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To assess the latter possibility, expression of pocket proteins (pRb, p107, and p130) were examined.
To investigate this possibility, expression levels of the ΔNPEA3En transgene in mammary glands and tumors were measured by RT-PCR.
To test this possibility, expression of brk was examined in dTIEGS14/Minute clones and compared to tkva12/Minute clones.
To examine this possibility, expression and methylation analyses were performed on two of the cancer related genes (Figures 4 and 5).
In line with this possibility, expression of an extra class of small RNAs molecules involved in gene silencing, so called piRNA, is expressed specifically in spermatogenic cells [ 59].
To explore this possibility, expression data from this cohort were analysed for associations between expression of EMMPRIN and S100A4 in primary tumour samples, and functional studies were carried out in two colorectal cancer cell lines.
Similar(53)
To study this possibility, expressions of CSIG and p33ING1 in early passage (young, ∼20 population doublings (pdl)) and late-passage (senescent, ∼60 pdl) 2BS cells were examined by western blot.
Considering these three possibilities, expression of each gene was classified into 3×3×3=27 patterns, 1− D D D,2− D D S,⋯,27− I I I, where the order of the letters corresponds to the transition.
To see them in collision — or in collaboration — is to witness intriguing new possibilities of expression opening up.
To address this possibility, the expression of doublecortin, a microtubule-associated protein expressed in immature neurons and involved in the regulation of neuronal migration, was investigated.
This raises the possibility that expression of long non-coding RNAs may play a role in modulating gene expression in domains that escape X-inactivation in mouse.
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