| 13:30-13:55 | 专题报告 |
细胞命运可塑性的遗传基础与调控机制 |
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| 13:55-14:20 | 专题报告 |
Tmem30b介导的耳蜗外毛细胞顶端膜稳态对听觉形成至关重要 |
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| 14:20-14:30 | 论文发言 |
KIF11 prevents retinal endothelial ferroptosis in familial exudative vitreoretinopathy by inhibiting phosphorylation-driven PRDX1 phase separation |
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| 14:30-14:40 | 论文发言 |
Glia-derived lipid metabolites drive pathological angiogenesis in ischemic retinopathy |
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| 14:40-14:50 | 论文发言 |
X-linked SYTL4 missense variant disrupt RAB27A-dependent vesicle trafficking and synaptic transmission in autism |
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| 14:50-15:00 | 论文发言 |
EFTUD2突变介导NIPBL异常剪接驱动下颌骨发育不良伴小头畸形综合征的分子机制研究 |
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| 15:00-15:10 | 论文发言 |
Uncoupled CD8+ T Cell Activation and FAS-L Mediated Pathogenesis in a Seronegative IPEX-like Syndrome Driven by a Novel FOXP3 splice-site mutation (IVS10+1G>A) |
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| 15:10-15:20 | 论文发言 |
利用碱基编辑器治疗β654地贫小鼠的研究 |
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| 15:20-15:30 | 论文发言 |
LINC01480 strengthens the STAT3/PRL-3 positive feedback loop to promote multiple myeloma progression |
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| 15:30-15:40 |
休息 |
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| 15:40-15:50 | 论文发言 |
膜蛋白KIDINS220调控AKT2通路重塑白色脂肪细胞代谢表型改善胰岛素抵抗 |
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| 15:50-16:00 | 论文发言 |
SCARF2基因突变通过影响BMP信号通路导致Van den Ende-Gupta综合征先天颅面畸形的机制研究 |
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| 16:00-16:10 | 论文发言 |
乳酸代谢重编程调控红白血病脾脏肿大的机制研究 |
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| 16:10-16:20 | 论文发言 |
HLF 调节人肝细胞中 CYP3A5 的表达 |
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| 16:20-16:30 | 论文发言 |
罕见EDA基因5'UTR区变异导致少汗型外胚层发育不良:一种uAUG介导的翻译调控机制 |
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| 16:30-16:40 | 论文发言 |
PRSS56基因变异与高度近视发生的系统性评估及干预策略开发 |
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| 16:40-16:50 | 论文发言 |
基于分子动力学模拟探究 SLCO2A1 基因点突变对其蛋白产物结构与功能的影响 |
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| 16:50-17:00 | 论文发言 |
WTAP-Mediated m6A Modification Preserves Retinal Photoreceptor Function Through Translational Regulation of REEP6, PDE6B, and RDH12 |
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| 17:00-17:10 | 论文发言 |
BLIMP1通过促进HsCDC6表达影响肿瘤进展的作用及机制研究 |
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| 17:10-17:20 | 论文发言 |
转录因子SIX1通过调控DLX家族调控牙胚间充质干细胞成牙分化的机制研究 |
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| 17:20-17:30 | 论文发言 |
NUSAP1 Mutations Induce Primary Microcephaly via KIF2C and Neural Stem/Progenitor cell Dysregulation |
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| 17:30-17:40 | 论文发言 |
In vivo Prime Editing Rescues Glycogen Storage Disease Type Ia in Humanized Mice with G6PC1 c.648G>T |
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| 17:40-17:50 | 论文发言 |
基于全基因组测序数据分析阿尔茨海默病生物标志物的遗传学基础 |
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| 17:50-18:00 | 论文发言 |
基于中国不同民族永生细胞库的GWAS研究揭示呼吸道合胞病毒遗传易感性新机制 |
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