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Journal ArticleDOI

High-throughput fluorescence microscopy for systems biology

Rainer Pepperkok, +1 more
- 19 Jul 2006 - 
- Vol. 7, Iss: 9, pp 690-696
TLDR
Fluorescence microscopy is making the transition to a quantitative and high-throughput technology to enable these techniques to be applied to functional genomics experiments.
Abstract
Fluorescence microscopy is a powerful tool to assay biological processes in intact living cells. Now, fluorescence microscopy is becoming a quantitative and high-throughput technology that can be applied to functional genomics experiments and can provide data for systems-biology approaches. In this post-genomic era, we need to define gene function on a genome-wide scale for model organisms and humans. The fundamental unit of biological processes is the cell. Among the most powerful tools to assay such processes in the physiological context of intact living cells are fluorescence microscopy and related imaging techniques. To enable these techniques to be applied to functional genomics experiments, fluorescence microscopy is making the transition to a quantitative and high-throughput technology.

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Citations
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Journal ArticleDOI

Highly fluorescent semiconducting polymer dots for biology and medicine.

TL;DR: Recent findings of the photophysical properties of Pdots which speak to the merits of these entities as fluorescent labels are summarized and the relationship between the physical properties and performance is discussed.
Journal ArticleDOI

Miniaturized integration of a fluorescence microscope

TL;DR: A miniature (1.9 g) integrated fluorescence microscope made from mass-producible parts, including a semiconductor light source and sensor enables high-speed cellular imaging across ∼0.5 mm2 areas in active mice and allows concurrent tracking of Ca2+ spiking in >200 Purkinje neurons across nine cerebellar microzones.
Journal ArticleDOI

Dynamic proteomics of individual cancer cells in response to a drug.

TL;DR: A dynamic-proteomics approach is presented that measures the levels and locations of nearly 1000 different endogenously tagged proteins in individual living cells at high temporal resolution, and identifies proteins whose dynamics differ widely between cells, in a way that corresponds to the outcomes—cell death or survival.
Journal ArticleDOI

Stochastic modelling for quantitative description of heterogeneous biological systems

TL;DR: Stochastic models are being used increasingly in preference to deterministic models to describe biochemical network dynamics at the single-cell level to adequately describe observed noise, variability and heterogeneity of biological systems over a range of scales of biological organization.
References
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BookDOI

Handbook of biological confocal microscopy

TL;DR: Methods for Three-Dimensional Imaging and Tutorial on Practical Confocal Microscopy and Use of the Confocal Test Specimen.
Journal ArticleDOI

Finishing the euchromatic sequence of the human genome

Chris P. Ponting, +1 more
- 21 Oct 2004 - 
TL;DR: The current human genome sequence (Build 35) as discussed by the authors contains 2.85 billion nucleotides interrupted by only 341 gaps and is accurate to an error rate of approximately 1 event per 100,000 bases.
Patent

High throughput screen

TL;DR: In this paper, a high throughput screen for determining the effect of test compounds on ion channel or transporter activity was proposed, and a method for monitoring ion channel activity in a membrane.
Journal ArticleDOI

Small Molecule Inhibitor of Mitotic Spindle Bipolarity Identified in a Phenotype-Based Screen

TL;DR: In vitro, monastrol specifically inhibited the motility of the mitotic kinesin Eg5, a motor protein required for spindle bipolarity, and will therefore be a particularly useful tool for studying mitotic mechanisms.
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