The phrase "artificial depletion" is correct and usable in written English.
It can be used in contexts discussing the intentional reduction of resources or quantities, often in economic, environmental, or technological discussions.
Example: "The company faced criticism for its role in the artificial depletion of natural resources in the region."
Alternatives: "man-made depletion" or "intentional depletion".
In a new and stressful environment, cellular demand for Hsp90 will increase beyond its supply, mimicking the effects of artificial depletion.
If Gln is not provided exogenously tumor cells can successfully manipulate host metabolism to cover their needs, therefore artificial depletion of Gln cannot stop, or even retard, tumor growth.
A closer analysis using a transcriptional repressor, KAP1, targeted to the synthetic centromere of the artificial chromosome resulted in the depletion of CENP-C and CENP-H followed by depletion of CENP-A, thus providing more evidence for a hierarchy of centromere disassembly in which CENP-A is one of the last proteins to be removed from a centromere that is being inactivated.
A solution to the problem of groundwater-level depletion is the artificial recharging of the aquifers.
This component can measure real-time energy consumption, emulate battery depletion, and generate artificial sensor data, hence emulating real-world application scenarios.
APCs were provided by either autologous CD3 depleted (RosetteSep CD3 depletion cocktail, StemCell) HLA-A2+ (irradiated 3300 rads) PBMC for polyclonal stimulation conditions or HLA-A2+/CD80+/CD83+ K562-cell derived artificial APCs (irradiated 10,000 rads) for antigen-specific suppression assays.
There was no evidence of yttrium depletion after 2.5 million cycles in artificial aging.
If this were true, artificial destruction of centrosome cohesion by C-Nap1 depletion should be sufficient to allow centrosome separation in the absence of Plk1 activity.
In order to enlighten the molecular basis of the KIAA1524/CIP2A-mediated inhibition of PP2A, we analyzed the activity of MTORC1-associated PP2A toward an artificial phosphopeptide substrate following amino acid starvation or KIAA1524/CIP2A depletion.
Because problems with cell elongation could be caused by defects in attachment to the extracellular matrix, we compared the efficiency of a variety of adhesion molecules and artificial substrates to affect cell spreading in an EB3-depletion background.
Production of gas evolved by depletion of the formation is not practical without using artificial lift.
