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To date, several studies have been published identifying temperature as a crucial parameter for protein crystallization (in addition to control of supersaturation via crystallization agent or pH).
Although the functional relationships among these outlier genes remain undetermined, observations are consistent with a previous study identifying temperature associations in a subset of these outliers and populations.
Our experiments confirm correlational studies and theoretical work, identifying temperature as an important determinant of PST epidemics (Rapilly 1979; Hau and de Vallavieille-Pope 2006).
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We used two methods for identifying temperature-sensitive mutants represented in the library.
We have therefore attempted to identify genes that mediate membrane dynamics during adult oogenesis by identifying temperature-sensitive, embryonic-lethal (TS-EL) C. elegans mutants that are both eggshell-defective (osmotically sensitive) after late larval up-shifts and adult sterile after early larval up-shifts (Eos/ Ste mutants), reasoning that both processes involve membrane trafficking.
The models consistently identified temperature and wind speed as significant factors.
The reactor design successfully met identified temperature limits for each of the transients analyzed.
The reactive distillation exhibits unique temperature sensitivities and the non-square relative gain (NRG) successfully identifies temperature control trays.
The analysis of the complex chemical equilibria helps to identify temperature zones corresponding to stability domains of certain molecules.
For example, Kurihara et al. (2009) identified temperature enhancement in the lower thermosphere in association with the auroral heating during the DELTA campaign.
For the four headstreams, we identified temperature thresholds in the time series of BFI and calculated regression relationships between temperature and BFI in the past 50 years.
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