2015
DOI: 10.1016/j.envres.2015.05.004
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Maternal hemochromatosis gene H63D single-nucleotide polymorphism and lead levels of placental tissue, maternal and umbilical cord blood

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Cited by 12 publications
(8 citation statements)
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“…The most related genes affecting lead toxicokinetics are delta-aminolevulinic acid dehydratase (ALAD) gene, Vitamin D receptor (VDR) gene and human hemochromatosis gene (HFE) [2,33,34]. The genetic polymorphisms in VDR gene are associated with lead toxicity due to the relationship between Ca 2þ and Pb 2þ .…”
Section: Discussionmentioning
confidence: 99%
“…The most related genes affecting lead toxicokinetics are delta-aminolevulinic acid dehydratase (ALAD) gene, Vitamin D receptor (VDR) gene and human hemochromatosis gene (HFE) [2,33,34]. The genetic polymorphisms in VDR gene are associated with lead toxicity due to the relationship between Ca 2þ and Pb 2þ .…”
Section: Discussionmentioning
confidence: 99%
“…Although the precise mechanisms through which heavy metals actively cross the placental barrier remain unclear, it is likely that these otherwise foreign trace metals usurp the roles of evolutionarily conserved methods for the transfer of essential elements to the developing fetus. Lead (Pb), for instance, is able to utilize existing mechanisms for Fe homeostasis to disperse throughout the human body, including across the placenta [7,8]. Even excessive exposure to otherwise essential metals can compromise the placental barrier; for example, high manganese (Mn) concentrations have been observed in placental tissues from children with neural tube defects [9].…”
Section: The Placenta As a Window Into Fetal Exposurementioning
confidence: 99%
“…It is well documented that lead can cause deleterious effects on the reproductive, haematological and cardiovascular systems, neurotoxicity, nephrotoxicity, genotoxicity and embryotoxicity in laboratory animals and humans (Anjum et al, 2011;Kayaalti et al, 2015;Skerfving et al, 2015;Szymańska-Chabowska et al, 2015). Lead exposure is an established cause of chronic kidney disease in adults and children, where adverse associations between blood Pb and kidney function have been observed (lee & Kim, 2012).…”
Section: Introductionmentioning
confidence: 99%