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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2012, Volume 109, Issue 16, pp. 6136 - 6141
Microscopic images of specific proteins in their cellular context yield important insights into biological processes and cellular architecture. The advent of... 
Mitochondria | Microscopy | Imaging | Correlatives | Cell lines | Fluorescence | Nuclear membrane | Mitochondrial DNA | P branes | Ion beams | Cryosection | Photoactivated localization microscopy | Electron microscopy | Correlative microscopy | OXIDATIVE-PHOSPHORYLATION | photoactivated localization microscopy | mitochondrial DNA | MULTIDISCIPLINARY SCIENCES | RESOLUTION | TRANSCRIPTION | NEWLY SYNTHESIZED PROTEINS | SECTIONS | OPTICAL RECONSTRUCTION MICROSCOPY | cryosection | ORGANIZATION | DNA | IN-VIVO | DYNAMICS | correlative microscopy | electron microscopy | Mitochondrial Proteins - ultrastructure | Mitochondria - ultrastructure | DNA-Binding Proteins - metabolism | DNA, Mitochondrial - genetics | Mitochondria - genetics | Mitochondrial Proteins - metabolism | Imaging, Three-Dimensional | Fibroblasts - metabolism | Reproducibility of Results | DNA, Mitochondrial - metabolism | High Mobility Group Proteins - metabolism | DNA, Mitochondrial - ultrastructure | Mitochondria - metabolism | DNA-Binding Proteins - genetics | Microscopy, Interference - methods | Mitochondrial Membranes - metabolism | Animals | Microscopy, Electron - methods | Microscopy, Fluorescence - methods | Mitochondrial Membranes - ultrastructure | Luminescent Proteins - genetics | Fibroblasts - cytology | Mice | 3T3 Cells | High Mobility Group Proteins - genetics | Luminescent Proteins - metabolism | Physiological aspects | Research | Membranes (Biology) | Methods | Biological Sciences
Journal Article
Methods and Applications in Fluorescence, ISSN 2050-6120, 07/2018, Volume 6, Issue 4, pp. 045002 - 045002
Superresolution microscopy based on localisation is usually performed in a buffer containing enzymatic oxygen scavenger, which facilitates reversible... 
STORM | correlative microscopy | AFM+STORM | imaging buffers | fluorescent probes | localisation microscopy | SYSTEM | LOCALIZATION | CHEMISTRY, ANALYTICAL | AFM plus STORM | CHEMISTRY, PHYSICAL | OPTICAL RECONSTRUCTION MICROSCOPY
Journal Article
Journal Article
JOURNAL OF GENERAL PHYSIOLOGY, ISSN 0022-1295, 08/2019, Volume 151, Issue 8, pp. 974 - 985
The plasma membrane separates a cell from its external environment. All materials and signals that enter or leave the cell must cross this hydrophobic barrier.... 
LOCALIZATION MICROSCOPY | SYNAPTIC VESICLES | PHYSIOLOGY | MOLECULAR SOCIOLOGY | CLATHRIN LATTICE | CRYOELECTRON TOMOGRAPHY | TISSUE SECTIONS | ACTIN CYTOSKELETON | RESOLUTION LIMIT | EMBEDDING MEDIUM | CORRELATIVE SUPERRESOLUTION FLUORESCENCE | Plasma | Hydrophobicity | Microscopy | Electron microscopy | Organelles
Journal Article
Methods in Cell Biology, ISSN 0091-679X, 2017, Volume 140, pp. 165 - 185
Atomic force microscopy (AFM) is becoming increasingly used in the biology field. It can give highly accurate topography and biomechanical quantitative data,... 
Atomic force microscopy | Scanning electron microscopy | Superresolution fluorescence microscopy | Transmission electron microscopy | Cell elasticity | Correlative microscopy | VISUALIZATION | CELLS | STIMULATED-EMISSION | SINGLE | FLUORESCENCE | CYTOSKELETON | RESOLUTION | ULTRASTRUCTURE | SURFACE<