Publications by authors named "Elizabeth A Yu"

Article Synopsis
  • The study investigates the role of the APOBEC3B (A3B) enzyme in lung cancer, specifically in non-small-cell lung cancer (NSCLC) driven by the epidermal growth factor receptor (EGFR).
  • It was found that A3B expression can limit tumor growth in mouse models but is linked to resistance against EGFR-targeted therapies in tumors.
  • The research suggests that A3B could be targeted to improve the effectiveness of cancer treatments, as its upregulation was observed in both preclinical models and patients undergoing EGFR-targeted therapy.
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Article Synopsis
  • * Scientists studied lung cancer from 30 patients using a special technique called single-cell RNA sequencing, which looks at individual cells, to see how cancer and its surroundings work together.
  • * They found that cancer cells change in response to treatment, showing different signs depending on whether they survived or got worse, and this can help predict how well treatments will work.
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We examined the role of basic psychological needs as a mediator of the association between future orientation and depressive symptoms in a sample of 202 (159 female and 43 male) multiethnoracial adults. Multiple mediation analysis with 10,000 bootstraps was conducted to test for mediation. The association between future orientation and depressive symptoms was found to be accounted for by dimensions of basic psychological needs.

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In this study, authors examined basic psychological needs (namely, competence, autonomy, and relatedness) as potential mediators of the association between sexual assault and depressive symptoms in a sample of 342 college students. Results from conducting a multiple mediation test provided support for partial mediation involving the indirect effects of competence and autonomy. In contrast, no support for mediation was found involving relatedness.

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This study examined for ethnic variations in the predictive utility of body discrepancy and self-construal in eating disturbances between 156 European American and 129 Asian American females. We found important ethnic variations in the prediction model between these two groups, especially in the value of self-construal. Some implications of the present findings are discussed.

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Insulinoma-associated protein (IA)-2 and IA-2β are transmembrane proteins involved in neurotransmitter secretion. Mice with targeted disruption of both IA-2 and IA-2β (double-knockout, or DKO mice) have numerous endocrine and physiological disruptions, including disruption of circadian and diurnal rhythms. In the present study, we have assessed the impact of disruption of IA-2 and IA-2β on molecular rhythms in the brain and peripheral oscillators.

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The circadian clock imparts 24-hour rhythmicity on gene expression and cellular physiology in virtually all cells. Disruption of the genes necessary for the circadian clock to function has diverse effects, including aging-related phenotypes. Some circadian clock genes have been described as tumor suppressors, while other genes have less clear functions in aging and cancer.

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Background: Casein kinase 1 delta (CK1delta) plays a more prominent role in the regulation of circadian cycle length than its homologue casein kinase 1 epsilon (CK1epsilon) in peripheral tissues such as liver and embryonic fibroblasts. Mice lacking CK1delta die shortly after birth, so it has not been possible to assess the impact of loss of CK1delta on behavioral rhythms controlled by the master circadian oscillator in the suprachiasmatic nuclei (SCN).

Methodology/principal Findings: In the present study, mPER2::LUCIFERASE bioluminescence rhythms were monitored from SCN explants collected from neonatal mice.

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Both casein kinase 1 delta (CK1delta) and epsilon (CK1epsilon) phosphorylate core clock proteins of the mammalian circadian oscillator. To assess the roles of CK1delta and CK1epsilon in the circadian clock mechanism, we generated mice in which the genes encoding these proteins (Csnk1d and Csnk1e, respectively) could be disrupted using the Cre-loxP system. Cre-mediated excision of the floxed exon 2 from Csnk1d led to in-frame splicing and production of a deletion mutant protein (CK1delta(Delta2)).

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