Searching journal content for articles similar to Garcia et al. 11 (6): 1043.

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  1. ...@wi.mit.eduAbstractRates of production and degradation together specify microRNA (miRNA) abundance and dynamics. Here, we used approach-to-steady-state metabolic labeling to assess these rates for 176 miRNAs in contact-inhibited mouse embryonic fibroblasts (MEFs), 182 miRNAs in dividing MEFs, and 127 miRNAs in mouse embryonic stem...
  2. ...), including those associated with increased fatty acid oxidation (Villanueva-Cañas et al. 2014), as hibernators rely on gradual fat utilization over winter. Research on shrew physiology indicates they also rely extensively on lipid metabolism in winter (Keicher et al. 2017) and may share some molecular...
  3. ..., as it alleviates lipid toxicity, mitigates ER stress, provides energy, and supports cell survival (Zadoorian et al. 2023). These findings suggest that TEs contribute to the diversity of the PLAAT4 gene products and function, thereby contributing to cancer metabolism remodeling (Fig. 6H).View larger version...
  4. ...coexpression modules with differential responses to environmental microbiota. Third, we link the microbial and host transcriptome data by predicting a global map of more than 2800 metabolic interactions. These interactions represent statistical associations between variation in bacterial metabolic potential...
  5. ...metabolitesGiven the significant influence of epigenetic mechanisms on lipid metabolism (Gomez-Alonso et al. 2021) and the observation that calorie restriction can modulate both epigenetic drift and metabolic pathways (Hahn et al. 2017; Maegawa et al. 2017), we further explored the impact of our EDS on serum...
  6. ..., becoming less constrained in lineages evolving more herbivorous diets. We further consider the biological functions associated with diet evolution and observe that pathways related to amino acid and lipid metabolism, biological oxidation, and small molecule transport experienced reduced purifying selection...
  7. ...has deficiency in lipid and 314 protein catabolism that influences phenotypic responses to diets (Gillette et al. 2020). As 315 validated by Sanger sequencing, honey bee spen has a p.322 Tyr>Cys recoding site with 316 significantly higher editing level in CV than in GF (Figure 6B). 317 Ly-6 protein XM...
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  8. ...(Long and Holtzman 2019). The accumulation of amyloid-β (Aβ) plaques and tau protein tangles are a hallmark of AD pathology. However, it is increasingly recognized that additional neuropathological processes, such as neuroinflammation, lipid metabolism dysfunction, mitochondrial impairment, axonal...
  9. ..., and metabolic responses to exercise, including glucose metabolism, lipid metabolism, and lactate production (Hultman et al. 1991; Romijn et al. 1993, 2000; Greenhaff et al. 1994; Bottinelli et al. 1999; Trappe et al. 2003, 2006; Kosek et al. 2006; Luden et al. 2008; Raue et al. 2009; Dickinson et al. 2010...
  10. ...the galactolipids in food, which is important for the lipid metabolism of herbivores.We recognized that although a number of complementary models were used in the present study, they may not adequately represent the general genetic basis of feeding habits in fish, as there are more than 32,000 species of fish...
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