Science, ISSN 0036-8075, 8/2013, Volume 341, Issue 6149, pp. 1005 - 1009
The development of multicellular animals is initially controlled by maternal gene products deposited in the oocyte. During the maternal-to-zygotic transition,...
Vertebrates | Transcription factors | Chromatin | Genes | Drosophila | REPORTS | Stem cells | Genomes | Embryos | Binding sites | Gene activation | TRANSITION | ZEBRAFISH | EVOLUTION | ENDODERM FORMATION | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | REGIONS | REGULATORY NETWORK | PLURIPOTENCY | EXPRESSION | DROSOPHILA | Pluripotent Stem Cells - cytology | Zebrafish Proteins - metabolism | Pluripotent Stem Cells - physiology | Transcriptional Activation | Zygote - metabolism | DNA Polymerase II - metabolism | Zebrafish - embryology | Zebrafish - genetics | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | Animals | Gene Expression Regulation, Developmental | Octamer Transcription Factor-3 - metabolism | Xenopus Proteins - metabolism | Zebrafish Proteins - genetics | Binding Sites | Physiological aspects | Genetic aspects | Research | Gene expression | Fracture mechanics | Zebrafish | Evolution | Cleavage | Activation | Mammals
Vertebrates | Transcription factors | Chromatin | Genes | Drosophila | REPORTS | Stem cells | Genomes | Embryos | Binding sites | Gene activation | TRANSITION | ZEBRAFISH | EVOLUTION | ENDODERM FORMATION | MULTIDISCIPLINARY SCIENCES | EMBRYONIC STEM-CELLS | REGIONS | REGULATORY NETWORK | PLURIPOTENCY | EXPRESSION | DROSOPHILA | Pluripotent Stem Cells - cytology | Zebrafish Proteins - metabolism | Pluripotent Stem Cells - physiology | Transcriptional Activation | Zygote - metabolism | DNA Polymerase II - metabolism | Zebrafish - embryology | Zebrafish - genetics | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | Animals | Gene Expression Regulation, Developmental | Octamer Transcription Factor-3 - metabolism | Xenopus Proteins - metabolism | Zebrafish Proteins - genetics | Binding Sites | Physiological aspects | Genetic aspects | Research | Gene expression | Fracture mechanics | Zebrafish | Evolution | Cleavage | Activation | Mammals
Journal Article
Journal of Materials Science: Materials in Medicine, ISSN 0957-4530, 11/2006, Volume 17, Issue 11, pp. 997 - 1002
Bioactive glasses have been shown to regulate gene expression in both hard and soft tissue repair. New resorbable bioactive glass constructs are now being...
Polymer Sciences | Chemistry | Ceramics, Glass, Composites, Natural Methods | Metallic Materials | Surfaces and Interfaces, Thin Films | Biomaterials | Characterization and Evaluation Materials | IONIC-DISSOLUTION PRODUCTS | MATERIALS SCIENCE, BIOMATERIALS | MESSENGER-RNA | BONE-FORMATION | ENGINEERING, BIOMEDICAL | EMBRYONIC STEM-CELLS | ENDOTHELIAL-CELLS | HUMAN FIBROBLASTS | SMOOTH-MUSCLE-CELLS | ALKALINE-PHOSPHATASE EXPRESSION | OSTEOBLASTS IN-VITRO | BETA-GLYCEROPHOSPHATE | Gene Expression Regulation - drug effects | Cell Line | Animals | Humans | Transcriptional Activation | Glass | Biocompatible Materials - pharmacology | Ceramics - pharmacology | Gene expression | Surface chemistry
Polymer Sciences | Chemistry | Ceramics, Glass, Composites, Natural Methods | Metallic Materials | Surfaces and Interfaces, Thin Films | Biomaterials | Characterization and Evaluation Materials | IONIC-DISSOLUTION PRODUCTS | MATERIALS SCIENCE, BIOMATERIALS | MESSENGER-RNA | BONE-FORMATION | ENGINEERING, BIOMEDICAL | EMBRYONIC STEM-CELLS | ENDOTHELIAL-CELLS | HUMAN FIBROBLASTS | SMOOTH-MUSCLE-CELLS | ALKALINE-PHOSPHATASE EXPRESSION | OSTEOBLASTS IN-VITRO | BETA-GLYCEROPHOSPHATE | Gene Expression Regulation - drug effects | Cell Line | Animals | Humans | Transcriptional Activation | Glass | Biocompatible Materials - pharmacology | Ceramics - pharmacology | Gene expression | Surface chemistry
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 07/2018, Volume 115, Issue 29, pp. E6780 - E6788
In mice, transcription initiates at the mid-one-cell stage and transcriptional activity dramatically increases during the two-cell stage, a process called...
Preimplantation mouse embryo | Minor zygotic gene activation | Gene expression | Maternal-to-zygotic transition | RNA-POLYMERASE-II | maternal-to-zygotic transition | preimplantation mouse embryo | HISTONE MODIFICATION | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | MAMMALIAN DEVELOPMENT | minor zygotic gene activation | DNA-REPLICATION | MESSENGER-RNA | EMBRYO | IN-VIVO | EXPRESSION | gene expression | MICROARRAY DATA | Animals | Zygote - cytology | Blastocyst - metabolism | Gene Expression Regulation, Developmental - drug effects | Zygote - metabolism | Embryonic Development - physiology | Blastocyst - cytology | Mice | Dichlororibofuranosylbenzimidazole - pharmacology | Histones - metabolism | Embryonic Development - drug effects | Gene Expression Regulation, Developmental - physiology | Embryonic development | Genetic aspects | Genetic transcription | Observations | Biological Sciences | PNAS Plus
Preimplantation mouse embryo | Minor zygotic gene activation | Gene expression | Maternal-to-zygotic transition | RNA-POLYMERASE-II | maternal-to-zygotic transition | preimplantation mouse embryo | HISTONE MODIFICATION | STEM-CELLS | MULTIDISCIPLINARY SCIENCES | MAMMALIAN DEVELOPMENT | minor zygotic gene activation | DNA-REPLICATION | MESSENGER-RNA | EMBRYO | IN-VIVO | EXPRESSION | gene expression | MICROARRAY DATA | Animals | Zygote - cytology | Blastocyst - metabolism | Gene Expression Regulation, Developmental - drug effects | Zygote - metabolism | Embryonic Development - physiology | Blastocyst - cytology | Mice | Dichlororibofuranosylbenzimidazole - pharmacology | Histones - metabolism | Embryonic Development - drug effects | Gene Expression Regulation, Developmental - physiology | Embryonic development | Genetic aspects | Genetic transcription | Observations | Biological Sciences | PNAS Plus
Journal Article
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Full Text
Nac1 facilitates pluripotency gene activation for establishing somatic cell reprogramming
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 10/2019, Volume 518, Issue 2, pp. 253 - 258
Transcription factors play a central role in pluripotency transcription circuitry for establishing pluripotent reprogramming. Master transcription factors...
Induced pluripotent stem cell | Embryonic stem cell | Nucleus accumbens-1 | Pluripotency | Anopheles | Genes | Genomics | Genetic transcription | DNA binding proteins | Embryonic stem cells | Biomedical engineering
Induced pluripotent stem cell | Embryonic stem cell | Nucleus accumbens-1 | Pluripotency | Anopheles | Genes | Genomics | Genetic transcription | DNA binding proteins | Embryonic stem cells | Biomedical engineering
Journal Article
Cell Stem Cell, ISSN 1934-5909, 05/2015, Volume 16, Issue 5, pp. 504 - 516
Long noncoding RNAs (lncRNAs) have been implicated in controlling various aspects of embryonic stem cell (ESC) biology, although the functions of specific...
NONCODING RNA | LINCRNAS | IDENTITY | EVOLUTION | CHROMATIN INTERACTOME | TRANSCRIPTION | SELF-RENEWAL | PLURIPOTENCY | ENHANCERS | EXPRESSION | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Cell Line | Homeodomain Proteins - metabolism | Transcriptional Activation | Gene Expression Regulation | Genetic Loci - genetics | Chromatin Assembly and Disassembly | RNA, Long Noncoding - genetics | Embryonic Stem Cells - physiology | Homeodomain Proteins - genetics | DNA - genetics | Cell Differentiation - genetics | Animals | CRISPR-Cas Systems | Enhancer Elements, Genetic - genetics | Mice | Genome | RNA, Long Noncoding - metabolism
NONCODING RNA | LINCRNAS | IDENTITY | EVOLUTION | CHROMATIN INTERACTOME | TRANSCRIPTION | SELF-RENEWAL | PLURIPOTENCY | ENHANCERS | EXPRESSION | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Cell Line | Homeodomain Proteins - metabolism | Transcriptional Activation | Gene Expression Regulation | Genetic Loci - genetics | Chromatin Assembly and Disassembly | RNA, Long Noncoding - genetics | Embryonic Stem Cells - physiology | Homeodomain Proteins - genetics | DNA - genetics | Cell Differentiation - genetics | Animals | CRISPR-Cas Systems | Enhancer Elements, Genetic - genetics | Mice | Genome | RNA, Long Noncoding - metabolism
Journal Article
Molecular Cell, ISSN 1097-2765, 11/2009, Volume 36, Issue 4, pp. 682 - 695
The transcription factor GATA-1 is required for terminal erythroid maturation and functions as an activator or repressor depending on gene context. Yet its...
DNA | MOUSE DEVELOPMENT | TRANSCRIPTION FACTOR GATA-1 | STEM-CELLS | DNA-BINDING FACTOR | N-RAS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | IN-VIVO | MAMMALIAN-CELLS | ERYTHROID MATURATION | EXPRESSION | CELL BIOLOGY | Chromatin - metabolism | Transcriptional Activation - genetics | Biotinylation | Computational Biology | Gene Silencing | Genome - genetics | Molecular Sequence Data | Gene Expression Profiling | Gene Expression Regulation, Leukemic | Polycomb-Group Proteins | GATA1 Transcription Factor - metabolism | Sequence Analysis, DNA | Regulatory Sequences, Nucleic Acid - genetics | Animals | Chromatin Immunoprecipitation | Streptavidin - metabolism | Base Sequence | Cell Line, Tumor | Protein Binding | Biotin - metabolism | Mice | Models, Genetic | Binding Sites | Repressor Proteins - metabolism | Computer science | Medical colleges | Chromatin | Anopheles | Genomics | Genetic research | Medical law | Gene expression | Artificial intelligence | erythroid | GATA-1 | ChIP-seq | Polycomb | Zbtb7a
DNA | MOUSE DEVELOPMENT | TRANSCRIPTION FACTOR GATA-1 | STEM-CELLS | DNA-BINDING FACTOR | N-RAS | BIOCHEMISTRY & MOLECULAR BIOLOGY | ZINC-FINGER | IN-VIVO | MAMMALIAN-CELLS | ERYTHROID MATURATION | EXPRESSION | CELL BIOLOGY | Chromatin - metabolism | Transcriptional Activation - genetics | Biotinylation | Computational Biology | Gene Silencing | Genome - genetics | Molecular Sequence Data | Gene Expression Profiling | Gene Expression Regulation, Leukemic | Polycomb-Group Proteins | GATA1 Transcription Factor - metabolism | Sequence Analysis, DNA | Regulatory Sequences, Nucleic Acid - genetics | Animals | Chromatin Immunoprecipitation | Streptavidin - metabolism | Base Sequence | Cell Line, Tumor | Protein Binding | Biotin - metabolism | Mice | Models, Genetic | Binding Sites | Repressor Proteins - metabolism | Computer science | Medical colleges | Chromatin | Anopheles | Genomics | Genetic research | Medical law | Gene expression | Artificial intelligence | erythroid | GATA-1 | ChIP-seq | Polycomb | Zbtb7a
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2015, Volume 112, Issue 15, pp. E1936 - E1945
Newborn granule neurons generated from neural progenitor cells (NPCs) in the adult hippocampus play a key role in spatial learning and pattern separation....
SOX2 | Epigenetics | Neurogenesis | PROGENITOR CELLS | ANOPHTHALMIA SYNDROME | MULTIDISCIPLINARY SCIENCES | ADULT DENTATE GYRUS | MOUSE | SELF-RENEWAL | PROLIFERATION | epigenetics | EMBRYONIC STEM-CELLS | IN-VIVO | neurogenesis | NEURONS | DIFFERENTIATION | Cell Cycle - genetics | Epigenesis, Genetic | SOXB1 Transcription Factors - deficiency | Transcriptional Activation | Promoter Regions, Genetic - genetics | SOXB1 Transcription Factors - metabolism | Neurogenesis - genetics | Basic Helix-Loop-Helix Transcription Factors - metabolism | RNA Interference | SOXB1 Transcription Factors - genetics | Neurons - physiology | Neurons - metabolism | Animals, Newborn | Cell Proliferation - genetics | Gene Expression | Basic Helix-Loop-Helix Transcription Factors - genetics | Mice, Inbred C57BL | Cells, Cultured | Mice, Transgenic | Hippocampus - cytology | Reverse Transcriptase Polymerase Chain Reaction | Nerve Tissue Proteins - genetics | Blotting, Western | Mice, Knockout | Nerve Tissue Proteins - metabolism | Hippocampus - metabolism | Patch-Clamp Techniques | Animals | Protein Binding | Neural Stem Cells - metabolism | Microscopy, Fluorescence | Influence | Transcription factors | Hippocampus (Brain) | Research | Analysis | Biological Sciences | PNAS Plus
SOX2 | Epigenetics | Neurogenesis | PROGENITOR CELLS | ANOPHTHALMIA SYNDROME | MULTIDISCIPLINARY SCIENCES | ADULT DENTATE GYRUS | MOUSE | SELF-RENEWAL | PROLIFERATION | epigenetics | EMBRYONIC STEM-CELLS | IN-VIVO | neurogenesis | NEURONS | DIFFERENTIATION | Cell Cycle - genetics | Epigenesis, Genetic | SOXB1 Transcription Factors - deficiency | Transcriptional Activation | Promoter Regions, Genetic - genetics | SOXB1 Transcription Factors - metabolism | Neurogenesis - genetics | Basic Helix-Loop-Helix Transcription Factors - metabolism | RNA Interference | SOXB1 Transcription Factors - genetics | Neurons - physiology | Neurons - metabolism | Animals, Newborn | Cell Proliferation - genetics | Gene Expression | Basic Helix-Loop-Helix Transcription Factors - genetics | Mice, Inbred C57BL | Cells, Cultured | Mice, Transgenic | Hippocampus - cytology | Reverse Transcriptase Polymerase Chain Reaction | Nerve Tissue Proteins - genetics | Blotting, Western | Mice, Knockout | Nerve Tissue Proteins - metabolism | Hippocampus - metabolism | Patch-Clamp Techniques | Animals | Protein Binding | Neural Stem Cells - metabolism | Microscopy, Fluorescence | Influence | Transcription factors | Hippocampus (Brain) | Research | Analysis | Biological Sciences | PNAS Plus
Journal Article
Science, ISSN 0036-8075, 7/2009, Volume 325, Issue 5939, pp. 471 - 473
Drosophila embryogenesis is characterized by rapid transitions in gene activity, whereby crudely distributed gradients of regulatory proteins give way to...
Ectoderm | Embryogenesis | Transcription factors | Genes | Drosophila | Mesoderm | Reports | Gene expression | Embryos | Gene activation | Genetic hybridization | MESODERM | PROTEIN | RNA | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | CONSEQUENCES | NOISE | EXPRESSION | GRADIENT | MELANOGASTER | DORSAL | Genes, Insect | Animals | Stochastic Processes | Gene Expression Regulation, Developmental | Transcriptional Activation | Embryo, Nonmammalian | RNA Polymerase II - metabolism | Drosophila - genetics | Embryonic development | Growth | Stochastic processes | Genetic aspects | Research | Insects | Evolution & development | DNA-directed RNA polymerase
Ectoderm | Embryogenesis | Transcription factors | Genes | Drosophila | Mesoderm | Reports | Gene expression | Embryos | Gene activation | Genetic hybridization | MESODERM | PROTEIN | RNA | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | CONSEQUENCES | NOISE | EXPRESSION | GRADIENT | MELANOGASTER | DORSAL | Genes, Insect | Animals | Stochastic Processes | Gene Expression Regulation, Developmental | Transcriptional Activation | Embryo, Nonmammalian | RNA Polymerase II - metabolism | Drosophila - genetics | Embryonic development | Growth | Stochastic processes | Genetic aspects | Research | Insects | Evolution & development | DNA-directed RNA polymerase
Journal Article
Cell Stem Cell, ISSN 1934-5909, 05/2014, Volume 14, Issue 5, pp. 575 - 591
The master transcription factors play integral roles in the pluripotency transcription circuitry of embryonic stem cells (ESCs). How they selectively activate...
OCT4 | CHROMATIN REMODELING COMPLEX | MEDIATOR | TRANSCRIPTIONAL NETWORK | MECHANISMS | DIFFERENTIATION | EXPRESSION | OCCUPANCY | GENOME | RNAI SCREEN | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Cell Line | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Pluripotent Stem Cells - cytology | Blastocyst - metabolism | Blastocyst - cytology | Chromatin Assembly and Disassembly - genetics | Embryo, Mammalian - metabolism | Octamer Transcription Factor-3 - genetics | Pluripotent Stem Cells - metabolism | Proteins - genetics | DNA Helicases - metabolism | Animals | Proteins - metabolism | Embryo, Mammalian - cytology | Models, Biological | Octamer Transcription Factor-3 - metabolism | Female | Mice | In Vitro Techniques | Cell Differentiation - physiology | DNA Helicases - genetics | Chromatin Assembly and Disassembly - physiology
OCT4 | CHROMATIN REMODELING COMPLEX | MEDIATOR | TRANSCRIPTIONAL NETWORK | MECHANISMS | DIFFERENTIATION | EXPRESSION | OCCUPANCY | GENOME | RNAI SCREEN | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Cell Line | Embryonic Stem Cells - metabolism | Embryonic Stem Cells - cytology | Pluripotent Stem Cells - cytology | Blastocyst - metabolism | Blastocyst - cytology | Chromatin Assembly and Disassembly - genetics | Embryo, Mammalian - metabolism | Octamer Transcription Factor-3 - genetics | Pluripotent Stem Cells - metabolism | Proteins - genetics | DNA Helicases - metabolism | Animals | Proteins - metabolism | Embryo, Mammalian - cytology | Models, Biological | Octamer Transcription Factor-3 - metabolism | Female | Mice | In Vitro Techniques | Cell Differentiation - physiology | DNA Helicases - genetics | Chromatin Assembly and Disassembly - physiology
Journal Article
Proceedings of the National Academy of Sciences of the United States, ISSN 0027-8424, 07/2018, Volume 115, Issue 29, p. 7463
Journal Article
Molecular Cell, ISSN 1097-2765, 09/2010, Volume 39, Issue 6, pp. 886 - 900
Epigenetic regulation of chromatin structure is essential for the expression of genes determining cellular specification and function. The Polycomb repressive...
HISTONE METHYLTRANSFERASE ACTIVITY | MOUSE DEVELOPMENT | TRANSCRIPTIONAL ACTIVATION | EPIGENETIC MARK | STEM-CELLS | METHYLATION | CHROMATIN | MAP KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHROMOSOME CONDENSATION | H3 VARIANTS | CELL BIOLOGY | Phosphorylation - physiology | Chromatin - metabolism | Embryonic Stem Cells - metabolism | Gene Expression - drug effects | Gene Expression - genetics | Humans | Neurons - cytology | Protein Transport - physiology | Promoter Regions, Genetic - genetics | Cell Differentiation - genetics | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Peptides - metabolism | Ribosomal Protein S6 Kinases, 90-kDa - antagonists & inhibitors | Antibodies - immunology | DNA Damage - genetics | Lysine - metabolism | Neurons - metabolism | Repressor Proteins - metabolism | Activating Transcription Factor 3 - genetics | Fibroblasts - metabolism | DNA Damage - drug effects | Histones - immunology | Gene Expression Regulation - physiology | Polycomb-Group Proteins | Serine - metabolism | Mitosis - physiology | Cell Differentiation - drug effects | Fibroblasts - drug effects | Ribosomal Protein S6 Kinases, 90-kDa - genetics | Cell Line, Tumor | Anisomycin - pharmacology | HeLa Cells | Histones - metabolism | Methylation | Chromatin - genetics | Protein Binding - physiology | Cell research | Chromatin | Lysine | Gene expression | Embryonic stem cells | Phosphotransferases | Tretinoin
HISTONE METHYLTRANSFERASE ACTIVITY | MOUSE DEVELOPMENT | TRANSCRIPTIONAL ACTIVATION | EPIGENETIC MARK | STEM-CELLS | METHYLATION | CHROMATIN | MAP KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHROMOSOME CONDENSATION | H3 VARIANTS | CELL BIOLOGY | Phosphorylation - physiology | Chromatin - metabolism | Embryonic Stem Cells - metabolism | Gene Expression - drug effects | Gene Expression - genetics | Humans | Neurons - cytology | Protein Transport - physiology | Promoter Regions, Genetic - genetics | Cell Differentiation - genetics | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Peptides - metabolism | Ribosomal Protein S6 Kinases, 90-kDa - antagonists & inhibitors | Antibodies - immunology | DNA Damage - genetics | Lysine - metabolism | Neurons - metabolism | Repressor Proteins - metabolism | Activating Transcription Factor 3 - genetics | Fibroblasts - metabolism | DNA Damage - drug effects | Histones - immunology | Gene Expression Regulation - physiology | Polycomb-Group Proteins | Serine - metabolism | Mitosis - physiology | Cell Differentiation - drug effects | Fibroblasts - drug effects | Ribosomal Protein S6 Kinases, 90-kDa - genetics | Cell Line, Tumor | Anisomycin - pharmacology | HeLa Cells | Histones - metabolism | Methylation | Chromatin - genetics | Protein Binding - physiology | Cell research | Chromatin | Lysine | Gene expression | Embryonic stem cells | Phosphotransferases | Tretinoin
Journal Article
Nature Cell Biology, ISSN 1465-7392, 05/2012, Volume 14, Issue 5, pp. 457 - 466
Transcription-factor-directed reprogramming from somatic cells to induced pluripotent stem cells (iPSCs) is by nature an epigenetic process of cell fate...
OCT4 | DOMAIN | MOUSE EMBRYONIC FIBROBLASTS | PATHWAY | SMALL-MOLECULE COMPOUNDS | STATE | E-CADHERIN | INDUCTION | IRF6 | LOCUS | CELL BIOLOGY | Promoter Regions, Genetic | Animals | Cell Proliferation | F-Box Proteins - physiology | Pluripotent Stem Cells - cytology | Epigenesis, Genetic | Gene Expression Regulation | Jumonji Domain-Containing Histone Demethylases - physiology | Polymerase Chain Reaction | Mice | Physiological aspects | Transcription factors | Genetic aspects | Research | Stem cells
OCT4 | DOMAIN | MOUSE EMBRYONIC FIBROBLASTS | PATHWAY | SMALL-MOLECULE COMPOUNDS | STATE | E-CADHERIN | INDUCTION | IRF6 | LOCUS | CELL BIOLOGY | Promoter Regions, Genetic | Animals | Cell Proliferation | F-Box Proteins - physiology | Pluripotent Stem Cells - cytology | Epigenesis, Genetic | Gene Expression Regulation | Jumonji Domain-Containing Histone Demethylases - physiology | Polymerase Chain Reaction | Mice | Physiological aspects | Transcription factors | Genetic aspects | Research | Stem cells
Journal Article
Development (Cambridge), ISSN 0950-1991, 2015, Volume 142, Issue 5, pp. 910 - 920
In mice, zygotic activation occurs for a wide variety of genes, mainly at the 2-cell stage. Long noncoding RNAs (lncRNAs) are increasingly being recognized as...
DNA demethylation | Epigenetic regulation | Early mouse preimplantation development | Long noncoding RNA | Zygotic gene activation | Pluripotency | APOPTOSIS | METHYLATION | DYNAMIC CPG | TRANSCRIPTION | DEVELOPMENTAL BIOLOGY | BLASTOCYST | PATERNAL GENOME | PROMOTERS | EMBRYONIC STEM-CELLS | EXPRESSION | Pluripotent Stem Cells - cytology | Oocytes - metabolism | Blastocyst - metabolism | Blastocyst - physiology | Data Mining | Male | DNA Methylation - genetics | RNA, Long Noncoding - genetics | Pluripotent Stem Cells - metabolism | Pregnancy | Animals | Epigenesis, Genetic - genetics | Polymerase Chain Reaction | Female | Mice | Spermatozoa - cytology
DNA demethylation | Epigenetic regulation | Early mouse preimplantation development | Long noncoding RNA | Zygotic gene activation | Pluripotency | APOPTOSIS | METHYLATION | DYNAMIC CPG | TRANSCRIPTION | DEVELOPMENTAL BIOLOGY | BLASTOCYST | PATERNAL GENOME | PROMOTERS | EMBRYONIC STEM-CELLS | EXPRESSION | Pluripotent Stem Cells - cytology | Oocytes - metabolism | Blastocyst - metabolism | Blastocyst - physiology | Data Mining | Male | DNA Methylation - genetics | RNA, Long Noncoding - genetics | Pluripotent Stem Cells - metabolism | Pregnancy | Animals | Epigenesis, Genetic - genetics | Polymerase Chain Reaction | Female | Mice | Spermatozoa - cytology
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2011, Volume 108, Issue 8, pp. 3116 - 3123
Histone methylation has an important role in transcriptional regulation. However, unlike H3K4 and H3K9 methylation, the role of H4K20 monomethylation...
Chromatin | Phenotypes | Messenger RNA | HEK293 cells | Transcriptional activation | Genes | Histones | Methylation | Gene expression | Embryos | Zebrafish embryonic development | Epigenetic regulation | COMPLEX |
Chromatin | Phenotypes | Messenger RNA | HEK293 cells | Transcriptional activation | Genes | Histones | Methylation | Gene expression | Embryos | Zebrafish embryonic development | Epigenetic regulation | COMPLEX |