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B. Christoffer Lagerholm

Researcher at University of Oxford

Publications -  46
Citations -  3160

B. Christoffer Lagerholm is an academic researcher from University of Oxford. The author has contributed to research in topics: Quantum dot & Biology. The author has an hindex of 22, co-authored 39 publications receiving 2886 citations. Previous affiliations of B. Christoffer Lagerholm include University of North Carolina at Chapel Hill & Carnegie Mellon University.

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Noninvasive Imaging of Quantum Dots in Mice

TL;DR: Long-term experiments demonstrated that these quantum dots remain fluorescent after at least four months in vivo, using only quantum dots for detection.
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Detecting microdomains in intact cell membranes.

TL;DR: In this review, a variety of experimental techniques that have been or might be used to look for lipid microdomains in intact cell membranes are described and the strengths and limitations of different techniques for microdomain identification and characterization are assessed.
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The Lateral Organization and Mobility of Plasma Membrane Components.

TL;DR: An overview of how cell-surface structure may give rise to the types of lateral mobility that are observed and some potentially fruitful future directions to elucidate the architecture of these structures in more molecular detail are presented.
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Methods to measure the lateral diffusion of membrane lipids and proteins.

TL;DR: In this paper, the authors discuss methods to measure lateral mobility of membrane lipids and proteins using techniques based on the light microscope, which typically sample lateral mobility in very small, micron-sized regions of the membrane so that they can be used to measure diffusion in regions of single cells.
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Bulk and micropatterned conjugation of extracellular matrix proteins to characterized polyacrylamide substrates for cell mechanotransduction assays

TL;DR: This simple conjugation method is especially effective in gel micropatterning by manual microcontact printing of protein patterns as small as 5 microm and enables numerous studies of constrained cell attachment and migration that were previously unfeasible due to high cost or difficulty in controlling the protein coating.