(Q41777861)

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Quantitative phosphoproteome analysis of lysophosphatidic acid induced chemotaxis applying dual-step (18)O labeling coupled with immobilized metal-ion affinity chromatography.

scientific article published on 12 September 2008

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scholarly article

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14 January 2020

Quantitative phosphoproteome analysis of lysophosphatidic acid induced chemotaxis applying dual-step (18)O labeling coupled with immobilized metal-ion affinity chromatography (English)

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14 January 2020

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Joshua N Adkins

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Richard D. Smith

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Samuel Owen Purvine

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Katrina M. Waters

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Jöns Jacob Berzelius

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Jon M Jacobs

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Matthew E Monroe

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Matthew E Monroe

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François-David Camps

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David G Camp

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Tyler H Heibeck

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14 January 2020

Aleksey V Tolmachev

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Aleksey V Tolmachev

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Ronald J Moore

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14 January 2020

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Shi-Jian Ding

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14 January 2020

Yingchun Wang

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14 January 2020

Feng Yang

5

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14 January 2020

Xiuxia Du

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14 January 2020

Wei Wang

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14 January 2020

Richard L Klemke

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14 January 2020

publication date

12 September 2008

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14 January 2020

Journal of Proteome Research

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14 January 2020

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14 January 2020

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14 January 2020

4215-4224

1 reference

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14 January 2020

PhosphoBlast, a computational tool for comparing phosphoprotein signatures among large datasets

1 reference

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6 June 2018

Profiling signaling polarity in chemotactic cells.

1 reference

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Mass measurement accuracy in analyses of highly complex mixtures based upon multidimensional recalibration

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6 June 2018

Global, in vivo, and site-specific phosphorylation dynamics in signaling networks

1 reference

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A probability-based approach for high-throughput protein phosphorylation analysis and site localization

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Phosphorylation of N-cadherin-associated cortactin by Fer kinase regulates N-cadherin mobility and intercellular adhesion strength

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Large-scale characterization of HeLa cell nuclear phosphoproteins

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Peptide and protein sequence analysis by electron transfer dissociation mass spectrometry

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Erk/Src phosphorylation of cortactin acts as a switch on-switch off mechanism that controls its ability to activate N-WASP

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Identification of novel phosphorylation sites on Xenopus laevis Aurora A and analysis of phosphopeptide enrichment by immobilized metal-affinity chromatography

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ERK and RhoA differentially regulate pseudopodia growth and retraction during chemotaxis

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[Mechanisms of cell adhesion and migration]

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Identifiers

10.1021/PR7007785

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14 January 2020

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Europe PubMed Central

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14 January 2020

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14 January 2020

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