Associated Papers
Transient growth factor expression via mRNA in lipid nanoparticles promotes hepatocyte cell therapy in mice.
Smith AR et al.
Nature Communications, 2024
Induced pluripotent stem cells model personalized variations in liver disease resulting from α1-antitrypsin deficiency.
Tafaleng EN et al.
Hepatology (baltimore, Md.), 2015
Long-term culture of genome-stable bipotent stem cells from adult human liver.
Huch M et al.
Cell, 2015
25533785 (PubMed )
Supplement: mmc6.pdf
Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells.
Rashid ST et al.
The Journal of Clinical Investigation, 2010
Gene targeted therapeutics for liver disease in alpha-1 antitrypsin deficiency.
McLean C et al.
Biologics : Targets & Therapy, 2009
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