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We next performed large scale in situ hybridization experiments to examine the expression patterns of the differentially expressed genes, and based on these patterns and homology, we chose 156 genes to knock down by RNAi.
HCA was used to examine the expression patterns of the 26 differentially expressed proteins across the study cohort with results depicted in heat map form.
To examine the expression patterns of the DEGs, we performed cluster analysis of 19,806 DEGs expressed in four CSILs.
Real-time qRT-PCR was performed to examine the expression patterns of autotetraploid rice hybrids.
This prompted us to examine the expression patterns of BMP4 and BMP receptors (BMPRs) at the apical region of the tooth germ during mouse tooth root development.
To examine the expression patterns of kinase genes in various rice tissues/organs as well as in response to abiotic/biotic stresses or hormone treatments, we used a meta-expression analysis based on 1150 Affymetrix array data plus GEO series GSE39429, which utilized the Agilent 44 K microarray platform (GEO platform GPL6854).
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Reverse transcription PCR (RT-PCR) was performed to examine the expression pattern of ASL3.
To examine the expression pattern of TCM5, we used RT-PCR to investigate the transcript levels of TCM5 in various tissues (Fig. 5).
In this paper we examine the expression pattern of the stam gene and the localisation of the STAM protein during D. melanogaster oogenesis.
The transformants were crossed with a MB-specific GAL4 driver line, OK107 [7], to examine the expression pattern.
Our results show that this approach can be adapted to examine the expression pattern of a microRNA in vivo.
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