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As previously demonstrated, Plk4 induction promotes the accumulation of centrosomal proteins such as hSAS-6 and CPAP around the mother centriole [3].
However, HIF-2 α induction promotes cell cycle progression by enhancing c-Myc function.
Other studies uncovered that angiogenic induction promotes neurogenesis, synaptogenesis, axonal sprouting and neuroblast migration to the lesion and further contributes to neurological recovery [ 51].
Because VEGF induction promotes tumour growth (Mohle et al, 1997; Khorana and Fine, 2004; Gorelick et al, 2009), thrombocytosis indirectly reflects tumour progression.
This induction promotes the expression of the antiapoptotic gene Bcl-2 and inhibits the expression of the proapoptotic gene Bax [ 21].
Because VEGF induction promotes tumour growth [ 74, 78], thrombocytosis indirectly reflects tumour progression; a high level of VEGF is found in serum, platelets, and leukocytes of patients with malignant disease [ 79], and platelet interactions with malignant cells promote metastasis [ 80].
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Nanog induction promoted reprogramming at high frequency (∼300 colonies/million NSCs fused) as previously reported (Silva et al., 2006, 2009).
Testosterone administration had a modest protective effect by offsetting SG shrinkage, reducing cleaved capase-3 induction, promoting SG AR activity and increasing FASN expression.
This supports that PIN1 might be involved in AR induction, promoting auxin lateral efflux from the hypocotyl vasculature towards the pericycle founder cells.
During reception, transduction and induction promoted by ABA in Arabidopsis several enzymes, proteins and small molecules are activated or inhibited within the cell.
Under these latter experimental conditions of prolonged treatment with oxalate, a slight induction of proliferation was observed in normal breast cells line but of a smaller magnitude than the induction promoted by treatment of these cells with FBS plus EGF.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com