The role of endogenous versus exogenous sources in the exposome of putative genotoxins and consequences for risk assessment | SpringerLink
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Toxicological aspects of the use of phenolic compounds in disease prevention. - Abstract - Europe PMC
Chemical repair of damaged leucine and tryptophane by thiophenols at close to diffusion‐controlled rates: Mechanisms and kinetics - Carreon‐Gonzalez - 2022 - Journal of Computational Chemistry - Wiley Online Library
Shared genetic etiology between Parkinson's disease and blood levels of specific lipids | npj Parkinson's Disease
Synthesis of new halogenated flavonoid-based isoxazoles: in vitro and in silico evaluation of a-amylase inhibitory potential, a SAR analysis and DFT studies - ScienceDirect
Cocrystals and a Salt of the Bioactive Flavonoid: Naringenin | Crystal Growth & Design
Consumption of flavonoids and risk of hormone-related cancers: a systematic review and meta-analysis of observational studies | Nutrition Journal | Full Text
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The N-terminal part of TIF1, a putative mediator of the ligand-dependent activation function (AF-2) of nuclear receptors, is fused to B-raf in the oncogenic protein T18. - Abstract - Europe PMC
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Frontiers | What Works for Whom: Patients' Psychological Resources and Vulnerabilities as Common and Specific Predictors of Working Alliance in Different Psychotherapies
Applied Sciences | Free Full-Text | Physiological Effects of Green-Colored Food-Derived Bioactive Compounds on Cardiovascular and Metabolic Diseases
Ring and Little Finger Metacarpal Fractures: Mechanisms, Locations, and Radiographic Parameters - Journal of Hand Surgery
Age and diet shape the genetic architecture of body weight in diversity outbred mice | eLife
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Persistent organic pollutants at the synapse: Shared phenotypes and converging mechanisms of developmental neurotoxicity - Latchney - 2021 - Developmental Neurobiology - Wiley Online Library
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Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity | Science
Quercetin acutely relaxes airway smooth muscle and potentiates β-agonist-induced relaxation via dual phosphodiesterase inhibition of PLCβ and PDE4. - Abstract - Europe PMC
