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Showing 1 to 8 of 8 for “"Liver Physiology"”.

  1. Elucidating the role of SRSF1, a prototypical splicing factor, in liver physiology

    … prototypical splicing factor, in the context of liver physiology. I began by generating and characterizing hepatocyte-specific SRSF1 knock-out mice models. These mice developed severe liver damage and exhibited pathology like the human disease Non-alcoholic steatohepatitis. Specifically, loss of …

    uiuc Repository record for Elucidating the role of SRSF1, a prototypical splicing factor, in liver physiology (opens in a new tab)

  2. Uncovering a novel role for FXR-SHP axis in liver physiology, diseases and beyond

    Liver performs a multitude of functions ranging from detoxification, metabolism and digestion. To execute these tasks, one of the mechanisms that the liver utilizes is nuclear receptor signaling, which in turn can transcriptionally regulate gene networks. My doctoral thesis focuses on studying the …

    uiuc Repository record for Uncovering a novel role for FXR-SHP axis in liver physiology, diseases and beyond (opens in a new tab)

  3. Use of gene expression to characterize heterogeneous liver cell populations

    … and necessary to maintain in vivo liver function. A variety of in vitro culture systems have been developed to address different aspects of liver physiology and architecture in order to recreate the microenvironment. These in vitro co-culture strategies have been limited by their …

    mit Repository record for Use of gene expression to characterize heterogeneous liver cell populations (opens in a new tab)

  4. Molecular Regulation of Maternal Hepatic Adaptations to Pregnancy

    The maternal liver exhibits robust adaptations to pregnancy to accommodate the metabolic needs of developing and growing placenta and fetus by largely unknown mechanisms. We found that achaete-scute homolog 1 (Ascl1), a basic helix-loop-helix transcription factor essential for neuronal development, …

    iupui Repository record for Molecular Regulation of Maternal Hepatic Adaptations to Pregnancy (opens in a new tab)

  5. The molecular genetic investigation of paediatric liver disease

    Liver disease in children is rare but often serious, life long, and in many cases leads to death. Advances in diagnosing and treating liver disease (including liver transplant) have improved the outlook for children in many cases however little is known about the molecular pathogenesis of the …

    birmingham Repository record for The molecular genetic investigation of paediatric liver disease (opens in a new tab)

  6. KUPFFER CELLS¿ MITOCHONDRIAL PLASTICITY AFFECTS SYSTEMIC IMMUNO-METABOLISM

    … resident macrophages that are essential for liver physiology and contribute to the development of metabolic-associated fatty liver disease (MAFLD). Due to their high plasticity, KCs can maintain immunotolerance and mediate cell-cell interaction within the hepatic niche, playing both an immune …

    milano Repository record for KUPFFER CELLS¿ MITOCHONDRIAL PLASTICITY AFFECTS SYSTEMIC IMMUNO-METABOLISM (opens in a new tab)

  7. Targeting LGALS3 to treat steatotic liver disease and hepatocarcinogenesis

    Non-alcoholic fatty liver disease (NAFLD), recently renamed as Metabolic dysfunction-associated steatotic liver disease (MASLD), is the leading cause of chronic liver disease (CLD) and liver-related morbidity and mortality worldwide. NAFLD, characterized by hepatic fat accumulation and coexisting …

    cagliari Repository record for Targeting LGALS3 to treat steatotic liver disease and hepatocarcinogenesis (opens in a new tab)

  8. Unfolded Protein Response (UPR) Signaling in Hepatic Stellate Cells (HSC) as a Key Regulator of Liver Fibrosis

    Liver cirrhosis is a leading cause of death worldwide, with the prevalence of cirrhosis on the rise. Cirrhosis is driven by various etiologies, including liver injuries from diabetes, obesity, metabolic disorders, and alcohol use. Central to the progression of chronic liver disease to cirrhosis is …

    iupui Repository record for Unfolded Protein Response (UPR) Signaling in Hepatic Stellate Cells (HSC) as a Key Regulator of Liver Fibrosis (opens in a new tab)