| 1 | 13:30-14:00 | 专题报告 | 
                                                                                                                     RNA剪接调控机制及靶向干预策略  | 
                                                    
                                                            
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| 2 | 14:00-14:30 | 专题报告 | 
                                                                                                                     东亚人群演化启发的精准医疗  | 
                                                    
                                                            
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| 3 | 14:30-14:45 | 论文发言 | 
                                                                                                                     Pin1 exacerbates nonalcoholic fatty liver disease by enhancing its activity through binding to ACC1  | 
                                                    
                                                            
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| 4 | 14:45-15:00 | 论文发言 | 
                                                                                                                     lnc-TSSK2-8通过调控线粒体功能与稳态导致先心病发生的机制  | 
                                                    
                                                            
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| 5 | 15:00-15:15 | 论文发言 | 
                                                                                                                     Activation of γ-globin expression by LncRNA-mediated ERF promoter hypermethylation in β-thalassemia  | 
                                                    
                                                            
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| 6 | 15:15-15:30 | 论文发言 | 
                                                                                                                     Signaling mechanisms governing early craniofacial develoment and genetic defects underling OFCs  | 
                                                    
                                                            
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| 1 | 15:40-15:55 | 论文发言 | 
                                                                                                                     遗传性糖尿病 MODY6 基因突变的特点、致病机制与精准诊疗  | 
                                                    
                                                            
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| 2 | 15:55-16:10 | 论文发言 | 
                                                                                                                     新型VDDR致病基因的发现及其功能的鉴定和研究  | 
                                                    
                                                            
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| 3 | 16:10-16:25 | 论文发言 | 
                                                                                                                     Single-cell RNA sequencing revealed up-regulation of MHC class-II gene expression in dendritic cells in patients with ankylosing spondylitis  | 
                                                    
                                                            
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| 4 | 16:25-16:40 | 论文发言 | 
                                                                                                                     单质子转移诱发碱基突变的理论计算与实验验证  | 
                                                    
                                                            
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| 5 | 16:40-16:55 | 论文发言 | 
                                                                                                                     Defective tRNA post-transcriptional modification dysregulated mitochondrial homeostasis in Leber’s hereditary optic neuropathy  | 
                                                    
                                                            
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| 6 | 16:55-17:10 | 论文发言 | 
                                                                                                                     Single-cell RNA-sequencing reveals the transcriptional landscape of ND-42 mediated spermatid elongation via mitochondrial derivative maintenance  | 
                                                    
                                                            
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| 7 | 17:10-17:25 | 论文发言 | 
                                                                                                                     A Homozygous Variant in NAA60 is Associated with Primary Familial Brain Calcification  | 
                                                    
                                                            
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