Design of isoform-selective phospholipase D inhibitors that modulate cancer cell invasiveness.
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FAM83B-mediated activation of PI3K/AKT and MAPK signaling cooperates to promote epithelial cell transformation and resistance to targeted therapiesFAM83B mediates EGFR- and RAS-driven oncogenic transformationHyperactivation of EGFR and downstream effector phospholipase D1 by oncogenic FAM83BEvidence that alpha-synuclein does not inhibit phospholipase DSrf1 is a novel regulator of phospholipase D activity and is essential to buffer the toxic effects of C16:0 platelet activating factorPhospholipase D as a therapeutic target in brain disordersA novel phospholipase D2-Grb2-WASp heterotrimer regulates leukocyte phagocytosis in a two-step mechanismMammalian phospholipase D physiological and pathological rolesDesign, synthesis, and biological evaluation of halogenated N-(2-(4-oxo-1-phenyl-1,3,8-triazaspiro[4.5]decan-8-yl)ethyl)benzamides: discovery of an isoform-selective small molecule phospholipase D2 inhibitorDiversity-oriented synthetic strategies applied to cancer chemical biology and drug discoveryFunctional regulation of phospholipase D expression in cancer and inflammationDrugs for allosteric sites on receptorsADP ribosylation factor 6 (ARF6) promotes acrosomal exocytosis by modulating lipid turnover and Rab3A activation.Mechanism of enzymatic reaction and protein-protein interactions of PLD from a 3D structural model.Membrane Tension Acts Through PLD2 and mTORC2 to Limit Actin Network Assembly During Neutrophil MigrationHow independent pharmacological screenings in plants and humans led to the discovery of a new family of lipid metabolism inhibitorsDesign and synthesis of isoform-selective phospholipase D (PLD) inhibitors. Part I: Impact of alternative halogenated privileged structures for PLD1 specificityAn Evolutionarily Conserved PLC-PKD-TFEB Pathway for Host DefenseTwo sites of action for PLD2 inhibitors: The enzyme catalytic center and an allosteric, phosphoinositide biding pocket.A phosphatidic acid binding/nuclear localization motif determines lipin1 function in lipid metabolism and adipogenesisCholine-releasing glycerophosphodiesterase EDI3 drives tumor cell migration and metastasisDiscovery of compounds blocking the proliferation of Toxoplasma gondii and Plasmodium falciparum in a chemical space based on piperidinyl-benzimidazolone analogs.Working towards an exegesis for lipids in biology.Positive feedback regulation between phospholipase D and Wnt signaling promotes Wnt-driven anchorage-independent growth of colorectal cancer cells.Expression proteomics study to determine metallodrug targets and optimal drug combinations.Comprehensive survey of chemical libraries for drug discovery and chemical biology: 2009.Molecular Effects of Doxorubicin on Choline Metabolism in Breast Cancer.PLD1 promotes dendritic spine development by inhibiting ADAM10-mediated N-cadherin cleavage.Quantitative analysis of glycerophospholipids by LC-MS: acquisition, data handling, and interpretation.ADP-ribosylation factor 6 regulates mammalian myoblast fusion through phospholipase D1 and phosphatidylinositol 4,5-bisphosphate signaling pathways.Cellular and physiological roles for phospholipase D1 in cancer.Francisella tularensis LVS induction of prostaglandin biosynthesis by infected macrophages requires specific host phospholipases and lipid phosphatasesPhosphatidic acid plays a regulatory role in clathrin-mediated endocytosis.Rebamipide-induced downregulation of phospholipase D inhibits inflammation and proliferation in gastric cancer cellsPhospholipase D facilitates efficient entry of influenza virus, allowing escape from innate immune inhibition¹⁹F NMR indicator displacement assay using a synthetic receptor with appended paramagnetic relaxation agent.2013 Philip S. Portoghese Medicinal Chemistry Lectureship: drug discovery targeting allosteric sites.Phospholipase D signaling pathways and phosphatidic acid as therapeutic targets in cancerDevelopment of allosteric modulators of GPCRs for treatment of CNS disordersPhospholipase D1 regulates autophagic flux and clearance of α-synuclein aggregates
P2860
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P2860
Design of isoform-selective phospholipase D inhibitors that modulate cancer cell invasiveness.
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Design of isoform-selective ph ...... late cancer cell invasiveness.
@ast
Design of isoform-selective ph ...... late cancer cell invasiveness.
@en
type
label
Design of isoform-selective ph ...... late cancer cell invasiveness.
@ast
Design of isoform-selective ph ...... late cancer cell invasiveness.
@en
prefLabel
Design of isoform-selective ph ...... late cancer cell invasiveness.
@ast
Design of isoform-selective ph ...... late cancer cell invasiveness.
@en
P2093
P2860
P356
P1476
Design of isoform-selective ph ...... late cancer cell invasiveness.
@en
P2093
Ashley L Thomas
Carlos L Arteaga
H Alex Brown
Hyekyung P Cho
Jason R Buck
Michelle D Armstrong
Paige E Selvy
Sarah A Scott
Tracy L Criswell
P2860
P2888
P304
P356
10.1038/NCHEMBIO.140
P577
2009-01-11T00:00:00Z