Karenliu
The Liu Lab | Department of Craniofacial Biology | Kings College London |
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Welcome to the Liu Lab!
We are interested in signal transduction in developmental biology.
In any intricate developmental process, the encoded genes are interpreted as myriad intercellular and intracellular interactions, all of which must occur at the right time and place. With this in mind, we are developing new methods to block or alter the activities of individual proteins in a drug-dependent manner. Our goal is to expand the repertoire of molecular tools available to developmental biologists. Rather than screen for small molecule-protein interactions we have chosen to use a directed approach to making chemically sensitive protein alleles, in which we use drug-dependent tags to regulate protein stability and localization.
The biological problem that we are interested in is the development of the neural crest and its derivatives, including the craniofacial skeleton. At present, we are developing chemical tools to study the roles of GSK-3 and Wnt signaling in the neural crest. We are using two model systems, the frog Xenopus laevis and the mouse. Xenopus embryos are abundant and live in an aquatic environment, allowing easy manipulation and drug accessibility; thus, we are using Xenopus to study early patterning and to rapidly test new tools. We then adapt these tools to mammalian systems. In the mouse, we are currently studying the development of the bony skull, using conventional and drug-dependent alleles of GSK-3β.
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28 April 2024
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15:09 | (Upload log) [Khiemle; CarterPaul (4×)] | |||
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15:09 CarterPaul talk contribs uploaded File:Sheet detatch.jpg (An illustration of standard cell detachment vs cell sheet detachment. (A) Cells harvested through enzymatic digestion. In this approach, cells lose their cell–cell junctions which cause them to float in a regular culture dish. (B) Cell sheet detachment through temperature control without any enzymatic digestion using temperature responsive culture dish. The temperature is lowered from 37 to 20 °C, which maintains the cell–cell junctions and ECM surface.) | ||||
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15:03 Khiemle talk contribs uploaded File:NGS Technology Illustration.png | ||||
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14:48 CarterPaul talk contribs uploaded File:Reactive coating.jpg (This image shows the steps to adding a reactive coating to a PDMS device) | ||||
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14:36 CarterPaul talk contribs uploaded File:Scaffold uses.jpg (This image shows the uses of 3D scaffold cell cultures and their current uses in cancer research) | ||||
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14:35 CarterPaul talk contribs uploaded File:Droplet hanging tech.jpg (image for 3D cell culture page) |
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15:09 | 3D Cell Culture - McLean Taggart, Emma Villares, Maximillian Marek, Scott LeBlanc, Adam Lyons and Jacob Belden 7 changes history +1,129 [CarterPaul (7×)] | |||
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15:08 | Nanoimprint Lithography (NIL) - Carter Paul 8 changes history +510 [CarterPaul (8×)] | |||
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