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Tillering requires the fine-tuning of expression of many genes such as MOC1 (Li et al. 2003), LRK1 (Zha et al. 2009), OsTB1 (Takeda et al. 2003), D10 (Arite et al. 2007), Htd1 (Zou et al. 2006), and D3 (Ishikawa et al. 2005).
PKCε activates many genes, such as RAS [30] [33] and STAT3 transcription factor, in various signal transduction pathways [34].
Oct4 also maintains the expression of many genes, such as Eif3c, Papola, Eif3b, Eif4e, Rbm3 and Cpsf4, that are involved in the post-transcriptional control.
In terms of embryonic development, many genes (such as ECE1, TGFBR3, CELSR1, and ACVR2A) have shown significant signs of positive selection in Tibetans.
In addition, many functions show a broad distribution across the day, often reflecting large functional classes with many genes such as hydrolase activity and signal transduction.
SRF activity is a key event during cellular differentiation of many processes and transcriptionally controls many genes such as actin isoforms (Actb, Actg, Acta2) and actin-binding proteins (ABPs; e.g., Gsn) [43], [44].
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In the absence of RUNX1 many regulator genes such as Tal1, Fli1, Lmo2 or Cebpb are already expressed and many haematopoietic genes are bound by C/EBPβ, SCL/TAL1 and FLI1 at this stage.
Analyses of Xenopus intestinal metamorphosis have led to the identification of many T3 response genes that are likely involved in the development of the adult stem cells and many such genes, such as those of the Shh and BMP-4 signaling pathways, likely have similar functions during the maturation of the adult intestine in mammals.
Exhaustive screening for IM screens will yield many genes with such a low contribution to oncogenesis that therapeutic targeting of these genes or gene products is ineffective.
Many cone genes such as Gnb3 were upregulated in both Nrl-/ and Crx-/ (Fig. 1D).
Many candidate genes, such as SLC6A4 and 5HTR2A, have been associated with MDD in recent decades [2].
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