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The encoded protein product is a phosphoprotein that travels between the nucleus and cytoplasm, which plays multiple roles in ribosomal RNA (rRNA) processing, ribosome assembly, transport of ribosomal subunits, centrosome duplication, regulation of p53, and cell growth and proliferation [ 5– 7].
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The purpose of negotiations is to achieve coherence between standards and avoid the duplication of regulation and process.
Finally, analysis of the mechanisms by which kallikreins are elevated in GBM, albeit by gene duplications, hormonal regulation, epigenetic changes, or other means, will be of interest and potentially important to understanding the differential expression and outcomes these novel serine proteases exert across a wide range of malignancies.
The pre-duplication orthologs of genes from the neo-functionalized class are most prominent in the 'unchanged' Module 3 and mildly induced Module 4 (Hyper-geometric test, p<10−3), suggesting that genes that were not regulated in glucose depletion prior to duplication, 'gain' such regulation de novo post-duplication, for at least one paralog.
It appears that the COX isoforms all arose through gene duplication and the regulation of complex IV activity occurs in-part through the expression of different isoforms of the nuclear-encoded subunits in different tissues and in response to different physiological conditions (for an extensive review, see Arnold 2012b).
AURKA, BRCA1, CCNE1 and CDK2 genes play pivotal roles in centrosome duplication and cell-cycle regulation.
Here, I review our understanding of Hox cluster architecture in different vertebrates and consider the implications of gene duplication for Hox gene regulation and function and the evolution of different body plans.
scMob1 binds Mps1p, a protein kinase essential for spindle pole body duplication and mitotic checkpoint regulation, which in turn plays a role in maintaining genome stability, again providing biological plausibility for loss of MOB3B in cancer.
Finally, global estimates on the processes maintaining the genetic and functional diversity in the samples (e.g. transposition, transfer, molecular regulation and duplication) can also be obtained by counting the relative proportions of OGF with duplicated sequences, homology to transposons[ 101, 109], phages[ 22, 33] or plasmids[ 110], or harbouring toxin/antitoxin systems[ 111].
This finding may be explained by three scenarios: 1) repeats are intrinsically involved in the gene family expansion process, 2) repeats accumulated immediately after the duplication to promote allelic regulation and 3) repeats accumulated as a result of an increase in tolerance due to an increase in redundancy.
High fitness and adaptation of diatoms to various Si levels in marine environments might arise in part by global regulations from gene (expression level) to genomic (organization in clusters, dosage compensation by gene duplication), and by post-transcriptional regulation and spatial distribution of SIT proteins.
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