ovarian Neoplasms - metabolism | Tumor Cells, Cultured | Fibroblasts - metabolism | Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase - genetics | Neoplasm Invasiveness | Spheroids, Cellular - metabolism | Transforming Growth Factor beta1 - genetics | Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase - metabolism | Cell Adhesion | Fibronectins - metabolism | Integrin beta1 - metabolism | Receptors, Urokinase Plasminogen Activator - metabolism | Collagen - metabolism | Phenotype | Transglutaminases - metabolism | Connective Tissue Growth Factor - genetics | Fibroblasts - cytology | Receptors, Urokinase Plasminogen Activator - genetics | Integrin beta1 - genetics | Extracellular Matrix - pathology | Connective Tissue Growth Factor - metabolism | Cell Movement | GTP-Binding Proteins - metabolism | Index Medicus
Journal Article
Nature Communications, ISSN 2041-1723, 02/2017, Volume 8, Issue 1, pp. 14450 - 14450
Journal Article
International Journal of Cancer, ISSN 0020-7136, 06/2014, Volume 134, Issue 12, pp. 2798 - 2807
Aberrant glucose metabolism characterized by high levels of glycolysis, even in the presence of oxygen, is an important hallmark of cancer. This metabolic... 
HIF‐1α | metabolism | NF‐κB | drug resistance | metastasis | EMT | NF-κB | HIF-1α | COMPLEX | HIF-1 alpha | INDUCIBLE FACTOR-I | HYPOXIA | DEHYDROGENASE | BREAST-CANCER | NF-kappa B | GENE | ONCOLOGY | GROWTH | NF-KAPPA-B | TISSUE TRANSGLUTAMINASE | EXPRESSION | Up-Regulation | Epithelial Cells - metabolism | Humans | Gene Expression Regulation, Neoplastic | Transglutaminases - genetics | Mammary Glands, Human - metabolism | GTP-Binding Proteins - genetics | Promoter Regions, Genetic - genetics | Oxygen - metabolism | Breast Neoplasms - metabolism | Signal Transduction - immunology | Cell Respiration - genetics | MCF-7 Cells | RNA Interference | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | Lactic Acid - biosynthesis | Female | Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis | Hypoxia-Inducible Factor 1, alpha Subunit - genetics | Down-Regulation | Transglutaminases - biosynthesis | Epithelial Cells - pathology | Mammary Glands, Human - pathology | Inflammation - immunology | Mitochondria - metabolism | Breast Neoplasms - genetics | Transcription Factor RelA - metabolism | Transcription Factor RelA - biosynthesis | Transglutaminases - metabolism | Cell Line, Tumor | Glucose - metabolism | Glycolysis | GTP-Binding Proteins - biosynthesis | RNA, Small Interfering | GTP-Binding Proteins - metabolism | Lactates | Glucose metabolism | Physiological aspects | Mitochondrial DNA | Glucose | Drug resistance | Dextrose | Rodents | Protein expression | Breast cancer | Metastasis | Metabolism | Cells | Index Medicus
Journal Article
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 11/2017, Volume 313, Issue 5, pp. L752 - L762
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 15, pp. 4064 - 4076
iRHOM2 is a highly conserved, catalytically inactive member of the Rhomboid family, which has recently been shown to regulate the maturation of the... 
CULTURED HUMAN KERATINOCYTES | GROWTH-FACTOR RECEPTOR | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEPARIN-BINDING EGF | PSORIATIC EPIDERMIS | GENETICS & HEREDITY | SQUAMOUS-CELL CARCINOMA | GENE-EXPRESSION | AUTOCRINE GROWTH | TGF-ALPHA | NECROSIS-FACTOR-ALPHA | ESOPHAGEAL CANCER | ADAM17 Protein | RNA, Small Interfering - genetics | Keratoderma, Palmoplantar - genetics | Staphylococcus aureus - physiology | Esophageal Neoplasms - microbiology | Humans | ErbB Receptors - genetics | Staphylococcal Skin Infections - metabolism | Transglutaminases - genetics | Male | Esophageal Neoplasms - pathology | Desmosomes - pathology | Epidermis - microbiology | Keratoderma, Palmoplantar - metabolism | Keratoderma, Palmoplantar - pathology | Esophageal Neoplasms - metabolism | Female | Keratinocytes - microbiology | Desmosomes - metabolism | Epidermis - metabolism | Epidermis - pathology | ADAM Proteins - antagonists & inhibitors | ErbB Receptors - metabolism | Signal Transduction | Epidermal Growth Factor - genetics | Gene Expression Regulation | Epidermal Growth Factor - metabolism | Staphylococcal Skin Infections - pathology | Carrier Proteins - genetics | ADAM Proteins - metabolism | Keratinocytes - pathology | Carrier Proteins - metabolism | Esophageal Neoplasms - genetics | Keratinocytes - metabolism | Transglutaminases - metabolism | Mutation | ADAM Proteins - genetics | Keratoderma, Palmoplantar - microbiology | Staphylococcal Skin Infections - microbiology | Cytokines - biosynthesis | RNA, Small Interfering - metabolism | Staphylococcal Skin Infections - genetics | Index Medicus
Journal Article
Diabetes, ISSN 0012-1797, 08/2016, Volume 65, Issue 8, pp. 2414 - 2428
Journal Article
Journal Article
Bioconjugate Chemistry, ISSN 1043-1802, 03/2014, Volume 25, Issue 3, pp. 569 - 578
Journal Article