نتایج جستجو برای: hbv genome cpg

تعداد نتایج: 253638  

2015
Jun Hu Yaxing Xu Changfei Li Junli Hao Shanxin Peng Xiaoyu Chu Dake Zhang Dongping Xu Songdong Meng

Hepatitis B virus (HBV) chronically infects approximately 350 million people worldwide. The replication of HBV which genome is only 3.2 kb long relies heavily on host factors. Previous studies demonstrated that a highly expressed liver-specific microRNA (miRNA) miR-122 suppresses HBV expression and replication in multiple ways. In this study, we found that the miR-122 response elements in viral...

2012
Francesca Bonvicini Elisabetta Manaresi Francesca Di Furio Luisa De Falco Giorgio Gallinella

CpG DNA methylation is one of the main epigenetic modifications playing a role in the control of gene expression. For DNA viruses whose genome has the ability to integrate in the host genome or to maintain as a latent episome, a correlation has been found between the extent of DNA methylation and viral quiescence. No information is available for Parvovirus B19, a human pathogenic virus, which i...

Journal: :Journal of Immunology 2023

Abstract An estimated 296 million people worldwide suffer from chronic hepatitis B virus (HBV) infection, with 1.5 new infections occurring each year despite the availability of an effective vaccine. Chronic HBV infection persists in a dysfunctional immune environment, manifested by ineffective T cell response to virus. Patient HBV-specific CD8 +T cells have diminished proliferative capacity an...

2000
Nir Avrahami

6.1.1 Preface: CpG islands It is known that due to biochemical considerations that CpG, the pair of nocleotides C and G, appearing successively, in this order, along one DNA starnd, is relatively rare in DNA sequences, excluding particular sub-sequences, which are several hundreds of nucleotides long, where the couple CpG is more frequent. These sub-sequences, called CpG islands, are known to a...

2013
Renáta Tóth István Mészáros Rajmund Stefancsik Dániel Bartha Ádám Bálint Zoltán Zádori

Based on GC content and the observed/expected CpG ratio (oCpGr), we found three major groups among the members of subfamily Parvovirinae: Group I parvoviruses with low GC content and low oCpGr values, Group II with low GC content and high oCpGr values and Group III with high GC content and high oCpGr values. Porcine parvovirus belongs to Group I and it features an ascendant CpG distribution by ...

Journal: :PLoS Computational Biology 2007
Christoph Bock Jörn Walter Martina Paulsen Thomas Lengauer

CpG islands were originally identified by epigenetic and functional properties, namely, absence of DNA methylation and frequent promoter association. However, this concept was quickly replaced by simple DNA sequence criteria, which allowed for genome-wide annotation of CpG islands in the absence of large-scale epigenetic datasets. Although widely used, the current CpG island criteria incur sign...

Journal: :The Journal of general virology 2001
T Nakano L Lu X Hu M Mizokami E Orito C Shapiro S Hadler B Robertson

The complete genome sequences of hepatitis B virus (HBV) from 12 HBV-infected Yucpa Indians of Venezuela, a group with highly endemic HBV, were amplified and sequenced. The 12 isolates were closely related to each other, with 98.6-100% nucleotide identity. A phylogenetic tree based on the complete genome indicated clearly that they were genotype F. Three individuals had evidence of infection wi...

Journal: :hepatitis monthly 0
sima besharat liver and pancreatobiliary diseases research center, digestive disease research institute, tehran university of medical sciences, tehran, ir iran; golestan research center of gastroentrology and hepatology, golestan university of medical sciences, gorgan, ir iran hossein poustchi liver and pancreatobiliary diseases research center, digestive disease research institute, tehran university of medical sciences, tehran, ir iran; liver and pancreatobiliary diseases research center, digestive diseases research institute, tehran university of medical sciences, north kargar ave., shariati hospital, p.o. box: 14117-13135, tehran, ir iran. tel: +98-2182415204, fax: +98-21 82415400 ashraf mohamadkhani liver and pancreatobiliary diseases research center, digestive disease research institute, tehran university of medical sciences, tehran, ir iran aezam katoonizadeh liver and pancreatobiliary diseases research center, digestive disease research institute, tehran university of medical sciences, tehran, ir iran abdolvahab moradi golestan research center of gastroentrology and hepatology, golestan university of medical sciences, gorgan, ir iran gholamreza roshandel liver and pancreatobiliary diseases research center, digestive disease research institute, tehran university of medical sciences, tehran, ir iran; golestan research center of gastroentrology and hepatology, golestan university of medical sciences, gorgan, ir iran

background although certain hbv mutations are known to affect the expression of hepatitis e antigen, their association with hbv viral level or clinical outcomes is less clear. objectives we evaluated associations between different mutations in the basal core promoter (bcp) and pre-core (pc) regions of hbv genome and subsequent changes in hbv viral dna level over seven years in a population of u...

2016
Yanan Pang Weixing Guo Jiaqi Wang Guixia Xu Kai Cheng Guangwen Cao Mengchao Wu Shuqun Cheng Shanrong Liu

Integration of hepatitis B virus (HBV) DNA into the human liver cell genome is believed to promote HBV-related carcinogenesis. This study aimed to quantify the integration of HBV DNA into the leukocyte genome in hepatocellular carcinoma (HCC) patients in order to identify potential biomarkers for HBV-related diseases. Whole-genome comparative genomic hybridization (CGH) chip array analyses were...

2017
Jie Wang Ran Chen Ruiyang Zhang Shanlong Ding Tianying Zhang Quan Yuan Guiwen Guan Xiangmei Chen Ting Zhang Hui Zhuang Frederick Nunes Timothy Block Shuang Liu Zhongping Duan Ningshao Xia Zhongwei Xu Fengmin Lu

The CRISPR/Cas9 system is a novel genome editing technology which has been successfully used to inhibit HBV replication. Here, we described a novel gRNA-microRNA (miRNA)-gRNA ternary cassette driven by a single U6 promoter. With an anti-HBV pri-miR31 mimic integrated between two HBV-specific gRNAs, both gRNAs could be separated from the long transcript of gRNA-miR-HBV-gRNA ternary cassette thro...

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