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As been shown for human [16], we found several distinct putative promoter regions for the mouse prominin-1 gene.
In response to CD137 ligand signaling the cells attached to the plates, spread and formed lamellipodia (Figure 1A), similar to what has been shown for human monocytes [7].
A relationship between SC-signatures and cancer signatures has been shown for human hepatocellular carcinoma where the fetal rodent SC signature has prognostic significance for human hepatocellular carcinoma [60].
It has been shown for human stem cells that cross sectional dimensions of EBs and/or the number of primarily seeded stem cells might affect lineage determination [18] and differentiation efficacy [19], we have therefore subsequently analysed the pluripotent differentiation potential of f-fEBs.
It has been known for more than a century that acidosis impairs cardiac contractility [ 7], and this has also been shown for human atrial and ventricular muscle [ 8].
Although other variants (H3mm6, H3mm15 and H3mm18) do not have such large deletions or additions, amino acid substitutions in the histone fold domain may drastically alter the nucleosome stability, as has been shown for human H3T [ 39].
Similar(46)
A similar relative efficacy difference has also been shown for humans [2], [3].
As has been shown for human-dispersed transatlantic populations of Carychium[ 26, 27], the transportation of only a few hermaphroditic individuals is needed for a successful population foundation.
Although a unity gain has been shown for humans between PIII and PII amplitudes [ 17, 18], it is not known if this is the case for rodent ERGs.
The effect of CDAP treatment on cell adhesion to the BNC surface is shown for human umbilical vein endothelial cells and the mouse mesenchymal stem cell line C3H10T1/2.
Similar results were shown for human bone marrow MSCs and MSCs derived from the hair follicle [25], [70].
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