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Although it has been reported that wild rice represents a major resource for disease resistance, relative to current cultivated varieties of rice, no studies have compared the immune responses of wild and cultivated roots of rice to M. oryzae.
It has been reported that wild salmon contains more nutrients per serving than farmed salmon, and several studies have been cited showing that farmed salmon contains more polychlorinated biphenyls (PCBs) than wild salmon.[2].
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In fact, it has been reported that wild-type mice derived from the late generation of mTR+/− heterozygous parents which had short telomeres display hematopoietic phenotypes resembling aplastic anemia and dyskeratosis congenita [50].
It has been reported that wild-type embryos treated from sphere stage (4.3 hpf) with DAPT display somitic and neuronal defects that are typical of Notch-depleted embryos [25].
It has been reported that wild-type WT1 protein has the ability to interact with the tumour suppressor p53 (22).
(18) It has been reported that wild-type p53 is abnormally sequestered in the cytoplasm in certain human tumor cells.
It has been reported that wild-card type mappers are better in mapping rate (percentage of reads being aligned) but struggle with mapping accuracy (percentage of reads mapped at correct positions) [ 12].
It has been reported that wild-type CDKN2A expression from an adenovirus vector (Adv/p16) in non-small-cell lung cancer cell line A549, which carries the wild-type p53 gene, results in activation of caspase-3, accompanied by the cleavage of its substrate PARP (Koh et al, 2002).
It has also been reported that wild-type (wt) BRAF is required for a successful response to panitumumab or cetuximab therapies in metastatic CRC (Di Nicolantonio et al, 2008; Laurent-Puig et al, 2009; Souglakos et al, 2009; De Roock et al, 2010).
However, it has also been reported that wild-type P53 may be aberrantly phosphorylated following ionising radiation (IR) and that there is a failure to promote cell cycle arrest or apoptosis, suggesting that signalling pathways downstream of P53 may be defective in melanoma [ 18].
In addition, it was reported that wild type myosin-VI and myosin-IX, both one-headed myosins, can also generate successive large steps.
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