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The effect of isoflurane on the uptake of FDG in the rat brain has been investigated using a motion compensation technique to scan fully conscious and unrestrained rats dynamically from the time of tracer infusion.
Indeed, the distribution of PR in both the male and female rat brain has been well described.
Although little is known about the ontogeny and distribution of D1 receptors in the neonatal rat brain, D1 receptor distribution within the adult rat brain has been characterized.
The expression of calcyon mRNA in the rat brain has been previously described in Sprague-Dawley rats [ 34].
Immunohistochemical staining of rat brain has shown that Oatp1a4 and 1c1 are localized in both the abluminal and luminal membrane of the BBB [ 9, 10].
The number of orexinergic neurons in the rat brain has been estimated to be only about 4,000 (Kilduff and Peyron 2000).
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Because the dependence on and the stimulation by calcium of base-exchange reactions is a well known mechanism and alterations in calcium levels in rat brain have been reported, we decided to investigate PS synthesis in the presence of endogenous and exogenous calcium (2.5 mM).
Extracts from ischemic rat brain have induced the production of BDNF, bFGF, VEGF and HGF in human MSCs in culture [73].
The cytosolic CSPα fraction extracts from the rat brain have been described to interact with HSC70 [ 26].
Furthermore, dividing endogenous progenitor cells in the adult rat brain have been shown to respond to demyelination by differentiating into myelin-forming oligodendrocytes [ 49].
Preclinical studies using stereotaxic injection of Aβ1-42 into rat brain have shown that Aβ can induce extensive white matter damage and oligodendrocyte death [ 25].
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