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MLL4 regulates postnatal palate growth and midpalatal suture development
Published 2025-01-01“…Mutations in the MLL4 gene are the major cause of Kabuki syndrome, a human developmental disorder that involves craniofacial birth defects, including anomalies in the palate. …”
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Pathogenetic, Clinical, and Prognostic Features of Adult t(4;11)(q21;q23)/MLL-AF4 Positive B-Cell Acute Lymphoblastic Leukemia
Published 2011-01-01“…Translocation t(4;11)(q21;q23) leading to formation of MLL-AF4 fusion gene is found in about 10% of newly diagnosed B-cell acute lymphoblastic leukemia (ALL) in adult patients. …”
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DNMT3A Mutations in Patients with Acute Myeloid Leukemia in South Brazil
Published 2012-01-01“…We found mutations in the DNMT3A gene in 6 patients (8%); 3 were type R882H. We found fusion transcripts in 19 patients, namely, AML1/ETO (n=5; 6.1%), PML/RARα (n=12; 14.6%), MLL/AF9 (0; 0%), and CBFβ/MYH11 (n=2; 2.4%). …”
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Germline Single-Nucleotide Polymorphism <i>GFI1-36N</i> Causes Alterations in Mitochondrial Metabolism and Leads to Increased ROS-Mediated DNA Damage in a Murine Model of Human Acu...
Published 2025-01-01“…<b>Methods</b>: We pursued this question in a murine model of human AML by knocking in human <i>GFI1-36S</i> or <i>GFI1-36N</i> variant constructs into the murine <i>Gfi1</i> gene locus and retrovirally expressing <i>MLL-AF9</i> to induce AML. …”
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Nuclear-localized HKDC1 promotes hepatocellular carcinoma through phosphorylating RBBP5 to upregulate H3K4me3
Published 2025-02-01“…This leads to the transcriptional activation of mitosis-related genes, thereby driving cell cycle progression and proliferation. …”
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