Dysregulation of cellular membrane homeostasis as a crucial modulator of cancer risk
A Erazo‐Oliveras, M Muñoz‐Vega… - The FEBS …, 2024 - Wiley Online Library
Cellular membranes serve as an epicentre combining extracellular and cytosolic
components with membranous effectors, which together support numerous fundamental …
components with membranous effectors, which together support numerous fundamental …
Biochemical Pathways of Cellular Mechanosensing/Mechanotransduction and Their Role in Neurodegenerative Diseases Pathogenesis
In this review, we shed light on recent advances regarding the characterization of
biochemical pathways of cellular mechanosensing and mechanotransduction with particular …
biochemical pathways of cellular mechanosensing and mechanotransduction with particular …
Multicolor Tuning of Perylene Diimides Dyes for Targeted Organelle Imaging In Vivo
Z Yang, X Li, T Sun, J Bian, X Bu, X Ge, J Sun… - Analytical …, 2024 - ACS Publications
The adjustment of the emission wavelengths and cell permeability of the perylene diimides
(PDI) for multicolor cell imaging is a great challenge. Herein, based on a bay-region …
(PDI) for multicolor cell imaging is a great challenge. Herein, based on a bay-region …
Label-free Super-resolution Microscopy for Long-term Monitoring the Dynamic Interactions of Cellular Organelles
L Shao, M Sun, J Zhang, H Xu, H Yang, H Li… - Chemical Research in …, 2024 - Springer
The ideal method for imaging living cells is one that allows for long-term, label-free
observation in real-time with super-resolution capabilities. Such a method would overcome …
observation in real-time with super-resolution capabilities. Such a method would overcome …
Local ionic conditions modulate the aggregation propensity and influence the structural polymorphism of alpha-synuclein
Parkinson's Disease (PD) is characterized by the aggregation of alpha-synuclein (aSyn), a
presynaptic protein that transitions from a disordered monomer into beta-sheet rich amyloid …
presynaptic protein that transitions from a disordered monomer into beta-sheet rich amyloid …
Super-resolution Fluorescence Imaging
HH Han, XP He - 2024 - books.rsc.org
Currently, our knowledge of living systems has been extended to the level of individual cells
and molecules, which makes the real-time visualization of subcellular structures and the …
and molecules, which makes the real-time visualization of subcellular structures and the …
Diffusive interactions play an important role in protein stability and mobility: Investigations of the intracellular milieu using in-cell NMR
T Sörensen - 2022 - diva-portal.org
Proteins are crucial for all cellular life. Every signal received by a cell, and every response to
it, is mediated by proteins. Inside cells, these proteins diffusively sample each other's …
it, is mediated by proteins. Inside cells, these proteins diffusively sample each other's …
Application of super-resolution microscopy in the study of organelle interactions (invited)
D Taiqiang, G Ye, M Ying, C Bolei, L Fuwei… - Infrared and Laser …, 2022 - irla.cn
Observing dynamic interaction between organelles and analyzing the law of action is of
great significance for revealing the mechanism behind the phenomenon of physiological …
great significance for revealing the mechanism behind the phenomenon of physiological …
[HTML][HTML] Computational Methods for the Study of Peroxisomes in Health and Disease
N van Wijk, M Linial - The Metabolic Role of Peroxisome in Health …, 2022 - intechopen.com
Peroxisomal dysfunction has been linked to severe human metabolic disorders but is also
linked to human diseases, including obesity, neurodegeneration, age-related diseases, and …
linked to human diseases, including obesity, neurodegeneration, age-related diseases, and …
[图书][B] Characterizing the Function of Neuronal Cells Derived from Induced Pluripotent Stem Cells Made from Patients with Lowe Syndrome
J Barnes - 2022 - search.proquest.com
Lowe Syndrome (LS) is a rare, X-linked disorder that occurs in 1 in 500,000 males. It is
typically caused by loss of function mutations in the gene OCRL, which codes for an inositol …
typically caused by loss of function mutations in the gene OCRL, which codes for an inositol …