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There are specific cellular proteins that regulate a protective immune response, for example the pro-inflammatory genes that were up-regulated to a greater extent in HP-PRRSV rJXwn06 than VR-2332 whenormalizeded to control samples as observed when comparing the pathogenicity of HP-PRRSV isolate rJXwn06 with the North American prototype strain VR-2332 PRRSV.
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These data advance our understanding of the immuno-protective function of IFN-γ within the synovial joint and go some way towards identifying mechanisms by which IFN-γ regulates a chondro-protective outcome during early inflammatory arthritis.
Nrf2 regulates a battery of protective genes by binding to regulatory antioxidant response elements (AREs).
Based on the current understanding, HO-1 confers protective actions by regulating a variety of downstream signaling molecules or signal transduction events.
Such observations suggest that EGFR may regulate the protective function of XPA.
So biologist Carole Peyssonnaux, microbiologist Victor Nizet, and colleagues at the University of California, San Diego, investigated how the cells might regulate their protective behavior.
Nuclear factors have been identified to regulate this protective response (Lee and Wei, 2005; Moreno-Loshuertos et al., 2006; Malik and Czajka, 2013).
HSF-1 and DAF-16 regulate opposing protective activities; HSF-1 influences disaggregation while DAF-16 mediates the formation of larger, plausibly less toxic aggregates (Cohen et al., 2006).
The mechanisms of action of fasting are best understood in the yeast Saccharomyces cerevisiae, in which a switch from glucose-containing medium to water causes the downregulation of the Tor S6K and Ras adenylate cyclase PKA pathways, and the consequent activation of the stress resistance transcription factors Msn2/4 and Gis1, which regulate many protective and metabolic genes (Wei et al., 2008).
Therefore, there is a need to elucidate factors that regulate protective immune responses against this pathogen and to identify targets for development of new drugs [3].
They encourage new studies of phenomena with enormous clinical importance, such as why males die younger than females and how selection shapes mechanisms that regulate protective responses such as pain and fever.
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