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A ZFN/piggyBac step closer to autologous liver cell therapy.
Hepatology (Baltimore, Md.), Jun-2012;55(6):2033-5.
A microRNA-21 surge facilitates rapid cyclin D1 translation and cell cycle progression in mouse liver regeneration.
The Journal of clinical investigation, Mar-1-2012;122(3):1097-108. Epub 2012 Feb 13.
Stem cells in liver diseases and cancer: recent advances on the path to new therapies.
Hepatology (Baltimore, Md.), Jan-2012;55(1):298-306.
Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration.
The Journal of clinical investigation, Dec-2011;121(12):4850-60. Epub 2011 Nov 21.
A simple code for installing hepatocyte function.
Cell stem cell, Aug-5-2011;9(2):89-91.
Mouse chimeras as a system to investigate development, cell and tissue function, disease mechanisms and organ regeneration.
Cell cycle (Georgetown, Tex.), Jul-1-2011;10(13):2091-9. Epub 2011 Jul 01.
Core promoter recognition complex changes accompany liver development.
Proceedings of the National Academy of Sciences of the United States of America, Mar-8-2011;108(10):3906-11. Epub 2011 Feb 22.
Transplanted nonviable human hepatocytes produce appreciable serum albumin levels in mice.
Stem cell research, Nov-2010;5(3):267-70. Epub 2010 Aug 5.
The MAP3K TAK1: a chock block to liver cancer formation.
Hepatology (Baltimore, Md.), Oct-2010;52(4):1506-9.
Induced pluripotent stem cell-derived hepatocytes have the functional and proliferative capabilities needed for liver regeneration in mice.
The Journal of clinical investigation, Sep-2010;120(9):3120-6. Epub 2010 Aug 25.
Therapeutic liver reconstitution with murine cells isolated long after death.
Gastroenterology, Sep-2010;139(3):1019-29. Epub 2010 Jun 2.
miRNAs regulate SIRT1 expression during mouse embryonic stem cell differentiation and in adult mouse tissues.
MicroRNAs control hepatocyte proliferation during liver regeneration.
Hepatology (Baltimore, Md.), May-2010;51(5):1735-43.
Loss of p21 permits carcinogenesis from chronically damaged liver and kidney epithelial cells despite unchecked apoptosis.
Cancer cell, Jul-8-2008;14(1):59-67.
A reproducible and well-tolerated method for 2/3 partial hepatectomy in mice.
Nature protocols, 2008;3(7):1167-70.