scholarly article | Q13442814 |
P2093 | author name string | Martin Thompson | |
P2860 | cites work | Rapid and phosphoinositol-dependent binding of the SWI/SNF-like BAF complex to chromatin after T lymphocyte receptor signaling | Q22008515 |
Reconstitution of a core chromatin remodeling complex from SWI/SNF subunits | Q22009033 | ||
Structure and ligand of a histone acetyltransferase bromodomain | Q22009928 | ||
Translating the Histone Code | Q22065840 | ||
HMG1 and 2: architectural DNA-binding proteins | Q22121969 | ||
The human SWI-SNF complex protein p270 is an ARID family member with non-sequence-specific DNA binding activity | Q22253861 | ||
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
Molecular characterization of celtix-1, a bromodomain protein interacting with the transcription factor interferon regulatory factor 2 | Q24290379 | ||
The human SWI/SNF-B chromatin-remodeling complex is related to yeast rsc and localizes at kinetochores of mitotic chromosomes | Q24290517 | ||
Transcription factors and nuclear receptors interact with the SWI/SNF complex through the BAF60c subunit | Q24303852 | ||
PBAF chromatin-remodeling complex requires a novel specificity subunit, BAF200, to regulate expression of selective interferon-responsive genes | Q24306301 | ||
The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors | Q24313036 | ||
Histone structure and the organization of the nucleosome | Q41548930 | ||
Essential and redundant functions of histone acetylation revealed by mutation of target lysines and loss of the Gcn5p acetyltransferase | Q41913369 | ||
Determinants of HMGB proteins required to promote RAG1/2-recombination signal sequence complex assembly and catalysis during V(D)J recombination | Q42839793 | ||
Crystal structure of the proximal BAH domain of the polybromo protein. | Q42928352 | ||
Structure of the Sir3 protein bromo adjacent homology (BAH) domain from S. cerevisiae at 1.95 A resolution | Q43043642 | ||
A key role of the hSNF5/INI1 tumour suppressor in the control of the G1-S transition of the cell cycle | Q44134109 | ||
The role of loop ZA and Pro371 in the function of yeast Gcn5p bromodomain revealed through molecular dynamics and experiment | Q46717356 | ||
Structure, dynamics, and function of chromatin in vitro | Q47910966 | ||
The RSC nucleosome-remodeling complex is required for Cohesin's association with chromosome arms | Q47946973 | ||
The bromodomain revisited. | Q48050242 | ||
Polybromo-1-bromodomains bind histone H3 at specific acetyl-lysine positions | Q53569429 | ||
Bromodomain factor 1 (Bdf1) protein interacts with histones | Q62019779 | ||
Expression, purification and characterization of individual bromodomains from human Polybromo-1 | Q80110257 | ||
The Swi2/Snf2 bromodomain is required for the displacement of SAGA and the octamer transfer of SAGA-acetylated nucleosomes | Q83222781 | ||
BAF60a mediates critical interactions between nuclear receptors and the BRG1 chromatin-remodeling complex for transactivation | Q24315628 | ||
Purification and biochemical heterogeneity of the mammalian SWI-SNF complex | Q24316969 | ||
Reading and function of a histone code involved in targeting corepressor complexes for repression | Q24322748 | ||
Diversity and specialization of mammalian SWI/SNF complexes | Q24322918 | ||
Targeting of SWI/SNF chromatin remodelling complexes to estrogen-responsive genes | Q24534273 | ||
Cell cycle arrest and repression of cyclin D1 transcription by INI1/hSNF5. | Q24537644 | ||
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
Bromodomain protein 4 mediates the papillomavirus E2 transcriptional activation function | Q24545850 | ||
From head to toes: the multiple facets of Sox proteins | Q24548730 | ||
A specificity and targeting subunit of a human SWI/SNF family-related chromatin-remodeling complex | Q24551058 | ||
The structural basis for the recognition of acetylated histone H4 by the bromodomain of histone acetyltransferase gcn5p | Q24596953 | ||
Structural insights into human KAP1 PHD finger-bromodomain and its role in gene silencing | Q24634118 | ||
Structure and function of a human TAFII250 double bromodomain module | Q27622657 | ||
Solution structure and acetyl-lysine binding activity of the GCN5 bromodomain | Q27628617 | ||
Structural basis of lysine-acetylated HIV-1 Tat recognition by PCAF bromodomain | Q27638717 | ||
Structure and function of the BAH-containing domain of Orc1p in epigenetic silencing | Q27639534 | ||
The S. cerevisiae architectural HMGB protein NHP6A complexed with DNA: DNA and protein conformational changes upon binding | Q27639828 | ||
Structural mechanism of the bromodomain of the coactivator CBP in p53 transcriptional activation | Q27643078 | ||
Solution structure of human Brg1 bromodomain and its specific binding to acetylated histone tails | Q27643720 | ||
Solution structure of BRD7 bromodomain and its interaction with acetylated peptides from histone H3 and H4 | Q27644757 | ||
Autoregulation of the Rsc4 Tandem Bromodomain by Gcn5 Acetylation | Q27647842 | ||
Structural Basis of Site-Specific Histone Recognition by the Bromodomains of Human Coactivators PCAF and CBP/p300 | Q27650290 | ||
Structure of the HMG box motif in the B-domain of HMG1 | Q27732133 | ||
The language of covalent histone modifications | Q27860931 | ||
The ctf13-30/CTF13 genomic haploinsufficiency modifier screen identifies the yeast chromatin remodeling complex RSC, which is required for the establishment of sister chromatid cohesion | Q27930793 | ||
RSC, an essential, abundant chromatin-remodeling complex | Q27933821 | ||
RSC2, encoding a component of the RSC nucleosome remodeling complex, is essential for 2 microm plasmid maintenance in Saccharomyces cerevisiae | Q27934780 | ||
The yeast RSC chromatin-remodeling complex is required for kinetochore function in chromosome segregation | Q27936620 | ||
Role of interactions between the origin recognition complex and SIR1 in transcriptional silencing | Q27937028 | ||
RSC exploits histone acetylation to abrogate the nucleosomal block to RNA polymerase II elongation | Q27938414 | ||
Two functionally distinct forms of the RSC nucleosome-remodeling complex, containing essential AT hook, BAH, and bromodomains | Q27939983 | ||
The bromodomain: a chromatin-targeting module? | Q28139513 | ||
The many faces of histone lysine methylation | Q34688382 | ||
The BAH domain facilitates the ability of human Orc1 protein to activate replication origins in vivo | Q35131006 | ||
Chromatin structure and transcription | Q35237465 | ||
Regulatory diversity among metazoan co-activator complexes | Q35762480 | ||
Actin up in the nucleus | Q35762484 | ||
Composition and functional specificity of SWI2/SNF2 class chromatin remodeling complexes | Q35997560 | ||
Kinetic analysis of acetylation-dependent Pb1 bromodomain-histone interactions | Q36844745 | ||
Nucleosome organization and targeting of SWI/SNF chromatin-remodeling complexes: contributions of the DNA sequence | Q36916642 | ||
High mobility group proteins and their post-translational modifications | Q37015673 | ||
Tandem bromodomains in the chromatin remodeler RSC recognize acetylated histone H3 Lys14 | Q37270587 | ||
Structure of Chromatin | Q39687258 | ||
The CBP bromodomain and nucleosome targeting are required for Zta-directed nucleosome acetylation and transcription activation | Q39743627 | ||
The SWI/SNF chromatin remodeling subunit BAF57 is a critical regulator of estrogen receptor function in breast cancer cells | Q40268747 | ||
Nucleosome structure | Q40289266 | ||
BAF57 governs androgen receptor action and androgen-dependent proliferation through SWI/SNF. | Q40451636 | ||
P16INK4a is required for hSNF5 chromatin remodeler-induced cellular senescence in malignant rhabdoid tumor cells | Q40618783 | ||
Differential requirement of SWI/SNF for androgen receptor activity | Q40643889 | ||
Osa associates with the Brahma chromatin remodeling complex and promotes the activation of some target genes | Q40911651 | ||
Signaling to chromatin through histone modifications | Q28142598 | ||
Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators | Q28143448 | ||
Histone acetylation and an epigenetic code | Q28143767 | ||
HMG1 and 2, and related 'architectural' DNA-binding proteins | Q28204610 | ||
Bromodomain: an acetyl-lysine binding domain | Q28209708 | ||
Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails | Q28216534 | ||
Selective recognition of acetylated histones by bromodomain proteins visualized in living cells | Q28239585 | ||
The multidomain structure of Orc1p reveals similarity to regulators of DNA replication and transcriptional silencing | Q28291160 | ||
Reconstitution of recombinant chromatin establishes a requirement for histone-tail modifications during chromatin assembly and transcription | Q28363122 | ||
An essential switch in subunit composition of a chromatin remodeling complex during neural development | Q28585238 | ||
A human BRCA2 complex containing a structural DNA binding component influences cell cycle progression | Q28590448 | ||
Polybromo protein BAF180 functions in mammalian cardiac chamber maturation | Q28591027 | ||
Baf60c is essential for function of BAF chromatin remodelling complexes in heart development | Q28593688 | ||
Histone acetylation and transcriptional regulatory mechanisms | Q29547707 | ||
Histone acetyltransferases | Q29547823 | ||
Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome | Q29618064 | ||
ATP-dependent nucleosome remodeling | Q29618979 | ||
Alteration of nucleosome structure as a mechanism of transcriptional regulation | Q29620047 | ||
Searching protein sequence libraries: Comparison of the sensitivity and selectivity of the Smith-Waterman and FASTA algorithms | Q30444379 | ||
Thermodynamic analysis of acetylation-dependent Pb1 bromodomain-histone H3 interactions | Q33314479 | ||
Identification of transcription complexes that contain the double bromodomain protein Brd2 and chromatin remodeling machines | Q33659363 | ||
Structural basis for origin recognition complex 1 protein-silence information regulator 1 protein interaction in epigenetic silencing | Q33853979 | ||
Structural basis of the Sir1-origin recognition complex interaction in transcriptional silencing | Q33854091 | ||
The BAH (bromo-adjacent homology) domain: a link between DNA methylation, replication and transcriptional regulation | Q33856691 | ||
Promoter targeting and chromatin remodeling by the SWI/SNF complex | Q33885075 | ||
Phosphatidylinositol-dependent actin filament binding by the SWI/SNF-like BAF chromatin remodeling complex | Q34014577 | ||
BAF180 is a critical regulator of p21 induction and a tumor suppressor mutated in breast cancer | Q34042035 | ||
Regulating SWI/SNF subunit levels via protein-protein interactions and proteasomal degradation: BAF155 and BAF170 limit expression of BAF57 | Q34097266 | ||
Characterization of human SMARCE1r high-mobility-group protein. | Q34127304 | ||
cDNA cloning of the human polybromo-1 gene on chromosome 3p21. | Q34165455 | ||
The BAH domain, polybromo and the RSC chromatin remodelling complex | Q34258291 | ||
The bromodomain: a chromatin browser? | Q34327281 | ||
The bromodomain: a regulator of ATP-dependent chromatin remodeling? | Q34327336 | ||
A region of the Sir1 protein dedicated to recognition of a silencer and required for interaction with the Orc1 protein in saccharomyces cerevisiae | Q34606092 | ||
The HMG-box: a versatile protein domain occurring in a wide variety of DNA-binding proteins | Q34643061 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 309-319 | |
P577 | publication date | 2008-12-03 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Biochimie | Q2904035 |
P1476 | title | Polybromo-1: the chromatin targeting subunit of the PBAF complex | |
P478 | volume | 91 |
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