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Jeroen L. A. Pennings

Researcher at Centre for Health Protection

Publications -  184
Citations -  4576

Jeroen L. A. Pennings is an academic researcher from Centre for Health Protection. The author has contributed to research in topics: Gene expression & Developmental toxicity. The author has an hindex of 37, co-authored 164 publications receiving 3787 citations. Previous affiliations of Jeroen L. A. Pennings include Maastricht University & Utrecht University.

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Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice

TL;DR: The findings establish the Ercc1∆/− mouse as a powerful model organism for health-sustaining interventions, reveal potential for reducing endogenous DNA damage, facilitate a better understanding of the molecular mechanism of dietary restriction and suggest a role for counterintuitive dietary-restriction-like therapy for human progeroid genome instability syndromes and possibly neurodegeneration in general.
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Chronically Alternating Light Cycles Increase Breast Cancer Risk in Mice

TL;DR: This study provides the first experimental proof that CRD increases breast cancer development, and suggests internal desynchronization and sleep disturbance as mechanisms linking shift work with cancer development and obesity.
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Evaluation of immunomodulation by Lactobacillus casei Shirota: Immune function, autoimmunity and gene expression

TL;DR: Experiments involving Lactobacillus casei Shirota (LcS) detected mainly enhancement of innate immune responses and promotion of Th1 mediated immune reactivity, which indicates that beneficial as well as harmful effects on immune related disorders could occur after LcS consumption.
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Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome

TL;DR: Comparison of corticogenesis, gene expression and behavior in three mouse models of Down syndrome revealed major differences between the models as well as significant limitations in each strain for understanding neurobiological changes in the human phenotype.
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Keratinocyte Gene Expression Profiles Discriminate Sensitizing and Irritating Compounds

TL;DR: In conclusion, KC expression profiling can identify contact sensitizers, providing opportunities for nonanimal testing for sensitizing potential and suggesting that contact Sensitizers induce the oxidative stress pathway in KC.