The endoplasmic reticulum (ER) is a compartment (organelle) in eukaryotic cells that consists of membrane sacs called cisternae. Because of the bound ribosomes, the 'rough' ER is the site of ...

Department of Chemistry, Indian Institute of Technology Gandhinagar, Palaj, Gandhinagar, Gujarat 382355, India ...

Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug ...

In Zika-infected cells, ANKLE2 clusters in pockets around the endoplasmic reticulum, a network used for protein production within the cell. Viral NS4A interacts with ANKLE2 to form pockets off the ...

The swollen axon segments or dystrophic axons were used as indicators of axonal injury and were identified with antibodies against axon-specific proteins under confocal microscopy ... mitochondrial, ...

We further verified the interaction between p30 and host proteins by laser confocal microscopy, co-immunoprecipitation ... ribosomal small subunit, polynucleosome, rough endoplasmic reticulum membrane ...

Abstract: The theory of the confocal resonator is extended to include the effect of unequal aperture size and unequal radii of curvature of the two reflectors. The latter is equivalent to a periodic ...

In flies defective for axonal transport of mitochondria, the authors report the upregulation of one subunit, the beta subunit, of the heterotrimeric eIF2 complex via mass spectroscopy proteome ...

Timlapse microscopy was performed with spinning disk confocal microscopy as described in Lewis et al. (2019). For all the above experiments, mitotic duration time was analyzed manually from prophase ...

Peer ReviewDownload a summary of the editorial decision process including editorial decision letters, reviewer comments and author responses to feedback. Disorders of surfactant protein biology cause ...

The paper investigates a potential cause of a type of severe epilepsy that develops in early life because of a defect in a gene called KCNQ2. The significance is fundamental because it substantially ...