Prevention and treatment of gerbil hepatitis E using the programmable CRISPR-Cas13d system  

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作  者:Chengcheng Zhao Chong Lia Sa Li Hanyu Wu Pengyao Ren Tianlong Liu Xiaoxiang Hu Ran Zhang 

机构地区:[1]State Key Laboratory of Animal Biotech Breeding,College of Biological Sciences,China Agricultural University,Beijing 100193,China [2]Laboratory of Veterinary Pathology and Nanopathology,College of Veterinary Medicine,China Agricultural University,Beijing 100193,China

出  处:《Genes & Diseases》2024年第4期94-97,共4页基因与疾病(英文)

基  金:supported by the National Transgenic Major Program of China(No.2016ZX08009-003-006);Plan 111(No.B12008).

摘  要:In recent years,the global incidence of hepatitis E virus(HEV)has been rising,leading to increased morbidity and mortality associated with hepatitis.Cas13,a CRISPR effector,shows promise as an antiviral agent against singlestranded RNA viruses.Cas13d,a type VI-D effector,exhibits higher efficiency in suppressing RNA viruses compared to other type VI variants.However,its in vivo activity against RNA viruses in mammals remains unknown.

关 键 词:MORTALITY HEPATITIS treatment 

分 类 号:R512.6[医药卫生—内科学]

 

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