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These findings demonstrate that tissue repair has distinguishable and different genomic expression patterns in mucosal and cutaneous sites.
The aim of this study was to determine if human immortalized keratinocytes cells (HaCaT) transfected with HPV18 E6 variants (E and AsAi) have different genomic expression patterns.
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This shows that different genomic organizations and expression modes have been adopted by the two major classes of snoRNA genes in N. crassa.
The feature values of all genomic data are finally normalized to have a zero mean and standard deviation of one across samples so that the relative impact of different genomic features on expression traits can be properly represented.
In addition, it has been observed in HPV16 E6 transfected human colon adenocarcinoma cells and human lung adenocarcinoma cells different genomic and proteomic expression patterns [ 63], in agreement with our results in cervix versus skin from K14E6 mice.
For example, medulloblastoma (MB) consists of four distinct subtypes – called WNT, Sonic Hedgehog (SHH), Group 3 and Group 4 – which exhibit different genomic alterations, gene expression profiles and response to treatment.
For example, MB consists of four distinct subtypes exhibiting different genomic alterations, gene expression profiles and response to treatment: WNT, Sonic Hedgehog (SHH), Group 3 and Group 4 (Taylor et al., 2012).
Early onset breast cancers are more likely to have arisen due to an inherited predisposition and tend to have a worse prognosis, possibly as a result of a different pattern of genomic expression compared with tumours developing in older women [ 19].
Medulloblastoma (MB) is the most common malignant primary pediatric brain tumor and is currently divided into four subtypes based on different genomic alterations, gene expression profiles and response to treatment: WNT, Sonic Hedgehog (SHH), Group 3 and Group 4. This extensive heterogeneity has made it difficult to assess the functional relevance of genes to malignant progression.
At both 20 and 60 post-natal days, we identified significant and comparable numbers of differentially expressed genes above experiment-specific noise levels in both pools (data not shown), thus demonstrating different strengths of genomic expression in the relevant histological compartments between mouse SOD1 and human SALS samples.
Although this classification is mainly based on histopathology, taking into account differences in the composition of the reactive infiltrate and stroma, recent studies have demonstrated that these disease entities are biologically different, with different genomic alterations, gene-expression patterns, cytokine milieu, and clinical behavior [ 6, 7].
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