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For example, in M. domestica, MEST exhibits imprinted expression while the adjacent COPG2 is expressed from both alleles.
We have previously described several genetic models that result in the complete loss of imprinting at mouse chromosome 12 (da Rocha et al., 2008), such that Dlk1, Rtl1 and Dio3 are fully expressed from both parental alleles and noncoding RNA expression was repressed.
Parent-specific expression analysis of nine other genes in this group demonstrated that all were expressed from both alleles.
Furthermore, not all genes on the X chromosome are inactivated; a small number escape modification and remain actively expressed from both X chromosomes in the cell.
Northern blots showed that single mRNAs of predicted length were expressed from both genes and the expected GFPuv protein was observed on Western immunoblots.
In human and in mouse, the JARID1C/Jarid1c gene escapes X inactivation, i.e. it is expressed from both alleles in females [9], [10].
ABL1 was chosen since it was ubiquitously expressed from both promoters at high levels across the 11 tissues, and was likely to show a similar trend in CD4+ T-cells.
Furthermore, in adult mouse choroid plexus, a brain tissue in which Igf2 is expressed from both alleles and H19 is not expressed, IC1 and the Igf2 DMRs are methylated on both parental chromosomes [24].
To determine whether the bacterially expressed IgG retained the same binding avidity as those expressed in mammalian cell culture, an ELISA of serially diluted purified IgG expressed from both bacterial and mammalian cell cultures was carried out against Dengue-2 and epsilon toxin using 4G2 and ET149 respectively.
It is noteworthy that the P1 transcript is reported to be expressed from both parental alleles in postnatal liver and fetal choroid plexus/leptomeninges [66], and that P1 promoter activity was observed not to be exclusively connected to IGF2 LOI in laryngeal squamous cell carcinoma [67].
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In female hESC in which XIST is repressed, XACT is expressed from and coats both Xs, and this correlates with significant reactivation of the inactive X chromosome.
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