Significados de cryo-electron tomography en inglés

Using cryo-electron tomography, we present the first structure-based localization model of the CSC.

The biggest challenge in cryo-electron tomography is the low signal-to-noise ratio.

Since the mid 2000s, cryo-electron tomography has provided us with new knowledge, concepts, and questions in the area of cilia research.

Using cryo-electron tomography and subtomogram averaging, we visualized the three-dimensional structure of the radial spokes in Chlamydomonas flagella in unprecedented detail.

However, the technology advances in cryo-electron tomography (CET) have made methods to identify proteins from their surface shapes extremely useful.

After negative staining and from preliminary studies by cryo-electron tomography, no clear evidence could be found for actin filament branching in lamellipodia.

The scientists used cryo-electron tomography, where cells are flash frozen, imaged from a variety of angles, then turned into a 3D image by a computer.

Cryo-electron tomography enabled us such a 3D structural analysis.

Cryo-electron tomography of phage 'infecting' outer membrane vesicles shows the tail needle contacting and indenting the outer membrane.

Cryo-electron tomography has been a valuable tool in the analysis of 3D structures of cilia at molecular and cellular levels.

Cryo-electron tomography shows ordered binding of part of the flexible receptor to the viral surface, with distal domains in multiple conformations.

Cryo-electron tomography of snap-frozen intact cells will be required to finally clarify the three-dimensional arrangement of actin filaments in lamellipodia in vivo.

Cryo-electron tomography revealed that the densities of two inner dynein arms were missing from at least 2 doublet microtubules in the axonemal structure.