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The 96 h LC50 lambda-cyhalothrin value for carp was reported at 0.5 μg L−1 [ 23], and the 96 h LC50 lambda-cyhalothrin value for juvenile Nile tilapia (Oreochromis niloticus) was 2.901 μg L−1 [ 24].
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In 1998, the first mass deaths of common and koi carp were reported in Israel and the United States (3).
Carp culture (Cyprinus spp). was reported in all the countries, the exception being Côte d'Ivoire.
In the Indian major carps, modulation of TLR2 expression was reported in PGN, zymosan, and LTA treatment [ 35, 36].
Inhibitory effect of deltamethrin at concentrations above 2 μg/L on the monooxygenase system of carp liver (Cyprinus carpio L). was reported by Deer et al. (1996).
Myoglobin is important for intracellular oxygen transportation upon oxygen scarcity and was reported to be up-regulated by hypoxia in various carp tissues [ 71, 72].
The accumulation of BPA glucuronid acid in the gall fluid before excretion was reported in rainbow trout (Larsson et al. 1999) and in carp (Mandich et al. 2007).
To date, no studies into the effects of SNPs on miRNA biogenesis and regulation in the common carp have been reported.
We found that 28 unigenes from head kidney in grass carp have been reported to be involved in the following pathways, Toll-like receptor signalling pathway, RIG-I-like receptor signalling pathway and the NOD-like receptor signalling pathway (Table 7).
Even though grass carps could live in both fresh and brackish waters, possible PZQ pharmacokinetic differences between freshwater-acclimated grass carps and brackish water grass carps have never been reported.
The genetic response in growth traits in a selection program for increased harvest weight in a common carp population in Vietnam is reported.
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