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NASH

Precancerous Liver Diseases Do Not Cause Increased Mutagenesis in Liver Stem Cells

[Communications Biology] Researchers performed whole-genome sequencing on clonally expanded single liver stem cells cultured as intrahepatic cholangiocyte organoids from patients with alcoholic cirrhosis, non-alcoholic steatohepatitis, and primary sclerosing cholangitis.

Elevar Therapeutics Receives Orphan Drug Designation from FDA for Rivoceranib for the Treatment of Hepatocellular Carcinoma (HCC)

[Hepatic Cell News] Elevar Therapeutics, Inc. announced that the US FDA has granted rivoceranib with orphan drug designation for the treatment of HCC, the most common primary liver malignancy and is a leading cause of cancer-related death worldwide.

Liver Sphingomyelin Synthase 1 Deficiency Causes Steatosis, Steatohepatitis, Fibrosis and Tumorigenesis: An Effect of Glucosylceramide Accumulation

[iScience] Investigators implicated that glucosylceramide accumulation was one of triggers promoting the development of nonalcoholic fatty liver disease into non-alcoholic steatohepatitis, then, fibrosis and tumorigenesis.

Immune Cell-Mediated Features of Non-Alcoholic Steatohepatitis

[Nature Reviews Immunology] Scientists discussed current concepts related to the role of immune cells in the onset and progression of non-alcoholic steatohepatitis.

Placental Extract Suppresses the Formation of Fibrotic Deposits by Tumor Necrosis Factor Alpha and Transforming Growth Factor Beta-Induced Epithelial–Mesenchymal Transition in ARPE-19 Cells

[BMC Research Notes] Scientists evaluated whether placental extract influences epithelial–mesenchymal transition (EMT) and fibrosis through cytokine-induced EMT in the retinal pigment epithelial cells, in vitro.

Gannex Announces US IND Approval of ASC43F, a First-in-Class Dual-Target Fixed-Dose Combination for NASH

[Gannex Pharma Co., Ltd.] Gannex Pharma Co., Ltd. announced the Investigational New Drug (IND) application approval by US FDA and initiation of global development of ASC43F, a fixed-dose combination with dual targets of thyroid hormone receptor beta and farnesoid X receptor for the treatment of non-alcoholic steatohepatitis (NASH).

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