scholarly article | Q13442814 |
review article | Q7318358 |
P6179 | Dimensions Publication ID | 1032800066 |
P356 | DOI | 10.1038/NG0496-363 |
P698 | PubMed publication ID | 8630488 |
P2093 | author name string | Bestor TH | |
Tycko B | |||
P2860 | cites work | Somatic mutations in the neurofibromatosis 1 gene in human tumors | Q24293243 |
A genetic map of the mouse with 4,006 simple sequence length polymorphisms | Q72702943 | ||
Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
Cytosine methylation: the pros and cons of DNA methylation | Q80505282 | ||
Chemistry. How are alkynes scrambled? | Q95780598 | ||
The crystal structure of Haelll methyltransferase covalently complexed to DNA: An extrahelical cytosine and rearranged base pairing | Q27729758 | ||
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality | Q28131773 | ||
Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability | Q33859871 | ||
X inactivation, differentiation, and DNA methylation | Q33999850 | ||
Silencing of the E-cadherin invasion-suppressor gene by CpG methylation in human carcinomas | Q34053843 | ||
Premeiotic instability of repeated sequences in Neurospora crassa | Q34179760 | ||
Unity in transposition reactions | Q34296425 | ||
Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications | Q34297548 | ||
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. | Q34314269 | ||
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage | Q34323420 | ||
Methylation and imprinting: from host defense to gene regulation? | Q34363070 | ||
HhaI and HpaII DNA methyltransferases bind DNA mismatches, methylate uracil and block DNA repair | Q34746885 | ||
CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro | Q34777507 | ||
Lack of expression from a retroviral vector after transduction of murine hematopoietic stem cells is associated with methylation in vivo | Q35123124 | ||
Inactivation of gene expression in plants as a consequence of specific sequence duplication | Q35179456 | ||
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma | Q35807817 | ||
Duplication-targeted DNA methylation and mutagenesis in the evolution of eukaryotic chromosomes | Q36819409 | ||
DNA methylation: evolution of a bacterial immune function into a regulator of gene expression and genome structure in higher eukaryotes | Q37581127 | ||
Alu repeated DNAs are differentially methylated in primate germ cells | Q37587525 | ||
Treatment of mice with 5-azacytidine efficiently activates silent retroviral genomes in different tissues | Q37679466 | ||
Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse | Q38291049 | ||
Sp1 sites in the mouse aprt gene promoter are required to prevent methylation of the CpG island | Q38303631 | ||
CpG methylation of the cAMP-responsive enhancer/promoter sequence TGACGTCA abolishes specific factor binding as well as transcriptional activation | Q38344762 | ||
Origins of replication and gene regulation | Q38581104 | ||
M.HhaI binds tightly to substrates containing mismatches at the target base | Q40393755 | ||
Gene number, noise reduction and biological complexity | Q40514856 | ||
Supercoiling-dependent sequence specificity of mammalian DNA methyltransferase | Q40566620 | ||
Homology-dependent gene silencing in transgenic plants: what does it really tell us? | Q40617697 | ||
DNA methyltransferases | Q40626444 | ||
It was a very good year for DNA repair | Q40804105 | ||
DNA methylation, genomic imprinting, and mammalian development | Q41586860 | ||
Sp1 elements protect a CpG island from de novo methylation | Q42497349 | ||
Specific Alu Binding Protein from Human Sperm Chromatin Prevents DNA Methylation | Q46112192 | ||
Epigenetic control of an endogenous gene family is revealed by a novel blue fluorescent mutant of Arabidopsis | Q48069018 | ||
Long-range cis preference in DNA homology search over the length of a Drosophila chromosome. | Q52543161 | ||
Epigenetic repeat-induced gene silencing (RIGS) in Arabidopsis. | Q54231411 | ||
Homology-dependent gene silencing in transgenic plants: epistatic silencing loci contain multiple copies of methylated transgenes | Q57756646 | ||
The evolutionary dynamics of repetitive DNA in eukaryotes | Q59090793 | ||
Regulated Synthesis and Localization of DNA Methyltransferase during Spermatogenesis1 | Q71787806 | ||
Perpetuation of cytosine methylation in Ascobolus immersus implies a novel type of maintenance methylase | Q72038617 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 363-367 | |
P577 | publication date | 1996-04-01 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | Creation of genomic methylation patterns | |
P478 | volume | 12 |
Q34581149 | 3-D DNA methylation phenotypes correlate with cytotoxicity levels in prostate and liver cancer cell models |
Q43206574 | A DNA target of 30 bp is sufficient for RNA-directed DNA methylation. |
Q56783008 | A Genome-Wide Screen for Normally Methylated Human CpG Islands That Can Identify Novel Imprinted Genes |
Q33872587 | A LINE-1 component to human aging: do LINE elements exact a longevity cost for evolutionary advantage? |
Q35033574 | A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13 |
Q34444089 | A gene essential for de novo methylation and development in Ascobolus reveals a novel type of eukaryotic DNA methyltransferase structure |
Q30304392 | A genetic program for deletion of foreign DNA from the mammalian genome |
Q30830058 | A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes |
Q42664087 | A histone H3 methyltransferase controls DNA methylation in Neurospora crassa |
Q30596872 | A new family of genes and pseudogenes potentially expressing testis- and brain-specific leucine zipper proteins in man and mouse |
Q61799565 | Aberrant DNA methylation of M1-macrophage genes in coronary artery disease |
Q30446005 | Activation of the lac repressor in the transgenic mouse |
Q35571297 | Age-related epigenetic changes and the immune system |
Q33787464 | Aging, DNA methylation and cancer |
Q34721216 | An 11bp region with stem formation potential is essential for de novo DNA methylation of the RPS element |
Q34606309 | An analysis of transvection at the yellow locus of Drosophila melanogaster. |
Q77406653 | An inverted repeat triggers cytosine methylation of identical sequences in Arabidopsis |
Q36414688 | Analysis of human peripheral blood T cells and single-cell-derived T cell clones uncovers extensive clonal CpG island methylation heterogeneity throughout the genome |
Q52892185 | Antibiotics induce genome-wide hypermethylation in cultured Nicotiana tabacum plants. |
Q41112950 | Base eversion and shuffling by DNA methyltransferases |
Q28396772 | Biomarkers of lead exposure and DNA methylation within retrotransposons |
Q33781581 | Characterization of novel parent-specific epigenetic modifications upstream of the imprinted mouse H19 gene. |
Q28143736 | Chimeric retroviral helper virus and picornavirus IRES sequence to eliminate DNA methylation for improved retroviral packaging cells |
Q35881189 | Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes |
Q34469056 | Cloning and analysis of a novel human putative DNA methyltransferase |
Q36844969 | Colorectal cancer epigenetics: the role of environmental factors and the search for molecular biomarkers |
Q33887777 | Competition--a common motif for the imprinting mechanism? |
Q37596549 | Conserved methylation patterns of human papillomavirus type 16 DNA in asymptomatic infection and cervical neoplasia |
Q33693362 | Context dependent substitution biases vary within the human genome |
Q29618264 | Cytosine methylation and the ecology of intragenomic parasites |
Q34385829 | Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomes |
Q44395792 | Cytosine methylation mediates sexual conflict |
Q77064368 | Cytosine methylation of repeated sequences in eukaryotes: the role of DNA pairing |
Q59506898 | DNA (cytosine-5) methyltransferase turnover and cellular localization in developing Paracentrotus lividus sea urchin embryo |
Q50042001 | DNA Tumor Virus Regulation of Host DNA Methylation and Its Implications for Immune Evasion and Oncogenesis |
Q33870798 | DNA hypermethylation in tumorigenesis: epigenetics joins genetics |
Q40288871 | DNA hypomethylation and aberrant expression of the human endogenous retrovirus ERVWE1/syncytin-1 in seminomas. |
Q44040981 | DNA hypomethylation and methyltransferase expression in atherosclerotic lesions |
Q33651436 | DNA methylation and DNA methyltransferases. |
Q34770507 | DNA methylation and gene silencing in cancer: which is the guilty party? |
Q41566233 | DNA methylation and imprinting: why bother? |
Q37311875 | DNA methylation and methyl-CpG binding proteins: developmental requirements and function |
Q96613313 | DNA methylation and the core pluripotency network |
Q41439642 | DNA methylation in genomic imprinting |
Q35647894 | DNA methylation topology: potential of a chromatin landmark for epigenetic drug toxicology |
Q30993657 | DNA methylation, methyltransferases, and cancer |
Q40388507 | DNA of Drosophila melanogaster contains 5-methylcytosine |
Q33368872 | De novo methylation and co-suppression induced by a cytoplasmically replicating plant RNA virus |
Q51983631 | Developmental acquisition of genome-wide DNA methylation occurs prior to meiosis in male germ cells. |
Q42489639 | Dietary selenomethionine increases exon-specific DNA methylation of the p53 gene in rat liver and colon mucosa. |
Q39596964 | Differential methylation of Epstein-Barr virus latency promoters facilitates viral persistence in healthy seropositive individuals. |
Q37241642 | Distal cis-regulatory elements are required for tissue-specific expression of enamelin (Enam). |
Q36772949 | Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis. |
Q34830485 | Epigenetic contributors to the discordance of monozygotic twins |
Q41566200 | Epigenetic phenomena in filamentous fungi: useful paradigms or repeat-induced confusion? |
Q41152824 | Epigenetic programming of developmental genome rearrangements in ciliates. |
Q22122053 | Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals |
Q35018423 | Epigenetic regulation of neuronal dendrite and dendritic spine development |
Q30498112 | Epigenetic silencing of engineered L1 retrotransposition events in human embryonic carcinoma cells. |
Q35094516 | Epigenetic variability and the evolution of human cancer. |
Q37240566 | Epigenetics in acute myeloid leukemia |
Q50104502 | Epigenetics: monoallelic expression in the immune system. |
Q37300382 | Existence of Two Distinct Infectious Endogenous Retroviruses in Domestic Cats and Their Different Strategies for Adaptation to Transcriptional Regulation. |
Q41439635 | Formation of methylation patterns in the mammalian genome |
Q36241447 | Gene identification and DNA sequence analysis in the GC-poor 20 megabase region of human chromosome 21 |
Q33843166 | Gene silencing as a threat to the success of gene therapy |
Q35207524 | Genetic therapy for HIV/AIDS. |
Q34587213 | Genome differentiation in a species pair of coregonine fishes: an extremely rapid speciation driven by stress-activated retrotransposons mediating extensive ribosomal DNA multiplications. |
Q49271010 | Genomic 5-mC contents in peripheral blood leukocytes were independent protective factors for coronary artery disease with a specific profile in different leukocyte subtypes |
Q33541538 | Genomic imprinting: implications for human disease |
Q36225308 | Host defenses to transposable elements and the evolution of genomic imprinting |
Q90189900 | Human Endogenous Retroviruses (HERVs): Shaping the Innate Immune Response in Cancers |
Q42804174 | Human polyomavirus BKV transcriptionally activates DNA methyltransferase 1 through the pRb/E2F pathway |
Q34145956 | Hypomethylation of an expanded FMR1 allele is not associated with a global DNA methylation defect |
Q35118465 | Hypomethylation: One Side of a Larger Picture |
Q42573261 | Identifying promoter elements necessary for enamelin tissue-specific expression |
Q52192434 | Imprinted expression of the Igf2r gene depends on an intronic CpG island. |
Q33852775 | Imprinted genes as potential genetic and epigenetic toxicologic targets |
Q33846679 | Infection of lymphoid cells by integration-defective human immunodeficiency virus type 1 increases de novo methylation |
Q36015063 | Inhibiting DNA Methylation Causes an Interferon Response in Cancer via dsRNA Including Endogenous Retroviruses |
Q45092709 | Intragenic DNA methylation alters chromatin structure and elongation efficiency in mammalian cells |
Q24562316 | Isolation and characterization of a novel DNA methyltransferase complex linking DNMT3B with components of the mitotic chromosome condensation machinery |
Q56814391 | LagoZ et LagZ, deux gènes appauvris en dinucléotides CpG dérivés du gène LacZ pour l'étude des contrôles épigénétiques |
Q35053056 | Loss of DNMT1o disrupts imprinted X chromosome inactivation and accentuates placental defects in females |
Q28594559 | Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans |
Q74312289 | Mechanisms of genomic imprinting |
Q28585211 | Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L |
Q74657204 | Mendel stayed home. Genomic imprinting and environmental disease susceptibility, National Institute of Environmental Health Sciences and Duke University Medical Center, Durham, NC, USA, 8-10 October 1998 |
Q28364163 | Methylation matters |
Q36565952 | Methylation of genomes and genes at the invertebrate-vertebrate boundary |
Q39585366 | Methylation of transcription factor binding sites in the Epstein-Barr virus latent cycle promoter Wp coincides with promoter down-regulation during virus-induced B-cell transformation |
Q40193786 | Methylation profile in benign, borderline and malignant ovarian tumors. |
Q39528996 | Methylation-mediated proviral silencing is associated with MeCP2 recruitment and localized histone H3 deacetylation |
Q33938490 | Mobile elements and the human genome |
Q45733925 | Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. |
Q36889966 | Molecular mechanisms of alcohol-mediated carcinogenesis |
Q77471629 | Murine de novo methyltransferase Dnmt3a demonstrates strand asymmetry and site preference in the methylation of DNA in vitro |
Q28114857 | New 5' regions of the murine and human genes for DNA (cytosine-5)-methyltransferase |
Q34093051 | Operomics: molecular analysis of tissues from DNA to RNA to protein |
Q46602155 | Organization, not duplication, triggers silencing in a complex transgene locus in rice |
Q92809345 | Oxidative DNA Damage Modulates DNA Methylation Pattern in Human Breast Cancer 1 (BRCA1) Gene via the Crosstalk between DNA Polymerase β and a de novo DNA Methyltransferase |
Q35671678 | Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome. |
Q34446607 | Pharmacological reactivation of inactive genes: the fragile X experience |
Q34447606 | Poly(ADP-ribosyl)ation acts in the DNA demethylation of mouse primordial germ cells also with DNA damage-independent roles |
Q34142627 | Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome |
Q53427610 | Polymorphisms, genomic imprinting and cancer susceptibility. |
Q33538759 | Position effects and epigenetic silencing of plant transgenes |
Q36144782 | Postnatal development- and age-related changes in DNA-methylation patterns in the human genome |
Q73401607 | Prognostic implications of epigenetic silencing of p15INK4B in acute promyelocytic leukemia |
Q34133548 | Protein transduction: a new tool for the study of cellular ageing and senescence |
Q39681923 | Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine |
Q39654059 | Quantitative comparison of genome-wide DNA methylation mapping technologies. |
Q34041209 | RNA-directed DNA methylation. |
Q35800504 | Retrotransposon-derived elements in the mammalian genome: a potential source of disease |
Q25255710 | Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line |
Q33751727 | Role of DNA methylation in the regulation of cell function |
Q58884458 | S1 SINE retroposons are methylated at symmetrical and non-symmetrical positions in Brassica napus: identification of a preferred target site for asymmetrical methylation |
Q40022520 | Sequence-specific epigenetic effects of the maternal somatic genome on developmental rearrangements of the zygotic genome in Paramecium primaurelia |
Q28392514 | Storage conditions and stability of global DNA methylation in placental tissue |
Q30881452 | Structural organization of the sea urchin DNA (cytosine-5)-methyltransferase gene and characterization of five alternative spliced transcripts. |
Q35198972 | Suppression of crossing-over by DNA methylation in Ascobolus |
Q35118484 | The Development of CpG Island Methylation Biomarkers Using Restriction Landmark Genomic Scanning |
Q24318274 | The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis |
Q57240725 | The Labyrinthine Ways of Cancer Immunotherapy–T Cell, Tumor Cell Encounter: “How Do I Lose Thee? Let Me Count the Ways” |
Q35646482 | The Role of Epigenetic Change in Autism Spectrum Disorders. |
Q39591112 | The cHS4 insulator increases the probability of retroviral expression at random chromosomal integration sites. |
Q35550046 | The contribution of <i>cis</i>-elements to disease-associated repeat instability: clinical and experimental evidence |
Q42418443 | The effect of DNA CpG methylation on the dynamic conformation of a nucleosome |
Q36783169 | The epigenetic basis of twin discordance in age-related diseases |
Q28201533 | The fragile X gene and its function |
Q36273365 | The potential cocarcinogenic effect of vitamin B12 deficiency |
Q48064741 | The role of DNA methylation during anoxia tolerance in a freshwater turtle (Trachemys scripta elegans). |
Q22122375 | The role of selfish genetic elements in eukaryotic evolution |
Q34762192 | Tracking an embryonic L1 retrotransposition event |
Q35207298 | Transgene integration into the same chromosome location can produce alleles that express at a predictable level, or alleles that are differentially silenced |
Q34041294 | Transgene silencing by the host genome defense: implications for the evolution of epigenetic control mechanisms in plants and vertebrates |
Q34041267 | Transgene silencing in monocots |
Q24816254 | Transgene-induced CCWGG methylation does not alter CG methylation patterning in human kidney cells |
Q37742436 | Transposable elements in the mammalian germline: a comfortable niche or a deadly trap? |
Q28143796 | Transvection and other homology effects |
Q28251486 | Tying it all together: epigenetics, genetics, cell cycle, and cancer |
Q32063623 | Undermethylation associated with retroelement activation and chromosome remodelling in an interspecific mammalian hybrid |
Q36150489 | Versatility of gene therapy vectors through viruses |
Q37264298 | Vitamin C increases viral mimicry induced by 5-aza-2'-deoxycytidine |
Q28511971 | Windows for sex-specific methylation marked by DNA methyltransferase expression profiles in mouse germ cells |
Q73013123 | X-linked mental retardation |
Q24297361 | Zinc-fingers and homeoboxes 1 (ZHX1) binds DNA methyltransferase (DNMT) 3B to enhance DNMT3B-mediated transcriptional repression |
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