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Yao et al. (2013) recently reported iAs contamination of commercial roxarsone formulations.
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A recent study of surgical samples from three coronary heart disease patients who lived in an arsenic area in Chile reported that iAs was the predominant arsenic species in cardiovascular tissue, whereas DMAs and MAs levels in the same samples were relatively low or undetectable (e.g., iAs concentration in the auricle was 49.2 µg/g, whereas MAs and DMAs were undetectable (Roman et al. 2011).
Only 1.7% of women in the general female population in Spain reported an IA during all their life [28].
Corda et al (1965) reported group Ia, Ib and II afferents in the phrenic nerve.
Iwabuchi et al. reported that IA injection of fasudil hydrochloride reduced time to peak in the CVS artery dose dependently [ 26].
For instance, previously reported DW-iAs from central-eastern regions of Mexico ranged up to 1,504 μg As/L (Valenzuela et al. 2005) and up to 215 μg/L (Del Razo et al. 2011) in Hidalgo and Zimapán, respectively.
Even under adequate antifungal therapy, mortality rates of between 30% and 80% are reported for IA, and antifungal drugs might be used for prophylaxis more often than for therapy [ 17].
Because AsIII can oxidize to AsV during sample transport, storage, and preparation, here we report total iAs (i.e., AsIII + AsV).
Methods: The Arsenic Health Risk Assessment and Molecular Epidemiology ASHRAMM) study, a case control study, was conducted in areas of Hungary, Romania, and Slovakia with reported presence of iAs in groundwater.
The reasons for variation in invasive potential of serotype Ia reported at different sites are unclear, however data from Portugal suggests that the high invasive index of this serotype can be attributed to a dominant clone (ST-23 and ST-24), suggesting that the underlying genotype can influence the invasive potential.
The estimated percentage of the genome that accounts for coding regions is larger than what has been previously reported for chromosome Ia (56.7%) and Ib (58.1%) [25], which could be a reflection of the increased number of false positive protein sequences that arise from a larger variety of analyzed gene prediction algorithms or possible characteristic differences among the T. gondii chromosomes.
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