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近日,重庆医科大学感染性疾病分子生物学教育部重点实验室在国际肝脏病学领域顶级期刊《HEPATOLOGY》在线发表了题为“A functional variant in UBE2L3 contributes to HBV infection and maintains cccDNA stability by inducing degradation of APOBEC3A protein”研究成果。这是数月来,该杂志又一次发表课题组相关研究工作。该课题组相继阐明了宿主调控乙型肝炎病毒cccDNA转录和稳定性的新机制,这为寻找新的抗病毒药物靶点提供了坚实的实验依据。
1. Zhou L, Ren J H, Cheng S T, et al. A functional variant in UBE 2L3 contributes to HBV infection and maintains ccc DNA stability by inducing degradation of APOBEC 3A protein[J]. Hepatology, 2019.
2.Ren J H, Hu J L, Cheng S T, et al. SIRT3 restricts hepatitis B virus transcription and replication through epigenetic regulation of covalently closed circular DNA involving suppressor of variegation 3‐9 homolog 1 and SET domain containing 1A histone methyltransferases[J]. Hepatology, 2018.作者: hantavirus 时间: 2019-1-18 10:30
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