References
- Stacey NH, Klaasen CD. Comparison of the effects of metals on cellular injury and lipid peroxidation in isolated rat hepatocytes. J Toxicol Environ Health. 1980; 7: 139-147. https://doi.org/10.1080/15287398109529965
- Roman HA, Walsh TL, Coull BA, Dewailly E, Guallar E, Hattis D, et al. Evaluation of the cardiovascular effects of methylmercury exposures: current evidence supports development of a doseresponse function for regulatory benefits analysis. Environ Health Perspect. 2011; 119: 607-614. https://doi.org/10.1289/ehp.1003012
- NIER (National Institute of Environmental Research). Annual report of the National Environmental Health Survey (KoNEHS). 2018.
- NIER (National Institute of Environmental Research). Annual report of the National Environmental Health Survey (KoNEHS). 2012.
- Rice DC, Schoeny R, Mahaffey K. Methods and rationale for derivation of a reference dose for methylmercury by the U.S. EPA. Risk analysis: an official publication of the Society for Risk Analysis. 2003; 23: 107-115. https://doi.org/10.1111/1539-6924.00294
- Yanga Z, Zhaoa Y, Lia Q, Shaoa Y, Yua X, Congb W, et al. Developmental exposure to mercury chloride impairs social behavior in male offspring dependent on genetic background and maternal autoimmune environment. Toxicology and Applied Pharmacology. 2019; 370: 1-13. https://doi.org/10.1016/j.taap.2019.03.006
- Kabuto M. Acute endocrine effects of a single administration of methylmercury chloride (MMC) in rats. Endocrinol Jpn. 1986; 33: 683-690. https://doi.org/10.1507/endocrj1954.33.683
- Vahter M, Akesson A, Lind B, Bjors U, Schutz A, Berglund M. Longitudinal study of methylmercury and inorganic mercury in blood and urine of pregnant and lactating women, as well as in 71 umbilical cord. Environmental Research. 2000; 84: 186-194. https://doi.org/10.1006/enrs.2000.4098
- Curle R, Persaud A. In vivo evaluation of teratogenesis and cytogenetic changes following methylmercuric chloride treatment. The Anatomical Record. 1987; 219: 289-295.
- Weng Z, Liu Z, Zhang S, Tao H, Ji X. Zinc Protection in Fetal Rats for Maternal Mercury Exposure-Induced Growth Retardation Is Probably Associated With S100B Expression. J Obstet Gynaecol Res. 2017; 43: 73-77. https://doi.org/10.1111/jog.13175
- Kim DS, Ahn SC, Chung HU, Kwon YM, Choi KH. A Study on Schoolchildren's Mercury Exposure and Related Health Effects in High Mercury Exposure Areas in Korea. J Environ Health Sci. 2015; 41: 268-276.
- Kim BM, Lee BE, Hong YC, Park H, Ha M, Kim YJ, et al. Mercury levels in maternal and cord blood and attained weight through the 24 months of life. Sci Total Environ. 2011; 410: 26-33. https://doi.org/10.1016/j.scitotenv.2011.08.060
- Robertson MC, Cosby H, Fresnoza A, Cattini PA, Shiu RP, et al. Expression, purification, and characterization of recombinant rat placental lactogen-I: a comparison with the native hormone. Endocrinology. 1994; 134: 393-400. https://doi.org/10.1210/en.134.1.393
- Dai G, Liu B, Szpirer C, Levan G, Kwok SC, et al. Prolactin-like protein-C variant: complementary deoxyribonucleic acid, unique six exon gene structure, and trophoblast cell-specific expression. Endocrinology. 1996; 137: 5009-5019. https://doi.org/10.1210/en.137.11.5009
- Forsyth I. Prolactin, growth hormones, and placental lactogens: an historical perspective. J Mammary Gland Biol Neoplasia. 1997; 2: 3-6.
- Lee CK, Kang SG, Lee JT, Lee SW, Kim JH, Son BC et al. Effects of perfluorooctane sulfuric acid on placental PRL-family hormone production and fetal growth retardation in mice. Molecular and Cellular Endocrinology. 2015; 401: 165-172. https://doi.org/10.1016/j.mce.2014.10.026
- Li J, Zhang N, Zhang Y, Hu X, Gao G, Ye Y, et al. Human placental lactogen mRNA in maternal plasma play a role in prenatal diagnosis of abnormally invasive placenta: yes or no? Gynecol Endocrinol. 2019; 35: 631-634. https://doi.org/10.1080/09513590.2019.1576607
- Lee JH. Methylmercuric chloride (MMC) and reduction of the fetal ossification in fisher-334 rats furing organogenesis. J Environ Health Sci. 2001; 27: 73-87.
- Oliveira CS, Oliveira VA, Costa LM, Pedroso TF, Fonseca MM, Bernardi JS, et al. Inorganic Mercury Exposure in Drinking Water Alters Essential Metal Homeostasis in Pregnant Rats Without Altering Rat Pup Behavior. Reprod Toxicol. 2016; 65: 18-23. https://doi.org/10.1016/j.reprotox.2016.06.013
- Simmons DG, Rawn S, Davies A, Hughes M, Cross JC. Spatial and temporal expression of the 23 murine Prolactin/Placental Lactogen-related genes is not associated with their position in the locus. BMC Genomics. 2008; 9: 352-373. https://doi.org/10.1186/1471-2164-9-352
- Thordarson G, Galosy S, Gudmundsson GO, Newcomer B, Sridaran R, et al. Interaction of mouse placental lactogens and androgens in regulating progesterone release in cultured mouse luteal cells. Endocrinology. 1997; 138: 3236-3241. https://doi.org/10.1210/en.138.8.3236
- Telleria CM, Zhong L, Deb S, Srivastava RK, Park KS, et al. Differential expression of the estrogen receptors alpha and beta in the rat corpus luteum of pregnancy: regulation by prolactin and placental lactogens. Endocrinology. 1998; 139: 2432-2442. https://doi.org/10.1210/en.139.5.2432
- Conliffe PR, Simmen RC, Buhi WC, Shiverick KT. Cloning of a novel rat placental prolactin-like protein C-related cDNA. Mol Reprod Dev. 1995; 41: 167-176. https://doi.org/10.1002/mrd.1080410207
- Cohick CB, Xu L, Soares MJ. Prolactin-like protein-B: heterologous expression and characterization of placental and decidual species. J Endocrinol. 1997; 152: 291-302. https://doi.org/10.1677/joe.0.1520291
- Rasmussen CA, Orwig KE, Vellucci S, Soares MJ. Dual expression of prolactin-related protein in decidua and trophoblast tissues during pregnancy in rats. Biol Reprod. 1997; 56: 647-654. https://doi.org/10.1095/biolreprod56.3.647
- Lee CK, Lee JT, Yu SJ, Kang SG, Moon CS et al. Effects of cadmium on the expression of placental lactogens and Pit-1 genes in the rat placental trophoblast cells. Molecular and Cellular Endocrinology. 2009; 298: 11-18. https://doi.org/10.1016/j.mce.2008.09.028
- Bodner M, Karin M. A pituitary-specific transacting factor can stimulate transcription from the growth hormone promoter in extracts of nonexpressing cells. Cell. 1987; 50: 267-275. https://doi.org/10.1016/0092-8674(87)90222-4
- Bamberger AM, Bamberger CM, Pu LP, Puy LA, Loh YP, et al. Expression of pit-1 messenger ribonucleic acid and protein in the human placenta. J Clin Endocrinol Metab. 1995; 80: 2021-2026. https://doi.org/10.1210/jc.80.7.2021
- Lee CK, Kang HS, Lee BJ, Kang HM, Choi WS, et al. Effects of dopamine and estrogen on the regulation of Pit-1 alpha, Pit-2 beta and PL-II gene expression in the rat placenta. Mol Cells. 1998; 8: 205-211.
- Roby KF, Soares MJ. Trophoblast cell differentiation and organization: role of fetal and ovarian signals. Placenta. 1993; 14: 529-545. https://doi.org/10.1016/S0143-4004(05)80206-1
- Cronier L, Guibourdenche J, Niger C, Malassine A. Oestradiol stimulates morphological and functional differentiation of human villous cytotrophoblast. Placenta. 1999; 20: 669-676. https://doi.org/10.1053/plac.1999.0423
- Zhanag X, Wang Y, Zhao Y, Chen X. Experimental study on the estrogen-like effect of mercuric chloride. Biometals. 2008; 21: 145-150.