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- W2028838235 endingPage "152" @default.
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- W2028838235 abstract "The number of genetic or acquired diseases of the liver treatable by organ transplantation is ever-increasing as transplantation techniques improve placing additional demands on an already limited organ supply. While cell and gene therapies are distinctly different modalities, they offer a synergistic alternative to organ transplant due to distinct architectural and physiological properties of the liver. The hepatic blood supply and fenestrated endothelial system affords relatively facile accessibility for cell and/or gene delivery. More importantly, however, the remarkable capacity of hepatocytes to proliferate and repopulate the liver creates opportunities for new treatments based on emerging technologies. This review will summarise current understanding of liver regeneration, describe clinical and experimental cell and gene therapeutic modalities and discuss critical challenges to translate these new technologies to wider clinical utility. This article is part of a Directed Issue entitled: Regenerative Medicine: the challenge of translation." @default.
- W2028838235 created "2016-06-24" @default.
- W2028838235 creator A5026215456 @default.
- W2028838235 creator A5051748845 @default.
- W2028838235 creator A5052717318 @default.
- W2028838235 creator A5061906652 @default.
- W2028838235 date "2014-11-01" @default.
- W2028838235 modified "2023-10-14" @default.
- W2028838235 title "Exploiting the unique regenerative capacity of the liver to underpin cell and gene therapy strategies for genetic and acquired liver disease" @default.
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