| scholarly article | Q13442814 |
| P50 | author | Onur Birol | Q86652207 |
| David J Katz | Q87164694 | ||
| Jadiel A Wasson | Q89259172 | ||
| P2093 | author name string | David J Katz | |
| Onur Birol | |||
| Jadiel A Wasson | |||
| P2860 | cites work | Critical evaluation of imprinted gene expression by RNA-Seq: a new perspective | Q21563370 |
| Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice | Q24293298 | ||
| KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints | Q24312768 | ||
| A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints | Q24322379 | ||
| dbSNP: the NCBI database of genetic variation | Q24608672 | ||
| High-resolution analysis of parent-of-origin allelic expression in the mouse brain | Q24626579 | ||
| Distinct physiological and behavioural functions for parental alleles of imprinted Grb10 | Q24632557 | ||
| Structure-function analysis reveals a novel mechanism for regulation of histone demethylase LSD2/AOF1/KDM1b | Q27675595 | ||
| WT1 proteins: functions in growth and differentiation | Q28191433 | ||
| Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation | Q28272845 | ||
| Bisphenol a exposure disrupts genomic imprinting in the mouse | Q28485979 | ||
| A novel mammalian flavin-dependent histone demethylase | Q28587686 | ||
| Role of Tet1 in erasure of genomic imprinting | Q28590791 | ||
| Epigenetic transgenerational actions of endocrine disruptors and male fertility | Q29547704 | ||
| Genomic imprinting: parental influence on the genome | Q29616227 | ||
| Mouse genomic variation and its effect on phenotypes and gene regulation | Q29617750 | ||
| dbSNP: a database of single nucleotide polymorphisms | Q30826134 | ||
| Genealogies of mouse inbred strains | Q33806120 | ||
| Principles and challenges of genomewide DNA methylation analysis | Q34096366 | ||
| Human LSD2/KDM1b/AOF1 regulates gene transcription by modulating intragenic H3K4me2 methylation. | Q34128674 | ||
| Mammalian epigenomics: reprogramming the genome for development and therapy. | Q34166723 | ||
| Imprinted genes … and the number is? | Q34221013 | ||
| Prader-Willi Syndrome: Obesity due to Genomic Imprinting | Q34229319 | ||
| Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns | Q34294949 | ||
| DNA methylation and mammalian epigenetics | Q34375355 | ||
| Genomic imprinting in mammals. | Q34453750 | ||
| Effects of endocrine disruptors on imprinted gene expression in the mouse embryo | Q35159064 | ||
| In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions | Q35534127 | ||
| Allele-specific binding of ZFP57 in the epigenetic regulation of imprinted and non-imprinted monoallelic expression | Q35819244 | ||
| Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders. | Q36010983 | ||
| Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans | Q36055767 | ||
| Sequence-based characterization of structural variation in the mouse genome | Q36193488 | ||
| Dynamic changes in histone modifications precede de novo DNA methylation in oocytes. | Q36406402 | ||
| Maternally provided LSD1/KDM1A enables the maternal-to-zygotic transition and prevents defects that manifest postnatally. | Q36791936 | ||
| Epigenetics in preimplantation mammalian development | Q36948545 | ||
| Regulation of imprinting in clusters: noncoding RNAs versus insulators | Q37087590 | ||
| Genomic imprinting: employing and avoiding epigenetic processes | Q37362832 | ||
| Prader–Willi syndrome and Angelman syndrome | Q37783981 | ||
| Genomic imprinting: a mammalian epigenetic discovery model | Q37937577 | ||
| Proteins involved in establishment and maintenance of imprinted methylation marks. | Q38023718 | ||
| Brain-expressed imprinted genes and adult behaviour: the example of Nesp and Grb10. | Q38131371 | ||
| A sequence-based variation map of 8.27 million SNPs in inbred mouse strains | Q43787849 | ||
| Next-generation sequencing data interpretation: enhancing reproducibility and accessibility | Q44853811 | ||
| Bisulfite modification for analysis of DNA methylation | Q44884117 | ||
| Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene | Q48371609 | ||
| Trim28 is required for epigenetic stability during mouse oocyte to embryo transition. | Q48652732 | ||
| Dnmt3L and the establishment of maternal genomic imprints | Q48874297 | ||
| Genomic imprinting: the emergence of an epigenetic paradigm. | Q51860651 | ||
| Mechanisms of imprinting of the Prader-Willi/Angelman region. | Q55050189 | ||
| P433 | issue | 1 | |
| P921 | main subject | DNA methylation | Q874745 |
| P304 | page(s) | 91-103 | |
| P577 | publication date | 2018-01-04 | |
| P1433 | published in | G3 | Q5512701 |
| P1476 | title | A Resource for the Allele-Specific Analysis of DNA Methylation at Multiple Genomically Imprinted Loci in Mice | |
| P478 | volume | 8 |
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