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On average, the antisense piRNA populations for these elements are 11.7% of those in the wild type, with the sense populations varying from 21 to 100% of those in wild type.
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In a strict sense, population size matters.
The quorum-sensing system from Vibrio fischeri [ 41, 42] enables cells to sense population density through a transcription factor protein LuxR which acts as a transcriptional activator of gene lacI when a small organic molecule, autoinducer (AI), binds to it.
In light of the identification of GK expression within additional neuronal and non-neuronal glucose-sensing populations [3,30,31], it is at present unclear whether NPY and ORX cells types represent first-order targets of GSN action.
We illustrate the concept by delineating the ZOI in three Indian PAs – Kanha, Ranthambore, and Nagarahole – using remote sensing, population census, and field data.
This makes intuitive sense; large populations will produce more mutations but fix fewer of them while small populations will produce few mutations but fix more of them.
This only makes sense for populations that are clearly distinguishable.
On average, the sense piRNA populations for these transposon families are 9.6% of those in the wild type.
In this sense, each population may consist of multiple "populations" if individuals are rarely outcrossing.
In that sense, the population mean adoption outcome measured by the ATE parameter is the population mean potential adoption outcome.
In a sense, as population ageing is almost an unavoidable fact of modern society, the policy of never-ending population growth merely postpones the inevitable problem, possibly a more severe one, to future generations.
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