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There was a high blood glucose level corresponding to high GLUT 1 protein level in HSD group.
High stocking density was responsible for high GLUT 1 protein levels in HSD individuals compared to LSD individuals (Fig. 2).
High GLUT 1 protein level in HSD individuals could be due to (1) higher number of erythrocytes which associatively enhanced levels of GLUT 1 protein (a transmembrane protein spanning the membranes of erythrocytes) in HSD individuals, (2) translocation of GLUT 1 protein from the intracellular pool to plasma membrane thereby increasing the level of GLUT 1 protein (Samih et al. 2000).
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Fifteen days after myocardial infarction, diabetic animals showed reduced infarct size and heart fibrosis area along with improved systolic function, increased expression of programmed cell survival genes, increased use of glucose as fuel (as suggested by high GLUT-1 expression), and reduced intensity of inflammation [ 7].
The results obtained indicate that HSD individuals had significantly higher GLUT 1 protein plasma levels than LSD individuals.
GLUT-1 expression and MCT4 expression showed an even stronger amount of colocalization with approximately six times higher GLUT-1 expression in MCT4 positive areas.
HSD individuals had significantly higher mean GLUT 1 protein level than LSD individuals, p < 0.05.
The plasma glucose lowering action of rhodiola-water extract is mainly mediated by β-endorphin release through an activation of opioid μ-receptors to achieve the higher of GLUT 4 gene expression and/or the decrease of hepatic PEPCK gene expression.
Immunofluorescent staining for Glut-1 (glucose transporter 1) showed high expression of Glut-1 in microvascular endothelia of the cervical and lumbar ventral horn of the spinal cords in C57BL/6J mice at 12 13 weeks of age (Figure 8A, B, H, I) and at 19 20 weeks of age (Figure 8C, J).
We may well discover there will be a high-rise condo glut.
The fish-stocked cultures at HSD showed a higher expression of GLUT 1 protein than those cultured at LSD as shown by Western blot immunoreactivity of the SDS PAGE resolved fish plasma proteins against IgG primary antibody for Nile tilapia GLUT 1.
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