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Previous study with CCR9 knockout mouse model has reported no adverse side effects of CCR9 gene ablation, besides the reduction in the γδ IELs which are characterized by their CCR9+ phenotype (Wurbel et al, 2001).
An apoE (apolipoprotien E -deficient mousE -deficientreported that a loss of TLR4 and its adaptor mouseule model (myeloid differentiation factor 88) decreased thassevereportedathatosclerosis and alossed atherofcleroTLR4plande formatits [ 22].
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Two studies using a mouse model have reported elevated ABR thresholds after chronic, low-dose exposure to MeHg (Chuu et al. 2001; Huang et al. 2008).
Other groups using the same model have reported similar findings of reduced perfused capillary density and increased heterogeneity in intestinal mucosa [ 5- 7].
In fact, previous studies using the same model have reported increases in iNOS mRNA (Juarranz et al., 2005) and plasma NOx (Sakaguchi et al., 2004).
In the low-salinity zone of the San Francisco Estuary mass balance calculations and models have reported that clams (especially the invasive Potamocorbula amurensis) suppress phytoplankton blooms.
However, few studies based on finite-element (FE) models have reported that the presence of FRP in shear-strengthened RC beams limits strain in the transverse-steel (e.g., Chen et al. 2010).
However, recent studies in healthy and pathological animal models have reported neural dynamics that do not match with this view of the GPe as a relay in the BG circuit.
Both IDDM and NIDDM animal models have reported decreased concentrations of BH4 in the vasculature [ 47, 48].
Studies using structural equation modeling have reported abnormalities in limbic prefrontal networks in MDD during emotional face processing (32).
Various studies using neurodegenerative disease models have reported that berberine possesses multiple neuroprotective effects including neurotrophin-mediated neuroprotection.
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