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ornithine carbamoyltransferase deficiency disease/albumin
Povezava se shrani v odložišče
3 rezultatov
Establishment of ornithine transcarbamylase deficiency-derived primary human hepatocyte with hepatic functions.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
A long-term hepatocyte culture maintaining liver-specific functions is very essential for both basic research and the development of bioartificial liver devices in clinical application. However, primary hepatocytes rapidly lose their proliferation and hepatic functions over a few days in culture.
Frequency and Pathophysiology of Acute Liver Failure in Ornithine Transcarbamylase Deficiency (OTCD).
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
BACKGROUND
Acute liver failure (ALF) has been reported in ornithine transcarbamylase deficiency (OTCD) and other urea cycle disorders (UCD). The frequency of ALF in OTCD is not well-defined and the pathogenesis is not known.
OBJECTIVE
To evaluate the prevalence of ALF in OTCD, we analyzed the Swiss
Isolation of Hepatic Progenitor Cells From Human Liver With Cirrhosis Secondary to Biliary Atresia Using EpCAM or Thy-1 Markers.
Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
We sought to determine whether hepatic progenitor cells can be isolated from cirrhotic liver using epithelial cell adhesion molecule (EpCAM) or Thy-1 markers. Liver tissue with cirrhosis secondary to biliary atresia (BA) was collagenase digested, and nonparenchymal cells (NPCs) were cultivated for
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