easyFRAP: an interactive, easy-to-use tool for qualitative and quantitative analysis of FRAP data. - Wikidata - awgldk - TriplyDB

easyFRAP: an interactive, easy-to-use tool for qualitative and quantitative analysis of FRAP data.

easyFRAP: an interactive, easy-to-use tool for qualitative and quantitative analysis of FRAP data.

http://www.wikidata.org/entity/Q34250463

about

Lytic immune synapse function requires filamentous actin deconstruction by Coronin 1A Primary ciliogenesis requires the distal appendage component Cep123.Poc1A and Poc1B act together in human cells to ensure centriole integrity The KLP-7 Residue S546 Is a Putative Aurora Kinase Site Required for Microtubule Regulation at the Centrosome in C. elegans Trafficking Dynamics of PCSK9-Induced LDLR Degradation: Focus on Human PCSK9 Mutations and C-Terminal Domain Context-dependent switch in chemo/mechanotransduction via multilevel crosstalk among cytoskeleton-regulated MRTF and TAZ and TGFβ-regulated Smad3 Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9 Snf2h-mediated chromatin organization and histone H1 dynamics govern cerebellar morphogenesis and neural maturation.Stem cell differentiation increases membrane-actin adhesion regulating cell blebability, migration and mechanics.Loss of function of the ALS protein SigR1 leads to ER pathology associated with defective autophagy and lipid raft disturbances Mechanistic determinants of MBNL activity Validation of Normalizations, Scaling, and Photofading Corrections for FRAP Data Analysis.Distinct prion strains are defined by amyloid core structure and chaperone binding site dynamics.An aberrant phase transition of stress granules triggered by misfolded protein and prevented by chaperone function.Mechanical stability of talin rod controls cell migration and substrate sensing.Prion-like proteins sequester and suppress the toxicity of huntingtin exon 1.CK1δ restrains lipin-1 induction, lipid droplet formation and cell proliferation under hypoxia by reducing HIF-1α/ARNT complex formation Luminal signalling links cell communication to tissue architecture during organogenesis.A novel approach for studying histone H1 function in vivo.ENDOCYTOSIS. Endocytic sites mature by continuous bending and remodeling of the clathrin coat.Generation of an alpaca-derived nanobody recognizing γ-H2AX Prion aggregate structure in yeast cells is determined by the Hsp104-Hsp110 disaggregase machinery.Remodeling nuclear architecture allows efficient transport of herpesvirus capsids by diffusion Analysis of Protein Kinetics Using Fluorescence Recovery After Photobleaching (FRAP).The Drosophila orthologue of the INT6 onco-protein regulates mitotic microtubule growth and kinetochore structure.Photobleaching studies reveal that a single amino acid polymorphism is responsible for the differential binding affinities of linker histone subtypes H1.1 and H1.5.Multi-step loading of human minichromosome maintenance proteins in live human cells From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.A murine retrovirus co-Opts YB-1, a translational regulator and stress granule-associated protein, to facilitate virus assembly.Frapbot: An open-source application for FRAP data.Dual recognition of chromatin and microtubules by INCENP is important for mitotic progression.The cationic small molecule GW4869 is cytotoxic to high phosphatidylserine-expressing myeloma cells.The serine protease-mediated increase in intestinal epithelial barrier function is dependent on occludin and requires an intact tight junction.Alternate RASSF1 Transcripts Control SRC Activity, E-Cadherin Contacts, and YAP-Mediated Invasion.Microdomain Formation Controls Spatiotemporal Dynamics of Cell-Surface Glycoproteins.PKC-mediated phosphorylation of nuclear lamins at a single serine residue regulates interphase nuclear size in Xenopus and mammalian cells Pak4 Is Required during Epithelial Polarity Remodeling through Regulating AJ Stability and Bazooka Retention at the ZA.Diffusion and retention are major determinants of protein targeting to the inner nuclear membrane Coactivators and general transcription factors have two distinct dynamic populations dependent on transcription Efficient protein targeting to the inner nuclear membrane requires Atlastin-dependent maintenance of ER topology.

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easyFRAP: an interactive, easy-to-use tool for qualitative and quantitative analysis of FRAP data.

http://www.wikidata.org/entity/Q34250463

description

2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... itative analysis of FRAP data.

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easyFRAP: an interactive, easy ...... titative analysis of FRAP data

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Ioanna-Eleni Symeonidou

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Maria Anna Rapsomaniki

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Nickolaos-Nikiforos Giakoumakis

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Zoi Lygerou

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P2860

Cdt1 associates dynamically with chromatin throughout G1 and recruits Geminin onto chromatin

Cdt1 interactions in the licensing process: a model for dynamic spatiotemporal control of licensing

Nuclear membrane dynamics and reassembly in living cells: targeting of an inner nuclear membrane protein in interphase and mitosis

From fixed to FRAP: measuring protein mobility and activity in living cells.

Dynamic recruitment of licensing factor Cdt1 to sites of DNA damage.

FRAP analysis of binding: proper and fitting.

Measurement of dynamic protein binding to chromatin in vivo, using photobleaching microscopy.

Using the Virtual Cell Simulation Environment for Extracting Quantitative Parameters from Live Cell Fluorescence Imaging Data

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1800-1801

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scholarly article

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10.1093/BIOINFORMATICS/BTS241

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13

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28

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Stavros Taraviras

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2012-04-27T00:00:00Z

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224867146

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