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Hepatitis B virus genetic mutations and evolution in liver diseases(Open Access)

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机构: [a]Institute of Basic and Clinical Medicine, Center of Clinical Molecular Biology, Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kumning Sci. and Tech. Univ, Kunming 650032, Yunnan Province, China [b]Medical Science College of Yunnan University, Kunming 650091, Yunnan Province, China
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关键词: Genotype Hepatitis B virus Liver disease Mutation Risk markers

摘要:
Hepatitis B virus (HBV) belongs to the genus Orthohepadnavirus of the Hepadnaviridae family and is approximately 3.2 kb in length. Owing to a lack of proofreading capacity during reverse transcription and a high replication rate, HBV exhibits as quasispecies. To detect the genetic mutations of HBV, many methods with different sensitivities and throughputs were developed. According to documentary records, HBV mutation and evolution were important vial parameters in predicting disease progression and therapeutic outcome. In this review, we separately discussed the correlation between HBV genomic mutations in four open reading frames and liver disease progression. Since some of the results were controversial from different laboratories, it remains to be seen whether functional analyses will confirm their role in modifying the course of infection. © 2014 Baishideng Publishing Group Co., Limited. All rights reserved.

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出版当年[2014]版:
大类 | 3 区 医学
小类 | 3 区 胃肠肝病学
最新[2023]版:
大类 | 3 区 医学
小类 | 3 区 胃肠肝病学
第一作者:
第一作者机构: [a]Institute of Basic and Clinical Medicine, Center of Clinical Molecular Biology, Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kumning Sci. and Tech. Univ, Kunming 650032, Yunnan Province, China [b]Medical Science College of Yunnan University, Kunming 650091, Yunnan Province, China [*1]Associate Professor, Center of Clinical Molecular Biology, Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People’s Hospital of Yunnan Province, Affiliated Hospital of Kumning Science and Technology University, 157 JinBi Road, Kunming 650032, Yunnan Province, China.
通讯作者:
通讯机构: [a]Institute of Basic and Clinical Medicine, Center of Clinical Molecular Biology, Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People's Hospital of Yunnan Province, Affiliated Hospital of Kumning Sci. and Tech. Univ, Kunming 650032, Yunnan Province, China [b]Medical Science College of Yunnan University, Kunming 650091, Yunnan Province, China [*1]Associate Professor, Center of Clinical Molecular Biology, Provincial Key Laboratory for Birth Defects and Genetic Diseases, the First People’s Hospital of Yunnan Province, Affiliated Hospital of Kumning Science and Technology University, 157 JinBi Road, Kunming 650032, Yunnan Province, China.
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