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We found a depletion of complex III and IV concentrations and relative increases in functional capacities of complex II and glycerol-3-phosphate dehydrogenase/complex III.
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The operation of all these soil processes regulated by B. aryabhattai strains resulted in a depletion of organically complexed and calcium carbonate bound zinc and an increase in exchangeable and sesquioxide bound zinc in soil.
In Madin-Darby canine kidney (MDCK) cells, siRNA-mediated reduction of DPAGT1 expression by only 40% results in a striking depletion of complex N-glycan modification of E-cadherin (Nita-Lazar et al. 2010).
Due to a lack of stability in the actin network caused by a depletion of cortactin, tubulobulbar complexes may not be able to elongate and acquire or maintain normal length and thereby fail to internalize the same amount of junctional membrane.
The resultant loss of polyadenylation causes a differential modulation of steady-state levels of specific mt-mRNAs and perturbs mitochondrial protein synthesis leading to profound depletion of complexes I and IV of the respiratory chain, resulting in a form of spastic ataxia and optic atrophy.
Because we have not used an alternative method of measuring mitochondrial content (e.g., electron microscopy), we cannot say whether the depletion of complexes III and IV occurred in isolation or as part of mitochondrial depletion.
The ability of aerobic ATP synthesis (OXPHOS) was reduced to ~54%% in ICU patients (p<0.01), in correlation with the depletion of complexes III (~38 % of control, p = 0.02) and IV (~26%% of controls, p<0.01) and without signs of mitochondrial uncoupling.
Quantitative analysis of western blotting revealed that double-siRNA treatment resulted in a more extensive depletion of Ska complex components than single-siRNA treatment, particularly when depletion efficiency was assessed at relatively early time points (Supplementary Figure 5A and B).
Failure of A-Complex recruitment due to mutation in the BRCT motif, or depletion of A-Complex components including BRCC36/45 (deubiquitinylases) would alter the chromatin ubiquitinylation pattern.
Despite the fact that CenH3CID levels at the centromeres were not altered by CHD1 depletion, it was possible that the association of CenH3CID with the chromatin was perturbed in a way similar to what has recently been reported for human CenH3CENP-A upon depletion of the chromatin remodeling complex RSF [21].
Accordingly, depletion of respiratory complex proteins has been described in the diaphragm in a rat model of sepsis [ 20].
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