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For example, during murine brain development, carnosine synthesis is only associated with the final stages of glial cell maturation [32].
We demonstrate that the d-peptides' concentrations in murine brain directly correlate with concentrations in cerebrospinal fluid.
a Raman spectra collected at two different positions of an ischemic murine brain in the core (red) or its contralateral region (blue).
Loss of NF2 function in the dorsal telencephalon of the murine brain also elicited increased Yap/TAZ activation and increased cell proliferation/expansion leading to developmental defects [101].
Here, we employed multiple models of murine brain malignancy and genetic lineage tracing to demonstrate that BMDMs are abundant in primary and metastatic brain tumors.
We show that UCP4 is present in fetal murine brain tissue as early as embryonic days 12 14 E12 E144), which coincides with the beginning of neuronal differentiation.
By using CircleSeq to analyze RNA-seq data generated by Salzman et al., Jeck et al. found that 44% (646/1477) of circRNAs in the murine brain were also present in the murine testis (Jeck et al., 2013).
Since data concerning system morphologies in murine brain are rarely available, mouse studies are usually designed and interpreted based on previous findings in rats, although interspecies differences are frequent.
RVG29 functionalized liposomes (RVG29-lip) showed significantly higher uptake efficiency in murine brain endothelial cells and dopaminergic cells, and high penetration efficiency across the blood brain barrier (BBB) in vitro.
In vitro transfection of murine brain capillary endothelial bEnd.3 cells with pSPE, pTETA, and pLPEI polyplexes was 2.3 4.9 times more effective compared with the non-degradable LPEI 22 kDa reagent (ExGen500) in the presence of serum.
RNA isolated from murine brain endothelial cell line (bEnd.3) was used a positive control.
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