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S

Sérgio Valente

Sapienza University of Rome
H指数:51
被引数:8,341

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Mutant Huntingtin disrupts neurogenic and astroglial programs via the EZH2–Let-7g–LIN28 axis with rescue by epigenetic modulators

突变亨廷蛋白通过EZH2–Let-7g–LIN28轴破坏神经发生和星形胶质细胞程序,并由表观遗传调节剂进行挽救

2026-07-160
OAAI
A synergistic interaction between PRMT5 and LSD1 inhibitors in AML

PRMT5与LSD1抑制剂的协同作用在AML中

2026-03-270
OA
Dynamic epigenetic regulation of BCLAF1 splicing in acute myeloid leukemia

急性髓系白血病中BCLAF1剪接的动态表观遗传调控

2026-03-240
OAAI
Simplification and Derivatization of Quinoline-Containing M41 Lead to the Discovery of NADPH Oxidase Isoform-Selective Inhibitors Effective in Cancer Cells

喹啉基M41的简化与衍生化导致NADPH氧化酶同工酶选择性抑制剂在癌细胞中的发现

2026-01-010
OA
Quinoline-Based DNA Methyltransferase Inhibitors Featuring Basic Side Chains: Design, Synthesis, and Insight in Biochemical and Anticancer Cell Properties

喹啉类DNA甲基转移酶抑制剂:含碱性侧链的设计、合成及对生化与抗癌细胞特性的见解

2025-11-010
PRE
TP53-Agnostic Lethality through Combined Pan-HDAC and CDK Inhibition in Acute Myeloid Leukemia

TP53非依赖性细胞死亡通过联合泛组蛋白去乙酰化酶和CDK抑制剂在急性髓系白血病中的作用

2025-09-010
PREAI
Long noncoding RNA H19 promotes the acquisition of a mesenchymal-like invasive phenotype in mesothelial primary cells through an HDAC1-mediated WT1/Sp1 switch

长链非编码RNA H19通过HDAC1介导的WT1/Sp1转换促进间皮源性细胞获得类间充质样侵袭表型。

2025-08-310
OAAI
Tranylcypromine-Based LSD1 Inhibitors as Useful Agents to Reduce Viability of Schistosoma mansoni

基于Tranylcypromine的LSD1抑制剂作为降低Schistosoma mansoni存活率的潜在有效药物

2025-07-020
OA
HDAC3 genetic and pharmacologic inhibition radiosensitizes fusion positive rhabdomyosarcoma by promoting DNA double-strand breaks
2024-08-062
OAAI
HDAC3 sustains resistance to hypofractionated radiotherapy in fusion positve rhabdomyosarcoma cells
2024-03-220
PRE
HDAC1/2 control mesothelium/ovarian cancer adhesive interactions impacting on Talin-1-α5β1-integrin-mediated actin cytoskeleton and extracellular matrix protein remodeling
2024-01-232
OAAI