Epigenetic balance of gene expression by Polycomb and COMPASS families.
about
Deciphering the Epigenetic Code in Embryonic and Dental Pulp Stem CellsMutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndromeMolecular architecture of polycomb repressive complexesDetection of Histone H3 mutations in cerebrospinal fluid-derived tumor DNA from children with diffuse midline glioma.Multi-omics approaches to disease.An Evolutionary Conserved Epigenetic Mark of Polycomb Response Elements Implemented by Trx/MLL/COMPASSEpigenetics of hematopoiesis and hematological malignancies.Inhibition of MLL1 histone methyltransferase brings the developmental clock back to naïve pluripotency.Three-Dimensional Genome Organization and Function in Drosophila.Role of remodeling and spacing factor 1 in histone H2A ubiquitination-mediated gene silencing.Therapeutic targeting of polycomb and BET bromodomain proteins in diffuse intrinsic pontine gliomas.The cancer epigenome: Concepts, challenges, and therapeutic opportunities.Selective targeting of epigenetic reader domains.MLL3/MLL4/COMPASS Family on Epigenetic Regulation of Enhancer Function and Cancer.Environmental and hormonal regulation of epigenetic enzymes in the hypothalamus.Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes.Somatic cancer mutations in the MLL1 histone methyltransferase modulate its enzymatic activity and dependence on the WDR5/RBBP5/ASH2L complexEpigenetic countermarks in mitotic chromosome condensation.Transcriptional Addiction in Cancer.Diverse roles of WDR5-RbBP5-ASH2L-DPY30 (WRAD) complex in the functions of the SET1 histone methyltransferase family.Modulation of gene expression dynamics by co-transcriptional histone methylations.Writing, erasing and reading histone lysine methylations.Histone H2A Monoubiquitination in Neurodevelopmental Disorders.Epigenetic plasticity and the hallmarks of cancer.RNA Binding by Histone Methyltransferases Set1 and Set2.Polycomb repressive complex 1 modifies transcription of active genes.Nuclear envelope-distributed CD147 interacts with and inhibits the transcriptional function of RING1 and promotes melanoma cell motility.Dual functionality of cis-regulatory elements as developmental enhancers and Polycomb response elementsDynamics of BAF-Polycomb complex opposition on heterochromatin in normal and oncogenic statesThe SET1 Complex Selects Actively Transcribed Target Genes via Multivalent Interaction with CpG Island Chromatin.SET1A/COMPASS and shadow enhancers in the regulation of homeotic gene expression.Dynamic changes in chromatin states during specification and differentiation of adult intestinal stem cellsMinireview: Epigenomic Plasticity and Vulnerability to EDC Exposures.Histone H3K4 monomethylation catalyzed by Trr and mammalian COMPASS-like proteins at enhancers is dispensable for development and viability.State of the Art: trxG Factor Regulation of Post-embryonic Plant Development.Polycomb and Trithorax Group Genes in Drosophila.Telomere repeats induce domains of H3K27 methylation in Neurospora.Trithorax dependent changes in chromatin landscape at enhancer and promoter regions drive female puberty.Nup98 recruits the Wdr82-Set1A/COMPASS complex to promoters to regulate H3K4 trimethylation in hematopoietic progenitor cells.Nervous system development and disease: A focus on trithorax related proteins and chromatin remodelers.
P2860
Q28080288-6801EB6B-6999-449C-8D0A-6A35A475047EQ29147388-55721130-ABF1-4276-8B70-2E17DBFA9FA8Q33364784-D562BDD6-0839-4551-8BEB-F37F54AD953EQ33568113-512EBA55-DEA4-47AE-A063-F35CD23AB35EQ33640903-4F332C22-941A-4238-8929-3C6B79F4BB62Q37201178-B53B5D0A-4452-4531-97CC-9E102DA2912DQ37343797-4C793B86-BBD1-4020-87DE-A181E2E323C7Q37407786-B2A6F85F-B1B8-4631-A406-AA62CB73867FQ37576480-4F4B3791-3959-4632-A26B-3194CBC9EC9FQ38601667-455AB21C-E787-474E-8B2F-46DABCE6785DQ38713523-9B5FCF99-CAB7-473E-9A1C-C0DCE761ABF1Q38743881-871902E1-5B40-43F6-A352-284A8D1996FAQ38748150-A9C61881-711B-433D-B7EE-1802C7BF78B5Q38800948-10565A38-DC24-4603-B69E-1C5BED37AC3AQ38859233-110EA7FD-79D2-4A44-93E4-845C3E1BC753Q38875147-30A63459-DCB2-4281-B6F6-FEE6C5FA439BQ38969866-F9A511B7-233C-48DE-AF1F-0BB32255F09FQ39043129-1250ACE7-FCC1-44ED-82F5-5789976C22D3Q39130428-26D49169-8D98-493A-BF0F-832C6E7B0573Q39147680-434CEA71-6889-4F9B-A512-96410E027FB1Q39268159-E621C3FC-1A7E-461E-B272-4149573A5D43Q39268171-BDB9C465-FAF8-4E54-9261-077C66120560Q39409765-F8092C05-53B1-4F3C-BC55-26A6513760EAQ39448979-BDB53B33-E799-45AC-AB6C-6E2E716B1A0DQ40994665-EDA2F2C2-63D1-4197-8F3F-7601AE49A6FAQ41212386-389C8CDC-3E54-48BF-972C-CD5CC87CDF61Q41498911-4573436B-4944-4C94-8CD0-7CCDD58A12B4Q41854220-E22C10CA-2F29-45D8-96A6-653A96B902C0Q41902469-CDA2C1DC-57E0-44AD-98E5-4F987344D962Q42048922-E61492CA-3EE9-493B-AD66-6FFB2E46BFA5Q42138584-B3B0B4C2-246B-49C4-B2AB-199CC01E7CE0Q42237145-309BF10B-DDB6-4557-A9E3-20EBAF161FB5Q42395101-0638C2CA-55F5-4BEA-A71D-3F2358FDAD35Q42596264-8613F300-D67C-4B71-972D-89E9D88684B3Q45941036-1EBB5D43-7243-429E-A956-FA7A5AEBF6B0Q46253902-A15BD9F2-1A19-4488-98BC-F30FFD083A03Q47107906-CD70F292-A495-49B2-AA24-5E067575C4B0Q47231120-42F74073-666F-49A1-8B3B-215861F2E6FCQ47263068-B24FB386-51F2-43A9-B93F-D1E89C29E5ACQ47340829-B88426D7-2D9A-4FA9-B4AA-F972B980906F
P2860
Epigenetic balance of gene expression by Polycomb and COMPASS families.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Epigenetic balance of gene expression by Polycomb and COMPASS families.
@en
type
label
Epigenetic balance of gene expression by Polycomb and COMPASS families.
@en
prefLabel
Epigenetic balance of gene expression by Polycomb and COMPASS families.
@en
P2860
P356
P1433
P1476
Epigenetic balance of gene expression by Polycomb and COMPASS families.
@en
P2093
Ali Shilatifard
Andrea Piunti
P2860
P304
P356
10.1126/SCIENCE.AAD9780
P407
P577
2016-06-01T00:00:00Z