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Nature (London), ISSN 1476-4687, 2010, Volume 464, Issue 7290, pp. 927 - 931
Journal Article
Journal Article
Journal Article
PloS one, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, p. e98176
Objective: Growing evidences indicate that the histone methyltransferase EZH2 (enhancer of zeste homolog 2) may be an appropriate therapeutic target in some... 
CANCER-CELLS | STEM-CELLS | METHYLATION | MULTIDISCIPLINARY SCIENCES | ZESTE HOMOLOG 2 | PROSTATE-CANCER | GROUP PROTEIN EZH2 | TUMOR | ENHANCER | PROLIFERATION | EXPRESSION | Apoptosis - drug effects | Humans | Enzyme Inhibitors - pharmacology | Adenosine - pharmacology | Reverse Transcriptase Polymerase Chain Reaction | Cell Movement - drug effects | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | Flow Cytometry | Histone Methyltransferases | Chondrosarcoma - enzymology | Adenosine - analogs & derivatives | Cell Line, Tumor | Chondrosarcoma - pathology | Immunohistochemistry | Enzymes | Epigenetic inheritance | Methyltransferases | Analysis | Histones | Hydrolases | Health aspects | Apoptosis | Adherent cells | Therapy | Flow cytometry | Chondrosarcoma | Leukemia | Homology | Metastasis | Cancer therapies | Metastases | Proteins | Cell cycle | DNA methylation | Histone methyltransferase | Cell survival | Wound healing | Hydrolase | Therapeutic applications | Poly(ADP-ribose) polymerase | Pharmacology | Gene expression | Cytometry | Inhibitors | Lysine | Cell death | Chondrocytes | Stem cells | Epigenetics | Methylation | Homocysteine | Cell migration | Histone H3 | Tumors | 3-deazaneplanocin | Histone-Lysine N-Methyltransferase | Epigenesis, Genetic | Biochemistry, Molecular Biology | Rhumatology and musculoskeletal system | Cellular Biology | EZH2 protein, human | Blotting, Western | Life Sciences | Human health and pathology | Polycomb Repressive Complex 2 | histone methyltransferase | Cell Death | Cancer
Journal Article
Nature (London), ISSN 1476-4687, 2015, Volume 520, Issue 7546, pp. 243 - 247
Journal Article
Nature (London), ISSN 0028-0836, 08/2018, Volume 560, Issue 7719, pp. 504 - 508
Histone H3 lysine 9 methylation (H3K9me) mediates heterochromatic gene silencing and is important for genome stability and the regulation of gene... 
SITE | METHYLATION | JMJC DOMAIN PROTEIN | STRUCTURAL BASIS | MULTIDISCIPLINARY SCIENCES | HETEROCHROMATIN | HISTONE LYSINE METHYLTRANSFERASE | DYNAMICS | INHERITANCE | EXPRESSION | Methyltransferases - chemistry | Schizosaccharomyces pombe Proteins - chemistry | Histones - chemistry | Epigenesis, Genetic | Humans | Methyltransferases - metabolism | Cell Cycle Proteins - metabolism | Gene Silencing | Heterochromatin - chemistry | Cell Cycle Proteins - chemistry | Histone-Lysine N-Methyltransferase - chemistry | Schizosaccharomyces - genetics | Heterochromatin - genetics | Histone Methyltransferases - chemistry | Heterochromatin - metabolism | Histone-Lysine N-Methyltransferase - metabolism | Schizosaccharomyces pombe Proteins - metabolism | Protein Conformation | Schizosaccharomyces - enzymology | Histone Methyltransferases - metabolism | Histones - metabolism | Methylation | Evolution, Molecular | Epigenetic inheritance | Methyltransferases | Analysis | Physiological aspects | Genetic research | Genetic regulation | Phosphorylation | Yeast | Peptides | Methyltransferase | Conservation | Amino acids | Homology | Genomes | Feedback loops | Catalytic activity | Positive feedback | Crystallography | Proteins | Demethylation | Heterochromatin | DNA methylation | Catalysis | Inhibition | Boundary element method | Deoxyribonucleic acid--DNA | Crystal structure | Enzymes | Stability | Gene expression | Substrates | Domains | Gene silencing | Hypotheses | Lysine | Proteomics | Epigenetics | Instability | Software | Scientific imaging | Mutation | Mass spectrometry | Histone H3 | Conformation
Journal Article
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 0027-8424, 9/2014, Volume 111, Issue 35, pp. 12853 - 12858
SET domain containing (lysine methyltransferase) 7 (SETD7) is implicated in multiple signaling and disease related pathways with a broad diversity of reported... 
Enzymes | Transcriptional regulatory elements | Genes | Cell lines | Histones | Gene expression regulation | Kinetics | Methylation | Inhibitory concentration 50 | Chemicals | Chemical biology | Epigenetics | Chemical probe | METHYLATION | STABILITY | MULTIDISCIPLINARY SCIENCES | TRANSCRIPTION | SET7/9 | epigenetics | LYSINE METHYLTRANSFERASE | ENZYME | chemical biology | PATHWAY | PURIFICATION | GENES | chemical probe | Humans | Methyltransferases - metabolism | Structure-Activity Relationship | Phosphoproteins - metabolism | Pyrrolidines - pharmacology | Dose-Response Relationship, Drug | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | MCF-7 Cells | Tetrahydroisoquinolines - chemistry | Enzyme Inhibitors - chemistry | Epigenesis, Genetic - drug effects | Protein Structure, Tertiary | Tetrahydroisoquinolines - pharmacology | Histone-Lysine N-Methyltransferase - genetics | Sulfonamides - chemistry | Enzyme Inhibitors - pharmacology | Protein-Serine-Threonine Kinases - genetics | Phosphoproteins - genetics | Sulfonamides - pharmacology | Pyrrolidines - chemistry | Methyltransferases - antagonists & inhibitors | Histone-Lysine N-Methyltransferase - metabolism | Signal Transduction - drug effects | Fibroblasts - drug effects | Adaptor Proteins, Signal Transducing - genetics | Mutation | Adaptor Proteins, Signal Transducing - metabolism | Protein research | Research | Methyltransferases | Lysine | Health aspects | Protein-protein interactions | Biological Sciences
Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 2012, Volume 122, Issue 4, pp. 1469 - 1486
Breast cancers are highly heterogeneous but can be grouped into subtypes based on several criteria, including level of expression of certain markers.... 
EPITHELIAL-MESENCHYMAL TRANSITION | MEDICINE, RESEARCH & EXPERIMENTAL | BASAL-LIKE | STEM-CELLS | DNA METHYLATION | CLAUDIN-LOW | TRANSCRIPTION FACTOR SNAIL | GENE-EXPRESSION | PHENOTYPE | TUMOR-CELLS | HISTONE METHYLATION | Histocompatibility Antigens - genetics | Neoplasm Transplantation | Adenocarcinoma - pathology | Humans | Middle Aged | Neoplasm Proteins - physiology | Recombinant Fusion Proteins - physiology | Neoplasm Proteins - antagonists & inhibitors | Cell Line, Tumor - transplantation | Gene Expression Profiling | Cadherins - biosynthesis | Breast Neoplasms - metabolism | Gene Knockdown Techniques | DNA (Cytosine-5-)-Methyltransferases - metabolism | DNA Methylation | Histone-Lysine N-Methyltransferase - antagonists & inhibitors | Adenocarcinoma - metabolism | Adult | Female | Cadherins - genetics | Neoplasm Proteins - genetics | Cell Line, Tumor - metabolism | Snail Family Transcription Factors | Gene Expression Regulation, Neoplastic - genetics | Histone-Lysine N-Methyltransferase - genetics | Transcription Factors - physiology | DNA (Cytosine-5-)-Methyltransferase 1 | Neoplasm Invasiveness | Histocompatibility Antigens - physiology | Transcription Factors - genetics | Mice, Inbred ICR | Animals | Histone-Lysine N-Methyltransferase - metabolism | Breast Neoplasms - pathology | Aged | Mice | Protein Processing, Post-Translational | Histones - metabolism | Methylation | Histone-Lysine N-Methyltransferase - physiology | Physiological aspects | Cadherins | Breast cancer | Genetic aspects | Research | Transforming growth factors
Journal Article