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At the same time, Yamamoto et al. (2011) reported salt stress susceptibility of NU2 among the NU varieties.
A new integrated catchment model for salinity has been developed to assess the transport of road salt from upland areas in watersheds to streams using readily accessible landscape, hydrologic, and meteorological data together with reported salt applications.
The reported salt tolerance of P. australis differs between studies.
No reported salt response motif was found in this region.
He reported salt craving but denied vomiting, diuretic use, pain, or persistent childhood diarrhea.
The reported salt intake did not include the salt added at the table or during cooking.
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All the reported salts, except ETH-2,3HBA exhibited charge assisted acid pyridine heterosynthon.
The candidate genes identified in the present study contained both the previously reported salt-responsive genes and some species-specific ones.
The candidate salt-responsive genes identified in M. pinnata contain both the previously reported salt-responsive genes and some species-specific genes which will be a new resource for molecular breeding in legumes or other crops.
Moreover, we reported salt-sensitive blood-pressure in this ZDF model, which may be attributable to inadequate high levels of aldosterone and altered expression of renal SGK-1 dependent sodium transporter under high-salt treatment [ 24].
It has been reported salt-adding would significantly cause the osmotic stress in the medium which results in a dramatic accumulation of glycerol in the microalga Chlamydomonas reinhardtii[ 36].
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