Hepatology - Higher soft drink consumption linked to increased risk of liver disease
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Developing a translational biomarker panel for in vitro NASH studiesDeveloping a translational biomarker panel for in vitro NASH studies

A pressing need for therapeutics to treat the metabolic disorder Non-alcoholic steatohepatitis (NASH) has led to the development of human liver microphysiological systems (MPS).Explore CN-Bio's MPS’ ability to recapitulate an advanced NASH phenotype (characterized by fibrosis), quantify biomarker expression and assess the efficacy of drugs that entered clinical trials.

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   Higher soft drink consumption linked to increased risk of liver diseaseHigher soft drink consumption linked to increased risk of liver disease
 
Study found that higher soft drink consumption is associated with an increased risk of nonalcoholic fatty liver disease, especially in males, within a cohort of Mexican adults.
 
   Beta Cells Alone Can Maintain Glycemic Balance Without Other Pancreatic CellsBeta Cells Alone Can Maintain Glycemic Balance Without Other Pancreatic Cells
 
Our glycemic balance is based on the ability of the pancreatic beta cells to detect glucose and secrete insulin to maintain our blood sugar levels.
 
   Breakthrough Nanoparticle Therapy Boosts Immune Response Against Aggressive Pancreatic CancerBreakthrough Nanoparticle Therapy Boosts Immune Response Against Aggressive Pancreatic Cancer
 
Innovative use of lipid nanoparticles to deliver immune agonists shows promise in activating anti-tumor immunity in pancreatic ductal adenocarcinoma models.
 
   Long-term air pollution exposure and poor lifestyle choices increase risk of non-alcoholic fatty liver diseaseLong-term air pollution exposure and poor lifestyle choices increase risk of non-alcoholic fatty liver disease
 
Long-term exposure to air pollution and poor lifestyle choices are key contributors to non-alcoholic fatty liver disease (NAFLD), affecting global liver health.
 
   Autophagy in HPCs modulates exosomal miRNAs to inhibit liver fibrosisAutophagy in HPCs modulates exosomal miRNAs to inhibit liver fibrosis
 
The study investigates the role of autophagy in hepatic progenitor cells (HPCs) and its potential to modulate exosomal microRNAs (miRNAs) to inhibit liver fibrosis in the context of schistosomiasis, a disease caused by parasitic flatworms that can lead to severe organ damage, particularly to the liver.
 
 
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