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Our data from real-time PCR and microarray analyses indicated that expression of the csgBAC operon was decreased to a greater degree than that of the csgDEFG operon upon deletion of dnaK (Fig. 2b, c), suggesting that the CsgD levels fell below their active concentration and/or that CsgD quality was compromised in the ΔdnaK strain.
A predicted stimulation of M1 growth by alcohols was demonstrated and microarray analyses indicated up-regulation of methanogenesis genes during co-culture with a hydrogen (H2) producing rumen bacterium.
Consistently, global transcriptional microarray analyses indicated that miR-195 primarily regulated genes associated with apoptosis in hESC-NPCs.
Comparative microarray analyses indicated that the phenanthrene response was closely related to other ROS conditions, including pathogen defense conditions.
Microarray analyses indicated that WrnΔ hel /Δ hel mouse embryonic fibroblasts respond very differently from wild type cells to exogenous H2O2.
Microarray analyses indicated that interferon-stimulated genes associated with antigen processing and presentation were enriched in ATII cells in COPD lungs.
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The qRT-PCR data together with DNA microarray analyses indicate that the ADAR1 mRNA levels are significantly higher than those of ADAR2 and ADAR3 in undifferentiated hESCs (Figure S3).
Our microarray analyses indicate that it is indeed the case.
Both the Sequenom MassArray and 70-mer oligonucleotide microarray analyses indicate that the majority of the DE profiles identified using the Affymetrix microarrays were valid.
First, 23 genes were selected from differentially expressed genes based on microarray analyses, indicating these 23 genes were more likely to be involved in anther development.
Approximately 80% of the up-regulated genes and 90% of the down-regulated genes were overlapped as shown by the first and second microarray analyses, indicating reproducible results.
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