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Published in 2022 at "Animal Cells and Systems"
DOI: 10.1080/19768354.2022.2139755
Abstract: ABSTRACT Glycogen storage disease type Ia (GSD-Ia) is caused by a deficiency in the glucose-6-phosphatase (G6Pase, G6pc) enzyme, which catalyses the final step of gluconeogenesis and glycogenolysis. Accumulation of G6pc can lead to an increase…
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Keywords:
crispr cas9;
disease;
g6pc mice;
yap signalling ... See more keywords
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2
Published in 2023 at "Hepatology"
DOI: 10.1097/hep.0000000000000026
Abstract: Background and Aims: Biliary atresia (BA), a congenital cholestatic liver disease, commonly culminates in end-stage liver disease. We previously demonstrated in BA that Prominin-1 (Prom1)-expressing hepatic progenitor cells (HPCs) expand within regions of developing fibrosis,…
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Keywords:
prom1;
tweak;
fn14;
ductular reactions ... See more keywords