Searching journal content for articles similar to Yang et al. 33 (11): 1906.

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  1. ...literature. By encouraging the inclusion of well-recognized and experimentally confirmed aging genes (Fig. 3B), SCALE is more explainable and robust to spurious correlation and technical variability, as shown in the external validation in aging-related diseases and rejuvenating interventions data (Fig. 4...
  2. ...malleable and could contribute to individual variability in heart aging.DiscussionIn this study, we examine the changes that occur with aging in the transcriptome and proteome of heart tissue from 185 genetically diverse mice. Most mice in this study are still healthy at 18 mo of age, and thus the age-related...
  3. ...to a joint PCA for all cells and ages in Fig. 3) showed that aging dominates the cell-to-cell variability within both of these cell types, and we could not find additional major independent sources of variability, such as additional subsets of cells. This suggests that most variations discernible within LT...
  4. ...that variation in -wide gene expression increases in aging worms. This agrees with findings by Bahar et al. (2006), who reported increased cell-to-cell variation in gene expression in agingmouse heart. Somel et al. (2006) used a number of microarray gene expression tissue data sets from humans and rats and found...
  5. .... (B) Barcode enrichment plot showing ranking of aging-related genes from the GenAge database (de Magalhaes et al. 2009) among the DE genes. Genes are ranked right to left from most up-regulated to most down-regulated in DKO cells. The rank of genes associated with increased lifespan is marked by red...
  6. ...an integrated read-out, allowing us to estimate the magnitude of age-related transcriptional change across cell identities. Using this approach, cell identities showed multifold differences in aging magnitude, and cell identity again explained the majority of variation. Our results are conceptually consistent...
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