Original data underlying the Fig 2A results.

NIAID Data Ecosystem2026-05-01 收录

肝炎病毒分子机制

纤维化信号通路

数据链接：

https://figshare.com/articles/dataset/Original_data_underlying_the_Fig_2A_results_/24027447 数据链接链接失效反馈

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Correction: Activation of the Connective Tissue Growth Factor (CTGF)-Transforming Growth Factor β 1 (TGF-β 1) Axis in Hepatitis C Virus-Expressing Hepatocytes

创建时间：

2023-08-24

The Hepatitis B Virus X Protein Transactivates Viral Core Gene Expression In Vivo

肝炎病毒分子机制

转基因动物模型

The function of the X protein in the life cycle of mammalian hepadnaviruses is unclear. Based on tissue culture experiments it has been suggested that this protein represents a transcriptional transac

PubMed Central60

Intestinal B cells license metabolic T-cell activation in NASH microbiota/antigen-independently and contribute to fibrosis by IgA-FcR signalling. Intestinal B cells license metabolic T-cell activation in NASH microbiota/antigen-independently and contribute to fibrosis by IgA-FcR signalling

非酒精性脂肪性肝炎(NASH)

纤维化信号通路

Non-alcoholic steatohepatitis (NASH), which is increasing in incidence due to the obesity epidemic, is a T-cell mediated, auto-aggressive condition that can result in progressive liver disease and hep

NIAID Data Ecosystem30

The m6A epitranscriptome of the HepAD38 cell line. The m6A epitranscriptome of the HepAD38 cell line

RNA表观遗传学

肝炎病毒分子机制

m6A modification appears in HepAD38 cell line Overall design: To investigate whether m6A modification is involved in evolution, we performed MeRIP-seq on HepAD38 cell line

NIAID Data Ecosystem20

Transcriptomic analysis of lipid biosynthesis pathways for HBV cure

肝炎病毒分子机制

代谢转录组学

RNAseq analysis of liver tissue samples from uninfected (n=5) and HBV-infected (n=5) humanized chimeric liver (uPA/SCID) mice was performed to identify potential new host factors and pathways modulate

NIAID Data Ecosystem50

La Autoantigen Specifically Recognizes a Predicted Stem-Loop in Hepatitis B Virus RNA

病毒蛋白相互作用

肝炎病毒分子机制

We recently identified three nuclear proteins (p45, p39, and p26) that bind to a 91-nucleotide (nt) RNA element between nt 1243 and 1333 in hepatitis B virus (HBV) RNA, and we showed that these protei

PubMed Central30

Original data underlying the Fig 2A results.

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