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In order to initiate this type of work for PPRV we constructed a PPRV minigenome and studied its expression in transfected cells.
To understand the role of beta-1 integrin in salivary gland development we have studied its expression in human foetal tissues.
To characterize the clinical antisense sequence, we studied its expression and explored the occurrence of its off-target effects in human in vitro models of skeletal muscle and liver.
To understand when and where LIF2 acted, we studied its expression by RT-PCR analyses.
In view of the role of ALCAM dynamics in some human tumors, we studied its expression in thyroid tumors, which had not been previously explored.
To evaluate whether or not DKK-1 is produced by cancer tissues, we studied its expression on CaP and healthy tissues by RQ-PCR.
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As a preliminary step in a functional study of SPAK in IBD, it is sensible to study its expression profile.
However, it is necessary to study its expression at protein level in HCC and its biological function for HCC cell growth.
Since CD24 is also expressed on neutrophils, we aimed to study its expression in sepsis and its putative role in apoptosis.
To investigate whether JAM-A is expressed in cultured primary HBMEC and to study its expression and subcellular localization under inflammatory conditions we first performed immunocytochemical staining of primary single donor HBMEC preparations employing M.Ab.F11 for JAM-A staining, the monoclonal antibody by which JAM-A was originally identified [1].
It is therefore critical to characterize the promoter and study its expression pattern.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com