Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors - Wikidata - awgldk - TriplyDB

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

http://www.wikidata.org/entity/Q27619648

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Sirtuins: Sir2-related NAD-dependent protein deacetylases The role of HDAC6 in cancer Identification of a transcriptional repressor related to the noncatalytic domain of histone deacetylases 4 and 5 Guide to the draft human genome Molecular cloning and characterization of a novel histone deacetylase HDAC10 Isolation and characterization of a novel class II histone deacetylase, HDAC10 Cloning and functional characterization of HDAC11, a novel member of the human histone deacetylase family Vitamin D stimulates apoptosis in gastric cancer cells in synergy with trichostatin A /sodium butyrate-induced and 5-aza-2'-deoxycytidine-induced PTEN upregulation A novel small molecule hydroxamate preferentially inhibits HDAC6 activity and tumour growth Loss of NKX3.1 favors vascular endothelial growth factor-C expression in prostate cancer Structural and functional analysis of the human HDAC4 catalytic domain reveals a regulatory structural zinc-binding domain Interphase nucleo-cytoplasmic shuttling and localization of SIRT2 during mitosis Cloning and characterization of a novel human histone deacetylase, HDAC8 Msx3 protein recruits histone deacetylase to down-regulate the Msx1 promoter Histone deacetylases (HDACs): characterization of the classical HDAC family Counterregulation of chromatin deacetylation and histone deacetylase occupancy at the integrated promoter of human immunodeficiency virus type 1 (HIV-1) by the HIV-1 repressor YY1 and HIV-1 activator Tat Crystal structure of a eukaryotic zinc-dependent histone deacetylase, human HDAC8, complexed with a hydroxamic acid inhibitor Expression, purification, assay, and crystal structure of perdeuterated human arginase I Regulation of BRCA2 gene expression by the SLUG repressor protein in human breast cells Negative regulation of histone deacetylase 8 activity by cyclic AMP-dependent protein kinase A A fully automatic evolutionary classification of protein folds: Dali Domain Dictionary version 3 Macrocyclic histone deacetylase inhibitors Functional proteomics establishes the interaction of SIRT7 with chromatin remodeling complexes and expands its role in regulation of RNA polymerase I transcription Evolution of the arginase fold and functional diversity A phase 2 study of vorinostat in acute myeloid leukemia Histone deacetylase inhibitors: Potential in cancer therapy Histone deacetylase inhibitor selectively induces p21WAF1 expression and gene-associated histone acetylation The human silent information regulator (Sir)2 homologue hSIRT3 is a mitochondrial nicotinamide adenine dinucleotide-dependent deacetylase Crystal structure of LpxC, a zinc-dependent deacetylase essential for endotoxin biosynthesis Substrate binding to histone deacetylases as shown by the crystal structure of the HDAC8-substrate complex DNA and the chromosome - varied targets for chemotherapy HDAC and HDAC Inhibitor: From Cancer to Cardiovascular Diseases Histone deacetylases as new therapy targets for platinum-resistant epithelial ovarian cancer HDAC8 substrates: Histones and beyond Small molecule inhibitors of zinc-dependent histone deacetylases Growing the growth cone: remodeling the cytoskeleton to promote axon regeneration Chemical probes in plant epigenetics studies HDAC inhibitors and immunotherapy; a double edged sword?Targeting histone deacetylases for cancer therapy: from molecular mechanisms to clinical implications Targeting JAK2 in the therapy of myeloproliferative neoplasms

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Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

http://www.wikidata.org/entity/Q27619648

description

1999 nî lūn-bûn

@nan

1999 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

1999年の論文

@ja

1999年論文

@yue

1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

name

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@ast

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@en

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@nl

type

label

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@ast

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@en

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@nl

prefLabel

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@ast

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@en

Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@nl

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Structures of a histone deacetylase homologue bound to the TSA and SAHA inhibitors

@en

P2093

A Cohen

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

J R Donigian

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

M S Finnin

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

N P Pavletich

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

P A Marks

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

R A Rifkind

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

R Breslow

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

V M Richon

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

P2860

Three proteins define a class of human histone deacetylases related to yeast Hda1p

The complete genome of the hyperthermophilic bacterium Aquifex aeolicus

Histone deacetylases, acetoin utilization proteins and acetylpolyamine amidohydrolases are members of an ancient protein superfamily

A role for histone deacetylase activity in HDAC1-mediated transcriptional repression

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

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors

Binding of hydroxamic acid inhibitors to crystalline thermolysin suggests a pentacoordinate zinc intermediate in catalysis

Structure determination and analysis of human neutrophil collagenase complexed with a hydroxamate inhibitor

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P304

188-93

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scholarly article

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1788689

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10.1038/43710

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P433

6749

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401

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1999-09-09T00:00:00Z

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1049319912

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10490031

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