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Blood, ISSN 0006-4971, 05/2014, Volume 123, Issue 19, pp. 3016 - 3026
Journal Article
STEM CELLS, ISSN 1066-5099, 06/2016, Volume 34, Issue 6, pp. 1664 - 1678
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, p. e98586
Journal Article
Blood, ISSN 0006-4971, 04/2005, Volume 105, Issue 7, pp. 2707 - 2716
Journal Article
Molecular Medicine Reports, ISSN 1791-2997, 12/2014, Volume 10, Issue 6, pp. 2786 - 2792
Various mechanisms have been proposed to underlie the cellular activity of genistein, based on biological experiments and epidemiological studies. The present... 
redox potential | genistein | cytoplasmic nicotinamide adenine dinucleotide phosphate-dependent isocitrate dehydrogenase | radiation | cell cycle transition | reactive oxygen species | Reactive oxygen species | Redox potential | Cell cycle transition | Genistein | Cytoplasmic nicotinamide adenine dinucleotide phosphate-dependent isocitrate dehydrogenase | Radiation | MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | STRAND BREAK REPAIR | INDUCED APOPTOSIS | CYCLE ARREST | INDUCTION | DAMAGE | LINES | IN-VITRO | ONCOLOGY | ANTIOXIDANT | PROSTATE-CANCER CELLS | Reactive Oxygen Species - metabolism | Apoptosis - drug effects | Humans | Gamma Rays - therapeutic use | Leukemia - drug therapy | Antioxidants - pharmacology | Down-Regulation - drug effects | Cell Division - drug effects | G2 Phase - drug effects | Up-Regulation - drug effects | Cell Cycle Checkpoints - drug effects | Lymphocytes - drug effects | Acetylcysteine - pharmacology | Genistein - pharmacology | Oxidation-Reduction - drug effects | Cell Line, Tumor | HL-60 Cells | Isocitrate Dehydrogenase - metabolism | Cell Proliferation - drug effects | Cell Death - drug effects | NADP - metabolism | GTP-binding protein | γ Radiation | NADPH-diaphorase | Leukemia | DNA damage | Acetylcysteine | Kinases | Antioxidants | Promyeloid leukemia | Ionizing radiation | Cell growth | Cell death | Lymphocytes | Penicillin | Cell cycle | NADP | Isocitrate dehydrogenase | Prostate cancer | Deoxyribonucleic acid--DNA | Apoptosis
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 6, p. e21077
The slow-releasing hydrogen sulfide (H2S) donor, GYY4137, caused concentration-dependent killing of seven different human cancer cell lines (HeLa, HCT-116, Hep... 
CELLS | APOPTOSIS | OXIDATIVE STRESS | INHIBITION | P38 | CASPASE-3 | BIOLOGY | Organothiophosphorus Compounds - therapeutic use | Humans | Antineoplastic Agents - therapeutic use | Organothiophosphorus Compounds - chemistry | Organothiophosphorus Compounds - pharmacology | Female | Antineoplastic Agents - pharmacology | Morpholines - therapeutic use | Cell Line | Cell Survival - drug effects | HCT116 Cells | Hydrogen Sulfide - chemistry | Morpholines - pharmacology | Antineoplastic Agents - chemistry | Mice, SCID | Blotting, Western | Morpholines - chemistry | Hep G2 Cells | Xenograft Model Antitumor Assays | Animals | Cell Line, Tumor | HL-60 Cells | Cell Proliferation - drug effects | Mice | Cell Cycle - drug effects | Hydrogen sulfide | Exhibitions | Care and treatment | Cancer | Sulfide | Cell culture | Biotechnology | Oxidative stress | Nuclear magnetic resonance--NMR | Hydrogen | Leukemia | Colorectal cancer | Smooth muscle | Biochemistry | Kinases | Anticancer properties | Ischemia | Rodents | Xenografts | Cell cycle | Fibroblasts | Sulfur | Hydrogen ion concentration | Killing | Enzymes | Incubation | Poly(ADP-ribose) polymerase | Caspase | Tumor cell lines | Releasing | Chemotherapy | Mutagenesis | Sodium | Lungs | Coronary vessels | Cell lines | Caspase-9 | Scientific imaging | Apoptosis | Nuclear magnetic resonance | NMR
Journal Article
BMC Cell Biology, ISSN 1471-2121, 01/2014, Volume 15, Issue 1, pp. 4 - 4
Background: Epigenetic regulation is known to affect gene expression, and recent research shows that aberrant DNA methylation patterning and histone... 
Histones | KG1 cells | Gene methylation/demethylation | Neutrophils | CD34+ cells | CHRONIC MYELOGENOUS LEUKEMIA | CD34+cells | DNA METHYLATION | HL-60 CELLS | E-CADHERIN | P16(INK4A) METHYLATION STATUS | CELL BIOLOGY | BREAST-CANCER CELLS | IN-VITRO | RETINOIC ACID | HISTONE DEACETYLASE INHIBITORS | STROMAL CELLS | Myeloid Cells - cytology | Neutrophils - cytology | Granulocytes - cytology | Antigens, CD34 - metabolism | Cadherins - metabolism | Epigenesis, Genetic | Humans | Receptors, Retinoic Acid - genetics | DNA Methylation | Cell Cycle Proteins - genetics | Phenylbutyrates - pharmacology | Granulocytes - metabolism | Cadherins - genetics | Neutrophils - metabolism | Promoter Regions, Genetic | Cell Cycle Proteins - metabolism | Cells, Cultured | Receptors, Retinoic Acid - metabolism | Hematopoietic Stem Cells - metabolism | Histones - genetics | Cell Differentiation - drug effects | Hematopoietic Stem Cells - cytology | Myeloid Cells - metabolism | Histone Deacetylase Inhibitors - pharmacology | Histones - metabolism | Physiological aspects | Methylation | Gene expression | Analysis | Hematopoietic stem cells | Epigenetic inheritance | DNA binding proteins | Research | Comparative analysis | Cell differentiation | Pathogenesis | DNA methylation | Epigenetics | Mutation | Experiments | Deoxyribonucleic acid--DNA | Methods
Journal Article
by Yoo, HJ and Lee, JS and Kim, JE and Gu, J and Koh, Y and Kim, I and Kim, HK
PLOS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0163982
Journal Article
Journal Article
Journal Article