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This process is largely accomplished through the function of importin proteins [1], which mediate the active import of protein cargoes through the nuclear pore complex [2].
It has been also demonstrated in model simulations that dual oscillations (i.e. subset of cells fire synchronously during a given gamma cycle) mediate the active maintenance of multiple short-term memories.
Carbon monoxide and NO may mediate the active decrease in energy demand that occurs in cells that lack oxygen [ 42, 43].
These integral membrane proteins mediate the active extrusion of antibiotics and toxic compounds from cells.
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The sodium/iodide symporter (NIS) is a plasma membrane glycoprotein that mediates the active transport of iodide in the thyroid and other NIS-expressing cells.
The dopamine transporter (DAT) plays a key role in the regulation of dopaminergic neurotransmission by mediating the active reuptake of synaptic dopamine.
Inhibition experiments in choroidal cell monolayers pointed to apical Slc22 carriers, likely Slc22a8, as mediating the active efflux of antiviral nucleoside analogs across the blood-CSF barrier [ 57].
In this study, we have reported a novel regulatory pathway mediating the active removal of prevailing prosurvival protein Survivin during the onset of apoptosis by the impairment of nuclear export machinery.
We further investigated the expression of ABCB1, which is the first ABC transport identified [ 19], ABCC2, which mediates the active efflux of glutathione-conjugated cisplatin [ 20], and GST-Pi.
It also assist to mediate the biodistribution of active compounds, drug loading, drug targeting, transport, release, and interaction with biological barriers.
Here, we discuss novel data that point to the ability of MyoD1 to mediate the assembly of active enhancers that augment the transcription of genes essential for muscle development and lineage specification.
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CEO of Professional Science Editing for Scientists @ prosciediting.com