PLoS genetics, ISSN 1553-7390, 12/2010, Volume 6, Issue 12, pp. e1001233 - 15
Human genome-wide association studies have linked single nucleotide polymorphisms (SNPs) on chromosome 9p21.3 near the INK4/ARF (CDKN2a/b) locus with...
SEQUENCE VARIANT | MYOCARDIAL-INFARCTION | GENETIC ASSOCIATION | ABDOMINAL AORTIC-ANEURYSM | GENETICS & HEREDITY | INK4A/ARF EXPRESSION | SUSCEPTIBILITY LOCI | CHROMOSOME 9P21 | CELL-PROLIFERATION | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Gene Expression | Genome-Wide Association Study | RNA, Untranslated - metabolism | Exons | Atherosclerosis - genetics | DNA, Circular - chemistry | Humans | Risk Factors | Cyclin-Dependent Kinase Inhibitor p16 - genetics | DNA, Circular - genetics | Atherosclerosis - epidemiology | DNA, Circular - metabolism | RNA, Untranslated - genetics | Atherosclerosis - metabolism | RNA Splicing | Cyclin-Dependent Kinase Inhibitor p15 - genetics | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | RNA, Untranslated - chemistry | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Nucleic Acid Conformation | RNA | Atherosclerosis | Physiological aspects | Tumor suppressor genes | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Mortality | Cell division | Genetics | Cardiovascular disease | Influence | Genomes
SEQUENCE VARIANT | MYOCARDIAL-INFARCTION | GENETIC ASSOCIATION | ABDOMINAL AORTIC-ANEURYSM | GENETICS & HEREDITY | INK4A/ARF EXPRESSION | SUSCEPTIBILITY LOCI | CHROMOSOME 9P21 | CELL-PROLIFERATION | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Gene Expression | Genome-Wide Association Study | RNA, Untranslated - metabolism | Exons | Atherosclerosis - genetics | DNA, Circular - chemistry | Humans | Risk Factors | Cyclin-Dependent Kinase Inhibitor p16 - genetics | DNA, Circular - genetics | Atherosclerosis - epidemiology | DNA, Circular - metabolism | RNA, Untranslated - genetics | Atherosclerosis - metabolism | RNA Splicing | Cyclin-Dependent Kinase Inhibitor p15 - genetics | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | RNA, Untranslated - chemistry | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Nucleic Acid Conformation | RNA | Atherosclerosis | Physiological aspects | Tumor suppressor genes | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Mortality | Cell division | Genetics | Cardiovascular disease | Influence | Genomes
Journal Article
Surgery, ISSN 0039-6060, 05/2019, Volume 165, Issue 5, pp. 946 - 952
The Jumonji-domain containing 3 has diverse roles in multiple cancers. Here, we investigated its prognostic significance in esophageal squamous cell carcinoma....
INK4A/ARF | SURGERY | ACTIVATION | HISTONE DEMETHYLASE JMJD3 | UTX | SENESCENCE | CANCER | CONTRIBUTES | Immunohistochemistry | Medical colleges | Care and treatment | Squamous cell carcinoma | Analysis | Esophageal cancer
INK4A/ARF | SURGERY | ACTIVATION | HISTONE DEMETHYLASE JMJD3 | UTX | SENESCENCE | CANCER | CONTRIBUTES | Immunohistochemistry | Medical colleges | Care and treatment | Squamous cell carcinoma | Analysis | Esophageal cancer
Journal Article
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, ISSN 1874-9399, 03/2015, Volume 1849, Issue 3, pp. 247 - 256
Inactivation of p14(ARF) and p16(INK4A) by epigenetic changes in cutaneous and uveal melanoma has been here investigated. Compared with melanocytes, p14(ARF)...
Human melanoma | METHYLATION ANALYSIS | PROMOTER HYPERMETHYLATION | LOW-FREQUENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | Promoter methylation | p14(ARF) | MALIGNANT-MELANOMA | Epi-drug | P53 | INACTIVATION | CIGARETTE-SMOKING | BIOPHYSICS | P16 | GROWTH ARREST | INK4A/ARF LOCUS | p16(INK4A) | Histone deacetylation
Human melanoma | METHYLATION ANALYSIS | PROMOTER HYPERMETHYLATION | LOW-FREQUENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | Promoter methylation | p14(ARF) | MALIGNANT-MELANOMA | Epi-drug | P53 | INACTIVATION | CIGARETTE-SMOKING | BIOPHYSICS | P16 | GROWTH ARREST | INK4A/ARF LOCUS | p16(INK4A) | Histone deacetylation
Journal Article
The EMBO Journal, ISSN 0261-4189, 08/2013, Volume 32, Issue 16, pp. 2217 - 2230
Cellular senescence is an intrinsic defense mechanism to various cellular stresses: while still metabolically active, senescent cells stop dividing and enter a...
senescence | DPY30 | ID proteins | chromatin | MLL | Chromatin | Senescence | INK4A-ARF LOCUS | P16(INK4A) EXPRESSION | SECRETORY PHENOTYPE | HISTONE-3 LYSINE-4 | DOSAGE COMPENSATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | LOOP-HELIX PROTEINS | TARGET GENES | SET1 COMPLEX | TUMOR-SUPPRESSOR | TRANSCRIPTION FACTOR | Humans | beta-Galactosidase | Cellular Senescence - physiology | Gene Expression Regulation - physiology | Nuclear Proteins - metabolism | Inhibitor of Differentiation Protein 1 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Gene Knockdown Techniques | Flow Cytometry | Chromatin Immunoprecipitation | RNA Interference | Microarray Analysis | Fluorescent Antibody Technique | Signal Transduction - physiology | Colony-Forming Units Assay | Nuclear Proteins - genetics | Protein expression | Cellular biology
senescence | DPY30 | ID proteins | chromatin | MLL | Chromatin | Senescence | INK4A-ARF LOCUS | P16(INK4A) EXPRESSION | SECRETORY PHENOTYPE | HISTONE-3 LYSINE-4 | DOSAGE COMPENSATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | LOOP-HELIX PROTEINS | TARGET GENES | SET1 COMPLEX | TUMOR-SUPPRESSOR | TRANSCRIPTION FACTOR | Humans | beta-Galactosidase | Cellular Senescence - physiology | Gene Expression Regulation - physiology | Nuclear Proteins - metabolism | Inhibitor of Differentiation Protein 1 - metabolism | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Gene Knockdown Techniques | Flow Cytometry | Chromatin Immunoprecipitation | RNA Interference | Microarray Analysis | Fluorescent Antibody Technique | Signal Transduction - physiology | Colony-Forming Units Assay | Nuclear Proteins - genetics | Protein expression | Cellular biology
Journal Article
BMC cancer, ISSN 1471-2407, 2012, Volume 12, Issue 1, pp. 470 - 470
Background: The histone H3K27 demethylases UTX and JMJD3 are important regulatory factors that modulate gene expression by altering the physical state of...
JMJD3 | INK4A/ARF | SUPPRESSOR | INK4A-ARF LOCUS | JMJD3 CONTRIBUTES | INDUCED SENESCENCE | CANCER | GENE | ONCOLOGY | Renal cell carcinoma | UTX | Epigenetics | Histone H3K27 demethylase | PROTEINS | Up-Regulation | Kidney Neoplasms - genetics | Polycomb Repressive Complex 2 - genetics | Histone Demethylases - biosynthesis | Cyclin-Dependent Kinase 4 - genetics | Humans | Middle Aged | Transcriptional Activation | Carcinoma, Renal Cell - genetics | Male | RNA, Messenger - metabolism | Histone Demethylases - genetics | Adult | Carcinoma, Renal Cell - enzymology | Female | Nuclear Proteins - genetics | RNA, Messenger - genetics | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Nuclear Proteins - metabolism | Cyclin-Dependent Kinase 4 - metabolism | Jumonji Domain-Containing Histone Demethylases - genetics | Enhancer of Zeste Homolog 2 Protein | Histone Demethylases - metabolism | Kidney Neoplasms - enzymology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Aged | Methylation | Polycomb Repressive Complex 2 - metabolism | Jumonji Domain-Containing Histone Demethylases - metabolism | Physiological aspects | Development and progression | Monoamine oxidase | Carcinoma, Renal cell | Research | Analysis | Epigenetic inheritance | Chromatin | RNA | Genes | Genetic research | Genetic aspects | Gene expression | Cancer | Index Medicus
JMJD3 | INK4A/ARF | SUPPRESSOR | INK4A-ARF LOCUS | JMJD3 CONTRIBUTES | INDUCED SENESCENCE | CANCER | GENE | ONCOLOGY | Renal cell carcinoma | UTX | Epigenetics | Histone H3K27 demethylase | PROTEINS | Up-Regulation | Kidney Neoplasms - genetics | Polycomb Repressive Complex 2 - genetics | Histone Demethylases - biosynthesis | Cyclin-Dependent Kinase 4 - genetics | Humans | Middle Aged | Transcriptional Activation | Carcinoma, Renal Cell - genetics | Male | RNA, Messenger - metabolism | Histone Demethylases - genetics | Adult | Carcinoma, Renal Cell - enzymology | Female | Nuclear Proteins - genetics | RNA, Messenger - genetics | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Nuclear Proteins - metabolism | Cyclin-Dependent Kinase 4 - metabolism | Jumonji Domain-Containing Histone Demethylases - genetics | Enhancer of Zeste Homolog 2 Protein | Histone Demethylases - metabolism | Kidney Neoplasms - enzymology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Aged | Methylation | Polycomb Repressive Complex 2 - metabolism | Jumonji Domain-Containing Histone Demethylases - metabolism | Physiological aspects | Development and progression | Monoamine oxidase | Carcinoma, Renal cell | Research | Analysis | Epigenetic inheritance | Chromatin | RNA | Genes | Genetic research | Genetic aspects | Gene expression | Cancer | Index Medicus
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 4/2010, Volume 67, Issue 7, pp. 1165 - 1176
Aging is linked to loss of the self-renewal capacity of adult stem cells. Here, we observed that human multipotent stem cells (MSCs) underwent cellular...
Life Sciences | Biochemistry, general | JMJD3 | Polycomb gene | Senescence | Life Sciences, general | Epigenetic | Biomedicine general | Cell Biology | Multipotent stem cell | TARGET | INK4A-ARF LOCUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROLIFERATION | P16(INK4A) | CELL BIOLOGY | HUMAN FIBROBLASTS | HETEROCHROMATIN FORMATION | DIFFERENTIATION | INHIBITOR | PROTEINS | Promoter Regions, Genetic | Up-Regulation | Adult Stem Cells - cytology | Histone Deacetylases - genetics | Down-Regulation | Epigenesis, Genetic | Humans | Multipotent Stem Cells - metabolism | Cells, Cultured | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Polycomb-Group Proteins | Jumonji Domain-Containing Histone Demethylases - genetics | Valproic Acid - pharmacology | Adult Stem Cells - metabolism | RNA Interference | Cellular Senescence | Multipotent Stem Cells - cytology | Histone Deacetylase Inhibitors - pharmacology | Jumonji Domain-Containing Histone Demethylases - metabolism | Repressor Proteins - metabolism | RNA, Small Interfering - metabolism | Stem cell research | Anopheles | Stem cells | Histones | Genetic research | Adults | Universities and colleges | Public health | Aging | Enzymes | Gene expression
Life Sciences | Biochemistry, general | JMJD3 | Polycomb gene | Senescence | Life Sciences, general | Epigenetic | Biomedicine general | Cell Biology | Multipotent stem cell | TARGET | INK4A-ARF LOCUS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROLIFERATION | P16(INK4A) | CELL BIOLOGY | HUMAN FIBROBLASTS | HETEROCHROMATIN FORMATION | DIFFERENTIATION | INHIBITOR | PROTEINS | Promoter Regions, Genetic | Up-Regulation | Adult Stem Cells - cytology | Histone Deacetylases - genetics | Down-Regulation | Epigenesis, Genetic | Humans | Multipotent Stem Cells - metabolism | Cells, Cultured | Repressor Proteins - genetics | Histone Deacetylases - metabolism | Polycomb-Group Proteins | Jumonji Domain-Containing Histone Demethylases - genetics | Valproic Acid - pharmacology | Adult Stem Cells - metabolism | RNA Interference | Cellular Senescence | Multipotent Stem Cells - cytology | Histone Deacetylase Inhibitors - pharmacology | Jumonji Domain-Containing Histone Demethylases - metabolism | Repressor Proteins - metabolism | RNA, Small Interfering - metabolism | Stem cell research | Anopheles | Stem cells | Histones | Genetic research | Adults | Universities and colleges | Public health | Aging | Enzymes | Gene expression
Journal Article
Developmental Cell, ISSN 1534-5807, 07/2009, Volume 17, Issue 1, pp. 142 - 149
Aging is a complex organismal process that is controlled by genetic, environmental, and behavioral factors. Accumulating evidence supports a role for different...
CELLCYCLE | SIGNALING | INK4A/ARF | APOPTOSIS | ACTIVATION | PATHWAY | MAP KINASE | TUMOR-SUPPRESSOR | WIP1 PHOSPHATASE | SENESCENCE | DEVELOPMENTAL BIOLOGY | P38-ALPHA | TUMORIGENESIS | CELL BIOLOGY | Islets of Langerhans - physiology | Humans | Liver - metabolism | Mice, Inbred C57BL | Phosphoprotein Phosphatases - metabolism | Protein Phosphatase 2C | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Repressor Proteins - genetics | p38 Mitogen-Activated Protein Kinases - genetics | Kidney - metabolism | Animals | Phosphoprotein Phosphatases - genetics | Aging - physiology | Spleen - metabolism | Islets of Langerhans - cytology | Cell Cycle - physiology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Lung - metabolism | Mice | p38 Mitogen-Activated Protein Kinases - metabolism | Enzyme Activation | Repressor Proteins - metabolism | Phosphatases | Cell cycle
CELLCYCLE | SIGNALING | INK4A/ARF | APOPTOSIS | ACTIVATION | PATHWAY | MAP KINASE | TUMOR-SUPPRESSOR | WIP1 PHOSPHATASE | SENESCENCE | DEVELOPMENTAL BIOLOGY | P38-ALPHA | TUMORIGENESIS | CELL BIOLOGY | Islets of Langerhans - physiology | Humans | Liver - metabolism | Mice, Inbred C57BL | Phosphoprotein Phosphatases - metabolism | Protein Phosphatase 2C | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Repressor Proteins - genetics | p38 Mitogen-Activated Protein Kinases - genetics | Kidney - metabolism | Animals | Phosphoprotein Phosphatases - genetics | Aging - physiology | Spleen - metabolism | Islets of Langerhans - cytology | Cell Cycle - physiology | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Lung - metabolism | Mice | p38 Mitogen-Activated Protein Kinases - metabolism | Enzyme Activation | Repressor Proteins - metabolism | Phosphatases | Cell cycle
Journal Article
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, ISSN 0925-4439, 11/2008, Volume 1782, Issue 11, pp. 642 - 648
We report here that the polycomb group protein Bmi1 promotes prostate tumorigenesis. Bmi1 is detected at higher levels in androgen-independent PC3 and DU145...
CANCER PATIENTS | METHYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | p14(ARF) | MOLECULAR MARKER | PROLIFERATION | Bmi1 | OVEREXPRESSION | BIOPHYSICS | EPITHELIAL-CELLS | GENE | CELL SELF-RENEWAL | MYC TRANSGENIC MICE | INK4A/ARF LOCUS | p16(INK4A) | Prostate cancer
CANCER PATIENTS | METHYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | p14(ARF) | MOLECULAR MARKER | PROLIFERATION | Bmi1 | OVEREXPRESSION | BIOPHYSICS | EPITHELIAL-CELLS | GENE | CELL SELF-RENEWAL | MYC TRANSGENIC MICE | INK4A/ARF LOCUS | p16(INK4A) | Prostate cancer
Journal Article
Molecular Biology of the Cell, ISSN 1059-1524, 09/2016, Volume 27, Issue 17, pp. 2726 - 2734
The tumor suppressor proteins p15(INK4B), p16(INK4A), and p14(ARF), encoded by the INK4AB/ARF locus, are crucial regulators of cellular senescence. The locus...
INK4A-ARF LOCUS | TARGET GENES | ACTIVATION | METHYLATION | ACETYLATION | CELL-CYCLE ARREST | STRESS | DEMETHYLASE JMJD3 CONTRIBUTES | HISTONE H3 PHOSPHORYLATION | IMMEDIATE-EARLY GENES | CELL BIOLOGY | Phosphorylation | Cell Proliferation | Humans | Transcriptional Activation | Polycomb-Group Proteins | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Aging - genetics | Cell Cycle | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Histones - metabolism | Ribosomal Protein S6 Kinases, 90-kDa - physiology | Tumor Suppressor Protein p14ARF - metabolism | Aging - metabolism | Life Sciences
INK4A-ARF LOCUS | TARGET GENES | ACTIVATION | METHYLATION | ACETYLATION | CELL-CYCLE ARREST | STRESS | DEMETHYLASE JMJD3 CONTRIBUTES | HISTONE H3 PHOSPHORYLATION | IMMEDIATE-EARLY GENES | CELL BIOLOGY | Phosphorylation | Cell Proliferation | Humans | Transcriptional Activation | Polycomb-Group Proteins | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Aging - genetics | Cell Cycle | Cell Line, Tumor | Cyclin-Dependent Kinase Inhibitor p16 - metabolism | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Histones - metabolism | Ribosomal Protein S6 Kinases, 90-kDa - physiology | Tumor Suppressor Protein p14ARF - metabolism | Aging - metabolism | Life Sciences
Journal Article
AGING CELL, ISSN 1474-9726, 08/2009, Volume 8, Issue 4, pp. 439 - 448
P>Expression of the p16(INK4a) tumor suppressor sharply increases with age in most mammalian tissues, and contributes to an age-induced functional decline of...
CDKN2a | LYMPHOCYTE SUBSETS | INK4A/ARF EXPRESSION | exercise | CHROMOSOME 9P21 | INK4 | CELLULAR SENESCENCE | IL-6 | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | frailty | ARF | smoking | IN-VIVO | GENE-EXPRESSION | TUMOR-SUPPRESSOR | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | TELOMERE LENGTH | Humans | Middle Aged | Gene Expression Regulation | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Male | Biomarkers - blood | Exercise | Aging - physiology | T-Lymphocytes - metabolism | Adolescent | Aged, 80 and over | Adult | Female | Transcription, Genetic | Aged | ADP-Ribosylation Factors - genetics | Cyclin-Dependent Kinase Inhibitor p16 - blood | Smoking
CDKN2a | LYMPHOCYTE SUBSETS | INK4A/ARF EXPRESSION | exercise | CHROMOSOME 9P21 | INK4 | CELLULAR SENESCENCE | IL-6 | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | frailty | ARF | smoking | IN-VIVO | GENE-EXPRESSION | TUMOR-SUPPRESSOR | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | TELOMERE LENGTH | Humans | Middle Aged | Gene Expression Regulation | Cyclin-Dependent Kinase Inhibitor p16 - genetics | Male | Biomarkers - blood | Exercise | Aging - physiology | T-Lymphocytes - metabolism | Adolescent | Aged, 80 and over | Adult | Female | Transcription, Genetic | Aged | ADP-Ribosylation Factors - genetics | Cyclin-Dependent Kinase Inhibitor p16 - blood | Smoking
Journal Article
Oncology Letters, ISSN 1792-1074, 2017, Volume 14, Issue 2, pp. 1550 - 1560
Previous studies have demonstrated abnormal H3K27 methylation status during clear cell renal cell carcinoma (ccRCC) carcinogenesis, and have suggested that the...
Jumonji domain-containing protein 3 | Clear cell renal cell carcinoma | Overall survival | Disease free survival | Prognostic biomarker | INK4A/ARF | clear cell renal cell carcinoma | ENHANCER | jumonji domain-containing protein 3 | CANCER | RADICAL NEPHRECTOMY | ONCOLOGY | overall survival | prognostic biomarker | disease free survival | CONTRIBUTES | EZH2 | TOOL
Jumonji domain-containing protein 3 | Clear cell renal cell carcinoma | Overall survival | Disease free survival | Prognostic biomarker | INK4A/ARF | clear cell renal cell carcinoma | ENHANCER | jumonji domain-containing protein 3 | CANCER | RADICAL NEPHRECTOMY | ONCOLOGY | overall survival | prognostic biomarker | disease free survival | CONTRIBUTES | EZH2 | TOOL
Journal Article
Stem Cell Reports, ISSN 2213-6711, 06/2018, Volume 10, Issue 6, pp. 1721 - 1733
Brain neurogenesis is severely impaired following exposure to ionizing radiation (IR). We and others have shown that the expression of the tumor suppressor...
senescence | neurogenesis | INK4a/ARF | DNA damage | irradiation | p53 | OXIDATIVE STRESS | CHILDHOOD-CANCER | ADULT NEUROGENESIS | HEMATOPOIETIC STEM-CELLS | ACUTE LYMPHOBLASTIC-LEUKEMIA | DNA-DAMAGE | CRANIAL IRRADIATION | IONIZING-RADIATION | HIPPOCAMPAL NEUROGENESIS | COGNITIVE DEFICITS | CELL & TISSUE ENGINEERING | CELL BIOLOGY
senescence | neurogenesis | INK4a/ARF | DNA damage | irradiation | p53 | OXIDATIVE STRESS | CHILDHOOD-CANCER | ADULT NEUROGENESIS | HEMATOPOIETIC STEM-CELLS | ACUTE LYMPHOBLASTIC-LEUKEMIA | DNA-DAMAGE | CRANIAL IRRADIATION | IONIZING-RADIATION | HIPPOCAMPAL NEUROGENESIS | COGNITIVE DEFICITS | CELL & TISSUE ENGINEERING | CELL BIOLOGY
Journal Article
Molecular and Cellular Endocrinology, ISSN 0303-7207, 08/2013, Volume 375, Issue 1-2, pp. 35 - 42
Microarray gene expression data were used to analyze the expression pattern of cyclin, cyclin-dependent kinase (CDKs) and cyclin-dependent kinase inhibitor...
Type 2 diabetes | Human islet | Cyclin | Beta-cell | Microarray | Cell cycle | INK4A/ARF EXPRESSION | PROLIFERATION | CANCER | CELL BIOLOGY | REPLICATION | HYPERGLYCEMIA | RETINOBLASTOMA PROTEIN | PRIMARY MECHANISM | INSULIN-RESISTANCE | IN-VIVO | ENDOCRINOLOGY & METABOLISM | Cyclin-Dependent Kinases - metabolism | Oligonucleotide Array Sequence Analysis | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Cyclins - genetics | Transcriptome | Male | Gene Expression Profiling | Cyclin-Dependent Kinase Inhibitor Proteins - metabolism | Diabetes Mellitus, Type 2 - metabolism | Case-Control Studies | Cyclin-Dependent Kinase Inhibitor Proteins - genetics | Cyclins - metabolism | Islets of Langerhans - metabolism | Aging | Female | Cyclin-Dependent Kinases - genetics | Insulin Secretion | Genetic Predisposition to Disease | Genetic Association Studies | Cells, Cultured | Insulin - metabolism | Aged | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - pathology | Genes, cdc | Human | Databases | Inhibitors | Genes | Diabetes | Kinases | Gene expression | Low level | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Type 2 diabetes | Human islet | Cyclin | Beta-cell | Microarray | Cell cycle | INK4A/ARF EXPRESSION | PROLIFERATION | CANCER | CELL BIOLOGY | REPLICATION | HYPERGLYCEMIA | RETINOBLASTOMA PROTEIN | PRIMARY MECHANISM | INSULIN-RESISTANCE | IN-VIVO | ENDOCRINOLOGY & METABOLISM | Cyclin-Dependent Kinases - metabolism | Oligonucleotide Array Sequence Analysis | Diabetes Mellitus, Type 2 - genetics | Humans | Middle Aged | Cyclins - genetics | Transcriptome | Male | Gene Expression Profiling | Cyclin-Dependent Kinase Inhibitor Proteins - metabolism | Diabetes Mellitus, Type 2 - metabolism | Case-Control Studies | Cyclin-Dependent Kinase Inhibitor Proteins - genetics | Cyclins - metabolism | Islets of Langerhans - metabolism | Aging | Female | Cyclin-Dependent Kinases - genetics | Insulin Secretion | Genetic Predisposition to Disease | Genetic Association Studies | Cells, Cultured | Insulin - metabolism | Aged | Polymorphism, Single Nucleotide | Diabetes Mellitus, Type 2 - pathology | Genes, cdc | Human | Databases | Inhibitors | Genes | Diabetes | Kinases | Gene expression | Low level | Clinical Medicine | Endokrinologi och diabetes | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Endocrinology and Diabetes
Journal Article
细胞研究:英文版, ISSN 1001-0602, 2015, Volume 25, Issue 11, pp. 1205 - 1218
ASXL1 mutations are frequently found in hematological tumors, and loss of Asxll promotes myeloid transforma- tion in mice. Here we present data supporting a...
转录激活 | 基因活性 | 增殖 | 肿瘤抑制 | 诱导表达 | 致癌 | 信号 | 活化作用 | Polycomb | tumor suppressor | INK4A | INK4B | H2A ubiquitylation | TRANSFORMATION | INK4A-ARF LOCUS | METHYLATION | FREQUENT MUTATION | P15(INK4B) | CANCER | CELL BIOLOGY | GENE | MYELODYSPLASTIC SYNDROMES | BAP1 | Cell Line | Promoter Regions, Genetic | Tumor Suppressor Proteins - metabolism | Cell Proliferation | Humans | Polycomb-Group Proteins - metabolism | Animals | Ubiquitin Thiolesterase - metabolism | Mice | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Histones - metabolism | Mutation | Ubiquitin-Specific Proteases - metabolism | Repressor Proteins - metabolism | Original
转录激活 | 基因活性 | 增殖 | 肿瘤抑制 | 诱导表达 | 致癌 | 信号 | 活化作用 | Polycomb | tumor suppressor | INK4A | INK4B | H2A ubiquitylation | TRANSFORMATION | INK4A-ARF LOCUS | METHYLATION | FREQUENT MUTATION | P15(INK4B) | CANCER | CELL BIOLOGY | GENE | MYELODYSPLASTIC SYNDROMES | BAP1 | Cell Line | Promoter Regions, Genetic | Tumor Suppressor Proteins - metabolism | Cell Proliferation | Humans | Polycomb-Group Proteins - metabolism | Animals | Ubiquitin Thiolesterase - metabolism | Mice | Cyclin-Dependent Kinase Inhibitor p15 - metabolism | Histones - metabolism | Mutation | Ubiquitin-Specific Proteases - metabolism | Repressor Proteins - metabolism | Original
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 10/2012, Volume 287, Issue 43, pp. 36179 - 36189
The polycomb group (PcG) proteins, Bmi-1 and Ezh2, are important epigenetic regulators that enhance skin cancer cell survival. We recently showed that Bmi-1...
MULTIPLE-MYELOMA | BREAST-CANCER | EZH2 HISTONE METHYLTRANSFERASE | SKIN-CANCER CELLS | BMI-1 ONCOPROTEIN | INK4A-ARF LOCUS | MECHANISM | SULFORAPHANE | COLORECTAL-CANCER | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROLIFERATION | Gene Expression Regulation, Enzymologic - drug effects | G2 Phase - genetics | Polycomb Repressive Complex 2 - genetics | Proteasome Inhibitors - pharmacology | Apoptosis - drug effects | Humans | Apoptosis - genetics | Nuclear Respiratory Factor 1 - genetics | Proteasome Endopeptidase Complex - biosynthesis | Enhancer of Zeste Homolog 2 Protein | G2 Phase - drug effects | Proteasome Endopeptidase Complex - genetics | Leupeptins - pharmacology | Ubiquitination - drug effects | Gene Expression Regulation, Enzymologic - genetics | Cysteine Proteinase Inhibitors - pharmacology | Nuclear Respiratory Factor 1 - metabolism | Cell Line, Tumor | Polycomb Repressive Complex 2 - metabolism | Ubiquitination - genetics | Nrf2 | Protein Synthesis and Degradation | Bmi-1 | Keratinocytes | Epidermis | Polycomb | Keratinocyte | Squamous Cell Carcinoma | Ezh2 | Proteasome
MULTIPLE-MYELOMA | BREAST-CANCER | EZH2 HISTONE METHYLTRANSFERASE | SKIN-CANCER CELLS | BMI-1 ONCOPROTEIN | INK4A-ARF LOCUS | MECHANISM | SULFORAPHANE | COLORECTAL-CANCER | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROLIFERATION | Gene Expression Regulation, Enzymologic - drug effects | G2 Phase - genetics | Polycomb Repressive Complex 2 - genetics | Proteasome Inhibitors - pharmacology | Apoptosis - drug effects | Humans | Apoptosis - genetics | Nuclear Respiratory Factor 1 - genetics | Proteasome Endopeptidase Complex - biosynthesis | Enhancer of Zeste Homolog 2 Protein | G2 Phase - drug effects | Proteasome Endopeptidase Complex - genetics | Leupeptins - pharmacology | Ubiquitination - drug effects | Gene Expression Regulation, Enzymologic - genetics | Cysteine Proteinase Inhibitors - pharmacology | Nuclear Respiratory Factor 1 - metabolism | Cell Line, Tumor | Polycomb Repressive Complex 2 - metabolism | Ubiquitination - genetics | Nrf2 | Protein Synthesis and Degradation | Bmi-1 | Keratinocytes | Epidermis | Polycomb | Keratinocyte | Squamous Cell Carcinoma | Ezh2 | Proteasome
Journal Article