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foxi3b, on the contrary, was sufficient to restore full NaRC (100%, n = 86) and partial HRC (24%, n = 86) differentiation in Notch-ON embryos (Figure 8E).

foxi3b misexpression was sufficient to restore NaRC (100%, n = 103) and partially HRC (21%, n = 103) differentiation in bmp7 morphants (Figure 8H).

Based on the differential expressions of foxi3a and foxi3b in differentiating NaRC (foxi3bhigh) and HRC (foxi3ahigh/foxi3blow) lineages, we speculated that they might have distinct functions in promoting the differentiation of NaRCs and HRCs.

However, when we forced foxi3a expression in bmp7 morphants, it was sufficient to restore both NaRC (100%, n = 62) and HRC (100%, n = 62) differentiation with high penetrance (Figure 8G).

However, when we forced foxi3a expression in Notch-ON embryos, it was sufficient to restore both NaRC (100%, n = 74) and HRC (100%, n = 74) differentiation with high penetrance (Figure 8D).

In 24-hpf bmp7 morphants, although we still could detect P63 expression, both NaRC (0%, n = 88) and HRC (0%, n = 88) differentiations were completely undetectable (Figure 8F) due to the loss of epidermal IC identity (detected by a foxi3a in situ study, data not shown).

Five wheat cultivars of diverse origin namely Tatara, NARC-2009, Sehar-2006, SKD-1 and F-Sarhad were planted on 19th November, at Islamabad during the years 2007 2011.

This observation suggests that both NaRCs (atp1b1b-positive cells) and HRCs (ca2a-positive cells) might come from common progenitors and then subsequently differentiate.

By counting the number of epidermal ICs (including both NaRCs and HRCs) and epidermal SCs (by P63 antibody staining) at 24 hpf, we detected significantly higher epidermal ICs (NaRCs, 41±5 vs. 28±5, n = 7, p<0.05; HRCs, 88±8 vs. 21±3, n = 7, p<0.05) and lower epidermal SCs (135±8 vs. 212±11, n = 7, p<0.05) in mibta52b mutants.

PCSK9, that was formerly known as NARC-1 is important for brain development, especially the cerebellum [ 128].

Lateral gene transfer out of the bacterial domain was deduced earlier from the genome sequence of the first sequenced Haloarchaeal genome, Halobacterium NARC-1, for six genes of menaquinone synthesis, cytochrome c oxidase, and NADH dehydrogenase (Kennedy et al. 2001).

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