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Through these mechanisms, the SWI/SNF complexes have powerful effects on transcriptional regulation, serving an important role in development through the coordinate activation and repression of critical gene expression programs.
Within an animal many genes act by coordinate activation and repression of specific biological pathways to elicit cumulative effects on the muscling trait.
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This plasticity is tightly regulated during embryonic development and mediated by the exquisitely coordinated activation and repression of groups of genes.
Taken together, coordinated activation and signaling through the complement system and the FcR system in a hierarchical manner leads to inflammation.
We propose that a network of transcription regulators and nuclear receptors including PPARG-target genes, INSIG1, and THRSP, coordinate activation of adipocyte differentiation and lipid synthesis.
We propose that a network of transcription regulators and nuclear receptors including PPARG-target genes, INSIG1, and THRSP, coordinate activation of adipocyte differentiation and lipid filling at an early age.
Nonetheless, the levels of activity achieved by the coordinate activation of endogenous ActRIIA and BMPRII homodimers in wild-type conditions may be sufficient to elicit a chemotactic response.
TNFR2 induction in TECs in organ culture results in a reciprocal coordinate activation of Etk, VEGFR2, and NF κB and promotes cell cycle entry (indicated by expression of nuclear phospho-Histone H3S10 and ki67), leading to activation of the PI3K/Akt pathway [ 47]. ki67-positive staining has been proposed as an independent prognostic factor for RCC [ 77, 78].
In light of the coordinate activation of both autophagic and apoptotic signals by PUMA and Bax, we examined whether autophagy could impact the apoptotic response.
As AKT activation but not MAPK is dependent on coordinate activation of EGFR, MET, and AXL, we investigated whether combination inhibition of PI3K and MAPK has additive or synergistic anti-proliferative effects in mesothelioma.
We propose that a network of transcription regulators and nuclear receptors, including SREBF1, SREBF2, PPARG, INSIG1, and PPARGC1A, coordinate activation of the genes driving the lipid synthesizing machinery.
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