In addition to dsx and fru, canonical regulators of Drosophila sex determination, we identified and further characterized the expression of fne and tango13 as genes expressed in a sex-biased manner.
As both Kir4.1 and aquaporin-4 are expressed heavily in Müller cells, we next characterized the expression of Kir4.1 and aquaporin-4 in more detail within the Müller cells themselves.
We characterized the expression of different genes of the BCL2 family either over expressed in oocytes (BCL2L1, BCL2L10, BCL2L11 (BIM), BCL2L14 (BCLG)) or in GCs (BCL2 BOK2L2, BOK) and that mainly prevent oocyte loss.
In addition to examining the level of AAEL010824 protein, we also characterized the expression of its gene.
In addition, Casu et al. [6] have recently characterized the expression of several cellulose synthase and cellulose synthase-like genes in sugarcane stem and found that their expression is highly variable depending on internode maturity [6].
To reveal the underlying basis of microRNA-driven complex subpopulation dynamics within the heterogeneous intra-tumoral ecosystem, we characterized the expression of the subtype-enriched microRNA-128 (miR-128) in transcriptionally and phenotypically diverse subpopulations of patient-derived glioblastoma stem-like cells.
In this study, we have characterized the expression of L1TD1 in hESC.
Here we have characterized the expression of a novel gene L1TD1 in hESC.
We first characterized the expression of dat-1 promoter-driven hαSyn by using immunohistochemistry and confocal microscopy.
Next, we characterized the expression of the CXCR4 receptor on NB4, HL60 cells, AML blasts and HT-29 cells.
Having determined that parp3 morphants have defective neural crest development, we next characterized the expression of sox9a, dlx3b and dlx4b.
