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Basal measures of fluid intake, food intake, and urine output and urine osmolality under EH conditions were unchanged in Azin1 shRNA-transduced animals compared with controls.
Basal measures of peripheral insulin resistance (HOMA-IR) in the absence of infused insulin correlate with peripheral glucose disposal rate measured during a glucose-insulin clamp (~r = 0.88) [ 69, 70].
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∆V = the values represent the mean difference of paw volume between the basal measure and others measures (1, 2, 3, 4 and 5 h) ± S.E.M.; n = 5-6.
∆V = the values represent the mean difference of paw volume between the basal measure and other measure (1 h) ± S.E.M.; n = 5-6.
Moreover, TEER measurements were not different from basal resistance measured in cell-free inserts.
Results: Cusp basal regions measured 0.69 to 0.86 mm in thickness, significantly thicker (P =.001) than the rest of the cusp, which measured 0.36 to 0.48 mm.
Basal secretion measured in the presence of 2 mM glucose was unaffected.
Plasma basal concentrations measured after stopping this were LH 9.4 IU/l, FSH 9.9 IU/l, testosterone 0.24 ng/ml and delta-4-androstenedione 1.2 ng/ml.
The basal proteolysis measured under control conditions was comparable in both cell lines and respectively set as the internal reference (white bars).
Data are expressed as the mean (×10−3) of relative luciferase units (RLU) normalized with β-galactosidase activity minus basal activity measured in empty vector-transfected cells.
Crown height, measured from the base of the tooth plicidentine to the crown tip if preserved (Figure 1, F). Basal width, measured from the anterior margin to the posterior margin of the base of the tooth (Figure 1, G).
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