Diverse chemical scaffolds support direct inhibition of the membrane-bound O-acyltransferase porcupine.
about
Wnt/beta-catenin signaling and small molecule inhibitorsDevelopment of anticancer agents targeting the Wnt/β-catenin signalingChemical Disruption of Wnt-dependent Cell Fate Decision-making Mechanisms in Cancer and Regenerative MedicineIdentification of key residues and regions important for porcupine-mediated Wnt acylationThe development of highly potent inhibitors for porcupine.The river blindness drug Ivermectin and related macrocyclic lactones inhibit WNT-TCF pathway responses in human cancer.Triple-negative breast cancer: new perspectives for targeted therapies.Fatty acyl donor selectivity in membrane bound O-acyltransferases and communal cell fate decision-making.Wnt acylation and its functional implication in Wnt signalling regulationSmall-molecule inhibitors of Wnt signaling pathway: towards novel anticancer therapeutics.Generation and application of signaling pathway reporter lines in zebrafishInhibition of the Wnt palmitoyltransferase porcupine suppresses cell growth and downregulates the Wnt/β-catenin pathway in gastric cancer.WNT Stimulation Dissociates a Frizzled 4 Inactive-State Complex with Gα12/13.Wnt secretion is required to maintain high levels of Wnt activity in colon cancer cellsStearoyl CoA desaturase is required to produce active, lipid-modified Wnt proteins.Targeting Wnt-driven cancer through the inhibition of Porcupine by LGK974.Biochemical Analysis of Tankyrase Activity in Zebrafish In Vitro and In Vivo.Palmitoylation of proteins in cancer.Revisiting the role of Wnt/β-catenin signaling in prostate cancer.Delivery of the Porcupine Inhibitor WNT974 in Mice.Monitoring Wnt Protein Acylation Using an In Vitro Cyclo-Addition ReactionDivergent effects of Porcupine and Wntless on WNT1 trafficking, secretion, and signaling.Identification of the WNT1 residues required for palmitoylation by Porcupine.Discovery of Pyridinyl Acetamide Derivatives as Potent, Selective, and Orally Bioavailable Porcupine Inhibitors.Development of a triazole class of highly potent Porcn inhibitors.Protein Lipidation: Occurrence, Mechanisms, Biological Functions, and Enabling Technologies.Bidirectional reporter assay using HAL promoter and TOPFLASH improves specificity in high-throughput screening of Wnt inhibitors.Monitoring Wnt Signaling in Zebrafish Using Fluorescent Biosensors.Wnt signaling in cancer.Mitsugumin 56 (hedgehog acyltransferase-like) is a sarcoplasmic reticulum-resident protein essential for postnatal muscle maturation.Separate roles for Med12 and Wnt signaling in regulation of oxytocin expression.
P2860
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P2860
Diverse chemical scaffolds support direct inhibition of the membrane-bound O-acyltransferase porcupine.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@ast
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@en
type
label
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@ast
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@en
prefLabel
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@ast
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@en
P2093
P2860
P50
P356
P1476
Diverse chemical scaffolds sup ...... d O-acyltransferase porcupine.
@en
P2093
Courtney M Karner
Francesco Argenton
Heping Shi
James F Amatruda
Jesung Moon
Jianming Lu
Lawrence Lum
Leni S Jacob
Li-shu Zhang
Michael E Dodge
P2860
P304
23246-23254
P356
10.1074/JBC.M112.372029
P407
P577
2012-05-15T00:00:00Z