[HTML][HTML] Quantitative fluorescence loss in photobleaching for analysis of protein transport and aggregation
Background Fluorescence loss in photobleaching (FLIP) is a widely used imaging
technique, which provides information about protein dynamics in various cellular regions. In …
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
The fluorescence microscopy methods presently used to characterize protein motion in cells
infer protein motion from indirect observables, rather than measuring protein motion directly …
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
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 …
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 …
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 …
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 …
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 …
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 …
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 …
treatment of post-infarction patients. Late gadolinium enhanced (LGE) MR visualizes …