[
    {
        "title": "DNMT3L modulates significant and distinct flanking sequence preference for DNA methylation by DNMT3A and DNMT3B in vivo.",
        "journal": "PLoS genetics",
        "date": "2010",
        "authors": "Wienholz BL, Kareta MS, Moarefi AH, Gordon CA, Ginno PA, Chedin F",
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            "url": "https://pubmed.ncbi.nlm.nih.gov/20838592"
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            {
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    {
        "title": "Identification of preferential target sites for human DNA methyltransferases.",
        "journal": "Nucleic acids research",
        "date": "2011",
        "authors": "Choi SH, Heo K, Byun HM, An W, Lu W, Yang AS",
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        "title": "Dynamic CpG island methylation landscape in oocytes and preimplantation embryos.",
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        "title": "Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation.",
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    {
        "title": "Structural insight into coordinated recognition of trimethylated histone H3 lysine 9 (H3K9me3) by the plant homeodomain (PHD) and tandem tudor domain (TTD) of UHRF1 (ubiquitin-like, containing PHD and RING finger domains, 1) protein.",
        "journal": "The Journal of biological chemistry",
        "date": "2013",
        "authors": "Cheng J, Yang Y, Fang J, Xiao J, Zhu T, Chen F, Wang P, Li Z, Yang H, Xu Y",
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                "uniprot_canonical_ac": "P58876-1",
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            {
                "uniprot_canonical_ac": "Q96A08-1",
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            },
            {
                "uniprot_canonical_ac": "P0C5Y9-1",
                "protein_name": "Histone H2A-Bbd type 1",
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            },
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                "uniprot_canonical_ac": "Q9BTM1-1",
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    {
        "title": "Multivalent histone engagement by the linked tandem Tudor and PHD domains of UHRF1 is required for the epigenetic inheritance of DNA methylation.",
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        "title": "Negative regulation of the forkhead transcription factor FKHR by Akt.",
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        "title": "GCUNC-45 is a novel regulator for the progesterone receptor/hsp90 chaperoning pathway.",
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        "title": "The transforming acidic coiled coil (TACC1) protein modulates the transcriptional activity of the nuclear receptors TR and RAR.",
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