Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1 - Wikidata - wikimedia - TriplyDB

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

http://www.wikidata.org/entity/Q27670771

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Apigenin sensitizes prostate cancer cells to Apo2L/TRAIL by targeting adenine nucleotide translocase-2 Epigallocatechin Gallate Nanodelivery Systems for Cancer Therapy Notes from the field: "green" chemoprevention as frugal medicine Cancer Preventive Activities of Tea Catechins Prediction of molecular targets of cancer preventing flavonoid compounds using computational methods Computational and Biochemical Discovery of RSK2 as a Novel Target for Epigallocatechin Gallate (EGCG)The flavonoid apigenin downregulates CDK1 by directly targeting ribosomal protein S9.Gene regulation mediated by microRNAs in response to green tea polyphenol EGCG in mouse lung cancer.ZBP-89 reduces histone deacetylase 3 by degrading IkappaB in the presence of Pin1 Active Pin1 is a key target of all-trans retinoic acid in acute promyelocytic leukemia and breast cancer Cancer therapy combination: green tea and a phosphodiesterase 5 inhibitor?Peptidyl-prolyl cis/trans-isomerase A1 (Pin1) is a target for modification by lipid electrophiles.Signal transduction and molecular targets of selected flavonoids.Cancer prevention by tocopherols and tea polyphenols.Lessons learned from cancer prevention studies with nutrients and non-nutritive dietary constituents.Mechanisms of body weight reduction and metabolic syndrome alleviation by tea.Green tea catechins: a fresh flavor to anticancer therapy.Pin1 dysregulation helps to explain the inverse association between cancer and Alzheimer's disease.Green tea polyphenols and their potential role in health and disease.The isomerase PIN1 controls numerous cancer-driving pathways and is a unique drug target.The role of Pin1 in the development and treatment of cancer.Effects of Tea Catechins on Cancer Signaling Pathways.Recent Advances in Anticancer Activities and Drug Delivery Systems of Tannins.Neighboring phosphoSer-Pro motifs in the undefined domain of IRAK1 impart bivalent advantage for Pin1 binding.Raf and PI3K are the molecular targets for the anti-metastatic effect of luteolin.Computational DNA binding studies of (-)-epigallocatechin-3-gallate.TPA-induced cell transformation provokes a complex formation between Pin1 and 90 kDa ribosomal protein S6 kinase 2.Computational Molecular Docking and X-ray Crystallographic Studies of Catechins in New Drug Design Strategies Prolyl isomerase Pin1: a promoter of cancer and a target for therapy Gears-In-Motion: The Interplay of WW and PPIase Domains in Pin1

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

http://www.wikidata.org/entity/Q27670771

description

2011 nî lūn-bûn

@nan

2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

name

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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type

label

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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prefLabel

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

@ast

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

@en

Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

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1940-6207.CAPR-11-0301

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Cancer Prevention Research

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Epigallocatechin-gallate Suppresses Tumorigenesis by Directly Targeting Pin1

@en

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Andria Carper

http://www.w3.org/2001/XMLSchema#string

Ann M Bode

http://www.w3.org/2001/XMLSchema#string

Darya V Urusova

http://www.w3.org/2001/XMLSchema#string

Dong Joon Kim

http://www.w3.org/2001/XMLSchema#string

Jung-Hyun Shim

http://www.w3.org/2001/XMLSchema#string

Sung Keun Jung

http://www.w3.org/2001/XMLSchema#string

Tatyana A Zykova

http://www.w3.org/2001/XMLSchema#string

Zigang Dong

http://www.w3.org/2001/XMLSchema#string

P2860

Function of WW domains as phosphoserine- or phosphothreonine-binding modules

Pin1 regulates turnover and subcellular localization of beta-catenin by inhibiting its interaction with APC

Pin1 is overexpressed in breast cancer and cooperates with Ras signaling in increasing the transcriptional activity of c-Jun towards cyclin D1.

Structure-function-folding relationship in a WW domain

The essential mitotic peptidyl-prolyl isomerase Pin1 binds and regulates mitosis-specific phosphoproteins

Improved methods for building protein models in electron density maps and the location of errors in these models

Structural basis for phosphoserine-proline recognition by group IV WW domains

Structural analysis of the mitotic regulator hPin1 in solution: insights into domain architecture and substrate binding

Structural Basis for High-Affinity Peptide Inhibition of Human Pin1

Structure-based design of novel human Pin1 inhibitors (I)

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1366-77

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scholarly article

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1465745

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10.1158/1940-6207.CAPR-11-0301

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9

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4

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2011-09-01T00:00:00Z

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51486698

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21750208

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3244823

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