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Timothy K. Lee

Researcher at Stanford University

Publications -  31
Citations -  4418

Timothy K. Lee is an academic researcher from Stanford University. The author has contributed to research in topics: Population & Cytoskeleton. The author has an hindex of 21, co-authored 30 publications receiving 4137 citations. Previous affiliations of Timothy K. Lee include University of California, San Francisco.

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Single-chain antigen-binding proteins

TL;DR: Three single-chain antigen-binding proteins are novel recombinant polypeptides, composed of an antibody variable light-chain amino acid sequence tethered to a variable heavy-chain sequence (VH) by a designed peptide that links the carboxyl terminus of the VL sequence to the amino terminusof the VH sequence.
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Single-cell NF-κB dynamics reveal digital activation and analogue information processing

TL;DR: In this paper, the authors used high-throughput microfluidic cell culture and fluorescence microscopy, quantitative gene expression analysis and mathematical modelling to investigate how single mammalian cells respond to different concentrations of the signalling molecule tumour-necrosis factor (TNF)-a, and relay information to the gene expression programs by means of the transcription factor nuclear factor (NF)-kB.
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A Noisy Paracrine Signal Determines the Cellular NF-κB Response to Lipopolysaccharide

TL;DR: It is shown that mammalian cells can create “noisy” environments to produce diversified responses to stimuli and be linked to a secondary paracrine signal secreted at low concentrations, such that not all cells undergo a second round of NF-κB activation.
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Rapid, precise quantification of bacterial cellular dimensions across a genomic-scale knockout library

TL;DR: Two software packages, Morphometrics and BlurLab, that together enable automated, computationally efficient, unbiased identification of cells and morphological features are introduced and suggest potential functions for unknown genes and differences in modes of action of antibiotics are suggested.
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Mechanical crack propagation drives millisecond daughter cell separation in Staphylococcus aureus

TL;DR: The ultrafast daughter cell separation in S. aureus appears to be driven by accumulation of stress in the peripheral ring and exhibits hallmarks of mechanical crack propagation.