| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Chris Barnett | |
| Jocelyn E Krebs | |||
| P2860 | cites work | Structure and ligand of a histone acetyltransferase bromodomain | Q22009928 |
| A novel family of bromodomain genes | Q22011208 | ||
| Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 | ||
| HuCHRAC, a human ISWI chromatin remodelling complex contains hACF1 and two novel histone-fold proteins | Q22254462 | ||
| Structure of the PHD zinc finger from human Williams-Beuren syndrome transcription factor | Q24290654 | ||
| NoRC--a novel member of mammalian ISWI-containing chromatin remodeling machines | Q24291631 | ||
| WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci | Q24295285 | ||
| The chromatin remodelling complex WSTF-SNF2h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription | Q24306527 | ||
| WSTF regulates the H2A.X DNA damage response via a novel tyrosine kinase activity | Q24309061 | ||
| Tyrosine dephosphorylation of H2AX modulates apoptosis and survival decisions | Q24313501 | ||
| Dephosphorylation of the C-terminal tyrosyl residue of the DNA damage-related histone H2A.X is mediated by the protein phosphatase eyes absent | Q24313879 | ||
| The Williams syndrome transcription factor interacts with PCNA to target chromatin remodelling by ISWI to replication foci | Q24314820 | ||
| ACF consists of two subunits, Acf1 and ISWI, that function cooperatively in the ATP-dependent catalysis of chromatin assembly | Q24602406 | ||
| A family of chromatin remodeling factors related to Williams syndrome transcription factor | Q24673669 | ||
| Megabase chromatin domains involved in DNA double-strand breaks in vivo | Q24680284 | ||
| Combined biochemical and electron microscopic analyses reveal the architecture of the mammalian U2 snRNP | Q24682070 | ||
| Chromatin modifications and their function | Q27861067 | ||
| INO80 and gamma-H2AX interaction links ATP-dependent chromatin remodeling to DNA damage repair. | Q27933934 | ||
| Phosphorylation of Williams syndrome transcription factor by MAPK induces a switching between two distinct chromatin remodeling complexes | Q28118804 | ||
| DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
| The bromodomain: a chromatin-targeting module? | Q28139513 | ||
| A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage | Q28144576 | ||
| The chromatin-remodeling complex WINAC targets a nuclear receptor to promoters and is impaired in Williams syndrome | Q28183858 | ||
| Anterior-posterior guidance of commissural axons by Wnt-frizzled signaling | Q28191111 | ||
| FACT facilitates transcription-dependent nucleosome alteration | Q28203107 | ||
| Nuclear receptor function requires a TFTC-type histone acetyl transferase complex | Q28212676 | ||
| ISWI remodeling complexes in Xenopus egg extracts: identification as major chromosomal components that are regulated by INCENP-aurora B | Q28216563 | ||
| Molecular basis for site-specific read-out of histone H3K4me3 by the BPTF PHD finger of NURF | Q28242466 | ||
| Functional diversity of ISWI complexes | Q28274890 | ||
| The dermatomyositis-specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities | Q28286772 | ||
| The DEK protein--an abundant and ubiquitous constituent of mammalian chromatin | Q28295129 | ||
| RETRACTED: Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF) | Q28512986 | ||
| A complex containing N-CoR, mSin3 and histone deacetylase mediates transcriptional repression | Q28578229 | ||
| Heterochromatin revisited | Q29614716 | ||
| The PHD finger: implications for chromatin-mediated transcriptional regulation | Q29620426 | ||
| Multiple ISWI ATPase complexes from xenopus laevis. Functional conservation of an ACF/CHRAC homolog | Q30903514 | ||
| Extrarenal expression of 25-hydroxyvitamin d(3)-1 alpha-hydroxylase | Q31831783 | ||
| ATP-dependent chromatin-remodeling complexes. | Q33786898 | ||
| Noncanonical Wnt-4 signaling and EAF2 are required for eye development in Xenopus laevis. | Q33937196 | ||
| Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene | Q34131820 | ||
| Natural history of Williams syndrome: physical characteristics | Q34406298 | ||
| Genome-scale identification of nucleosome positions in S. cerevisiae | Q34427114 | ||
| Functional interaction between RNA helicase II/Gu(alpha) and ribosomal protein L4. | Q34437211 | ||
| Purification and characterization of CAF-I, a human cell factor required for chromatin assembly during DNA replication in vitro | Q34451628 | ||
| A novel human gene, WSTF, is deleted in Williams syndrome | Q34481307 | ||
| The WSTF-SNF2h chromatin remodeling complex interacts with several nuclear proteins in transcription | Q34512121 | ||
| Williams-Beuren syndrome. | Q34615997 | ||
| A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development | Q34909016 | ||
| Regulation of eye development by frizzled signaling in Xenopus | Q35043171 | ||
| Chromatin remodelling and transcription: be-WICHed by nuclear myosin 1. | Q36436099 | ||
| ATP-dependent chromatin remodeling complexes in Drosophila. | Q36527443 | ||
| A new transcriptional-activation motif restricted to a class of helix-loop-helix proteins is functionally conserved in both yeast and mammalian cells | Q36660430 | ||
| Chromatin remodeling and repair of DNA double-strand breaks | Q36660520 | ||
| Mechanisms of ATP dependent chromatin remodeling | Q36738573 | ||
| How eukaryotic genes are transcribed | Q37514183 | ||
| Chromosomal landscape of nucleosome-dependent gene expression and silencing in yeast. | Q38317749 | ||
| The SNF2 domain protein family in higher vertebrates displays dynamic expression patterns in Xenopus laevis embryos. | Q38463369 | ||
| Identification of Myb-binding protein 1A (MYBBP1A) as a novel substrate for aurora B kinase | Q39736403 | ||
| Transrepression by a liganded nuclear receptor via a bHLH activator through co-regulator switching | Q40413870 | ||
| Transcriptional activation of a constitutive heterochromatic domain of the human genome in response to heat shock. | Q40509160 | ||
| Structure-function relationships in the vitamin D endocrine system | Q40545127 | ||
| Topoisomerase II, not topoisomerase I, is the proficient relaxase of nucleosomal DNA. | Q42410346 | ||
| A comparative study of neurogenesis in the retinal ciliary marginal zone of homeothermic vertebrates | Q43955517 | ||
| Distinct strategies to make nucleosomal DNA accessible | Q44455871 | ||
| The transcription factor Eyes absent is a protein tyrosine phosphatase | Q44662320 | ||
| Nucleosome binding by the bromodomain and PHD finger of the transcriptional cofactor p300. | Q44806809 | ||
| The CSB protein actively wraps DNA. | Q45153429 | ||
| Histone H2A.X Tyr142 phosphorylation: a novel sWItCH for apoptosis? | Q46009519 | ||
| Neural and eye-specific defects associated with loss of the imitation switch (ISWI) chromatin remodeler in Xenopus laevis | Q46709205 | ||
| Sunlight, season, skin pigmentation, vitamin D, and 25-hydroxyvitamin D: integral components of the vitamin D endocrine system | Q46727296 | ||
| Cloning and developmental expression of WSTF during Xenopus laevis embryogenesis | Q48666812 | ||
| RETRACTED: Nuclear Receptor Function Requires a TFTC-Type Histone Acetyl Transferase Complex | Q55920649 | ||
| Efficient Inhibition of Escherichia Coli RNA Polymerase by the Bacteriophage T4 AsiA Protein Requires that AsiA Binds First to Free σ70 | Q57078236 | ||
| Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome | Q68427180 | ||
| Ligand-induced transrepressive function of VDR requires a chromatin remodeling complex, WINAC | Q79971397 | ||
| Isthmus organizer for midbrain and hindbrain development | Q81088754 | ||
| Diverse regulation of SNF2h chromatin remodeling by noncatalytic subunits | Q81455683 | ||
| Primers on chromatin | Q81557015 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 12-23 | |
| P577 | publication date | 2011-02-01 | |
| P1433 | published in | Biochemistry and Cell Biology | Q4914719 |
| P1476 | title | WSTF does it all: a multifunctional protein in transcription, repair, and replication | |
| P478 | volume | 89 |
| Q107515230 | B-WICH chromatin remodelling complex |
| Q107602852 | B-WICH chromatin remodelling complex |
| Q38930069 | A cis-acting element in the promoter of human ether à go-go 1 potassium channel gene mediates repression by calcitriol in human cervical cancer cells. |
| Q38185355 | Bromodomains and their pharmacological inhibitors |
| Q35391240 | DGCR14 induces Il17a gene expression through the RORγ/BAZ1B/RSKS2 complex |
| Q91995541 | Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication |
| Q89538003 | Elevated Levels of 1,25-Dihydroxyvitamin D in Plasma as a Missing Risk Factor for Celiac Disease |
| Q93080999 | Epigenetic Mechanisms in Hirschsprung Disease |
| Q34663839 | Epigenetic regulation in neural crest development |
| Q38870288 | Epigenetics in ENS development and Hirschsprung disease |
| Q43441639 | FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination. |
| Q35739715 | Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes |
| Q46069709 | Haploinsufficiency of BAZ1B contributes to Williams syndrome through transcriptional dysregulation of neurodevelopmental pathways. |
| Q37395824 | Helicase CHD4 is an epigenetic coregulator of PAX3-FOXO1 in alveolar rhabdomyosarcoma |
| Q33910348 | ISWI remodels nucleosomes through a random walk |
| Q37619715 | KRASG12 mutant induces the release of the WSTF/NRG3 complex, and contributes to an oncogenic paracrine signaling pathway |
| Q30560450 | Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression |
| Q26775935 | Multiple Functions of the Eya Phosphotyrosine Phosphatase |
| Q38804461 | PTH and Vitamin D. |
| Q91906236 | Potential risk factors for celiac disease in childhood: a case-control epidemiological survey |
| Q33910372 | Quantitative determination of binding of ISWI to nucleosomes and DNA shows allosteric regulation of DNA binding by nucleotides |
| Q34981653 | Screen identifies bromodomain protein ZMYND8 in chromatin recognition of transcription-associated DNA damage that promotes homologous recombination. |
| Q35081686 | Subnuclear domain proteins in cancer cells support the functions of RUNX2 in the DNA damage response |
| Q34107107 | The HARE-HTH and associated domains: novel modules in the coordination of epigenetic DNA and protein modifications |
| Q34482956 | The WSTF-ISWI chromatin remodeling complex transiently associates with the human inactive X chromosome during late S-phase prior to BRCA1 and γ-H2AX |
| Q96230063 | WSTF acetylation by MOF promotes WSTF activities and oncogenic functions |
| Q36282251 | Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis |
Search more.