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It suggests that tanshinone biosynthesis-related genes may be responsive to exogenous GA3 treatment.
In addition to ferritin, many of the genes that we identified in this group have also been shown to be responsive to exogenous H2O2 in Arabidopsis [ 30].
This study is well performed and does indicate that ductal cells may be responsive to exogenous transcription factors that can drive towards an islet cell fate.
Analyzing the responses of SmKSL1 and SmKSL2 to GA3 treatment showed that both SmKSL1 and SmKSL2 were significantly up-regulated in roots, stems and leaves of S. miltiorrhiza plants treated with exogenous GA3 (Fig. 10j– 10o), confirming that tanshinone biosynthesis-related genes may be responsive to exogenous GA3 treatment.
In support of this model, the MM14 myoblast line was found to be responsive to exogenous FGF-2 ligand, but not endogenous, and ectopic expression of oncogenic ras was found to be required to liberate or activate the endogenous extracellular FGF-2 for signaling [ 28].
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Half of ' early response' bHLH genes were responsive to exogenous H2O2 and their profiles were characterized by multiple waves reflecting possible roles in combinatorial control mechanisms (see Additional file 3).
We also confirmed that a representative subset of ' early response' genes containing as1/ocs-like promoter elements were responsive to exogenous H2O2.
We have identified a putative abscisic acid-response element (ABRE) in the 5'-untranslated region of the A. thaliana L-isoaspartyl methyltransferase gene and have shown that the expression of the mRNA is responsive to exogenous abscisic acid (ABA), but not to the environmental stresses of salt or drought.
We first showed that Met is present in the neonatal cardiomyocytes and is responsive to exogenous HGF.
Splice variants showed tissue-specific expression patterns and were responsive to exogenous GA3 treatement.
The expressions of maize ARF genes are responsive to exogenous auxin treatment.
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