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However, a deeper analysis of the expression patterns of three redundant, fully functional, and simultaneously expressed Sultr1 2 forms (BjSultr1 2a, BjSultr1 2b, BjSultr1 2c) revealed that sulfate limitation induced the expression of all the variants, whilst BjSultr1 2b and BjSultr1 2c only seemed to have the capacity to respond to Cd.
Comparative analysis of the expression patterns of immune-related genes revealed a total of 217 differentially expressed (DE) protein-coding genes and 50 DE novel transcripts, in which 40 DE protein-coding genes were related to the immune system.
The detailed analysis of the expression patterns of the dystrophin isoforms and their spatial and temporal co-expression relationships provide a better understanding of the role of dystrophin in the development and function of the human brain.
To gain more insights into the role of dystrophin in this cognitive phenotype, we performed a comprehensive analysis of the expression patterns of dystrophin isoforms across human brain development, using unique transcriptomic data from Allen Human Brain and BrainSpan atlases.
Therefore, we provided a detailed analysis of the expression patterns of genes involved in endocytosis.
A more limited analysis of the expression patterns of Cldn3 and Cldn4 (which lie close to Cldn13 on mouse chromosome 5) showed different profiles.
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Fig. 7 qRT-PCR analysis of the expression pattern of REL2.
Small RNA blot analysis was performed to determine the expression patterns of conserved and new miRNAs.
Next, DNA microarray analysis can be used to study the expression patterns of genes, and to understand the function of all genes and their interactions.
Analysis of the tissue expression patterns of xPKD1 demonstrated a high level of expression in the kidney.
In this study, we provide detailed analysis of the spatial and temporal expression patterns of the dystrophin isoforms in the pathology-free adult and developing human brain.
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