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Pentao Liu

Researcher at Li Ka Shing Faculty of Medicine, University of Hong Kong

Publications -  153
Citations -  13957

Pentao Liu is an academic researcher from Li Ka Shing Faculty of Medicine, University of Hong Kong. The author has contributed to research in topics: Induced pluripotent stem cell & Stem cell. The author has an hindex of 52, co-authored 138 publications receiving 12137 citations. Previous affiliations of Pentao Liu include Wellcome Trust Sanger Institute & National Institutes of Health.

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piggyBac transposition reprograms fibroblasts to induced pluripotent stem cells

TL;DR: It is shown that the individual PB insertions can be removed from established iPS cell lines, providing an invaluable tool for discovery, and the traceless removal of reprogramming factors joined with viral 2A sequences delivered by a single transposon from murine iPS lines is demonstrated.
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A Highly Efficient Recombineering-Based Method for Generating Conditional Knockout Mutations

TL;DR: This method is fast, efficient, and reliable and makes it possible to generate cko-targeting vectors in less than 2 wk and should also facilitate the generation of knock-in mutations and transgene constructs, as well as expedite the analysis of regulatory elements and functional domains in or near genes.
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Requirement for Wnt3 in vertebrate axis formation

TL;DR: It is shown that Wnt3 is expressed before gastrulation in the proximal epiblast of the egg cylinder, then is restricted to the posterior proximalEpiblast and its associated visceral endoderm and subsequently to the primitive streak and mesoderm, and the subsequent establishment of anterior-posterior neural pattern in the ectoderm is dependent on derivatives of the primitive streaks.
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The Merlin/NF2 Tumor Suppressor Functions through the YAP Oncoprotein to Regulate Tissue Homeostasis in Mammals

TL;DR: It is demonstrated that the Merlin/NF2 tumor suppressor and the YAP oncoprotein function antagonistically to regulate liver development and implicate YAP activation as a mediator of pathologies relevant to Neurofibromatosis 2.
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Chromosome engineering in mice

TL;DR: It is reported here that defined deficiencies, inversions and duplications extending to 3-4 cM can be constructed in embryonic stem cells by consecutive targeting of loxP recombination substrates to the end points of a genetic interval followed by Cre-induced recombination, which reconstructs a positive selectable marker which facilitates direct selection of clones with a chromosome structure specific to the relative orientation of theloxP sites.