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Topf, U. et al. Quantitative proteomics identifies redox switches for global translation modulation by mitochondrially produced reactive oxygen species.
These previous data indicate a conserved mechanism of translation modulation by organizing ribosomes into resting higher-order assemblies.
The long-range RNA-RNA interaction of the 5′- and 3′-UTRs which is mediated by direct interaction of the 5′- and 3′-UTRs or by trans factors, is thought to play a role in viral translation modulation and in the switch from protein synthesis to RNA replication.
This observation therefore suggests that the mTOR pathway mediates some of the translation modulation effects induced by Myc.
Given the heterogeneous nature of cancer, it is unlikely that transcription and translation modulation is homogenous in different cancers.
At present, it is largely unknown whether beyond the global enhancement of protein synthesis, Myc activation results in translation modulation of specific genes.
Similar(52)
Similar ideas led to the development of transforms based on groups generated by translations, modulations, and dilation of a mother wavelet [25].
Our approach is to first define generalized convolution, translation, and modulation operators for signals on graphs, and explore related properties such as the localization of translated and modulated graph kernels.
Both transformations intertwine translation with modulation, and both rely on a new group-theoretic tool: for a closed subgroup Γ⊆G, we produce a measure on the space Γ\G of right cosets that gives a measure space isomorphism G≅Γ×Γ\G.
In order to obtain a translation and modulation invariant operator on the space of signals, the corresponding operator on the reproducing kernel space of Gabor transforms must be left-invariant, i.e. it should commute with the left-regular action of the reduced Heisenberg group Hr.
Let (T_{b}f( cdot )=f( cdot -b)) and (M_{a}f( cdot )=e^{2pi i a cdot}f( cdot)), (a,binmathbb {R} ^{n} ) denote the translation and modulation operators, respectively.
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