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In four exocyst mutant lines with the most severe root growth defects (exo84b-1, sec8-3, sec8-4, and sec8-4 exo70A1), we predicted a more profound alteration in the distribution/pattern of DR5 expression if the exocyst mutant's slower root growth was due to a defect in auxin response in the stem cell niche or MZ.
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Cerebral autoregulation, however, has been shown to be influenced by carbon dioxide levels in patients with septic shock, with more profound alterations in autoregulation detected in hypercapnic (pCO2 > 40 mmHg) than hypocapnic (pCO2 < 40 mmHg) patients[14].
More profound alterations and a higher incidence of structural defects in HLA Class I expression were found in post-BCG-recurrent tumors.
It would seem to me overall, that as a whole the metabolic effects of CR in table 3, are much attenuated in the GHRko mice, i.e. WT mice have much more profound alterations in metabolic parameters in response to CR than do GHRko mice to CR.
Together, in addition to an altered phosphorylation pattern, inhibition of CD11b/CD18-mediated CD11b/CD18-mediatedcts the expression levels of the kinadherenceng TPalsoduced differentiaffectsuggestheg much morexpression alevelsiofs in the overall cell function and fate since phosphorylation signals can be adapted and changed much faster than a kinasesprotein expression profile.
This increase in the number of new neurons has been associated to some beneficial effects on cognitive functions and affective behavior, thus raising the key question to which extent this experience-dependent form of plasticity may also involve more profound alterations in the connectivity of newly-generated neurons.
This is also logical diffuse patterns of inflammation that are likely to reflect a more profound physiologic alteration than a more specific inflammatory response.
The more severe the insult, the more profound is the alteration and the more chance the patients have to develop adverse clinical outcome.
These alterations are more profound in postural, "antigravity" muscles and, to a lesser extent, in muscles involved in fast movements [ 3, 4].
Transcriptomic alterations were more profound in STZ-WKY than in GK and involved largely non-overlapping sets of genes, thus underlining the importance of investigating gene expression in very different, but complementary, contexts of diabetes aetiology and pathogenesis.
WM alterations are much more profound in the hereditary SVDs such as CADASIL and CARASIL.
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