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Altered histone modification, in turn, is associated with altered gene expression (Pal-Bhadra et al. 2007).
Affective disorders are associated with altered cognitive performance.
Both are associated with altered immune regulation and share several risk factors.
Accordingly, various diseases such as cardiomyopathies, neurodegenerative and inflammatory disorders, and cancer are associated with altered S100 protein levels.
Vitamin D status [25(OH D] has recently been reported to be associated with altered cellular bioenergetic profiles of peripheral blood mononuclear cells (PBMCs).
CYP2D6, CYP1A2, and CYP3A4/5 are major enzymes in the metabolism of antipsychotics and polymorphisms of alleles for these proteins are associated with altered plasma levels.
Therefore the BDNF Val66Met variant, which affects secretion of BDNF, may interact with early exposure to pain-related stress in children born very preterm, to differentially affect HPA regulation that in turn may be associated with altered cognitive performance.
Protein intake during the first and second trimesters of gestation has a sexually dimorphic effect on progeny plasma thyroid hormone concentrations, and these changes are associated with altered milk intake and postnatal growth pathway.
Senescence is associated with altered gene expression signatures that are cell- and context-dependent [22].
Genetic polymorphisms related to cardiovascular functions have been associated with altered HRV [8], [9], [10], [11].
Previous studies suggest that these SNPs are associated with altered TLR gene function and susceptibility to different infections.
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