The above hydrodynamic equations can be expressed as a general expression shown below frac{partial }{partial {x}^left varphi {u}^right)+frac{partial }{partial {y}^left varphi {v}^right)=S+frac{partial }{partial {y}^left(Nfrac{partial varphi }{partial {y}^right) (8 where φ is the dependent variable, N is the diffusion, and S is the source term.
In addition, as we show below, the expression levels of genes within a particular pathway are fairly consistent, indicating that there was little bias in our RNA-Seq library construction.
Fragments used for gene disruption and expression experiments are shown below the genes.
The expressions show curiosity, fatigue, bemusement, tolerance.
These cells have been previously identified by their lack of expression of Sirp-α, and as shown below, intermediate expression of CD45RA.
The expression of RMSE is shown below: {text{RMSE = }}sqrt {frac{{sumnolimits_{{i{ = 1}}}^{N} { (q_{{t, {text{expt}}}} - q_{{t, {text{theo}}}} )^{ 2} } }}{N}} (5 where, (q_{{t, {text{expt}}}} ) solid phase concentration obtained experimentally at time t (mg/g), (q_{{t, {text{theo}}}} ) simulated solid phase concentration at time t (mg/g), N = number of experiments.
Thus, we can presume that NAL1 allele could also be involved in enhancing flag leaf area in the qGN4.1 QTL-NILs for enhanced photosynthetic efficiency, and grain number per panicle traits, but as shown below, the expression of NAL1 gene was down-regulated in the high grain number lines in our material.
Growth curve with CDK11p58 stable expression and controls was also shown below.
Parental-specific expression across all replicates is shown below transcript models in natural log of TPM units (ln TPM)), with the posterior distribution of the parental biases across replicates indicated in the right inset boxes with corresponding PPs on top.
