The LA-ICP-MS method presented here fulfils these requirements, and will facilitate interpretation of changes in element supply and incorporation, as well as the comparison between different regions via concretion analyses.
The BES-tagging data presented here redefine the requirement for a minimal BES, which appears only to entail functional copies of ESAGs 1, 2 and 6, although ESAG1 is not essential within an active BES [16], [17] and ESAG2 is absent from the BES encoding SRA, the T. b. rhodesiense gene able to confer resistance to human serum in infections [36].
Because all non-redundant genes are advantageous, and all combinations are allowed, in contrast to models like the hypercycle [ 19] or the Stochastic Corrector Model [ 21], the model presented here has no requirement for a specific combination of genes to be present for the system (i.e. cells) to operate.
However, we are not aware of a true, heralded source of single photons that meets the requirements of repetition rate and pulse width presented here.
In fact, the linear geometry of the glottis presented here is not a requirement of the current study, rather, it is assumed to simplify analytical integration calculations and does not essentially affect the onset mechanism described below.
This study presented here identifies an endogenous requirement for notch1b in development of the mCP and a functional role for any Notch ligand (dla and dld) in the mCP.
The results presented here demonstrate an absolute requirement for Gab1 in EGF-induced activation of the PI-3 kinase/Akt signaling pathway.
The optimised method presented here considerably reduces the input requirements for performing native ChIP-seq.
The mathematical model presented here exhibits many of the requirements of such a theoretical investigation, although it does not currently represent adequate regions of the host anatomy.
Not an absolute requirement, but rather a suggestion: the PRIME method presented here makes heavy use of MOMA.
