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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
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
American Journal of Physiology - Lung Cellular and Molecular Physiology, ISSN 1040-0605, 10/2014, Volume 307, Issue 7, pp. L576 - L585
We previously reported that transglutaminase 2 (TG2) activity is markedly elevated in lungs of hypoxia-exposed rodent models of pulmonary hypertension (PH).... 
CaSR | HIF-1α | TRPV4 | TG2 | Pulmonary artery smooth muscle cells | COBALT CHLORIDE | INDUCIBLE FACTOR-1-ALPHA | PHYSIOLOGY | HIF-1 alpha | RECEPTOR | pulmonary artery smooth muscle cells | INTRACELLULAR CA2 | RESPIRATORY SYSTEM | CALCIUM | HYPERTENSION | TISSUE TRANSGLUTAMINASE | EXPRESSION | VASOCONSTRICTION | MAMMARY EPITHELIAL-CELLS | Cell Proliferation | GTP-Binding Proteins - antagonists & inhibitors | Humans | Receptors, Calcium-Sensing - metabolism | Muscle, Smooth, Vascular - physiopathology | Cell Hypoxia | TRPV Cation Channels - metabolism | Cattle | Hypoxia-Inducible Factor 1, alpha Subunit - metabolism | TRPV Cation Channels - antagonists & inhibitors | Calcium Signaling | Hypertension, Pulmonary - enzymology | Receptors, Calcium-Sensing - antagonists & inhibitors | Transglutaminases - antagonists & inhibitors | GTP-Binding Proteins - physiology | Myocytes, Smooth Muscle - enzymology | Cells, Cultured | Enzyme Inhibitors - pharmacology | Myocytes, Smooth Muscle - physiology | Enzyme Induction | Pulmonary Artery - physiopathology | Muscle, Smooth, Vascular - pathology | Animals | Transglutaminases - physiology | Enzyme Activation | Hypertension, Pulmonary - pathology | Pulmonary Artery - pathology | Cell proliferation | Cell research | Smooth muscle | Muscle cells | Research | Health aspects | Pulmonary artery | Glutamine | Lungs | Pulmonary arteries | Rodents | Hypoxia | Gene expression | Enzyme kinetics | Cells | Index Medicus
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 04/2014, Volume 289, Issue 14, pp. 10115 - 10125
Background: Tissue transglutaminase (tTG) promotes various aspects of oncogenesis, including cell survival. Results: Ectopically expressed tTG in... 
Transformation | TYROSINE PHOSPHORYLATION | Src | Cell Survival | INDUCED APOPTOSIS | PHOSPHATIDYLINOSITOL 3-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | FACTOR-KAPPA-B | Akt | DRUG-RESISTANCE | p70 S6-kinase | BREAST-CANCER CELLS | MIDDLE T-ANTIGEN | PI3-kinase (PI3K) | EXPRESSION | BINDING | Apoptosis | Tissue Transglutaminase | NIH 3T3 Cells | Fibroblasts - enzymology | TOR Serine-Threonine Kinases - metabolism | GTP-Binding Proteins - antagonists & inhibitors | Humans | Transglutaminases - genetics | Multiprotein Complexes - genetics | Phosphatidylinositol 3-Kinases - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Cadaverine - pharmacology | GTP-Binding Proteins - genetics | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - metabolism | TOR Serine-Threonine Kinases - genetics | src-Family Kinases - metabolism | Chromones - pharmacology | Cell Survival - physiology | Transglutaminases - antagonists & inhibitors | Cell Survival - drug effects | Cadaverine - analogs & derivatives | Ribosomal Protein S6 Kinases, 70-kDa - metabolism | src-Family Kinases - antagonists & inhibitors | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Ribosomal Protein S6 Kinases, 70-kDa - genetics | Pyrimidines - pharmacology | Phosphatidylinositol 3-Kinases - genetics | Animals | Transglutaminases - metabolism | Mice | src-Family Kinases - genetics | GTP-Binding Proteins - metabolism | Index Medicus | Cell Biology
Journal Article
Journal Article
Oncogene, ISSN 0950-9232, 05/2017, Volume 36, Issue 21, pp. 2981 - 2990
Journal Article
Circulation Research, ISSN 0009-7330, 07/2010, Volume 107, Issue 1, pp. 117 - 125
Journal Article
2005, Methods in enzymology, ISBN 0121828069, Volume 401., xxxvii, 560, [6]
Book
Journal Article
Journal of Periodontology, ISSN 0022-3492, 10/2013, Volume 84, Issue 10, pp. 1469 - 1475
Background: Transglutaminase‐2 (TGM‐2) has been implicated in several fibrotic disorders and can be induced by reactive oxygen species (ROS). Hence, the... 
fibroblasts | Cyclosporin | gingival overgrowth | transglutaminase‐2 | reactive oxygen species | Fibroblasts | Gingival overgrowth | Reactive oxygen species | Transglutaminase-2 | TRANSCRIPTION | 2 EXPRESSION | PROLIFERATION | HYPERPLASIA | PLASMINOGEN-ACTIVATOR INHIBITOR | OVERGROWTH | ANTIOXIDANT | DENTISTRY, ORAL SURGERY & MEDICINE | MESANGIAL CELLS | transglutaminase-2 | ERK 1/2 | TISSUE TRANSGLUTAMINASE | Free Radical Scavengers - pharmacology | GTP-Binding Proteins - drug effects | Reactive Oxygen Species - metabolism | Cyclosporine - pharmacology | GTP-Binding Proteins - antagonists & inhibitors | Humans | Oxidative Stress - physiology | Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors | Male | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Transglutaminases - drug effects | Dose-Response Relationship, Drug | Protease Inhibitors - pharmacology | Gingiva - drug effects | Adult | Female | Flavonoids - pharmacology | Cell Culture Techniques | Catechin - pharmacology | Immunosuppressive Agents - pharmacology | Transglutaminases - antagonists & inhibitors | Cells, Cultured | Curcumin - pharmacology | Enzyme Inhibitors - pharmacology | Imidazoles - pharmacology | Antioxidants - pharmacology | Immunosuppressive Agents - toxicity | Morpholines | Up-Regulation - drug effects | Cyclosporine - toxicity | Fibroblasts - drug effects | Acetylcysteine - pharmacology | Gingiva - cytology | Catechin - analogs & derivatives | Pyridines - pharmacology | Chromones | Index Medicus | Dentistry
Journal Article
Cell death & disease, ISSN 2041-4889, 07/2017, Volume 8, Issue 7, pp. e2931 - e2931
Filaggrin (FLG) mutation is a well-confirmed genetic aberration in atopic dermatitis (AD). Genome-wide association studies on AD have revealed other... 
POPULATION | HAIR | SUSCEPTIBILITY LOCI | MECHANISMS | DIFFERENTIATION | EPIDERMAL PROGENITOR CELLS | PROTEINS | SKIN BARRIER | GENOME-WIDE ASSOCIATION | AXIS | CELL BIOLOGY | Receptors, Aryl Hydrocarbon - antagonists & inhibitors | Humans | Transglutaminases - genetics | DNA-Binding Proteins - metabolism | Interleukin-4 - pharmacology | Cell Nucleus - metabolism | RNA Interference | Intermediate Filament Proteins - genetics | Receptors, Aryl Hydrocarbon - metabolism | Membrane Proteins - metabolism | Cell Culture Techniques | Cell Line | DNA-Binding Proteins - antagonists & inhibitors | Protein Precursors - genetics | Membrane Proteins - genetics | Receptors, Aryl Hydrocarbon - genetics | Transcription Factors - antagonists & inhibitors | Dermatitis, Atopic - pathology | Keratinocytes - cytology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Tars - pharmacology | Protein Precursors - metabolism | Receptors, Aryl Hydrocarbon - agonists | Transcription Factors - metabolism | Up-Regulation - drug effects | Keratinocytes - metabolism | Transglutaminases - metabolism | Carbazoles - pharmacology | Dermatitis, Atopic - metabolism | Intermediate Filament Proteins - metabolism | RNA, Small Interfering - metabolism | Tar | Hydrocarbons | Keratinocytes | Genomes | Filaggrin | Gene expression | Dermatitis | Carbazole | Nuclear transport | Interleukin 4 | Cellular biology | Atopic dermatitis | Ligands | Skin | Receptor mechanisms | Mutation | Index Medicus | Original
Journal Article
Pediatric Diabetes, ISSN 1399-543X, 11/2015, Volume 16, Issue 7, pp. 504 - 509
Journal Article