David J. Williamson

发表

Development of 2-colour and 3D SMLM data analysis methods for fibrous spatial point patterns

Juliette Griffié, Jesse Aaron, Ruby Peters, 2018, Journal of Physics D: Applied Physics.

Blinking statistics and molecular counting in direct stochastic reconstruction microscopy (dSTORM)

Lekha Patel, Edward A. K. Cohen, David J. Williamson, 2021, Bioinform..

Semiparametric point process modeling of blinking artifacts in PALM

Ute Hahn, David J. Williamson, Louis G. Jensen, 2021, The Annals of Applied Statistics.

Bayesian cluster identification in single-molecule localization microscopy data

David J. Williamson, Patrick Rubin-Delanchy, G. Burn, 2015, Nature Methods.

Three-dimensional total-internal reflection fluorescence nanoscopy with nanometric axial resolution by photometric localization of single molecules

David J. Williamson, D. Owen, N. Unsain, 2019, Nature Communications.

Three-dimensional total internal reflection fluorescence nanoscopy with sub-10 nm resolution

David J. Williamson, D. Owen, N. Unsain, 2019, bioRxiv.

Pre-existing clusters of the adaptor Lat do not participate in early T cell signaling events

Astrid Magenau, Katharina Gaus, Dylan M Owen, 2011, Nature Immunology.

Conformational states of the kinase Lck regulate clustering in early T cell signaling

Katharina Gaus, Dylan M Owen, David J. Williamson, 2012, Nature Immunology.

The integration of signaling and the spatial organization of the T cell synapse

Katharina Gaus, David J. Williamson, K. Gaus, 2012, Front. Immun..

Dynamic Bayesian Cluster Analysis of Live-Cell Single Molecule Localization Microscopy Datasets

Patrick Rubin-Delanchy, Juliette Griffié, Ruby Peters, 2018, Small Methods.

3D Bayesian cluster analysis of super-resolution data reveals LAT recruitment to the T cell synapse

Patrick Rubin-Delanchy, Juliette Griffié, Lies Boelen, 2017, Scientific Reports.

Membrane lipid order of sub‐synaptic T cell vesicles correlates with their dynamics and function

David J. Williamson, Nathan Day, G. Burn, 2018, Traffic.

Blinking Statistics and Molecular Counting in direct Stochastic Reconstruction Microscopy (dSTORM)

David J. Williamson, D. Owen, E. Cohen, 2019, bioRxiv.

Functional Implications of Plasma Membrane Condensation for T Cell Activation

David J. Williamson, K. Gaus, C. Rentero, 2008, PloS one.

Quantitative Microscopy: Protein Dynamics and Membrane Organisation

Katharina Gaus, Dylan M Owen, David J. Williamson, 2009, Traffic.

Differential nanoscale organisation of LFA-1 modulates T-cell migration

Michael J. Shannon, David J. Williamson, J. Griffié, 2019, Journal of Cell Science.

A Bayesian cluster analysis method for single-molecule localization microscopy data

Patrick Rubin-Delanchy, Juliette Griffié, Michael Shannon, 2016, Nature Protocols.

The lipid raft hypothesis revisited – New insights on raft composition and function from super‐resolution fluorescence microscopy

David J. Williamson, K. Gaus, D. Owen, 2012, BioEssays : news and reviews in molecular, cellular and developmental biology.

Correction of multiple-blinking artifacts in photoactivated localization microscopy

David J. Williamson, D. Sage, Patrick Rubin-Delanchy, 2022, Nature Methods.

VAMP7 controls T cell activation by regulating the recruitment and phosphorylation of vesicular Lat at TCR-activation sites

Katharina Gaus, Lydia Danglot, David J. Williamson, 2013, Nature Immunology.

Evidence for annexin A6‐dependent plasma membrane remodelling of lipid domains

David J. Williamson, K. Gaus, D. Owen, 2015, British journal of pharmacology.

PALM imaging and cluster analysis of protein heterogeneity at the cell surface

Astrid Magenau, Katharina Gaus, David J. Williamson, 2010, Journal of biophotonics.

Machine learning for cluster analysis of localization microscopy data

Juliette Griffié, Ruby Peters, David J. Williamson, 2020, Nature Communications.

Sub-resolution lipid domains exist in the plasma membrane and regulate protein diffusion and distribution

Astrid Magenau, Katharina Gaus, Dylan M Owen, 2012, Nature Communications.

Multi-color Molecular Visualization of Signaling Proteins Reveals How C-Terminal Src Kinase Nanoclusters Regulate T Cell Receptor Activation.

David J. Williamson, J. Griffié, A. Cope, 2020, Cell reports.

Multi-colour DNA-qPAINT reveals how Csk nano-clusters regulate T-cell receptor signalling

David J. Williamson, J. Griffié, A. Cope, 2019, bioRxiv.

Structural synaptic signatures of Alzheimer's disease and dementia with Lewy bodies in the male brain

David J. Williamson, D. Aarsland, C. Troakes, 2021, medRxiv.

Live-Cell Super-resolution Reveals F-Actin and Plasma Membrane Dynamics at the T Cell Synapse.

David J. Williamson, H. Ewers, G. Burn, 2017, Biophysical journal.

How does the kinase Lck phosphorylate the T cell receptor? Spatial organization as a regulatory mechanism

David J. Williamson, K. Gaus, Jérémie Rossy, 2012, Front. Immun..

Optical techniques for imaging membrane domains in live cells (live-cell palm of protein clustering).

David J. Williamson, K. Gaus, D. Owen, 2012, Methods in enzymology.

Differential nanoscale organisation of LFA-1 modulates T-cell migration

Michael J. Shannon, David J. Williamson, J. Griffié, 2019, Journal of Cell Science.

Quantitative fibre analysis of single-molecule localization microscopy data

Juliette Griffié, Garth L Burn, Dylan M Owen, 2018, Scientific Reports.

Multicolor lifetime imaging and its application to HIV-1 uptake

David J. Williamson, S. Padilla-Parra, I. Carlon-Andres, 2023, Nature communications.

Correction of multiple-blinking artifacts in photoactivated localization microscopy

David J. Williamson, D. Sage, Patrick Rubin-Delanchy, 2022, Nature Methods.

PRODAN differentially influences its local environment.

David J. Williamson, C. Lorenz, D. Owen, 2018, Physical chemistry chemical physics : PCCP.