1994, Di 1 ban., Gu dai wen shi ming zhu xuan yi cong shu, ISBN 9787805236377, 4, 3, 10, 304
Book
Nature Medicine, ISSN 1078-8956, 07/2017, Volume 23, Issue 7, pp. 859 - 868
Emerging evidence has linked the gut microbiome to human obesity. We performed a metagenome-wide association study and serum metabolomics profiling in a cohort...
MEDICINE, RESEARCH & EXPERIMENTAL | THETAIOTAOMICRON | RICHNESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Y GASTRIC BYPASS | MARKERS | DIET-INDUCED OBESITY | CELL BIOLOGY | MONOSODIUM GLUTAMATE | IMPACT | GLUCOSE | GENES | BARIATRIC SURGERY | Humans | Male | Dysbiosis - microbiology | Obesity - microbiology | Bacteroides thetaiotaomicron - genetics | Case-Control Studies | Young Adult | Adiposity | Adult | DNA, Bacterial - analysis | Female | Weight Gain | Bariatric Surgery | Obesity - surgery | Metabolome | Fusobacterium - genetics | Gastrectomy | Gastrointestinal Microbiome - genetics | Dysbiosis - metabolism | Obesity - metabolism | Bacteroides - genetics | Animals | Glutamic Acid - blood | Mice | Metagenome | Obesity | Usage | Microbiota (Symbiotic organisms) | Patient outcomes | Analysis | Surgery | Weight loss | Glutamate | Health aspects | Intervention | Glutamic acid | Metabolomics | Stomach | Profiling | Adipose tissue | Amino acids | Abundance | Alterations | Microorganisms | Weight control | Metabolites | Intestine | Human performance | Rodents | Weight reduction | Links | Gastrointestinal surgery | Intestinal microflora | Digestive tract
MEDICINE, RESEARCH & EXPERIMENTAL | THETAIOTAOMICRON | RICHNESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | Y GASTRIC BYPASS | MARKERS | DIET-INDUCED OBESITY | CELL BIOLOGY | MONOSODIUM GLUTAMATE | IMPACT | GLUCOSE | GENES | BARIATRIC SURGERY | Humans | Male | Dysbiosis - microbiology | Obesity - microbiology | Bacteroides thetaiotaomicron - genetics | Case-Control Studies | Young Adult | Adiposity | Adult | DNA, Bacterial - analysis | Female | Weight Gain | Bariatric Surgery | Obesity - surgery | Metabolome | Fusobacterium - genetics | Gastrectomy | Gastrointestinal Microbiome - genetics | Dysbiosis - metabolism | Obesity - metabolism | Bacteroides - genetics | Animals | Glutamic Acid - blood | Mice | Metagenome | Obesity | Usage | Microbiota (Symbiotic organisms) | Patient outcomes | Analysis | Surgery | Weight loss | Glutamate | Health aspects | Intervention | Glutamic acid | Metabolomics | Stomach | Profiling | Adipose tissue | Amino acids | Abundance | Alterations | Microorganisms | Weight control | Metabolites | Intestine | Human performance | Rodents | Weight reduction | Links | Gastrointestinal surgery | Intestinal microflora | Digestive tract
Journal Article
Nature Communications, ISSN 2041-1723, 12/2017, Volume 8, Issue 1, pp. 1785 - 12
Antidiabetic medication may modulate the gut microbiota and thereby alter plasma and faecal bile acid (BA) composition, which may improve metabolic health....
METFORMIN | ENTEROTYPES | METAGENOME | INSULIN-RESISTANCE | GLUCOSE | MULTIDISCIPLINARY SCIENCES | FARNESOID-X-RECEPTOR | BARIATRIC SURGERY | RANDOMIZED-TRIAL | SERUM METABOLOME | ACARBOSE | Hypoglycemic Agents - therapeutic use | Acarbose - therapeutic use | Bile Acids and Salts - blood | Diabetes Mellitus, Type 2 - microbiology | Humans | Middle Aged | Bacteroides - physiology | Glycoside Hydrolase Inhibitors - therapeutic use | Male | Glipizide - therapeutic use | Diabetes Mellitus, Type 2 - metabolism | Feces - chemistry | Gastrointestinal Microbiome - drug effects | Female | Lactobacillus - physiology | Diabetes Mellitus, Type 2 - drug therapy | Bifidobacterium - physiology | Population Dynamics | Drugs | Acarbose | Bile acids | Diabetes mellitus | Abundance | Metabolism | Patients | Microorganisms | Microbiota | Acids | Relative abundance | Plasma levels | Bile
METFORMIN | ENTEROTYPES | METAGENOME | INSULIN-RESISTANCE | GLUCOSE | MULTIDISCIPLINARY SCIENCES | FARNESOID-X-RECEPTOR | BARIATRIC SURGERY | RANDOMIZED-TRIAL | SERUM METABOLOME | ACARBOSE | Hypoglycemic Agents - therapeutic use | Acarbose - therapeutic use | Bile Acids and Salts - blood | Diabetes Mellitus, Type 2 - microbiology | Humans | Middle Aged | Bacteroides - physiology | Glycoside Hydrolase Inhibitors - therapeutic use | Male | Glipizide - therapeutic use | Diabetes Mellitus, Type 2 - metabolism | Feces - chemistry | Gastrointestinal Microbiome - drug effects | Female | Lactobacillus - physiology | Diabetes Mellitus, Type 2 - drug therapy | Bifidobacterium - physiology | Population Dynamics | Drugs | Acarbose | Bile acids | Diabetes mellitus | Abundance | Metabolism | Patients | Microorganisms | Microbiota | Acids | Relative abundance | Plasma levels | Bile
Journal Article
ENDOCRINE JOURNAL, ISSN 0918-8959, 2010, Volume 57, Issue suppl.2-1, pp. S398 - S398
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2019, Volume 58, Issue 40, pp. 14140 - 14145
Provided here is evidence showing that the stacking between triplet chromophores plays a critical role in ultralong organic phosphorescence (UOP) generation...
phosphorescence | noncovalent interactions | fluorescence | crystal engineering | solid-state structures | Carbazoles | Stacking | Fluorescence | Chromophores | Phosphorescence | Carbazole | Crystal structure
phosphorescence | noncovalent interactions | fluorescence | crystal engineering | solid-state structures | Carbazoles | Stacking | Fluorescence | Chromophores | Phosphorescence | Carbazole | Crystal structure
Journal Article
Hepatology, ISSN 0270-9139, 02/2014, Volume 59, Issue 2, pp. 671 - 682
Fulminant hepatic failure (FHF) is a clinical syndrome characterized by sudden and severe impairment of liver function. Mesenchymal stem cells (MSCs) have been...
HEPATOCELLULAR-CARCINOMA | ACTIVATION | IN-VIVO | DISEASE | GENERATION | FULMINANT HEPATIC-FAILURE | GASTROENTEROLOGY & HEPATOLOGY | PRECURSORS | PIVOTAL ROLE | TRANSPLANTATION | ANTIGEN | Th1 Cells - pathology | T-Lymphocytes, Regulatory - metabolism | Liver - pathology | Liver Failure, Acute - microbiology | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Dendritic Cells - pathology | Liver Failure, Acute - chemically induced | Cell- and Tissue-Based Therapy | Liver Failure, Acute - therapy | Lipopolysaccharides - adverse effects | T-Lymphocytes, Regulatory - pathology | Th1 Cells - metabolism | Animals | Mice | Mesenchymal Stromal Cells - pathology | Gram-Positive Bacterial Infections - complications | Propionibacterium acnes | Transforming Growth Factor beta - metabolism | Dendritic Cells - metabolism | Mesenchymal Stem Cell Transplantation | Disease Models, Animal | Receptors, Prostaglandin E, EP4 Subtype - metabolism | Rodents | Liver | Hepatology | Stem cells | Regeneration | Liver Injury
HEPATOCELLULAR-CARCINOMA | ACTIVATION | IN-VIVO | DISEASE | GENERATION | FULMINANT HEPATIC-FAILURE | GASTROENTEROLOGY & HEPATOLOGY | PRECURSORS | PIVOTAL ROLE | TRANSPLANTATION | ANTIGEN | Th1 Cells - pathology | T-Lymphocytes, Regulatory - metabolism | Liver - pathology | Liver Failure, Acute - microbiology | Signal Transduction | Liver - metabolism | Mice, Inbred C57BL | Dendritic Cells - pathology | Liver Failure, Acute - chemically induced | Cell- and Tissue-Based Therapy | Liver Failure, Acute - therapy | Lipopolysaccharides - adverse effects | T-Lymphocytes, Regulatory - pathology | Th1 Cells - metabolism | Animals | Mice | Mesenchymal Stromal Cells - pathology | Gram-Positive Bacterial Infections - complications | Propionibacterium acnes | Transforming Growth Factor beta - metabolism | Dendritic Cells - metabolism | Mesenchymal Stem Cell Transplantation | Disease Models, Animal | Receptors, Prostaglandin E, EP4 Subtype - metabolism | Rodents | Liver | Hepatology | Stem cells | Regeneration | Liver Injury
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 04/2014, Volume 111, Issue 17, pp. 6389 - 6394
A critical challenge for chemotherapy is the development of chemoresistance in breast cancer. However, the underlying mechanisms and validated predictors...
PROMOTE TUMOR-GROWTH | CELLS | MEMBRANE-VESICLES | MULTIDISCIPLINARY SCIENCES | EXOSOMES | CA15.3 | MICROVESICLES | GENERATION | MEDIATORS | MICROPARTICLES | P-GLYCOPROTEIN | Breast Neoplasms - ultrastructure | Cytoplasmic Vesicles - drug effects | Doxorubicin - therapeutic use | Humans | TRPC Cation Channels - blood | Treatment Outcome | Breast Neoplasms - drug therapy | Breast Neoplasms - metabolism | Xenograft Model Antitumor Assays | Animals | Breast Neoplasms - pathology | Mice, Nude | Cytoplasmic Vesicles - ultrastructure | Cytoplasmic Vesicles - metabolism | TRPC Cation Channels - metabolism | Cell Line, Tumor | Female | Mice | Doxorubicin - pharmacology | Drug Resistance, Neoplasm - drug effects | Pharmaceutical research | Chemotherapy | Oncology, Experimental | Breast cancer | Research | Drug therapy | Drug resistance | Cancer | Biological Sciences
PROMOTE TUMOR-GROWTH | CELLS | MEMBRANE-VESICLES | MULTIDISCIPLINARY SCIENCES | EXOSOMES | CA15.3 | MICROVESICLES | GENERATION | MEDIATORS | MICROPARTICLES | P-GLYCOPROTEIN | Breast Neoplasms - ultrastructure | Cytoplasmic Vesicles - drug effects | Doxorubicin - therapeutic use | Humans | TRPC Cation Channels - blood | Treatment Outcome | Breast Neoplasms - drug therapy | Breast Neoplasms - metabolism | Xenograft Model Antitumor Assays | Animals | Breast Neoplasms - pathology | Mice, Nude | Cytoplasmic Vesicles - ultrastructure | Cytoplasmic Vesicles - metabolism | TRPC Cation Channels - metabolism | Cell Line, Tumor | Female | Mice | Doxorubicin - pharmacology | Drug Resistance, Neoplasm - drug effects | Pharmaceutical research | Chemotherapy | Oncology, Experimental | Breast cancer | Research | Drug therapy | Drug resistance | Cancer | Biological Sciences
Journal Article
Journal of Photochemistry and Photobiology. A, Chemistry, ISSN 1010-6030, 02/2017, Volume 335, p. 268
Niflumic acid (NFC) and surfactant 1-octane sulfonic acid sodium (OS) are intercalated into the gallery of NO3- type layered europium hydroxide (NO3-LEuH) by...
Rare earth metals | Hybrids | Hydroxides | Luminescence | Atoms & subatomic particles | Emission | Layered materials | Thermal stability | Sulfonic acid | Emissions | Studies | Fabrication | Diffraction | Sodium | Acids | Synergistic effect | Ion exchange | Europium
Rare earth metals | Hybrids | Hydroxides | Luminescence | Atoms & subatomic particles | Emission | Layered materials | Thermal stability | Sulfonic acid | Emissions | Studies | Fabrication | Diffraction | Sodium | Acids | Synergistic effect | Ion exchange | Europium
Journal Article
DIABETES, ISSN 0012-1797, 10/2019, Volume 68, Issue 10, pp. 1950 - 1964
Immature pancreatic beta-cells are highly proliferative, and the expansion of beta-cells during the early neonatal period largely determines functional...
ACTIVATION | PANCREATIC-ISLETS | REPLICATION | ALPHA-CELLS | REGENERATION | MTOR PATHWAY | ENDOCRINOLOGY & METABOLISM | CYCLE PROGRESSION | MASS EXPANSION | MATURATION | GLUCAGON
ACTIVATION | PANCREATIC-ISLETS | REPLICATION | ALPHA-CELLS | REGENERATION | MTOR PATHWAY | ENDOCRINOLOGY & METABOLISM | CYCLE PROGRESSION | MASS EXPANSION | MATURATION | GLUCAGON
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 7285 - 8
Type 2 diabetes mellitus (T2DM) is closely related to depression; however, the exact molecular mechnisms of this association are unknown. Here, we investigated...
DISORDER | ANXIETY | TYPE-2 | ASSOCIATION | MULTIDISCIPLINARY SCIENCES | Wnt protein | Mental disorders | ErbB protein | Diabetes mellitus | MiRNA | Reverse transcription | MAP kinase | Mental depression | Gene expression | Kinases | Polymerase chain reaction | Signal transduction | DNA microarrays | Protein kinase | Circular RNA | Diabetes | Thyroid
DISORDER | ANXIETY | TYPE-2 | ASSOCIATION | MULTIDISCIPLINARY SCIENCES | Wnt protein | Mental disorders | ErbB protein | Diabetes mellitus | MiRNA | Reverse transcription | MAP kinase | Mental depression | Gene expression | Kinases | Polymerase chain reaction | Signal transduction | DNA microarrays | Protein kinase | Circular RNA | Diabetes | Thyroid
Journal Article
Nature communications, ISSN 2041-1723, 06/2017, Volume 8, Issue 1, p. 15755
Diabetes is associated with beta cell mass loss and islet dysfunctions. mTORC1 regulates beta cell survival, proliferation and function in physiological and...
LACTATE-DEHYDROGENASE | MAMMALIAN TARGET | RAPAMYCIN | ENDOCRINE PANCREAS | MESSENGER-RNA TRANSLATION | MULTIDISCIPLINARY SCIENCES | HEXOKINASE-I | MICE | INDUCED INSULIN-SECRETION | GLUCOSE-TOLERANCE | MTOR | Diabetes Mellitus, Type 2 - genetics | Humans | Mice, Inbred C57BL | Male | Diabetes Mellitus, Type 2 - metabolism | Mechanistic Target of Rapamycin Complex 1 - metabolism | Mice, Knockout | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA (Cytosine-5-)-Methyltransferases - genetics | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Mechanistic Target of Rapamycin Complex 1 - genetics | Animals | Glucose - metabolism | Female | Cell Differentiation | Insulin-Secreting Cells - cytology | Mice | Regulatory-Associated Protein of mTOR - genetics | Regulatory-Associated Protein of mTOR - metabolism
LACTATE-DEHYDROGENASE | MAMMALIAN TARGET | RAPAMYCIN | ENDOCRINE PANCREAS | MESSENGER-RNA TRANSLATION | MULTIDISCIPLINARY SCIENCES | HEXOKINASE-I | MICE | INDUCED INSULIN-SECRETION | GLUCOSE-TOLERANCE | MTOR | Diabetes Mellitus, Type 2 - genetics | Humans | Mice, Inbred C57BL | Male | Diabetes Mellitus, Type 2 - metabolism | Mechanistic Target of Rapamycin Complex 1 - metabolism | Mice, Knockout | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA (Cytosine-5-)-Methyltransferases - genetics | Insulin - metabolism | Insulin-Secreting Cells - metabolism | Mechanistic Target of Rapamycin Complex 1 - genetics | Animals | Glucose - metabolism | Female | Cell Differentiation | Insulin-Secreting Cells - cytology | Mice | Regulatory-Associated Protein of mTOR - genetics | Regulatory-Associated Protein of mTOR - metabolism
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 02/2019, Volume 23, Issue 2, pp. 1470 - 1485
Focal inflammation and remyelination failure are major hallmarks of multiple sclerosis and its animal model, experimental autoimmune encephalomyelitis (EAE)....
EAE | CNS inflammation | oligodendrocyte differentiation | leonurine | remyelination | MEDICINE, RESEARCH & EXPERIMENTAL | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | STEM-CELLS | ACTIVATION | THYROID-HORMONE | CNS | CELL BIOLOGY | MULTIPLE-SCLEROSIS | INFLAMMATION | GENE-EXPRESSION | CUPRIZONE | Multiple sclerosis | Disease susceptibility | T cells | Analysis | Animal models | Encephalomyelitis | Maturation | Myelin | Pathogenesis | Central nervous system | Nervous system | Lymphocytes T | Inflammation | Experimental allergic encephalomyelitis | Microglia | Proteins | Myelination | Cuprizone | Demyelination | Lysine | Lymphocytes | Oligodendrocytes | Methylation | Histone H3 | Original
EAE | CNS inflammation | oligodendrocyte differentiation | leonurine | remyelination | MEDICINE, RESEARCH & EXPERIMENTAL | EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS | STEM-CELLS | ACTIVATION | THYROID-HORMONE | CNS | CELL BIOLOGY | MULTIPLE-SCLEROSIS | INFLAMMATION | GENE-EXPRESSION | CUPRIZONE | Multiple sclerosis | Disease susceptibility | T cells | Analysis | Animal models | Encephalomyelitis | Maturation | Myelin | Pathogenesis | Central nervous system | Nervous system | Lymphocytes T | Inflammation | Experimental allergic encephalomyelitis | Microglia | Proteins | Myelination | Cuprizone | Demyelination | Lysine | Lymphocytes | Oligodendrocytes | Methylation | Histone H3 | Original
Journal Article
BIOMED RESEARCH INTERNATIONAL, ISSN 2314-6133, 2019, Volume 2019, pp. 3939720 - 9
Background. Tumor immunotherapy and immunological checkpoint-related proteins are research hotspots. Intensity-modulated radiotherapy (IMRT) is the main...
MEDICINE, RESEARCH & EXPERIMENTAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | Interleukin 22 | CD223 antigen | Metastasis | Gender | Interleukin 6 | Proteins | Nasopharyngeal carcinoma | Immunology | Interleukin 5 | Immunotherapy | Deoxyribonucleic acid--DNA | Age | Target detection | Medical research | Statistical analysis | Cytokines | Interleukin 12 | Radiation therapy | Tumor necrosis factor-α | Gene expression | IL-1β | Survival | Patients | Cell death | Pancreatic cancer | Medical prognosis | γ-Interferon | PD-L1 protein | Interleukin 10 | Biomarkers | Ligands | Software | Apoptosis | Tumors
MEDICINE, RESEARCH & EXPERIMENTAL | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | Interleukin 22 | CD223 antigen | Metastasis | Gender | Interleukin 6 | Proteins | Nasopharyngeal carcinoma | Immunology | Interleukin 5 | Immunotherapy | Deoxyribonucleic acid--DNA | Age | Target detection | Medical research | Statistical analysis | Cytokines | Interleukin 12 | Radiation therapy | Tumor necrosis factor-α | Gene expression | IL-1β | Survival | Patients | Cell death | Pancreatic cancer | Medical prognosis | γ-Interferon | PD-L1 protein | Interleukin 10 | Biomarkers | Ligands | Software | Apoptosis | Tumors
Journal Article
Molecular Medicine, ISSN 1076-1551, 06/2019, Volume 25, Issue 1, pp. 25 - 7
Background: Tumor necrosis factor (TNF) blockers have a high efficacy in treating Ankylosing Spondylitis (AS), yet up to 40% of AS patients show poor or even...
TNF blocker | Ankylosing spondylitis | Drug response prediction | IgG-gal ratio | MYOM2-rs2294066 | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOSYLATION | CELL BIOLOGY | ALPHA BLOCKERS | POLYMORPHISMS | DISEASE | ASSOCIATION
TNF blocker | Ankylosing spondylitis | Drug response prediction | IgG-gal ratio | MYOM2-rs2294066 | MEDICINE, RESEARCH & EXPERIMENTAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOSYLATION | CELL BIOLOGY | ALPHA BLOCKERS | POLYMORPHISMS | DISEASE | ASSOCIATION
Journal Article
Diabetes, ISSN 0012-1797, 03/2011, Volume 60, Issue 3, pp. 827 - 837
OBJECTIVE-We examined the role of Rictor/mammalian target of rapamycin complex 2 (mTORC2), a key component of the phosphotidylinositol-3-kinase...
MAMMALIAN TARGET | SURVIVAL | DISRUPTION | GENE | ISLET MASS | TRANSCRIPTION FACTOR FOXO1 | GROWTH | EXPANSION | ENDOCRINOLOGY & METABOLISM | MICE | PDK1 | Glucose Intolerance - metabolism | Phosphorylation - physiology | Cell Proliferation | Hyperglycemia - genetics | Proto-Oncogene Proteins c-akt - genetics | Insulin-Secreting Cells - metabolism | Insulin-Secreting Cells - cytology | Proto-Oncogene Proteins c-akt - metabolism | Rapamycin-Insensitive Companion of mTOR Protein | PTEN Phosphohydrolase - genetics | Glucose Intolerance - genetics | PTEN Phosphohydrolase - metabolism | Cell Size | Genotype | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Hyperglycemia - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Analysis of Variance | Alleles | Fluorescent Antibody Technique | Glucose - metabolism | Signal Transduction - physiology | Mice | Apoptosis - physiology | Islet Studies
MAMMALIAN TARGET | SURVIVAL | DISRUPTION | GENE | ISLET MASS | TRANSCRIPTION FACTOR FOXO1 | GROWTH | EXPANSION | ENDOCRINOLOGY & METABOLISM | MICE | PDK1 | Glucose Intolerance - metabolism | Phosphorylation - physiology | Cell Proliferation | Hyperglycemia - genetics | Proto-Oncogene Proteins c-akt - genetics | Insulin-Secreting Cells - metabolism | Insulin-Secreting Cells - cytology | Proto-Oncogene Proteins c-akt - metabolism | Rapamycin-Insensitive Companion of mTOR Protein | PTEN Phosphohydrolase - genetics | Glucose Intolerance - genetics | PTEN Phosphohydrolase - metabolism | Cell Size | Genotype | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Hyperglycemia - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Analysis of Variance | Alleles | Fluorescent Antibody Technique | Glucose - metabolism | Signal Transduction - physiology | Mice | Apoptosis - physiology | Islet Studies
Journal Article
EMBO reports, ISSN 1469-221X, 12/2017, Volume 18, Issue 12, pp. 2131 - 2143
The histone H3 N‐terminal protein domain (N‐tail) is regulated by multiple posttranslational modifications, including methylation, acetylation,...
N‐tail cleavage | H3K9me1 | Histone H3 | JMJD5 | N-tail cleavage | CHROMATIN | DOMAIN-CONTAINING PROTEIN | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLIPPING ACTIVITY | PROTEOLYSIS | IDENTIFICATION | H2AX PHOSPHORYLATION | CELL BIOLOGY | DEMETHYLASE | CATHEPSIN-L | EMBRYONIC STEM-CELLS | A549 Cells | Phosphorylation | Humans | Protein Processing, Post-Translational - genetics | Gene Expression Regulation | Histone Demethylases - genetics | Histone Demethylases - metabolism |
N‐tail cleavage | H3K9me1 | Histone H3 | JMJD5 | N-tail cleavage | CHROMATIN | DOMAIN-CONTAINING PROTEIN | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLIPPING ACTIVITY | PROTEOLYSIS | IDENTIFICATION | H2AX PHOSPHORYLATION | CELL BIOLOGY | DEMETHYLASE | CATHEPSIN-L | EMBRYONIC STEM-CELLS | A549 Cells | Phosphorylation | Humans | Protein Processing, Post-Translational - genetics | Gene Expression Regulation | Histone Demethylases - genetics | Histone Demethylases - metabolism |