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There was an increase in mitochondrial electron transport (GO 0006120), which includes NADH-dehydrogenase genes and NADH-plastoquinon oxidoreductase subunits, both members of Complex I of the electron transport chain, known to be high producers of reactive oxygen species (ROS) [ 52].
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Gtr2 and Ego3 are both members of complexes, Gtr1/ 2 and Ego1/ 3. Normally one would expect that abolishing one member of a two-member complex would generate a functional phenotype similar to abolishing the other member.
But because amino acid replacements in the TF are permissive for mutations in the RE, and subsequent RE mutations are permissive for replacements in the protein, both members of the complex can explore regions of their own sequence space and reach genotypes that were not previously available to either.
In the current study, T. denticola and T. forsythia, both members of the red complex, did show significant association with periodontitis, which is consistent with the literature.
More recently, two mTOR kinase domain inhibitors (TORKinibs; AZD8055 and INK128) targeting both members of the mTOR complex (mTORC1 and mTORC2), have been developed and are currently being evaluated in several clinical trials [ 6, 7].
Together, these studies identified the components of the TBM-specific 30 kD antigen: two mycobacterial antigens, Rv 3804c and Rv1886c (Ag 85 A and B respectively, both members of Ag 85 complex), and one host-derived protein (immunoglobulin [Ig] Kappa light chain VLJ region; accession no. BAC01690.1) [ 16].
Analysis of peptide evolutionary rates between Cxqdsx and Cxpipdsx (both members of the Culex pipiens complex) shows the male-specific portion of the transcript to have evolved rapidly with respect to female-specific and common regions.
Another instance of this cooperative functional role of repressive modifications in XCI involves the histone variant macroH2A as well as Cullin3 and SPOP (both members of an E3 ligase complex that ubiquitinates macroH2A) [ 21, 22].
C. jejuni 81 176 and isolates 1967 are both members of the ST-42 clonal complex.
Clade 1 basal lineages were sourced from the south central part of the island and most were obtained from P. mooreana and P. tohiveana, both members of the P. suturalis species complex [ 23].
Moorean Clade 3 was almost exclusively (36/40 snails) composed of P. suturalis (including nominal subspecies) and P. aurantia, both members of the P. suturalis species complex [ 23, 32] that readily hybridized in the laboratory [ 22].
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