Modular scanning FCS quantifies receptor-ligand interactions in living multicellular organisms.
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Cross-Scale Integrin Regulation Organizes ECM and Tissue Topology.Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevisLive imaging of Xwnt5A-ROR2 complexesBranch mode selection during early lung developmentDigit patterning during limb development as a result of the BMP-receptor interactionFluorescence fluctuation approaches to the study of adhesion and signalingWnt-dependent epithelial transitions drive pharyngeal pouch formation.In vivo single-molecule imaging identifies altered dynamics of calcium channels in dystrophin-mutant C. elegans.Single cell visualization of transcription kinetics variance of highly mobile identical genes using 3D nanoimaging.Dual-color fluorescence lifetime correlation spectroscopy to quantify protein-protein interactions in live cell.Imaging molecular dynamics in vivo--from cell biology to animal models.Computational modelling of bovine ovarian follicle development.Dual-color dual-focus line-scanning FCS for quantitative analysis of receptor-ligand interactions in living specimensFactors affecting the quantification of biomolecular interactions by fluorescence cross-correlation spectroscopy.Cellular response to heat shock studied by multiconfocal fluorescence correlation spectroscopy.Lessons in fluctuation correlation spectroscopy.Quantitative imaging reveals real-time Pou5f3-Nanog complexes driving dorsoventral mesendoderm patterning in zebrafishPromoting convergence: The integrated graduate program in physical and engineering biology at Yale University, a new model for graduate education.The SUN protein Mps3 controls Ndc1 distribution and function on the nuclear membrane.Recent developments in fluorescence correlation spectroscopy for diffusion measurements in planar lipid membranes.FRET and FCS--friends or foes?Fluorescence techniques to study lipid dynamics.Computational modelling of the BRI1 receptor system.The control of branching morphogenesis.Quantifying intracellular dynamics using fluorescence fluctuation spectroscopy.Endocytosis and signaling during developmentRecent applications of fluorescence correlation spectroscopy in live systems.Self-segregation of myelin membrane lipids in model membranes.Simulations demonstrate a simple network to be sufficient to control branch point selection, smooth muscle and vasculature formation during lung branching morphogenesis.Measuring fast stochastic displacements of bio-membranes with dynamic optical displacement spectroscopy.Precise measurement of protein interacting fractions with fluorescence lifetime imaging microscopy.Educated natural killer cells show dynamic movement of the activating receptor NKp46 and confinement of the inhibitory receptor Ly49A.Feedback, receptor clustering, and receptor restriction to single cells yield large Turing spaces for ligand-receptor-based Turing models.There and back again: from the origin of life to single molecules.Optimal fluorescent protein tags for quantifying protein oligomerization in living cells.
P2860
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P2860
Modular scanning FCS quantifies receptor-ligand interactions in living multicellular organisms.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
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2009年學術文章
@zh-hant
name
Modular scanning FCS quantifie ...... iving multicellular organisms.
@en
Modular scanning FCS quantifie ...... iving multicellular organisms.
@nl
type
label
Modular scanning FCS quantifie ...... iving multicellular organisms.
@en
Modular scanning FCS quantifie ...... iving multicellular organisms.
@nl
prefLabel
Modular scanning FCS quantifie ...... iving multicellular organisms.
@en
Modular scanning FCS quantifie ...... iving multicellular organisms.
@nl
P2860
P50
P356
P1433
P1476
Modular scanning FCS quantifie ...... iving multicellular organisms.
@en
P2093
Markus Burkhardt
Shuizi Rachel Yu
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P2888
P304
P356
10.1038/NMETH.1355
P577
2009-08-02T00:00:00Z