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hepatitis

HCV Infection Alters Salivary Gland Histology and Saliva Composition

[Journal of Dental Research] Researchers investigated if xerostomia associated with salivary gland (SG) and hepatitis C virus (HCV) infection and characterized the structural changes in SG and saliva composition.

Recapitulating Hepatitis E Virus–Host Interactions and Facilitating Antiviral Drug Discovery in Human Liver–Derived Organoids

[Science Advances] Scientists demonstrated that 3D cultured organoids from fetal and adult human liver with cholangiocyte or hepatocyte phenotype supported hepatitis E virus replication.

Ascletis Announces US IND Approval of ASC22 (Envafolimab), a Subcutaneously Administered PD-L1 Antibody for Functional Cure of Chronic Hepatitis B

[Ascletis Pharma, Inc.] Ascletis Pharma, Inc. announced the Investigational New Drug (IND) application approval by US FDA and initiation of global development of ASC22, a first-in-class, subcutaneously administered PD-L1 antibody for functional cure of chronic hepatitis B.

Oral Cyanobacteria and Hepatocellular Carcinoma

[Cancer Epidemiology Biomarkers & Prevention] Bacterial 16S rRNA sequences were evaluated in oral samples from 90 hepatocellular carcinoma (HCC) cases and 90 controls who were a part of a larger US case–control study of HCC among patients diagnosed from 2011 to 2016. The authors provides novel evidence that oral Cyanobacteria may be an independent risk factor for HCC.

Aligos Therapeutics Expands Collaboration with Merck to Develop Oligonucleotide Therapies for NASH

[Aligos Therapeutics, Inc.] Aligos Therapeutics, Inc. announced that it has expanded its ongoing collaboration agreement with Merck to discover and develop oligonucleotide therapies for non-alcoholic steatohepatitis (NASH).

CRISPR Screens Uncover Protective Effect of PSTK as a Regulator of Chemotherapy-Induced Ferroptosis in Hepatocellular Carcinoma

[Molecular Cancer] CRISPR-based loss-of-function genetic screens were used to target 18,053 protein-coding genes in hepatocellular carcinoma cells to identify chemotherapy-related synthetic lethal genes in these cells.

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