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By targeted metabolomics and isotope tracing experiments in loss- and gain-of-function cell and mouse models of Slc22a1, we uncovered a role of SLC22A1 in the efflux of acylcarnitines from the liver to the circulation.
In this study, we uncovered a role of LRRK2 in modulating the innate immune response in macrophages.
The same study then also uncovered a role of Sir2 for the efficient retention of aggregates by mother cells and the clearance of daughter cells from aggregates via polarisome-dependent retrograde transport along actin cables.
Second, we uncovered a role of the PI3K-Akt pathway in hSKPs.
We have also uncovered a role of X-linked inhibitor of apoptosis protein in the regulation of endogenous Par-4 levels through inhibition of caspase-mediated cleavage.
Our findings revealed the essential roles of GATA2 in EHT and granulocyte development through regulating SPI1, and uncovered a role of Notch signaling in granulocyte generation during hematopoiesis modeled by human ESCs.
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Mechanistic studies further uncovered a role for SUMOylation of the PAF1 complex component, parafibromin (CDC73), in potentiating antiviral gene expression.
Our data uncover a role of keratins, which to our knowledge is previously unreported, in the maintenance of HDs upstream of plectin, with implications for epidermal homeostasis and pathogenesis.
Together, our results uncover a role of LRRK2 in modulating innate immunity by enhancing the signaling strength of the Nod2-Rip2 pathway.
By uncovering a role of the src-substrate cortactin in AChR clustering this study suggests a previously unappreciated way by which src could regulate AChR aggregation at the NMJ.
However, these screens failed to uncover a role of DUBs in the regulation of Notch signaling, probably attributable to the fact that many DUBs exhibit pleiotropic effects in early development.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com