scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1000070031 |
P356 | DOI | 10.1007/S00018-016-2157-6 |
P932 | PMC publication ID | 4819931 |
P698 | PubMed publication ID | 26883803 |
P5875 | ResearchGate publication ID | 294919595 |
P50 | author | Hsiao Phin Joanna Voon | Q80310067 |
Richard J Gibbons | Q37830276 | ||
P2093 | author name string | Richard J Gibbons | |
Hsiao P J Voon | |||
P2860 | cites work | Genome-wide analysis of KAP1 binding suggests autoregulation of KRAB-ZNFs | Q21563454 |
The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9 | Q24297608 | ||
Histone H3.1 and H3.3 complexes mediate nucleosome assembly pathways dependent or independent of DNA synthesis | Q24304348 | ||
KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints | Q24312768 | ||
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 | Q24312925 | ||
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints | Q24322379 | ||
Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes | Q24539228 | ||
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome | Q24644175 | ||
DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA | Q24645346 | ||
The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase | Q24678267 | ||
An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus | Q24678820 | ||
SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteins | Q24685694 | ||
Spotting the enemy within: Targeted silencing of foreign DNA in mammalian genomes by the Krüppel-associated box zinc finger protein family | Q26782206 | ||
New insights into establishment and maintenance of DNA methylation imprints in mammals | Q26852971 | ||
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 | ||
Structure of the variant histone H3.3–H4 heterodimer in complex with its chaperone DAXX | Q27675056 | ||
Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 | ||
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain | Q27860477 | ||
Set2 methylation of histone H3 lysine 36 suppresses histone exchange on transcribed genes | Q27929868 | ||
Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription | Q27932406 | ||
ATRX interacts with H3.3 in maintaining telomere structural integrity in pluripotent embryonic stem cells | Q28114801 | ||
Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferases | Q51598430 | ||
Imprinted expression of the Igf2r gene depends on an intronic CpG island | Q52192434 | ||
Epigenetic reprogramming in mouse primordial germ cells | Q57086629 | ||
HIRA Is Critical for a Nucleosome Assembly Pathway Independent of DNA Synthesis | Q57549500 | ||
Demethylation of the zygotic paternal genome | Q59066150 | ||
Mitochondria and the death of oocytes | Q59075483 | ||
Airn transcriptional overlap, but not its lncRNA products, induces imprinted Igf2r silencing | Q85652146 | ||
Histone tails regulate DNA methylation by allosterically activating de novo methyltransferase. | Q35348766 | ||
In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions | Q35534127 | ||
In vivo targeting of de novo DNA methylation by histone modifications in yeast and mouse. | Q35545732 | ||
Zinc finger protein ZFP57 requires its co-factor to recruit DNA methyltransferases and maintains DNA methylation imprint in embryonic stem cells via its transcriptional repression domain | Q35694053 | ||
Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression | Q35819244 | ||
Global profiling of DNA methylation erasure in mouse primordial germ cells | Q35864711 | ||
A unique regulatory phase of DNA methylation in the early mammalian embryo | Q35903352 | ||
Genome-wide bisulfite sequencing in zygotes identifies demethylation targets and maps the contribution of TET3 oxidation. | Q35973407 | ||
The KRAB-ZFP/KAP1 system contributes to the early embryonic establishment of site-specific DNA methylation patterns maintained during development | Q36915286 | ||
SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell state | Q37426752 | ||
Defending the genome from the enemy within: mechanisms of retrotransposon suppression in the mouse germline | Q37698311 | ||
DAXX co-folds with H3.3/H4 using high local stability conferred by the H3.3 variant recognition residues | Q37701297 | ||
Genomic profiling of DNA methyltransferases reveals a role for DNMT3B in genic methylation | Q38918003 | ||
Distinctive chromatin in human sperm packages genes for embryo development | Q40137854 | ||
Regulation of the large (approximately 1000 kb) imprinted murine Ube3a antisense transcript by alternative exons upstream of Snurf/Snrpn. | Q40540300 | ||
Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoa | Q46329417 | ||
Asymmetric regulation of imprinting on the maternal and paternal chromosomes at the Dlk1-Gtl2 imprinted cluster on mouse chromosome 12. | Q48231351 | ||
Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin | Q28187783 | ||
A mouse model for Prader-Willi syndrome imprinting-centre mutations | Q28271033 | ||
Distinct factors control histone variant H3.3 localization at specific genomic regions | Q28275277 | ||
PGC7/Stella protects against DNA demethylation in early embryogenesis | Q28506319 | ||
The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin | Q28506981 | ||
PGC7 binds histone H3K9me2 to protect against conversion of 5mC to 5hmC in early embryos | Q28508667 | ||
Histone H3-K9 methyltransferase ESET is essential for early development | Q28513000 | ||
KDM5B regulates embryonic stem cell self-renewal and represses cryptic intragenic transcription | Q28513535 | ||
Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine | Q28585429 | ||
Identification of PGC7, a new gene expressed specifically in preimplantation embryos and germ cells | Q28589532 | ||
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 | Q28589840 | ||
The role of Tet3 DNA dioxygenase in epigenetic reprogramming by oocytes | Q28595016 | ||
DAXX envelops a histone H3.3-H4 dimer for H3.3-specific recognition | Q28658254 | ||
Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation | Q29614333 | ||
Partitioning and plasticity of repressive histone methylation states in mammalian chromatin | Q29614513 | ||
Histone H3 lysine 4 methylation patterns in higher eukaryotic genes | Q29614678 | ||
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 | ||
Allelome.PRO, a pipeline to define allele-specific genomic features from high-throughput sequencing data. | Q30982170 | ||
Identifying genes preferentially expressed in undifferentiated embryonic stem cells | Q33295361 | ||
Regulation of DNA methylation turnover at LTR retrotransposons and imprinted loci by the histone methyltransferase Setdb1 | Q33606891 | ||
Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome. | Q33760054 | ||
The function of non-coding RNAs in genomic imprinting | Q33761870 | ||
Characterization of the contradictory chromatin signatures at the 3' exons of zinc finger genes | Q33828243 | ||
Relationship between Gene Body DNA Methylation and Intragenic H3K9me3 and H3K36me3 Chromatin Marks | Q33883693 | ||
The Dnmt3a PWWP domain reads histone 3 lysine 36 trimethylation and guides DNA methylation | Q34074317 | ||
Transcription Is Required to Establish Maternal Imprinting at the Prader-Willi Syndrome and Angelman Syndrome Locus | Q34126322 | ||
Dynamic chromatin modifications characterise the first cell cycle in mouse embryos. | Q34402750 | ||
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 | ||
Histone variant H3.3 provides the heterochromatic H3 lysine 9 tri-methylation mark at telomeres | Q34490850 | ||
Epigenetic events in mammalian germ-cell development: reprogramming and beyond | Q34736397 | ||
Chromosome-wide analysis of parental allele-specific chromatin and DNA methylation. | Q35077074 | ||
Dynamic CpG island methylation landscape in oocytes and preimplantation embryos | Q35135165 | ||
The KRAB zinc finger protein ZFP809 is required to initiate epigenetic silencing of endogenous retroviruses | Q35173298 | ||
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 9 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
regulation of gene expression | Q411391 | ||
gene silencing | Q1431332 | ||
P304 | page(s) | 1871-1879 | |
P577 | publication date | 2016-05-01 | |
P13046 | publication type of scholarly work | review article | Q7318358 |
P1433 | published in | Cellular and Molecular Life Sciences | Q5058352 |
P1476 | title | Maintaining memory of silencing at imprinted differentially methylated regions | |
P478 | volume | 73 |
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Q40292496 | Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome |
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