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A more recent example of ERF-type transcription factors that directly target defense-related genes in rice is OsERF922, which acts on GCC-box containing genes to negatively regulate resistance to Magnaporthe oryzae (Liu et al., 2012).
Our results verify the important effect of C5-deficiency in inbred mouse strains, and further identify two novel loci, Carg3 and Carg4, which regulate resistance to C. albicans infection in a C5-independent manner.
Finally, we show that NPHP1 trafficking to cilia does not require PC-1 and that PC-1 may require NPHP1 to regulate resistance to apoptosis, but not to regulate cell cycle progression.
The TCS CopRS and the modified CorRSP system regulate resistance to copper [ 53] and coronatine synthesis [ 43, 44], respectively.
However, an understanding of how small G proteins regulate resistance to P. infestans in potato is lacking.
The latter induces interferon (IFN) γ-activated MΦs to kill Leishmania parasites, promote disease healing and regulate resistance to re-infection as well as vaccine-induced immunity [ 3].
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A third example is Arabidopsis enhanced disease resistance 4 (EDR4) negatively regulating resistance to powdery mildew.
Rice MPK12 positively regulates resistance to Xoo (Seo et al. 2011).
Our study revealed that OsHsp18.0-CI positively regulates resistance to bacterial leaf streak in rice.
These results suggested that OsHsp18.0-CI positively regulates resistance to Xoc in rice.
Our results suggest that the sHSP OsHsp18.0-CI positively regulates resistance to Xoc in rice.
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