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Pseudogenes for genomic Cox1 and Cox3 are present and they may have been affected with expression of FLAG-NLS-Cas9 targeting mtCox1 and mtCox3 regions.
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In Notch-deficient mib mutants the first phase of this process is affected with premature GFP expression, deficient cell recruitment into TC and abnormal patterning of ChP.
mRNA expression for NeuroD/Beta2, Isl-1, Ras, Metalloproteinase-2 (MMP-2), −9 and −7 also were affected, with PLL inducing increased expression of NeuroD/Beta2 of Isl-1, and no difference between C and control.
Comparison of the 127 genes whose expression is affected with those that are bound by CREM identifies 58 genes as direct targets.
The directional expression changes indicated how these processes were being affected, with a general increase in the expression of immune related and protein metabolism genes, whereas growth, structural proteins and cell cycle showed a negative trend, with a majority of genes being down regulated in expression.
To assess whether or not the expression of SPRY4 has been affected in pLenti-miR-411 H1299 and SPC-A1 cells in comparison with that in pLenti cells, we investigated the SPRY4 protein expression.
We further examined whether peripheral blood cells were affected using gene expression analysis with DNA microarray.
We tested whether anti-RRxpS/T recognized phopshorylated dCREB, and whether phosphorylation of dCREB was affected by Aβ42 expression by immunoprecipitation with anti-RRxpS/T followed by Western blotting with anti-dCREB antibody.
To examine whether the altered methylation patterns in SVs from mice treated neonatally with DES might be affected by the expression level of the epigenetic modifiers, we used real-time PCR to investigate the RNA levels of DNA methyltransferases, including DNMTs (DNMT1, DNMT3A, and DNMT3B) and MBDs (MeCP2, MBD2, and MBD3), as well as two histone modifiers (HDAC1 and HDAC2).
Protein function is affected by its expression level, localization, interaction with other proteins, and its posttranslational modifications.
We found that the fraction of mitotic cells is strongly reduced in mutant (UAS-dicer2/+; sal EPv-Gal4 UAS-GFP/UAS-salm-i; UAS-salr-i/+; Fig. 3H,H′,I) compared to wild type discs (UAS-dicer2/+; sal EPv-Gal4 UAS-GFP/+; Fig. 3G,G′,I), indicating that entering into mitosis is affected in cells with reduced expression of sal located in the central domain of the wing blade.
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