Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
about
Global profiling of co- and post-translationally N-myristoylated proteomes in human cellsOpen access chemical probes for epigenetic targetsSmall-molecule based musculoskeletal regenerative engineeringChemical probes of histone lysine methyltransferasesDelivery of small molecules for bone regenerative engineering: preclinical studies and potential clinical applicationsA potent and highly specific FN3 monobody inhibitor of the Abl SH2 domainSmall-molecule p21-activated kinase inhibitor PF-3758309 is a potent inhibitor of oncogenic signaling and tumor growthChemical genetic strategy for targeting protein kinases based on covalent complementarityInhibition of RNA polymerase I transcription initiation by CX-5461 activates non-canonical ATM/ATR signalingThe potent Cdc7-Dbf4 (DDK) kinase inhibitor XL413 has limited activity in many cancer cell lines and discovery of potential new DDK inhibitor scaffoldsA High-Throughput Screening-Compatible Strategy for the Identification of Inositol Pyrophosphate Kinase InhibitorsConversion of a Single Polypharmacological Agent into Selective Bivalent Inhibitors of Intracellular Kinase ActivityNetworks inferred from biochemical data reveal profound differences in toll-like receptor and inflammatory signaling between normal and transformed hepatocytes.Synthetic lethality: emerging targets and opportunities in melanoma.Prostanoid receptor EP2 as a therapeutic targetA genome-wide RNA interference screen reveals an essential CREB3L2-ATF5-MCL1 survival pathway in malignant glioma with therapeutic implications.Probing the probes: fitness factors for small molecule tools.Regulation of HPV16 E6 and MCL1 by SF3B1 inhibitor in head and neck cancer cells.Phosphoproteomics by mass spectrometry: insights, implications, applications and limitations.Analyzing fission yeast multidrug resistance mechanisms to develop a genetically tractable model system for chemical biology.Target validation using chemical probes.Evaluating the feasibility of utilizing the small molecule phenamil as a novel biofactor for bone regenerative engineering.The role of small molecules in musculoskeletal regeneration.Unraveling the mechanism of cell death induced by chemical fibrils.The Plk1-dependent phosphoproteome of the early mitotic spindleThe promise and peril of chemical probes.An activating transcription factor 5-mediated survival pathway as a target for cancer therapy?Complex regulation of PKCβ2 and PDK-1/AKT by ROCK2 in diabetic heart.Mechanism of Action of 2-Aminobenzamide HDAC Inhibitors in Reversing Gene Silencing in Friedreich's Ataxia.Preconditioning with endoplasmic reticulum stress ameliorates endothelial cell inflammation.Development of a High-Throughput Screening Assay to Identify Inhibitors of the Lipid Kinase PIP5K1CCombining targeted therapies: practical issues to consider at the bench and bedside.Targeting of KRAS mutant tumors by HSP90 inhibitors involves degradation of STK33.CD40 ligand induces RIP1-dependent, necroptosis-like cell death in low-grade serous but not serous borderline ovarian tumor cells.A Class of Diacylglycerol Acyltransferase 1 Inhibitors Identified by a Combination of Phenotypic High-throughput Screening, Genomics, and GeneticsCharacterization of a series of 4-aminoquinolines that stimulate caspase-7 mediated cleavage of TDP-43 and inhibit its function.Development of a chemical genetic approach for human aurora B kinase identifies novel substrates of the chromosomal passenger complexLigand and Target Discovery by Fragment-Based Screening in Human Cells.A Role for Widely Interspaced Zinc Finger (WIZ) in Retention of the G9a Methyltransferase on Chromatin.A SIRT2-Selective Inhibitor Promotes c-Myc Oncoprotein Degradation and Exhibits Broad Anticancer Activity.
P2860
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P2860
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@ast
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@en
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@nl
type
label
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@ast
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@en
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@nl
prefLabel
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@ast
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@en
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@nl
P2093
P2860
P356
P1476
Recognizing and exploiting differences between RNAi and small-molecule inhibitors.
@en
P2093
Kevan M Shokat
Stephen S Taylor
William A Weiss
P2860
P2888
P304
P356
10.1038/NCHEMBIO1207-739
P577
2007-12-01T00:00:00Z
P5875
P6179
1050191010