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VVOs often extend to inter-endothelial cell interfaces and their individual vesicles (unlike caveolae) commonly open to the inter-endothelial cell cleft.
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The first degenerative changes such as increased cell death, cleft and radial tear formation, and cracks in the endplates can be seen already at 11 years of age at the time when the discs start to become avascular as the vessels penetrating into the disc through the endplates are obliterated [ 17].
Microtubules have several surface helices with which microtubule-binding proteins interact, as well as cell surface clefts bound by KLD/KID-containing proteins such as kinesins, Tau, and MAP2C [33], [33].
However, if Dorsomorphin exposure occured prior to the initiation of cell death, clefting was prevented (Fig. 9b).
Other membrane proteins that were both up-regulated in superficial hyperplastic zones in our study and that have been detected at the surface of C2C12 cells included cleft lip and palate transmembrane protein1, trophoblast glycoprotein, tissue factor/CD142, Ephrin type A receptor 2, tetraspanin 3 and 4 and fibroblast growth factor 4 (FGFR4) [ 33].
OSE cells in clefts and cysts also express the AR; and these cells are potentially in closer proximity to the androgen producing cells of the ovarian cortex.
Cells overlaying the cleft between two underlying cortex cells are short and differentiate into hair cells (H file) [ 68].
Interestingly, inhibition of Bmp signaling prior to the initiation of interdigital cell death prevented cleft formation.
Measurements of 10 traits were initially used to characterize SAM architecture: height, arc length, width, and midpoint width from the P1 cleft; cell number in the L1 layer along the arc length; length of P1; PIL; and the derived traits of cell size, height.width ratio, and volume.
For example, a basal FN matrix polarizes N-cadherin to the apical domain of zebrafish myocardial cells [58] and downregulates E-cadherin basally in cleft cells of branching epithelia [57].
When the leaf explants were cultured on 1/2 MS medium supplemented with suitable concentrations of cytokinins (the details will be discussed in the following paragraph) for 60 days in darkness, transparent somatic proembryos directly formed from the epidermal cells (Fig. 1a) or from the mesophyll cells through a cleft (Fig. 1b).
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