| scholarly article | Q13442814 |
| P2093 | author name string | Maria M Viveiros | |
| Claudia Baumann | |||
| Rabindranath De La Fuente | |||
| P2860 | cites work | Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association | Q22253267 |
| Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres | Q24292850 | ||
| The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3 | Q24315621 | ||
| The cohesin complex is required for the DNA damage-induced G2/M checkpoint in mammalian cells | Q24317260 | ||
| Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo | Q27345576 | ||
| DNA double-strand breaks in heterochromatin elicit fast repair protein recruitment, histone H2AX phosphorylation and relocation to euchromatin | Q28236172 | ||
| Dynamic molecular linkers of the genome: the first decade of SMC proteins | Q28254733 | ||
| Distinct factors control histone variant H3.3 localization at specific genomic regions | Q28275277 | ||
| Specific interaction between human kinetochore protein CENP-C and a nucleolar transcriptional regulator | Q28284336 | ||
| DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors | Q28303693 | ||
| Histone variant H3.3 maintains a decondensed chromatin state essential for mouse preimplantation development | Q28507170 | ||
| PRC1 and Suv39h specify parental asymmetry at constitutive heterochromatin in early mouse embryos | Q28513185 | ||
| Epigenetic reprogramming in mammalian reproduction: contribution from histone variants | Q37400944 | ||
| Epigenetic transitions in germ cell development and meiosis | Q37809239 | ||
| Heterochromatin establishment in the context of genome-wide epigenetic reprogramming | Q37865899 | ||
| Heterochromatin maintenance and establishment: lessons from the mouse pericentromere | Q37937379 | ||
| Chromothripsis: chromosomes in crisis | Q38059925 | ||
| Objective scoring of transformed foci in BALB/c 3T3 cell transformation assay by statistical image descriptors. | Q39131569 | ||
| Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase | Q39835411 | ||
| Rapid and transient recruitment of DNMT1 to DNA double-strand breaks is mediated by its interaction with multiple components of the DNA damage response machinery. | Q41122376 | ||
| Loss of ATRX leads to chromosome cohesion and congression defects | Q41825660 | ||
| Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNA. | Q43966668 | ||
| Heterochromatin reorganization during early mouse development requires a single-stranded noncoding transcript | Q44595549 | ||
| ATRX in chromatin assembly and genome architecture during development and disease. | Q50790126 | ||
| Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos. | Q51590622 | ||
| A strand-specific burst in transcription of pericentric satellites is required for chromocenter formation and early mouse development. | Q51897792 | ||
| CENP-C is a structural platform for kinetochore assembly. | Q52716239 | ||
| Chromosome instability is common in human cleavage-stage embryos. | Q53398239 | ||
| DNA double-strand breaks trigger genome-wide sister-chromatid cohesion through Eco1 (Ctf7). | Q53541157 | ||
| New Epigenetic Drivers of Cancers | Q56929412 | ||
| Mitochondria and the death of oocytes | Q59075483 | ||
| Analysis of a malsegregating mouse Y chromosome: evidence that the earliest cleavage divisions of the mammalian embryo are non-disjunction-prone | Q73773749 | ||
| Heterochromatin formation in the mouse embryo requires critical residues of the histone variant H3.3 | Q28589235 | ||
| ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes | Q28591500 | ||
| Dicer-deficient mouse embryonic stem cells are defective in differentiation and centromeric silencing | Q28594776 | ||
| To err (meiotically) is human: the genesis of human aneuploidy | Q29618613 | ||
| On the road to cancer: aneuploidy and the mitotic checkpoint | Q29619455 | ||
| Dissection of CENP-C-directed centromere and kinetochore assembly | Q30437632 | ||
| Aurora B is enriched at merotelic attachment sites, where it regulates MCAK. | Q30441483 | ||
| Tracking epigenetic histone modifications in single cells using Fab-based live endogenous modification labeling | Q30503605 | ||
| Double-strand breaks in heterochromatin move outside of a dynamic HP1a domain to complete recombinational repair. | Q30524137 | ||
| Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage | Q30531076 | ||
| ATRX tolerates activity-dependent histone H3 methyl/phos switching to maintain repetitive element silencing in neurons | Q30653780 | ||
| Active demethylation of the paternal genome in the mouse zygote | Q33901068 | ||
| Hira-mediated H3.3 incorporation is required for DNA replication and ribosomal RNA transcription in the mouse zygote | Q34051667 | ||
| Cohesin protects genes against γH2AX Induced by DNA double-strand breaks | Q34140001 | ||
| Histone variants in metazoan development | Q34149623 | ||
| Centromeres: unique chromatin structures that drive chromosome segregation | Q34179745 | ||
| Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes | Q34257086 | ||
| Molecular-clinical spectrum of the ATR-X syndrome | Q34306141 | ||
| Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway | Q34350929 | ||
| Dynamic chromatin modifications characterise the first cell cycle in mouse embryos. | Q34402750 | ||
| Somatic genomic variations in early human prenatal development | Q34479598 | ||
| Accumulation of small murine minor satellite transcripts leads to impaired centromeric architecture and function | Q34695366 | ||
| Histone H2A ubiquitination in transcriptional regulation and DNA damage repair | Q34859357 | ||
| Unrepaired clustered DNA lesions induce chromosome breakage in human cells | Q35002550 | ||
| Role of ATRX in chromatin structure and function: implications for chromosome instability and human disease | Q35661042 | ||
| CENP-C is required for maintaining proper kinetochore size and for a timely transition to anaphase. | Q36233891 | ||
| SUV39H1 orchestrates temporal dynamics of centromeric methylation essential for faithful chromosome segregation in mitosis. | Q36297890 | ||
| Spatial separation of parental genomes in preimplantation mouse embryos | Q36316386 | ||
| Transcription in the maintenance of centromere chromatin identity | Q36478032 | ||
| Centromere mitotic recombination in mammalian cells | Q36718343 | ||
| The origin of human aneuploidy: where we have been, where we are going | Q36958145 | ||
| Heterochromatin tells CENP-A where to go. | Q37163174 | ||
| Kinetochore asymmetry defines a single yeast lineage | Q37167774 | ||
| DNMT3B interacts with constitutive centromere protein CENP-C to modulate DNA methylation and the histone code at centromeric regions | Q37295052 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 1806-1817 | |
| P577 | publication date | 2015-04-29 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | ATRX contributes to epigenetic asymmetry and silencing of major satellite transcripts in the maternal genome of the mouse embryo | |
| P478 | volume | 142 |
| Q92636236 | Decoding the Role of Satellite DNA in Genome Architecture and Plasticity-An Evolutionary and Clinical Affair |
| Q94591294 | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
| Q99233799 | Helicase LSH/Hells regulates kinetochore function, histone H3/Thr3 phosphorylation and centromere transcription during oocyte meiosis |
| Q39038126 | Heterochromatin and the molecular mechanisms of 'parent-of-origin' effects in animals. |
| Q39155966 | How can zygotes segregate entire parental genomes into distinct blastomeres? The zygote metaphase revisited |
| Q36955138 | Inheritance of the CENP-A chromatin domain is spatially and temporally constrained at human centromeres |
| Q34550716 | Integrity of the human centromere DNA repeats is protected by CENP-A, CENP-C, and CENP-T. |
| Q27309180 | Kinetochore function is controlled by a phospho-dependent coexpansion of inner and outer components |
| Q35844163 | Postovulatory aging affects dynamics of mRNA, expression and localization of maternal effect proteins, spindle integrity and pericentromeric proteins in mouse oocytes |
| Q41673553 | Satellite DNA: An Evolving Topic |
| Q37693989 | Silencing markers are retained on pericentric heterochromatin during murine primordial germ cell development |
| Q37699534 | Stress and the Emerging Roles of Chromatin Remodeling in Signal Integration and Stable Transmission of Reversible Phenotypes. |
| Q55036381 | TERRA and the state of the telomere. |
| Q48103225 | Telomere chromatin establishment and its maintenance during mammalian development. |
| Q57060639 | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
| Q38592335 | Transcription of tandemly repetitive DNA: functional roles |
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