Chem-seq permits identification of genomic targets of drugs against androgen receptor regulation selected by functional phenotypic screens.
about
Targeting molecular resistance in castration-resistant prostate cancerDrug resistance in castration resistant prostate cancer: resistance mechanisms and emerging treatment strategiesKDM4C, a H3K9me3 Histone Demethylase, is Involved in the Maintenance of Human ESCC-Initiating Cells by Epigenetically Enhancing SOX2 ExpressionTargeting Aberrant Epigenetic Networks Mediated by PRMT1 and KDM4C in Acute Myeloid Leukemia.Molecular pathways and targets in prostate cancerUnravelling the genomic targets of small molecules using high-throughput sequencing.Genome-wide Mapping of Drug-DNA Interactions in Cells with COSMIC (Crosslinking of Small Molecules to Isolate Chromatin)Multiplexed barcoded CRISPR-Cas9 screening enabled by CombiGEM.Regulators of Androgen Action Resource: a one-stop shop for the comprehensive study of androgen receptor action.Jmjd2/Kdm4 demethylases are required for expression of Il3ra and survival of acute myeloid leukemia cells.Epigenomic Regulation of Androgen Receptor Signaling: Potential Role in Prostate Cancer Therapy.Overview on the complexity of androgen receptor-targeted therapy for prostate cancerTargeting epigenetic regulators for cancer therapy: modulation of bromodomain proteins, methyltransferases, demethylases, and microRNAs.The Y-located proto-oncogene TSPY exacerbates and its X-homologue TSPX inhibits transactivation functions of androgen receptor and its constitutively active variants.Deciphering the function of non-coding RNAs in prostate cancer.Histone Lysine Demethylase Inhibitors.Rationale for the development of alternative forms of androgen deprivation therapy.Genome-Wide Assessment of the Binding Effects of Artificial Transcriptional Activators by High-Throughput Sequencing.A comprehensive analysis of coregulator recruitment, androgen receptor function and gene expression in prostate cancer.DNA Sequence Constraints Define Functionally Active Steroid Nuclear Receptor Binding Sites in Chromatin.Inhibitors of both the N-methyl lysyl- and arginyl-demethylase activities of the JmjC oxygenases.H3K14me3 genomic distributions and its regulation by KDM4 family demethylases
P2860
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P2860
Chem-seq permits identification of genomic targets of drugs against androgen receptor regulation selected by functional phenotypic screens.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Chem-seq permits identificatio ...... functional phenotypic screens.
@ast
Chem-seq permits identificatio ...... functional phenotypic screens.
@en
type
label
Chem-seq permits identificatio ...... functional phenotypic screens.
@ast
Chem-seq permits identificatio ...... functional phenotypic screens.
@en
prefLabel
Chem-seq permits identificatio ...... functional phenotypic screens.
@ast
Chem-seq permits identificatio ...... functional phenotypic screens.
@en
P2093
P2860
P356
P1476
Chem-seq permits identificatio ...... functional phenotypic screens.
@en
P2093
Bogdan Tanasa
Christopher P Evans
Chunru Lin
Chunyu Jin
Daria Merkurjev
Hongyan Zhou
Joy C Yang
Kenneth A Ohgi
Liuqing Yang
P2860
P304
P356
10.1073/PNAS.1404303111
P407
P577
2014-06-13T00:00:00Z