[HTML][HTML] Quantitative fluorescence loss in photobleaching for analysis of protein transport and aggregation

D Wüstner, LM Solanko, FW Lund, D Sage… - BMC …, 2012 - Springer
Background Fluorescence loss in photobleaching (FLIP) is a widely used imaging
technique, which provides information about protein dynamics in various cellular regions. In …

[PDF][PDF] Measurement of rapid protein diffusion in the cytoplasm by photo-converted intensity profile expansion

RG Sadovsky, S Brielle, D Kaganovich, JL England - Cell reports, 2017 - cell.com
The fluorescence microscopy methods presently used to characterize protein motion in cells
infer protein motion from indirect observables, rather than measuring protein motion directly …

Non-rigid contour-based registration of cell nuclei in 2-D live cell microscopy images using a dynamic elasticity model

DV Sorokin, I Peterlik, M Tektonidis… - IEEE transactions on …, 2017 - ieeexplore.ieee.org
The analysis of the pure motion of subnuclear structures without influence of the cell nucleus
motion and deformation is essential in live cell imaging. In this paper, we propose a 2-D …

Diffeomorphic multi-frame non-rigid registration of cell nuclei in 2D and 3D live cell images

M Tektonidis, K Rohr - IEEE Transactions on Image Processing, 2017 - ieeexplore.ieee.org
To gain a better understanding of cellular and molecular processes, it is important to
quantitatively analyze the motion of subcellular particles in live cell microscopy image …

Non-rigid multi-frame registration of cell nuclei in live cell fluorescence microscopy image data

M Tektonidis, IH Kim, YCM Chen, R Eils… - Medical image …, 2015 - Elsevier
The analysis of the motion of subcellular particles in live cell microscopy images is essential
for understanding biological processes within cells. For accurate quantification of the particle …

Denoisereg: Unsupervised joint denoising and registration of time-lapse live cell microscopy images using deep learning

K Celikay, VO Chagin, MC Cardoso… - 2022 IEEE 19th …, 2022 - ieeexplore.ieee.org
Image registration is important for analysing time-lapse live cell microscopy images.
However, this is challenging due to significant image noise and complex cell movement. We …

Model-based alignment of look-locker MRI sequences for calibrated myocardical scar tissue quantification

M van de Giessen, Q Tao… - 2013 IEEE 10th …, 2013 - ieeexplore.ieee.org
The characterization of myocardial scar tissue in Late Gadolinium Enhancement (LGE) MRI
volumes is hampered by the nonquantitative nature of MRI image intensities. Using the …

[PDF][PDF] Совмещение изображений флуоресцентной микроскопии для компенсации движения живых клеток: обзор

ДВ Сорокин - GraphiCon 2017, 2017 - graphicon.ru
Совмещение изображений является базовой задачей в области обработки и анализа
микроскопических изображений живых клеток. С помощью совмещения изображений …

Combining magnetic resonance late gadolinium enhanced and Look-Locker sequences for myocardial scar characterization

Q Tao, M van de Giessen, S Piers… - 2013 IEEE 10th …, 2013 - ieeexplore.ieee.org
Characterization of myocardial scar has important diagnostic and prognostic value for
treatment of post-infarction patients. Late gadolinium enhanced (LGE) MR visualizes …

[引用][C] Signature redacted

RG Sadovsky - 2016 - Massachusetts Institute of …