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In this study, we generated iPSCs from a patient with dilated cardiomyopathy (DCM) caused by a missense mutation S635A in RNA-binding motif protein 20 (RBM20) and investigated the functionality and cell biology of cardiomyocytes (CMs) derived from patient-specific iPSCs (RBM20-iPSCs).
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Here we sought to identify and investigate the functionality of T-UCRs differentially expressed in NB cell lines following ATRA-treatment.
This study systematically investigated the functionality and mechanism of miR-26a and miR-26b in estrogen-promoted ER+ breast cancer cell proliferation.
Here we investigated the functionality of the two GH7 cellobiohydrolases and focus on whether the CBD domain is an essential domain for typical cellobiohydrolase function.
In addition, we also investigated the functionality of the ancestral form of TRPV6 and the putatively-selected, derived form of TRPV6.
Group 5 investigated the functionality of future SNS such as Facebook.
In this connection, we investigated the functionality of IL-12R on in vitro expanded NBEC since immunohistochemical studies disclosed IL-12Rβ2 expression in NBEC surrounding the tumor.
In addition, we investigated the functionality of SR Ca2+ ATPase (SERCA) pumps, which serve as an important SR Ca2+ sequestration pathway.
We then investigated the functionality of such pathways through direct chemical stimulation of the InM.
Next, we investigated the functionality of our suicide vector pLtBid INS 2R in the context of infectious HIV-1 particles.
Next, we investigated the functionality of p35 expressed in the adenovirus-infected tumor cells, as judged by its inhibition of both basal and CPA-induced caspase activity.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com