| scholarly article | Q13442814 |
| P2093 | author name string | Lori A McEachern | |
| P2860 | cites work | Genomic imprinting in mammals: emerging themes and established theories | Q21145256 |
| DNA methylation patterns and epigenetic memory | Q22065780 | ||
| Parental imprinting of the mouse H19 gene | Q22122365 | ||
| CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2 | Q24295238 | ||
| Human SRCAP and Drosophila melanogaster DOM are homologs that function in the notch signaling pathway | Q24529979 | ||
| Central role of Drosophila SU(VAR)3-9 in histone H3-K9 methylation and heterochromatic gene silencing | Q24536235 | ||
| Regulation of chromatin by histone modifications | Q24635070 | ||
| On the origin and functions of RNA-mediated silencing: from protists to man | Q24657546 | ||
| The role of chromatin during transcription | Q27860995 | ||
| The Arabidopsis thaliana MEDEA Polycomb group protein controls expression of PHERES1 by parental imprinting | Q59510192 | ||
| Genotype-specific modifiers of transgene methylation and expression in the zebrafish, Danio rerio | Q72237925 | ||
| Deletion of a nuclease-sensitive region between the Igf2 and H19 genes leads to Igf2 misregulation and increased adiposity | Q73707646 | ||
| Genomic imprinting in Drosophila is maintained by the products of Suppressor of variegation and trithorax group, but not Polycomb group, genes | Q74813438 | ||
| A human H19 transgene exhibits impaired paternal-specific imprint acquisition and maintenance in mice | Q77658784 | ||
| Establishing the epigenetic status of the Prader-Willi/Angelman imprinting center in the gametes and embryo | Q80563734 | ||
| Maternal and paternal alleles exhibit differential histone methylation and acetylation at maize imprinted genes | Q81768504 | ||
| Polycomb group complexes self-regulate imprinting of the Polycomb group gene MEDEA in Arabidopsis | Q82780023 | ||
| Tissue- and expression level-specific chromatin looping at maize b1 epialleles. | Q51741969 | ||
| The human and mouse H19 imprinting control regions harbor an evolutionarily conserved silencer element that functions on transgenes in Drosophila. | Q52005553 | ||
| Polycomb, pairing and PIWI--RNA silencing and nuclear interactions. | Q52011214 | ||
| Differential acetylation of histones H3 and H4 in paternal and maternal germline chromosomes during development of sciarid flies. | Q52112409 | ||
| Disruption of mesodermal enhancers for Igf2 in the minute mutant. | Q52122005 | ||
| Elucidation of the minimal sequence required to imprint H19 transgenes. | Q52135344 | ||
| mediator of paramutation1 is required for establishment and maintenance of paramutation at multiple maize loci. | Q52144523 | ||
| Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19. | Q52164786 | ||
| Imprinting of Igf2 and H19 from a 130 kb YAC transgene. | Q52192416 | ||
| Comparative analysis of Igf-2/H19 imprinted domain: identification of a highly conserved intergenic DNase I hypersensitive region. | Q52213159 | ||
| Function of the Polycomb protein is conserved in mice and flies. | Q52536715 | ||
| An imprinting element from the mouse H19 locus functions as a silencer in Drosophila. | Q52553227 | ||
| Directional gene silencing induced by a complex subtelomeric satellite from Drosophila. | Q52567651 | ||
| DNA methylation in Drosophila melanogaster. | Q52584665 | ||
| Polycomb-group proteins are involved in silencing processes caused by a transgenic element from the murine imprinted H19/Igf2 region in Drosophila. | Q52606062 | ||
| Methylation of histone H3 at Lys4 differs between paternal and maternal chromosomes in Sciara ocellaris germline development. | Q52673568 | ||
| CTCF binding is not the epigenetic mark that establishes post-fertilization methylation imprinting in the transgenic H19 ICR. | Q54156030 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| The two-domain hypothesis in Beckwith–Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster | Q58134238 | ||
| Sequence specificity of methylation in higher plant DNA | Q59066718 | ||
| Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene | Q28145754 | ||
| CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus | Q28145756 | ||
| Regulation of heterochromatin by histone methylation and small RNAs | Q28261891 | ||
| Paramutation in maize: RNA mediated trans-generational gene silencing | Q28273129 | ||
| An enhancer deletion affects both H19 and Igf2 expression | Q28288348 | ||
| Paramutation: from maize to mice | Q28289966 | ||
| Genome regulation by polycomb and trithorax proteins | Q28289984 | ||
| RNAi-mediated pathways in the nucleus | Q28300961 | ||
| Intergenic transcripts regulate the epigenetic state of rRNA genes | Q28593840 | ||
| The role of DNA methylation, nucleosome occupancy and histone modifications in paramutation | Q29400675 | ||
| Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
| Epigenetics in cancer | Q29617139 | ||
| Meiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegans | Q30411914 | ||
| An upstream repressor element plays a role in Igf2 imprinting | Q30684867 | ||
| A dominant mutation in mediator of paramutation2, one of three second-largest subunits of a plant-specific RNA polymerase, disrupts multiple siRNA silencing processes | Q30912369 | ||
| Two-step recruitment of RNA-directed DNA methylation to tandem repeats | Q33263577 | ||
| The Drosophila homolog of the mammalian imprint regulator, CTCF, maintains the maternal genomic imprint in Drosophila melanogaster | Q33645894 | ||
| H19 imprinting control region methylation requires an imprinted environment only in the male germ line. | Q33648826 | ||
| An intragenic methylated region in the imprinted Igf2 gene augments transcription. | Q33757992 | ||
| Transgenic expression of CBBP, a CXC domain protein, establishes paramutation in maize | Q33777880 | ||
| Genomic imprinting in plants: observations and evolutionary implications | Q33918746 | ||
| Conservation and divergence of methylation patterning in plants and animals | Q33928315 | ||
| Paramutation, an allelic interaction, is associated with a stable and heritable reduction of transcription of the maize b regulatory gene | Q33961926 | ||
| Investigation of elements sufficient to imprint the mouse Air promoter | Q33969040 | ||
| Transgene repeat arrays interact with distant heterochromatin and cause silencing in cis and trans | Q33971190 | ||
| Conservation of heterochromatin protein 1 function | Q33975076 | ||
| The properties, origin, and mechanism of conversion-type inheritance at the B locus in maize | Q33983138 | ||
| RNA polymerase IV directs silencing of endogenous DNA. | Q33984841 | ||
| Allele-specific non-CpG methylation of the Nf1 gene during early mouse development | Q34108779 | ||
| Genome-wide evolutionary analysis of eukaryotic DNA methylation. | Q34110385 | ||
| CTCF is conserved from Drosophila to humans and confers enhancer blocking of the Fab-8 insulator | Q34166628 | ||
| Parental imprinting in Drosophila | Q34213001 | ||
| Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes. | Q34363546 | ||
| Gardening the genome: DNA methylation in Arabidopsis thaliana | Q34414767 | ||
| Profiling epigenetic alterations in disease | Q37882670 | ||
| Non-coding transcripts in the H19 imprinting control region mediate gene silencing in transgenic Drosophila | Q38297213 | ||
| Transcriptional repression by Drosophila and mammalian Polycomb group proteins in transfected mammalian cells | Q38310778 | ||
| Control elements within the PWS/AS imprinting box and their function in the imprinting process | Q40590108 | ||
| Reinforcement of silencing at transposons and highly repeated sequences requires the concerted action of two distinct RNA polymerases IV in Arabidopsis. | Q41807998 | ||
| The transcriptional status but not the imprinting control region determines allele-specific histone modifications at the imprinted H19 locus | Q41910878 | ||
| Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops | Q42632085 | ||
| Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component | Q43890842 | ||
| Repeat-induced gene silencing in mammals. | Q44031048 | ||
| RNA polymerase IV functions in paramutation in Zea mays. | Q45984611 | ||
| Two regulatory genes of the maize anthocyanin pathway are homologous: isolation of B utilizing R genomic sequences. | Q46598592 | ||
| RNAi components are required for nuclear clustering of Polycomb group response elements. | Q47072703 | ||
| Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus | Q48061527 | ||
| Atypical RNA polymerase subunits required for RNA-directed DNA methylation | Q48136173 | ||
| Plant nuclear RNA polymerase IV mediates siRNA and DNA methylation-dependent heterochromatin formation | Q48146967 | ||
| A skeletal muscle-specific mouse Igf2 repressor lies 40 kb downstream of the gene | Q48562987 | ||
| Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch | Q48563204 | ||
| Appropriate expression of the mouse H19 gene utilises three or more distinct enhancer regions spread over more than 130 kb. | Q48563905 | ||
| A paternal-specific methylation imprint marks the alleles of the mouse H19 gene | Q49057890 | ||
| A census of mammalian imprinting. | Q34430259 | ||
| Chromatin conversations: mechanisms and implications of paramutation | Q34548805 | ||
| The human HYMAI/PLAGL1 differentially methylated region acts as an imprint control region in mice | Q34559930 | ||
| An RNA-dependent RNA polymerase is required for paramutation in maize | Q34569244 | ||
| The chromatin remodeling factor Bap55 functions through the TIP60 complex to regulate olfactory projection neuron dendrite targeting | Q34573656 | ||
| In the loop: long range chromatin interactions and gene regulation | Q34580688 | ||
| Rmr6 maintains meiotic inheritance of paramutant states in Zea mays | Q34589702 | ||
| Noncoding transcription by RNA polymerase Pol IVb/Pol V mediates transcriptional silencing of overlapping and adjacent genes | Q34881670 | ||
| Paramutation: the tip of an epigenetic iceberg? | Q35108507 | ||
| A transcriptional insulator at the imprinted H19/Igf2 locus | Q35199693 | ||
| Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
| Element 1360 and RNAi components contribute to HP1-dependent silencing of a pericentric reporter | Q35239502 | ||
| RNA at the steering wheel | Q35605953 | ||
| DNA methylation in insects | Q35729179 | ||
| Differential chromatin structure within a tandem array 100 kb upstream of the maize b1 locus is associated with paramutation | Q35780093 | ||
| Analysis of the H19ICR insulator | Q35856849 | ||
| Towards a mechanism for histone chaperones | Q35861914 | ||
| Identification of a silencing element in the human 15q11-q13 imprinting center by using transgenic Drosophila | Q35884190 | ||
| RNA meets chromatin | Q36197886 | ||
| DNA methylation and histone modifications: teaming up to silence genes | Q36228564 | ||
| CTCF is the master organizer of domain-wide allele-specific chromatin at the H19/Igf2 imprinted region | Q36421340 | ||
| Genomic imprinting in the mealybugs | Q36436510 | ||
| The Prader-Willi/Angelman imprinted domain and its control center | Q36436601 | ||
| Gene regulation by chromatin structure: paradigms established in Drosophila melanogaster | Q36553584 | ||
| Deeper into the maize: new insights into genomic imprinting in plants | Q36660578 | ||
| RNA interference guides histone modification during the S phase of chromosomal replication. | Q36692156 | ||
| Noncoding RNAs and gene silencing | Q36744484 | ||
| Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. | Q36820044 | ||
| CTCF regulates allelic expression of Igf2 by orchestrating a promoter-polycomb repressive complex 2 intrachromosomal loop | Q36959918 | ||
| Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a. | Q36967574 | ||
| Epigenetic interplay between histone modifications and DNA methylation in gene silencing | Q37137074 | ||
| Roles of RNA polymerase IV in gene silencing | Q37178200 | ||
| Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain | Q37238842 | ||
| Repeat elements and the Arabidopsis DNA methylation landscape | Q37749496 | ||
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P921 | main subject | transgenic organism | Q123738417 |
| epigenetics | Q26939 | ||
| P304 | page(s) | 689819 | |
| P577 | publication date | 2012-03-27 | |
| P1433 | published in | Genetics Research International | Q26842364 |
| P1476 | title | Transgenic epigenetics: using transgenic organisms to examine epigenetic phenomena | |
| P478 | volume | 2012 |
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