The phrase "all possible complexes" is correct and usable in written English.
It can be used when discussing a range of different combinations or structures in a specific context, such as chemistry, biology, or project management.
Example: "In our research, we aim to analyze all possible complexes that can form between the two compounds."
Alternatives: "every conceivable complex" or "all conceivable combinations".
We consider the three proteins known to participate in this inhibition: Mad2, Mad3 and Bub3, as well as all possible complexes that can be formed between them totaling to seven inhibitory factors (figure 3C).
We considered all possible complexes with RRp as possible activators (shown as RRactive).
This method can work well and is often applied [ 8- 15], but there are also cases in which the resulting models show poor accuracy when compared to a model which considers all possible complexes and reactions.
Only recently, methods have been discovered for the systematic generation and evaluation of all possible complex column configurations for the separation of multi-component mixtures.
This consideration of all four possible complexes between phosphorylated and non-phosphorylated forms of Ft and Ds is a key distinguishing feature of our model, when compared to previous computational approaches which only considered a single binding species essentially equivalent to our complex A (Abley et al., 2013; Mani et al., 2013; Jolly et al., 2014).
Researchers at our laboratory have proposed a potential link through which the SHR Y chromosome can increase sympathetic nervous system activity and adrenal TH activity (rate-limiting enzyme of the catecholamine pathway), as well as an early rise in prepubertal T, all of which suggest a possible complex interaction to yield a hypertensive phenotype in SHR animals [ 7, 14, 50].
These results imply a possible complex pathophysiology for anthrax associated shock.
The determination of a possible complex genetic interaction between alleles MDS3 and GCN1 requires further characterization of this QTL structure.
Surprisingly, the dag1gai-t6 double mutant proved embryo-lethal, suggesting an unexpected involvement of (a possible complex between) DAG1 and GAI in embryo development.
Given the depth and breath of the field of enzyme kinetics, it is surprising that the basic flux expression for the ordered ternary-complex mechanism with inhibition at all possible enzyme complexes has not been previously presented.
We reduce the problem to the case where the point x 0 has a hyperplane tangent to the boundary at the point x 0. We use Calderón's exponential solutions for all the possible complex frequencies ρ such that ρ · ρ = 0 (previously we used in Sects. 1.4 and 1.5.3 the cancellation of the real parts when taking the products).
