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Molecular complexity is becoming a crucial concept in drug discovery.
This, in all its molecular complexity, is what the bulging end of a single neuron looks like.
The thing is, none of this molecular complexity is present in the Lewis model.
Understanding of its molecular complexity is incomplete and there is a need to identify new therapeutic targets and to optimize criteria for its diagnosis, assessment and prognosis.
This molecular complexity is mirrored by the manifold roles of FGF signaling in vertebrate physiology, ranging from mesoderm induction during gastrulation to control of hair follicle growth in postnatal life (82, 83).
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Synthetic scaffold modifications leading to an increase in molecular complexity were studied.
Through the analysis of various reference compound databases, common pitfalls and workarounds of the quantification of molecular complexity are discussed.
It is found that simple molecules, such as propane and propene, are the optimal ORC working fluids for a low-grade (150 °C) heat source, whilst molecules with increasing molecular complexity are favoured at higher temperatures.
A simple numerical method for seekingsolitary wavesolutions of a permanent profile in molecular systems of big complexity is presented.
These recursive clauses (called "truth conditions") can be reapplied until the truth of a non-elementary, molecular sentence of arbitrary complexity is reduced to the truth or falsehood of its elementary, atomic constituents.
Different oligos have such drastically different annealing and ligation efficiency especially since they can also form various inter- and intra-molecular interactions when the complexity is increased.
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morphological complexity is
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moderate complexity is
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genomic complexity is
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