By using methylated DNA immunoprecipitation, methylation and CGH arrays, we show that global DNA hypomethylation is associated with genes hypomethylation, hypomethylation of DNA repeat element and chromosomal instability.
By using in-house fabricated arrays, we show resistance of HyPer5 signal to repeat exposures of ozone pulses of 300 ppb over time.
Using the crossed fiber arrays, we showed that neuronal cell bodies contacted the silk fibers and formed ganglion-like structures within 4 weeks.
Previously (using Illumina 1M arrays) we showed that stringent CNVs >30 kb detected by both iPattern and QuantiSNP were confirmed by quantitative PCR (qPCR) to be true events at 95% confidence (Pinto et al. 2010).
Using cDNA array analysis, we show that this cell wall component triggers the synthesis of MMP-3 by FLSs and may therefore contribute to joint destruction.
In our SNP array study, we show that NFIB, which lies 9.1MB centromeric to the JAK2 locus, is amplified as a result of trisomy 9 in 6/87 MPN patients and gain of 9p23 13.3 in 1/87 MPN patients.
According to our transcriptomic profiling results (Supplemental Table 1) and using cytometric bead array analysis, we show in Fig. 2 that the secretions of IL-6 and IL-8 cytokines were strongly induced in P-NALD fibroblasts, whereas secretion of TNFα was not significantly changed (data not shown).
Instead of Priess and Hirsh, 1986, we had referenced another paper from the Priess lab that describes the epidermal microtubule arrays in the larval stages (Costa et al., Dev. Biol. 1997), which are the arrays that we show here are required for larval growth.
Here we describe OPEN (Oligomerized Pool ENgineering), a rapid, publicly available strategy for constructing multifinger arrays, which we show is more effective than the previously published modular assembly method.
