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Specifically, we evaluated the developmental transitions of the four neuronal subtypes from their most proximate progenitors: different NSC species into mature neuronal subtypes (CHOLNs and MSNs), radial glia (RG) into GLUTNs, and bipotent neuronal-OL progenitors (N/OPs) into GABANs (Table 3).
We then evaluated the developmental potential of the PGCLCs.
W. Watanabe et al. evaluated the developmental immunotoxicity of methamidophos using a respiratory syncytial virus (RSV) infection mouse model.
However, no study has thoroughly evaluated the developmental patterns of the hip joint in patients with HME.
Previous work that evaluated the developmental requirement for exon IIIb in mice used a mouse allele in which exon IIIb was deleted.
To reveal unknown effects of methamidophos on human health, we evaluated the developmental immunotoxicity of methamidophos using a respiratory syncytial virus (RSV) infection mouse model.
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Currently it is common practice to evaluate the developmental toxicity hazard of chemicals or pharmaceuticals by evaluation of fetuses after administration of the compound to pregnant animals.
The objective of this work was to evaluate the developmental level of children aged 1-59 months living in poverty (PROSPERA program beneficiaries) through application of the CDE test.
This study aimed to evaluate the developmental occurrence of inspiratory phonations (IPs) in the spontaneous cries of healthy infants across the first 10 weeks of life.
Previous studies to evaluate the developmental potential of candidate hESC-derived progenitors have delivered these cells into murine and porcine cardiac tissue, with inconclusive evidence regarding the capacity of these human cells to physiologically engraft in xenotransplantation assays.
To evaluate the developmental occurrence of subharmonic (SH) and noise (N) phenomena and to quantify their extent in the spontaneous cries of healthy infants across the first 3 months.
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