Coactivators necessary for transcriptional output of the hypoxia inducible factor, HIF, are directly recruited by ARNT PAS-B
about
Hypoxia-inducible aryl hydrocarbon receptor nuclear translocator (ARNT) (HIF-1β): is it a rare exception?Regulating the ARNT/TACC3 Axis: Multiple Approaches to Manipulating Protein/Protein Interactions with Small MoleculesAllosteric inhibition of hypoxia inducible factor-2 with small moleculesCrystal Structure of the Heterodimeric CLOCK:BMAL1 Transcriptional Activator ComplexEmerging models for the molecular basis of mammalian circadian timingHypoxia-inducing factors as master regulators of stemness properties and altered metabolism of cancer- and metastasis-initiating cellsDistinct roles for aryl hydrocarbon receptor nuclear translocator and ah receptor in estrogen-mediated signaling in human cancer cell lines.XTACC3-XMAP215 association reveals an asymmetric interaction promoting microtubule elongation.Cryptochrome 1 regulates the circadian clock through dynamic interactions with the BMAL1 C terminus.TACC3 is essential for EGF-mediated EMT in cervical cancerCoiled-coil coactivators play a structural role mediating interactions in hypoxia-inducible factor heterodimerization.Single-molecule experiments reveal the flexibility of a Per-ARNT-Sim domain and the kinetic partitioning in the unfolding pathway under force.A cell-penetrating peptide suppresses the hypoxia inducible factor-1 function by binding to the helix-loop-helix domain of the aryl hydrocarbon receptor nuclear translocatorRare variants in single-minded 1 (SIM1) are associated with severe obesity.Genome-wide analysis of HIF-2α chromatin binding sites under normoxia in human bronchial epithelial cells (BEAS-2B) suggests its diverse functionsEpigenetic regulation of hypoxia-responsive gene expression: focusing on chromatin and DNA modifications.Transcriptional regulation by hypoxia inducible factors.Aryl hydrocarbon receptor repressor and TiPARP (ARTD14) use similar, but also distinct mechanisms to repress aryl hydrocarbon receptor signaling.Oncogenic FGFR3 gene fusions in bladder cancer.Regulation of heme oxygenase expression by alcohol, hypoxia and oxidative stress.Hypoxia inducible factor (HIF) as a model for studying inhibition of protein-protein interactions.The centrosomal adaptor TACC3 and the microtubule polymerase chTOG interact via defined C-terminal subdomains in an Aurora-A kinase-independent manner.Formation of a repressive complex in the mammalian circadian clock is mediated by the secondary pocket of CRY1.Unsaturated fatty acids as high-affinity ligands of the C-terminal Per-ARNT-Sim domain from the Hypoxia-inducible factor 3α.Zinc finger nuclease-mediated knockout of AHR or ARNT in human breast cancer cells abolishes basal and ligand-dependent regulation of CYP1B1 and differentially affects estrogen receptor α transactivation.Assembly and function of bHLH-PAS complexes.Recent Advances in Comprehending the Signaling Pathways Involved in the Progression of Breast Cancer.TACC3 deregulates the DNA damage response and confers sensitivity to radiation and PARP inhibition.TACC3 transcriptionally upregulates E2F1 to promote cell growth and confer sensitivity to cisplatin in bladder cancer.
P2860
Q27027475-3E0FFD8E-E9A6-49BC-A7BE-89CFC8E52D45Q27675499-FFAEBBE6-73ED-4E6E-8979-4323BAF78EDFQ27676596-E678D47D-0C7E-4FEC-AB4D-46C7F8F397AFQ27679392-1CBA3858-3232-401E-8495-DFB029A36654Q28249506-C5807491-8C37-4D50-A269-5781D7019D5BQ28393898-7DB8ED91-5CB0-40F7-B4D8-166BD31392DAQ34123737-FD3DF9E5-5CE0-4087-B7D7-1D055B47118CQ34357171-4A55F46A-AFD7-408B-ABFA-6851D134BE14Q34475929-C6F6D582-399E-4A3B-9B67-C3DB7E09A644Q34925509-D0FC9088-DADE-40F8-BCC0-1F14F9C0AB3CQ35199417-E205CDBD-BA8A-4590-993F-E3EC902DC304Q35926219-093182D3-FDBC-400C-9470-737EE80DB058Q36865718-7413080C-4DD6-453A-A88C-E90807BA35DEQ36966937-3A0E0EAD-44A2-4364-B41A-DA52956C433BQ37062066-025041B1-814D-41A4-B57E-B8F128C805C2Q38096949-A59C68DD-FD87-45E5-BE82-1D20B6CE97D6Q38149945-809DA4D9-3300-4E36-984B-807D183C33D9Q38997390-A9603252-E74D-4CEA-9A17-3EB38121C13EQ39240290-362F1380-0D4C-4B81-A693-18900E06B2E6Q40032274-F673E06B-28E9-4085-B92C-B5C14A2E218FQ41559175-DBEB3D57-356E-4A6F-B3F0-EE7A0C4FF074Q41848433-6EF6F2CE-0FE6-4914-A111-3013E8DC1F31Q41908841-C1E91939-B2D0-4A5A-87BF-3CBDB143CDA5Q42411828-9882FDED-22BF-4957-A1F2-DB4B8518CCC7Q42450380-780024B3-2E85-45A0-9387-66774BD34822Q45141795-17F0B0EE-9331-489B-BAEB-A3236E07B188Q47143199-F34014F8-77DC-41C1-9068-371E3DD4D0A8Q48314165-4EF47E7A-3607-426D-BB02-90E99A4CA72CQ49865845-7B31E387-D401-44F0-9E1D-70D5E0838908
P2860
Coactivators necessary for transcriptional output of the hypoxia inducible factor, HIF, are directly recruited by ARNT PAS-B
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին 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
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@ast
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@en
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@nl
type
label
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@ast
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@en
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@nl
prefLabel
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@ast
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@en
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@nl
P2860
P356
P1476
Coactivators necessary for tra ...... rectly recruited by ARNT PAS-B
@en
P2093
Carrie L Partch
P2860
P304
P356
10.1073/PNAS.1101357108
P407
P577
2011-04-21T00:00:00Z