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PLoS ONE, ISSN 1932-6203, 02/2009, Volume 4, Issue 2, p. e4352
Background: Genomic imprinting is an exception to Mendelian genetics in that imprinted genes are expressed monoallelically, dependent on parental origin. In... 
MULTIDISCIPLINARY SCIENCES | Multigene Family | Oligonucleotide Array Sequence Analysis | Chromosomes, Mammalian - genetics | Parthenogenesis - genetics | DNA, Complementary - genetics | Antibodies | Molecular Sequence Data | RNA, Messenger - metabolism | Embryo, Mammalian - metabolism | Base Sequence | Cloning, Molecular | Female | Fibroblasts - metabolism | Telomere - genetics | Alternative Splicing - genetics | RNA, Messenger - genetics | Intercellular Signaling Peptides and Proteins - genetics | Genomic Imprinting - genetics | Proteins - genetics | Polyadenylation - genetics | Animals | Centromere - genetics | Embryo, Mammalian - cytology | RNA, Long Noncoding | Mice | MicroRNAs - genetics | Iodide Peroxidase - genetics | RNA | Analysis | Genes | Sheep | Genetics | Genetic aspects | Book publishing | Genetic transcription | Transcription | Architects | Disorders | Biology | Thyroid gland | Preadipocyte factor 1 | Genomic imprinting | Immunology | Imprinting | DNA methylation | Fibroblasts | Chromosome 12 | Chromosomes | Medical research | Prader-Willi syndrome | Introns | Cloning | Abnormalities | Underpotential deposition | MiRNA | Embryo fibroblasts | Gene expression | Embryos | Virology | Northern blotting | Polymerase chain reaction | Ribonucleic acids | MicroRNAs | Cell lines | Alleles | Epigenetics | Aberration | Cancer
Journal Article
Molecular Immunology, ISSN 0161-5890, 07/2013, Volume 54, Issue 3-4, pp. 482 - 492
► Oral treatment with α,β-amyrin ameliorate disease activity in DSS-induced colitis. ► α,β-Amyrin treatment decrease leukocyte influx to the colon. ► The... 
Inflammatory bowel disease | α,β-Amyrin | Dextran sodium sulfate | Inflammatory cytokines | Cannabinoid system | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | alpha,beta-amyrin | MECHANISMS | BETA-AMYRIN | ADHESION MOLECULES | IMMUNOLOGY | PROTIUM-HEPTAPHYLLUM | ALPHA-AMYRIN | INFLAMMATORY-BOWEL-DISEASE | MOUSE MODEL | RECEPTORS | EXPRESSION | P-Selectin - metabolism | Colitis - genetics | Tumor Necrosis Factor-alpha - genetics | Colon - drug effects | Body Weight - drug effects | Ki-67 Antigen - metabolism | Male | Interleukin-1beta - genetics | Antigens, CD - genetics | Body Weight - genetics | Antigens, CD - metabolism | Lectins, C-Type - metabolism | Interleukin-1beta - metabolism | Cannabinoids - genetics | Colitis - drug therapy | Cannabinoids - metabolism | Administration, Oral | CD18 Antigens - genetics | Membrane Proteins - genetics | Asialoglycoproteins - metabolism | P-Selectin - genetics | Cell Adhesion Molecules - metabolism | Chemokines - genetics | Colon - metabolism | CD18 Antigens - metabolism | Intercellular Adhesion Molecule-1 - metabolism | Receptor, Cannabinoid, CB1 - genetics | Ki-67 Antigen - genetics | Intercellular Adhesion Molecule-1 - genetics | Colitis - metabolism | Chemokines - metabolism | Mice | Vascular Cell Adhesion Molecule-1 - metabolism | Tumor Necrosis Factor-alpha - metabolism | Dextran Sulfate | Cell Adhesion Molecules - genetics | Oleanolic Acid - analogs & derivatives | Oleanolic Acid - pharmacology | Lectins, C-Type - genetics | Receptor, Cannabinoid, CB2 - genetics | Asialoglycoproteins - genetics | Colitis - chemically induced | Vascular Cell Adhesion Molecule-1 - genetics | Membrane Proteins - metabolism | Interleukin-4 - genetics | Amidohydrolases - metabolism | Amidohydrolases - genetics | Interleukin-4 - metabolism | RNA, Messenger - genetics | Up-Regulation - genetics | Antigens, Differentiation, Myelomonocytic - genetics | Up-Regulation - drug effects | Receptor, Cannabinoid, CB1 - metabolism | Receptor, Cannabinoid, CB2 - metabolism | Animals | Antigens, Differentiation, Myelomonocytic - metabolism | Peroxidase - genetics | Peroxidase - metabolism
Journal Article
Nature Biotechnology, ISSN 1087-0156, 06/2004, Volume 22, Issue 6, pp. 695 - 700
Journal Article
Molecular Carcinogenesis, ISSN 0899-1987, 02/2014, Volume 53, Issue 2, pp. 85 - 97
As a link between inflammation and cancer has been reported in many studies, we established an in vitro model of prostatic inflammation to investigate the loss... 
androgen | loss of p53 | inflammation | DNA damage | ROS | prostate | NFkB | Loss of p53 | Androgen | Inflammation | Prostate | OXIDATIVE STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLUTATHIONE-PEROXIDASE | CANCER | ONCOLOGY | GENES | NKX3.1 | LINK | EXPRESSION | Proto-Oncogene Proteins c-mdm2 - genetics | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Antioxidants - metabolism | Homeodomain Proteins - metabolism | Humans | Transcriptional Activation - drug effects | Tumor Necrosis Factor-alpha - genetics | Apoptosis - genetics | Male | NF-kappa B - metabolism | Interleukin-1beta - genetics | Prostatitis - metabolism | Inflammation - metabolism | Matrix Metalloproteinase 9 - metabolism | Phosphorylation - genetics | Acetylcysteine - analogs & derivatives | Interleukin-1beta - metabolism | Matrix Metalloproteinase 9 - genetics | U937 Cells | Prostate-Specific Antigen - metabolism | Phosphorylation - drug effects | Interleukin-6 - metabolism | Prostate-Specific Antigen - genetics | Glutathione Peroxidase - metabolism | Lysine - analogs & derivatives | Interleukin-6 - genetics | Down-Regulation - genetics | Glutathione Peroxidase - genetics | Prostatitis - drug therapy | Androgens - genetics | Macrophages - metabolism | Receptors, Androgen - genetics | Signal Transduction - drug effects | Cell Line, Tumor | Androgens - metabolism | Tumor Necrosis Factor-alpha - metabolism | Prostatic Neoplasms - metabolism | Receptors, Androgen - metabolism | I-kappa B Proteins - metabolism | I-kappa B Proteins - genetics | Prostatitis - pathology | Tumor Suppressor Protein p53 - genetics | Cell Differentiation - genetics | Prostatic Neoplasms - genetics | Inflammation Mediators - metabolism | Proto-Oncogene Proteins c-mdm2 - metabolism | Prostatic Neoplasms - pathology | Kallikreins - genetics | Tumor Suppressor Protein p53 - metabolism | Antioxidants - pharmacology | Transcription Factors - genetics | Down-Regulation - drug effects | Homeodomain Proteins - genetics | Transcription Factors - metabolism | Up-Regulation - drug effects | Lysine - pharmacology | NF-kappa B - genetics | Cell Differentiation - drug effects | Acetylcysteine - pharmacology | Inflammation - genetics | Macrophages - drug effects | Kallikreins - metabolism | Ubiquitin | Analysis | Kallikrein | Hormones, Sex | Tumor proteins | Mitogens | Androgens | Cytokines | Molecular biology | Gene expression | Prostate cancer | Index Medicus
Journal Article
Circulation, ISSN 0009-7322, 04/2007, Volume 115, Issue 16, pp. 2178 - 2187
Background - Recent clinical studies have suggested a major protective role for the antioxidant enzyme glutathione peroxidase-1 ( GPx1) in diabetes-associated... 
Antioxidants | Aorta | Free radicals | Cardiovascular diseases | Diabetes mellitus | Atherosclerosis | atherosclerosis | INTIMA-MEDIA THICKNESS | free radicals | OXIDATIVE STRESS | CARDIAC & CARDIOVASCULAR SYSTEMS | antioxidants | CARDIOVASCULAR COMPLICATIONS | diabetes mellitus | FACTOR-KAPPA-B | cardiovascular diseases | REACTIVE OXYGEN | ENDOTHELIAL-CELLS | VASCULAR INFLAMMATION | PERIPHERAL VASCULAR DISEASE | aorta | PLATELET ACTIVATION | HEMATOLOGY | CORONARY-ARTERY-DISEASE | GLYCATION END-PRODUCTS | Superoxide Dismutase - genetics | Apolipoproteins E - deficiency | Atherosclerosis - genetics | Membrane Glycoproteins - biosynthesis | Male | Aorta - metabolism | Vascular Endothelial Growth Factor A - genetics | Tyrosine - analogs & derivatives | NADPH Oxidases - genetics | Diabetes Mellitus, Experimental - complications | Glutathione Peroxidase - deficiency | NADPH Oxidases - biosynthesis | Receptor for Advanced Glycation End Products | Atherosclerosis - pathology | Macrophages - pathology | Oxidation-Reduction | Tyrosine - biosynthesis | Isoenzymes - genetics | Immediate-Early Proteins - biosynthesis | Glutathione Peroxidase - genetics | Mice, Knockout | Aorta - pathology | Aortic Diseases - genetics | Immediate-Early Proteins - genetics | NF-kappa B - biosynthesis | Fibrosis | Glutathione Peroxidase - physiology | Vascular Cell Adhesion Molecule-1 - biosynthesis | Mice | Receptors, Immunologic - genetics | Inflammation - enzymology | Vascular Endothelial Growth Factor A - biosynthesis | Superoxide Dismutase - biosynthesis | Glutathione - metabolism | Streptozocin | Intercellular Signaling Peptides and Proteins - biosynthesis | Atherosclerosis - etiology | Atherosclerosis - enzymology | Receptors, Immunologic - biosynthesis | Diabetic Angiopathies - complications | Diabetic Angiopathies - enzymology | Vascular Cell Adhesion Molecule-1 - genetics | Aortic Diseases - enzymology | Sinus of Valsalva - pathology | Aortic Diseases - pathology | Hyperlipoproteinemia Type II - complications | Mice, Inbred C57BL | Gene Expression Regulation | Intercellular Signaling Peptides and Proteins - genetics | Glutathione Peroxidase - biosynthesis | NADPH Oxidase 2 | Membrane Glycoproteins - genetics | Animals | NF-kappa B - genetics | Apolipoproteins E - genetics | Inflammation - genetics | Isoenzymes - biosynthesis | Aortic Diseases - etiology | Connective Tissue Growth Factor | Hyperlipoproteinemia Type II - genetics | Animal models in research | Physiological aspects | Development and progression | Peroxidase | Research | Apolipoproteins | Glutathione
Journal Article
Journal Article
Journal Article
BMC Plant Biology, ISSN 1471-2229, 07/2012, Volume 12, Issue 1, pp. 118 - 118
Background: The eukaryotic translation initiation factor 5A (eIF5A) promotes formation of the first peptide bond at the onset of protein synthesis. However,... 
EIF5A | YEAST | SALT STRESS | ARABIDOPSIS-THALIANA | GENE | TRANSCRIPTION FACTOR | PROTEIN-SYNTHESIS | EXPRESSION | BINDING | CELL-DEATH | PLANT SCIENCES | Adaptation, Physiological | RNA-Binding Proteins - genetics | Superoxide Dismutase - genetics | Saccharomyces cerevisiae - genetics | Sodium Chloride - pharmacology | Regulatory Sequences, Nucleic Acid | Stress, Physiological | Cell Membrane - genetics | Chlorophyll - genetics | Saccharomyces cerevisiae - metabolism | Cloning, Molecular | Gene Expression Regulation, Plant | Abscisic Acid - metabolism | Cell Membrane - metabolism | Plant Proteins - metabolism | Superoxide Dismutase - metabolism | Tamaricaceae - physiology | Transformation, Genetic | Plants, Genetically Modified - physiology | Promoter Regions, Genetic | Salt-Tolerant Plants - metabolism | Plants, Genetically Modified - genetics | Signal Transduction | Solubility | Tamaricaceae - metabolism | Chlorophyll - metabolism | Transcription Factors - genetics | Tamaricaceae - genetics | Peptide Initiation Factors - metabolism | Transcription Factors - metabolism | Abscisic Acid - pharmacology | Peptide Initiation Factors - genetics | Plant Proteins - genetics | Plants, Genetically Modified - metabolism | Peroxidase - genetics | Genetic Vectors | RNA-Binding Proteins - metabolism | Peroxidase - metabolism | Salt-Tolerant Plants - genetics | Salt-Tolerant Plants - physiology | Physiological aspects | Transcription factors | Genetic aspects | Stress (Physiology) | Research | Peptides | Chlorophyll | Abscisic acid | Protein biosynthesis | Superoxide | Genetic engineering | DNA binding proteins | Genetic translation | Protein binding | Trees | Yeast | Microbiology | Abiotic stress | Cloning | Molecular weight | Proteins | Studies | Signal transduction | Protein synthesis | Cell cycle | Phylogenetics | Apoptosis
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e63456
Introduction: The gastrointestinal tract is frequently exposed to noxious stimuli that may cause oxidative stress, inflammation and injury. Intraluminal... 
BREAST-CANCER CELLS | IN-VITRO | OXYGEN RADICALS | KAPPA B ACTIVATION | INDUCED OXIDATIVE STRESS | MULTIDISCIPLINARY SCIENCES | ULCERATIVE-COLITIS | GENE-EXPRESSION | HYDROGEN-PEROXIDE | SUPEROXIDE-DISMUTASE | CACO-2 CELLS | Inflammation - chemically induced | Intestines - drug effects | Superoxide Dismutase - genetics | Epithelial Cells - metabolism | Gene Expression - drug effects | Gene Expression - genetics | Antioxidants - metabolism | Epithelial Cells - drug effects | Humans | Cell Survival - genetics | Intestines - embryology | NF-kappa B - metabolism | Free Radicals - adverse effects | Iron - adverse effects | Promoter Regions, Genetic - drug effects | Promoter Regions, Genetic - genetics | Ascorbic Acid - adverse effects | Inflammation - metabolism | I-kappa B Kinase - metabolism | Cyclooxygenase 2 - genetics | Lipid Peroxidation - drug effects | Free Radicals - metabolism | Epigenesis, Genetic - drug effects | Interleukin-6 - metabolism | Superoxide Dismutase - metabolism | Caco-2 Cells | Malondialdehyde - metabolism | Cell Survival - drug effects | Glutathione Peroxidase - metabolism | Up-Regulation - genetics | DNA Methylation - genetics | I-kappa B Kinase - genetics | Glutathione Peroxidase - genetics | Up-Regulation - drug effects | NF-kappa B - genetics | Epigenesis, Genetic - genetics | Cyclooxygenase 2 - metabolism | Cell Line, Tumor | Inflammation - genetics | Lipid Peroxidation - genetics | DNA Methylation - drug effects | Type 2 diabetes | Antioxidants | Epigenetic inheritance | Enzymes | Interleukins | Gastrointestinal system | Lipid peroxidation | Superoxide | Inflammation | Methylation | Organic acids | Health sciences | Pediatrics | Oxidative stress | Salts | Ascorbic acid | Disease | Epithelial cells | Interleukin | Oxidizing agents | Colorectal cancer | Superoxide dismutase | Iron | Interleukin 6 | Proteins | Cell growth | Oxidants | Vitamin E | Intestine | Rodents | DNA methylation | Nutrients | Peroxidase | Catalysis | Deoxyribonucleic acid--DNA | Glutathione | Peroxidation | Glutathione peroxidase | Medical research | NF-κB protein | Pain perception | Oxygen | Free radicals | Incubation | Gastrointestinal tract | Metabolism | Gene expression | Malondialdehyde | Medicine | Cellular biology | Epigenetics | Diabetes | Deoxyribonucleic acid | DNA
Journal Article