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Gene expression analysis indicated that PfPDCT is expressed ubiquitously in developing seeds and other organs examined.
Cited2 expression analysis indicated that it is highly expressed in long-term HSCs (LT-HSCs; Lin−Sca-1+c-kit+(LSK CD34−Flt3− cells), less abundantly in short-term HSCs (ST-HSCs; LSKCD34+Flt3− cells), and profoundly downregulated in lymphoid-primed multipotent progenitors (LMPPs; LSKCD34+Flt3+ cells).
Result of gene expression analysis indicated that both genes were expressed at a similar level in most samples examined, including leaf, stem, flower bud, and developing seeds from 14 DAP to 42 DAP, with the exception of PfLPAT2 levels in stem tissue, where expression was only about 50% that detected in leaf.
Expression analysis indicated that both genes are ubiquitously expressed in vegetative and reproductive organs, including the root, stem, leaf, anther, ovule, and seed.
Relative expression analysis indicated that CYP707A and NCED are both expressed both in embryos and endosperm, and are expressed at higher levels in embryos than in endosperm.
Initial expression analysis indicated that mi-er1 mRNA was differentially expressed in breast carcinoma cell lines and breast tumours (Paterno et al, 1998); however this study did not distinguish between the two MI-ER1 isoforms.
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Expression analysis indicates that Hha and Hhb are expressed in a Sonic Hh-like pattern.
Our gene expression analysis indicates that some of them are expressed in different regions at various developmental stages of feathers.
Expression analysis indicates that a subset of histone genes were expressed in a similar pattern and many of them responded to stress conditions.
Gene expression analysis indicates that the major CRC molecular subtypes are represented.
In summary, our gene expression analysis indicates that ablation of UPF2 during fetal organogenesis is incompatible with the development of a metabolically functional competent liver able to sustain postnatal life.
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