| scholarly article | Q13442814 |
| P50 | author | Lee H Wong | Q56438118 |
| Jeffrey R Mann | Q63698596 | ||
| P2093 | author name string | Philippe Collas | |
| Hilda A Pickett | |||
| F Lyn Chan | |||
| Maheshi Udugama | |||
| Lynne Mayne | |||
| James D R McGhie | |||
| Fiona T M Chang | |||
| Michelle C Tang | |||
| P2860 | cites work | Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres | Q24292850 |
| Histone H3.1 and H3.3 complexes mediate nucleosome assembly pathways dependent or independent of DNA synthesis | Q24304348 | ||
| The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3 | Q24315621 | ||
| The HP1alpha-CAF1-SetDB1-containing complex provides H3K9me1 for Suv39-mediated K9me3 in pericentric heterochromatin | Q24317426 | ||
| Somatic histone H3 alterations in pediatric diffuse intrinsic pontine gliomas and non-brainstem glioblastomas | Q24629777 | ||
| Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin | Q27670415 | ||
| ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome | Q27670417 | ||
| Chromatin modifications and their function | Q27861067 | ||
| ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells | Q28114801 | ||
| Conditional allelic replacement applied to genes encoding the histone variant H3.3 in the mouse. | Q50765147 | ||
| Dynamics of histone H3 deposition in vivo reveal a nucleosome gap-filling mechanism for H3.3 to maintain chromatin integrity. | Q51543312 | ||
| Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferases. | Q51598430 | ||
| Stable G-quadruplexes are found outside nucleosome-bound regions. | Q54687435 | ||
| Genome-wide analysis predicts DNA structural motifs as nucleosome exclusion signals | Q66777985 | ||
| DNA C-circles are specific and quantifiable markers of alternative-lengthening-of-telomeres activity | Q84946960 | ||
| Telomeric repeat containing RNA and RNA surveillance factors at mammalian chromosome ends | Q28116571 | ||
| Regulation of replication fork progression through histone supply and demand | Q28261912 | ||
| Distinct factors control histone variant H3.3 localization at specific genomic regions | Q28275277 | ||
| The G4 genome | Q28289973 | ||
| DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors | Q28303693 | ||
| PML bodies provide an important platform for the maintenance of telomeric chromatin integrity in embryonic stem cells | Q28587544 | ||
| Contribution of the two genes encoding histone variant h3.3 to viability and fertility in mice | Q28591185 | ||
| Rif1 maintains telomere length homeostasis of ESCs by mediating heterochromatin silencing | Q28591651 | ||
| The histone variant H3.3 marks active chromatin by replication-independent nucleosome assembly | Q29618256 | ||
| Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability | Q29620365 | ||
| Histone H3.3 is enriched in covalent modifications associated with active chromatin | Q33196967 | ||
| Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues | Q33240549 | ||
| Regulation of DNA methylation turnover at LTR retrotransposons and imprinted loci by the histone methyltransferase Setdb1 | Q33606891 | ||
| Altered telomeres in tumors with ATRX and DAXX mutations | Q34196696 | ||
| Molecular pathology and genetics of pancreatic endocrine tumours. | Q34274982 | ||
| Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway | Q34350929 | ||
| ATRX Plays a Key Role in Maintaining Silencing at Interstitial Heterochromatic Loci and Imprinted Genes. | Q34471329 | ||
| Histone H3.3 is required for endogenous retroviral element silencing in embryonic stem cells | Q34474887 | ||
| Loss of wild-type ATRX expression in somatic cell hybrids segregates with activation of Alternative Lengthening of Telomeres | Q34490971 | ||
| Loss of Atrx sensitizes cells to DNA damaging agents through p53-mediated death pathways | Q34533223 | ||
| PTMs on H3 variants before chromatin assembly potentiate their final epigenetic state | Q34575324 | ||
| Developmentally regulated transcription of mammalian telomeres by DNA-dependent RNA polymerase II. | Q34729916 | ||
| Prevalence of the alternative lengthening of telomeres telomere maintenance mechanism in human cancer subtypes | Q35235698 | ||
| In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions | Q35534127 | ||
| Active transcription and essential role of RNA polymerase II at the centromere during mitosis | Q35751023 | ||
| Nucleosome-depleted chromatin gaps recruit assembly factors for the H3.3 histone variant | Q36438477 | ||
| Association of age at diagnosis and genetic mutations in patients with neuroblastoma. | Q36480024 | ||
| Loss of ATRX or DAXX expression and concomitant acquisition of the alternative lengthening of telomeres phenotype are late events in a small subset of MEN-1 syndrome pancreatic neuroendocrine tumors | Q36541359 | ||
| Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span. | Q36793436 | ||
| DNA secondary structures: stability and function of G-quadruplex structures | Q37051064 | ||
| Histone H3.3 incorporation provides a unique and functionally essential telomeric chromatin in embryonic stem cells | Q37142011 | ||
| H3.3 actively marks enhancers and primes gene transcription via opening higher-ordered chromatin. | Q37362553 | ||
| Rapid induction of alternative lengthening of telomeres by depletion of the histone chaperone ASF1. | Q37624289 | ||
| Epigenetic regulation of telomere chromatin integrity in pluripotent embryonic stem cells | Q37961786 | ||
| The chromatin remodeller ATRX: a repeat offender in human disease | Q38126641 | ||
| Transcription recovery after DNA damage requires chromatin priming by the H3.3 histone chaperone HIRA. | Q39090477 | ||
| Telomeric repeats act as nucleosome-disfavouring sequences in vivo | Q41941289 | ||
| Selective RNA versus DNA G-quadruplex targeting by in situ click chemistry. | Q41945558 | ||
| Transcriptional activation triggers deposition and removal of the histone variant H3.3. | Q42122747 | ||
| Suv39h-dependent H3K9me3 marks intact retrotransposons and silences LINE elements in mouse embryonic stem cells. | Q42209064 | ||
| Atrx promotes heterochromatin formation at retrotransposons | Q42389920 | ||
| DNA methylation and SETDB1/H3K9me3 regulate predominantly distinct sets of genes, retroelements, and chimeric transcripts in mESCs | Q42826399 | ||
| A subset of the histone H3 lysine 9 methyltransferases Suv39h1, G9a, GLP, and SETDB1 participate in a multimeric complex. | Q43175284 | ||
| Prdm3 and Prdm16 are H3K9me1 methyltransferases required for mammalian heterochromatin integrity. | Q45262911 | ||
| Epigenetic memory of an active gene state depends on histone H3.3 incorporation into chromatin in the absence of transcription | Q46861232 | ||
| Step-wise methylation of histone H3K9 positions heterochromatin at the nuclear periphery. | Q47068818 | ||
| ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner. | Q47407852 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 4.0 International | Q34179348 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 10227-10237 | |
| P577 | publication date | 2015-08-24 | |
| P1433 | published in | Nucleic Acids Research | Q135122 |
| P1476 | title | Histone variant H3.3 provides the heterochromatic H3 lysine 9 tri-methylation mark at telomeres | |
| P478 | volume | 43 |
| Q58727164 | ATRX loss induces multiple hallmarks of the alternative lengthening of telomeres (ALT) phenotype in human glioma cell lines in a cell line-specific manner |
| Q47766696 | Accumulation of histone variant H3.3 with age is associated with profound changes in the histone methylation landscape. |
| Q92443471 | Alternative Lengthening of Telomeres and Chromatin Status |
| Q51645621 | Alternative Lengthening of Telomeres and Loss of DAXX/ATRX Expression Predicts Metastatic Disease and Poor Survival in Patients with Pancreatic Neuroendocrine Tumors. |
| Q47108479 | Aurora Kinase B, a novel regulator of TERF1 binding and telomeric integrity |
| Q47137522 | CENP-B protects centromere chromatin integrity by facilitating histone deposition via the H3.3-specific chaperone Daxx |
| Q64889834 | Centromeric and ectopic assembly of CENP-A chromatin in health and cancer: old marks and new tracks. |
| Q50193501 | Epigenetic regulation in cell senescence |
| Q47352829 | Functional Redundancy of Variant and Canonical Histone H3 Lysine 9 Modification in Drosophila |
| Q30043364 | H3.3 demarcates GC-rich coding and subtelomeric regions and serves as potential memory mark for virulence gene expression in Plasmodium falciparum |
| Q38882222 | H3.Y discriminates between HIRA and DAXX chaperone complexes and reveals unexpected insights into human DAXX-H3.3-H4 binding and deposition requirements. |
| Q38733118 | HIRA deficiency in muscle fibers causes hypertrophy and susceptibility to oxidative stress |
| Q64104141 | Histone Modifications and the Maintenance of Telomere Integrity |
| Q37143027 | Histone turnover and chromatin accessibility: Critical mediators of neurological development, plasticity, and disease |
| Q39031041 | Histone variants on the move: substrates for chromatin dynamics |
| Q40292496 | Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome |
| Q39021931 | Life and cancer without telomerase: ALT and other strategies for making sure ends (don't) meet. |
| Q106089349 | Local Enrichment of HP1alpha at Telomeres Alters Their Structure and Regulation of Telomere Protection |
| Q58765323 | Local enrichment of HP1alpha at telomeres alters their structure and regulation of telomere protection |
| Q26765418 | Maintaining memory of silencing at imprinted differentially methylated regions |
| Q26775163 | Markers of cellular senescence. Telomere shortening as a marker of cellular senescence |
| Q91949069 | Molecular effects of dADD1 misexpression in chromatin organization and transcription |
| Q98735817 | Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function |
| Q26771668 | New players in heterochromatin silencing: histone variant H3.3 and the ATRX/DAXX chaperone |
| Q91843058 | PML is recruited to heterochromatin during S phase and represses DAXX-mediated histone H3.3 chromatin assembly |
| Q38877286 | PML protein organizes heterochromatin domains where it regulates histone H3.3 deposition by ATRX/DAXX. |
| Q33674324 | Quantitative chromatin proteomics reveals a dynamic histone post-translational modification landscape that defines asexual and sexual Plasmodium falciparum parasites |
| Q27306288 | RNase P protein subunit Rpp29 represses histone H3.3 nucleosome deposition |
| Q52579677 | Ribosomal DNA copy loss and repeat instability in ATRX-mutated cancers. |
| Q64062855 | SETDB1-dependent heterochromatin stimulates alternative lengthening of telomeres |
| Q39119025 | Silencing of endogenous retroviruses by heterochromatin |
| Q48103225 | Telomere chromatin establishment and its maintenance during mammalian development. |
| Q39025713 | The molecular basis of the organization of repetitive DNA-containing constitutive heterochromatin in mammals. |
| Q52532574 | The tale of a tail: histone H4 acetylation and the repair of DNA breaks. |
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