Perinatal exposure to bisphenol-A impairs learning-memory by concomitant down-regulation of N-methyl-d-aspartate receptors of hippocampus in male offspring mice

Morris water maze: procedures for assessing spatial and related forms of learning and memory

Vorhees, C. V., & Williams, M. T. (2006) · Nature Protocols · doi:10.1038/nprot.2006.116 · Cited by 4,629 · see citing works

Long-Term Potentiation and Memory

Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,001 · see citing works

In vivo effects of bisphenol A in laboratory rodent studies

Richter, C. A., Birnbaum, L. S., Farabollini, F., Newbold, R. R., Rubin, B. S., Talsness, C. E., Vandenbergh, J. G., Walser-Kuntz, D. R., & vom Saal, F. S. (2007) · Reproductive Toxicology · doi:10.1016/j.reprotox.2007.06.004 · Cited by 1,147 · see citing works

Large Effects from Small Exposures. III. Endocrine Mechanisms Mediating Effects of Bisphenol A at Levels of Human Exposure

Welshons, W. V., Nagel, S. C., & Saal, F. S. V. (2006) · Endocrinology · doi:10.1210/en.2005-1159 · Cited by 968 · see citing works

Memory Formation: The Sequence of Biochemical Events in the Hippocampus and Its Connection to Activity in Other Brain Structures

Izquierdo, I., & Medina, J. H. (1997) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1997.3799 · Cited by 959 · see citing works

Estradiol and the Developing Brain

McCARTHY, M. M. (2008) · Physiological Reviews · doi:10.1152/physrev.00010.2007 · Cited by 885 · see citing works

Developmental changes in distribution of NMDA receptor channel subunit mRNAs

Watanabe, M., Inoue, Y., Sakimura, K., & Mishina, M. (1992) · Neuroreport · doi:10.1097/00001756-199212000-00027 · Cited by 721 · see citing works

Estradiol regulates hippocampal dendritic spine density via an N-methyl- D-aspartate receptor-dependent mechanism

Woolley, C. S., & McEwen, B. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07680.1994 · Cited by 679 · see citing works

Rapid bidirectional switching of synaptic NMDA receptors.

Bellone, C., & Nicoll, R. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.035 · Cited by 357 · see citing works

Low dose effects of bisphenol A on sexual differentiation of the brain and behavior in rats

Kubo, K., Arai, O., Omura, M., Watanabe, R., Ogata, R., & Aou, S. (2003) · Neuroscience Research · doi:10.1016/s0168-0102(02)00251-1 · Cited by 311 · see citing works

Morphological abnormalities in the brains of estrogen receptor β knockout mice

Wang, L., Andersson, S., Warner, M. N., & Gustafsson, J.-Α. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.041617498 · Cited by 272 · see citing works

Effects of perinatal exposure to bisphenol A on sociosexual behavior of female and male rats.

Farabollini, F., Porrini, S., Seta, D. D., Bianchi-Jassir, F., & Dessì‐Fulgheri, F. (2002) · Environmental Health Perspectives · doi:10.1289/ehp.02110s3409 · Cited by 204 · see citing works

NMDA Receptors and Learning and Memory Processes

Castellano, C., Cestari, V., & Ciamei, A. (2001) · Current Drug Targets · doi:10.2174/1389450013348515 · Cited by 197 · see citing works

The Environmental Estrogen Bisphenol A Inhibits Estradiol-Induced Hippocampal Synaptogenesis

MacLusky, N. J., Hajszan, T., & Leranth, C. (2005) · Environmental Health Perspectives · doi:10.1289/ehp.7633 · Cited by 196 · see citing works

The role of N ‐methyl‐ D ‐asparate receptors in neurogenesis

Nácher, J., & McEwen, B. S. (2006) · Hippocampus · doi:10.1002/hipo.20160 · Cited by 189 · see citing works

Perinatal Exposure to the Estrogenic Pollutant Bisphenol A Affects Behavior in Male and Female Rats

Farabollini, F. (1999) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(99)00136-7 · Cited by 183 · see citing works

Developmental exposure to environmental estrogens alters anxiety and spatial memory in female mice

Ryan, B. C., & Vandenbergh, J. G. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.01.007 · Cited by 180 · see citing works

Developmental exposure to low-dose estrogenic endocrine disruptors alters sex differences in exploration and emotional responses in mice.

Gioiosa, L., Fissore, E., Ghirardelli, G., Parmigiani, S., & Palanza, P. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.05.006 · Cited by 160 · see citing works

Prenatal exposure to bisphenol A impairs sexual differentiation of exploratory behavior and increases depression-like behavior in rats

Fujimoto, T., Kubo, K., & Aou, S. (2005) · Brain Research · doi:10.1016/j.brainres.2005.11.028 · Cited by 157 · see citing works

A neuronal analogue of state-dependent learning

Shulz, D. E., Sosnik, R., Ego‐Stengel, V., Haidarliu, S., & Ahissar, E. (2000) · Nature · doi:10.1038/35000586 · Cited by 153 · see citing works

Exposure to bisphenol A during the fetal and suckling periods disrupts sexual differentiation of the locus coeruleus and of behavior in the rat

Kubo, K., Arai, O., Ogata, R., Omura, M., Hori, T., & Aou, S. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)01760-8 · Cited by 150 · see citing works

NMDA receptor activation limits the number of synaptic connections during hippocampal development

Lüthi, A., Schwyzer, L., Mateos, J. M., Gähwiler, B. H., & McKinney, R. A. (2001) · Nature Neuroscience · doi:10.1038/nn744 · Cited by 138 · see citing works

Estrogen modulates synaptic N‐methyl‐ D ‐aspartate receptor subunit distribution in the aged hippocampus

Adams, M. M., Fink, S. E., Janssen, W. G. M., Shah, R. A., & Morrison, J. H. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20148 · Cited by 137 · see citing works

Behavioral Alterations in Response to Fear-Provoking Stimuli and Tranylcypromine Induced by Perinatal Exposure to Bisphenol A and Nonylphenol in Male Rats

Negishi, T., Kawasaki, K., Suzaki, S., Maeda, H., Ishii, Y., Kyuwa, S., Kuroda, Y., & Yoshikawa, Y. (2004) · Environmental Health Perspectives · doi:10.1289/ehp.6961 · Cited by 126 · see citing works

Sex Differences in Hippocampal Estradiol-Induced N-Methyl-D-Aspartic Acid Binding and Ultrastructural Localization of Estrogen Receptor-Alpha

Romeo, R. D., McCarthy, J. B., Wang, A. C., Milner, T. A., & McEwen, B. S. (2005) · Neuroendocrinology · doi:10.1159/000089557 · Cited by 115 · see citing works

NR2B‐ and NR2D‐containing synaptic NMDA receptors in developing rat substantia nigra pars compacta dopaminergic neurones

Brothwell, S., Barber, J., Monaghan, D. T., Jane, D. E., Gibb, A., & Jones, S. (2008) · Journal of Physiology · doi:10.1113/jphysiol.2007.144618 · Cited by 112 · see citing works

Estradiol Targets Synaptic Proteins to Induce Glutamatergic Synapse Formation in Cultured Hippocampal Neurons: Critical Role of Estrogen Receptor-

Jelks, K. B., Wylie, R., Floyd, C. L., McAllister, A. K., & Wise, P. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.0909-07.2007 · Cited by 111 · see citing works

Perinatal bisphenol A affects the behavior and SRC-1 expression of male pups but does not influence on the thyroid hormone receptors and its responsive gene

Xu, X., Liu, Y., Sadamatsu, M., Tsutsumi, S., Akaike, M., Ushijima, H., & Kato, N. (2007) · Neuroscience Research · doi:10.1016/j.neures.2007.02.011 · Cited by 110 · see citing works

Memory impairment associated with a dysfunction of the hippocampal cholinergic system induced by prenatal and neonatal exposures to bisphenol-A

Miyagawa, K., Narita, M., Narita, M., Akama, H., & Suzuki, T. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.01.088 · Cited by 108 · see citing works

Developmental Exposure to Bisphenol A Impairs the Uterine Response to Ovarian Steroids in the Adult

Varayoud, J., Ramos, J. G., Bosquiazzo, V. L., Muñoz‐de‐Toro, M., & Luque, E. H. (2008) · Endocrinology · doi:10.1210/en.2008-0651 · Cited by 97 · see citing works

Prenatal exposure to bisphenol A affects adult murine neocortical structure

Nakamura, K., Itoh, K., Sugimoto, T., & Fushiki, S. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.02.093 · Cited by 87 · see citing works

Effect of Neonatal Rat Bisphenol a Exposure on Performance in the Morris Water Maze

Carr, R. L., Bertasi, F., Betancourt, A. M., Bowers, S. D., Gandy, B. S., Ryan, P. L., & Willard, S. T. (2003) · Journal of Toxicology and Environmental Health Part A · doi:10.1080/713853983 · Cited by 85 · see citing works

Aqueous Extract of Black Maca (Lepidium meyenii) on Memory Impairment Induced by Ovariectomy in Mice

Rubio, J., Wang, Q., Liu, X., Jiang, Z., Dang, H., Chen, S., & Gonzales, G. F. (2008) · Evidence-based Complementary and Alternative Medicine · doi:10.1093/ecam/nen063 · Cited by 83 · see citing works

Effects of estradiol benzoate on learning-memory behavior and synaptic structure in ovariectomized mice

Xu, X., & Zhang, Z. (2006) · Life Sciences · doi:10.1016/j.lfs.2006.04.020 · Cited by 78 · see citing works

Beta estrogen receptor knockout (BERKO) mice present attenuated hippocampal CA1 long-term potentiation and related memory deficits in contextual fear conditioning

Day, M., Sung, A., Logue, S. F., Bowlby, M. R., & Arias, R. L. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.05.011 · Cited by 74 · see citing works

Bisphenol-A differently affects estrogen receptors-α in estrous-cycling and lactating female rats

Aloisi, A. M., Seta, D. D., Ceccarelli, I., & Farabollini, F. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02092-4 · Cited by 70 · see citing works

Assembly and forward trafficking of NMDA receptors (Review)

Stephenson, F. A., Cousins, S. L., & Kenny, A. V. (2008) · Molecular Membrane Biology · doi:10.1080/09687680801971367 · Cited by 67 · see citing works

Effects of pre- and neonatal exposure to bisphenol A on murine brain development

Tando, S., Itoh, K., Yaoi, T., Ikeda, J., Fujiwara, Y., & Fushiki, S. (2006) · Brain and Development · doi:10.1016/j.braindev.2006.10.003 · Cited by 62 · see citing works

Distribution of N-methyl-d-aspartate receptors (NMDARs) in the developing rat brain

Takai, H., Katayama, K., Uetsuka, K., Nakayama, H., & Doi, K. (2003) · Experimental and Molecular Pathology · doi:10.1016/s0014-4800(03)00030-3 · Cited by 61 · see citing works

AMPA, kainate, and NMDA receptor densities in the hippocampus of untreated male rats and females in estrus and diestrus

Palomero‐Gallagher, N., Bidmon, H. J., & Zilles, K. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10638 · Cited by 61 · see citing works

Environmental Enrichment Induces Synaptic Structural Modification After Transient Focal Cerebral Ischemia in Rats

Xu, X., Ye, L., & Ruan, Q. (2009) · Experimental Biology and Medicine · doi:10.3181/0804-rm-128 · Cited by 60 · see citing works

Effects of perinatal exposure to bisphenol A on the behavior of offspring in F344 rats

Negishi, T., Kawasaki, K., Takatori, A., Ishii, Y., Kyuwa, S., Kuroda, Y., & Yoshikawa, Y. (2003) · Environmental Toxicology and Pharmacology · doi:10.1016/s1382-6689(03)00044-9 · Cited by 57 · see citing works

Changes in estrogen receptors α and β expression in the brain of mice exposed prenatally to bisphenol A

Kawai, K., Murakami, S., Senba, E., Yamanaka, T., Fujiwara, Y., Arimura, C., Nozaki, T., Takii, M., & Kubo, C. (2007) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2006.04.002 · Cited by 53 · see citing works

Presynaptic N‐methyl‐D‐aspartate receptor expression is increased by estrogen in an aromatase‐rich area of the songbird hippocampus

Saldanha, C. J., Schlinger, B. A., Micevych, P. E., & Horváth, T. L. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.11035 · Cited by 52 · see citing works

Estrogen receptor beta is expressed in human embryonic brain cells and is regulated by 17β‐estradiol

Fried, G. M., Andersson, E. R., Csöregh, L., Enmark, E., Gustafsson, J.-Α., Aanesen, A., & Österlund, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03693.x · Cited by 40 · see citing works

Glycine site of the excitatory amino acid N-methyl-D-aspartate receptor in neonatal and adult brain.

D'Souza, S. W., McConnell, S. E., Slater, P., & Barson, A. J. (1993) · Archives of Disease in Childhood · doi:10.1136/adc.69.2.212 · Cited by 40 · see citing works

Hippocampal NMDA receptor subunit expression and watermaze learning in estrogen deficient female mice

Boon, W. C., Diepstraten, J., van der Burg, J. M. M., Jones, M. E. E., Simpson, E. R., & van den Buuse, M. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.07.004 · Cited by 33 · see citing works

Developmental regulation of subunit composition of extrasynaptic NMDA receptors in neocortical neurones

Mohrmann, R., Hatt, H. H., & Gottmann, K. (2000) · Neuroreport · doi:10.1097/00001756-200004270-00012 · Cited by 32 · see citing works

Extracellular levels of brain aspartate, glutamate and GABA during an inhibitory avoidance response in the rat

Ballini, C., Corte, L., Pazzagli, M., Colivicchi, M. A., Pepeu, G., Tipton, K. F., & Giovannini, M. G. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05452.x · Cited by 25 · see citing works

Environmental impacts on brain functions: Low dose effects of bisphenol A during perinatal critical period

Fujimoto, T., Kubo, K., & Aou, S. (2007) · International Congress Series · doi:10.1016/j.ics.2006.12.002 · Cited by 17 · see citing works

N-methyl-D-aspartate receptors are involved in lithium-induced state-dependent learning in mice

Rezayat, S. M., Niasari, H., Ahmadi, S., Parsaei, L., & Zarrindast, M. (2009) · Journal of Psychopharmacology · doi:10.1177/0269881108100093 · Cited by 11 · see citing works

Untitled work

(1997) · doi:10.1002/(sici)1096-9861(19971201)388:4

Scientific Opinion on the risks to public health related to the presence of bisphenol A (BPA) in foodstuffs

EFSA Panel on Food Contact Materials, E. (2015) · EFSA Journal · doi:10.2903/j.efsa.2015.3978 · Cited by 1,026 · see citing works

Are Structural Analogues to Bisphenol A Safe Alternatives?

Rosenmai, A. K., Dybdahl, M., Pedersen, M., van Vugt‐Lussenburg, B. M. A., Wedebye, E. B., Taxvig, C., & Vinggaard, A. M. (2014) · Toxicological Sciences · doi:10.1093/toxsci/kfu030 · Cited by 430 · see citing works

Non-Monotonic Dose Responses in Studies of Endocrine Disrupting Chemicals: Bisphenol a as a Case Study

Vandenberg, L. N. (2013) · Dose-Response · doi:10.2203/dose-response.13-020.vandenberg · Cited by 406 · see citing works

Gestational Exposure to Bisphenol A Produces Transgenerational Changes in Behaviors and Gene Expression

Wolstenholme, J. T., Edwards, M., Shetty, S. R. J., Gatewood, J. D., Taylor, J. A., Rissman, E. F., & Connelly, J. J. (2012) · Endocrinology · doi:10.1210/en.2012-1195 · Cited by 319 · see citing works

The role of bisphenol A in shaping the brain, epigenome and behavior

Wolstenholme, J. T., Rissman, E. F., & Connelly, J. J. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.10.001 · Cited by 309 · see citing works

Epigenetic perspective on the developmental effects of bisphenol A

Kundaković, M., & Champagne, F. A. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.02.005 · Cited by 270 · see citing works

Bisphenol A and its analogues: A comprehensive review to identify and prioritize effect biomarkers for human biomonitoring

Mustieles, V., D’Cruz, S. C., Couderq, S., Rodríguez‐Carrillo, A., Fini, J., Hofer, T., Steffensen, I., Dirven, H. A. A. M., Barouki, R., Olea, N., et al. (2020) · Environment International · doi:10.1016/j.envint.2020.105811 · Cited by 269 · see citing works

Current Knowledge on Endocrine Disrupting Chemicals (EDCs) from Animal Biology to Humans, from Pregnancy to Adulthood: Highlights from a National Italian Meeting

Street, M. E., Angelini, S., Bernasconi, S., Burgio, E., Cassio, A., Catellani, C., Cirillo, F., Deodati, A., Fabbrizi, E., Fanos, V., et al. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19061647 · Cited by 261 · see citing works

Multigenerational and transgenerational effects of endocrine disrupting chemicals: A role for altered epigenetic regulation?

Xin, F., Susiarjo, M., & Bartolomei, M. S. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.05.008 · Cited by 238 · see citing works

Low dose effects of bisphenol A

Vandenberg, L. N., Ehrlich, S., Belcher, S. M., Ben‐Jonathan, N., Dolinoy, D. C., Hugo, E. R., Hunt, P. A., Newbold, R. R., Rubin, B. S., Saili, K. S., et al. (2013) · Endocrine Disruptors · doi:10.4161/endo.26490 · Cited by 238 · see citing works

Biomonitoring of bisphenol A concentrations in maternal and umbilical cord blood in regard to birth outcomes and adipokine expression: a birth cohort study in Taiwan

Chou, W., Chen, J., Lin, C.-F., Chen, Y., Shih, F.-C., & Chuang, C. (2011) · Environmental Health · doi:10.1186/1476-069x-10-94 · Cited by 206 · see citing works

Neurodevelopmental low-dose bisphenol A exposure leads to early life-stage hyperactivity and learning deficits in adult zebrafish

Saili, K. S., Corvi, M. M., Weber, D. N., Patel, A. U., Das, S. R., Przybyla, J., Anderson, K. A., & Tanguay, R. L. (2011) · Toxicology · doi:10.1016/j.tox.2011.11.001 · Cited by 195 · see citing works

Prenatal exposure to bisphenol A and phthalates and infant neurobehavior

Yolton, K. A., Xu, Y. Y., Strauss, D., Altaye, M., Calafat, A. M., & Khoury, J. C. (2011) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2011.08.003 · Cited by 192 · see citing works

Neurodevelopmental Disorders and Environmental Toxicants: Epigenetics as an Underlying Mechanism

Tran, N. Q. V., & Miyake, K. (2017) · International Journal of Genomics · doi:10.1155/2017/7526592 · Cited by 183 · see citing works

Disruption of adult expression of sexually selected traits by developmental exposure to bisphenol A

Jašarević, E., Sieli, P. T., Twellman, E. E., Welsh, T. H., Schachtman, T. R., Roberts, R. M., Geary, D. C., & Rosenfeld, C. S. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107958108 · Cited by 177 · see citing works

Bisphenol A exposure and children’s behavior: A systematic review

Ejaredar, M., Lee, Y., Roberts, D. J., Sauve, R. S., & Dewey, D. (2016) · Journal of Exposure Science & Environmental Epidemiology · doi:10.1038/jes.2016.8 · Cited by 170 · see citing works

Gestational Exposure to Low Dose Bisphenol A Alters Social Behavior in Juvenile Mice

Wolstenholme, J. T., Taylor, J. A., Shetty, S. R. J., Edwards, M., Connelly, J. J., & Rissman, E. F. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025448 · Cited by 168 · see citing works

Scientific Opinion on Bisphenol A: evaluation of a study investigating its neurodevelopmental toxicity, review of recent scientific literature on its toxicity and advice on the Danish risk assessment of Bisphenol A

EFSA Panel on food contact materials, E. (2010) · EFSA Journal · doi:10.2903/j.efsa.2010.1829 · Cited by 165 · see citing works

Neurological Effects of Bisphenol A and its Analogues

Inadera, H. (2015) · International Journal of Medical Sciences · doi:10.7150/ijms.13267 · Cited by 159 · see citing works

Transgenerational effects of prenatal bisphenol A on social recognition

Wolstenholme, J. T., Goldsby, J. A., & Rissman, E. F. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.09.007 · Cited by 157 · see citing works

Current concepts in neuroendocrine disruption

León‐Olea, M., Martyniuk, C. J., Orlando, E. F., Ottinger, M. A., Rosenfeld, C. S., Wolstenholme, J. T., & Trudeau, V. L. (2014) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2014.02.005 · Cited by 144 · see citing works

Neurotoxicity of Endocrine Disruptors: Possible Involvement in Brain Development and Neurodegeneration

Masuo, Y., & Ishido, M. (2011) · Journal of Toxicology and Environmental Health Part B · doi:10.1080/10937404.2011.578557 · Cited by 137 · see citing works

Lifestyle, Pregnancy and Epigenetic Effects

Barua, S., & Junaid, M. A. (2015) · Epigenomics · doi:10.2217/epi.14.71 · Cited by 129 · see citing works

Gestational exposure to bisphenol A and cross-fostering affect behaviors in juvenile mice.

Cox, K. H., Gatewood, J. D., Howeth, C., & Rissman, E. F. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.07.008 · Cited by 127 · see citing works

Human health risk assessment of bisphenol A (BPA) through meat products

Wang, X., Nag, R., Brunton, N. P., Siddique, M. A. B., Harrison, S. M., Monahan, F. J., & Cummins, E. (2022) · Environmental Research · doi:10.1016/j.envres.2022.113734 · Cited by 125 · see citing works

Sex and dose-dependent effects of developmental exposure to bisphenol A on anxiety and spatial learning in deer mice (Peromyscus maniculatus bairdii) offspring

Jašarević, E., Williams, S. A., Vandas, G. M., Ellersieck, M. R., Liao, C., Kannan, K., Roberts, R. M., Geary, D. C., & Rosenfeld, C. S. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.09.009 · Cited by 124 · see citing works

Effect of triclosan, triclocarban, 2,2′,4,4′-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis

Wu, Y., Beland, F. A., & Fang, J. (2016) · Toxicology in Vitro · doi:10.1016/j.tiv.2016.01.014 · Cited by 122 · see citing works

Effects of perinatal exposure to low dose of bisphenol A on anxiety like behavior and dopamine metabolites in brain

Matsuda, S., Matsuzawa, D., Ishii, D., Tomizawa, H., Sutoh, C., Nakazawa, K., Amano, K., Sajiki, J., & Shimizu, E. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.06.016 · Cited by 122 · see citing works

Estrogen-Induced Memory Enhancements Are Blocked by Acute Bisphenol A in Adult Female Rats: Role of Dendritic Spines

Inagaki, T., Frankfurt, M., & Luine, V. N. (2012) · Endocrinology · doi:10.1210/en.2012-1121 · Cited by 117 · see citing works

Low‐dose effect of developmental bisphenol A exposure on sperm count and behaviour in rats

Hass, U., Christiansen, S., Boberg, J., Rasmussen, M., Mandrup, K. R., & Axelstad, M. (2016) · Andrology · doi:10.1111/andr.12176 · Cited by 112 · see citing works

Bisphenol A in relation to behavior and learning of school‐age children

Hong, S., Hong, Y., Kim, J., Park, E. J., Shin, M., Kim, B., Yoo, H., Cho, I., Bhang, S., & Cho, S.-C. (2013) · Journal of Child Psychology and Psychiatry · doi:10.1111/jcpp.12050 · Cited by 111 · see citing works

Perinatal exposure of rats to Bisphenol A affects fertility of male offspring—An overview

Salian, S., Doshi, T., & Vanage, G. R. (2010) · Reproductive Toxicology · doi:10.1016/j.reprotox.2010.10.008 · Cited by 103 · see citing works

Detrimental Effects of Bisphenol Compounds on Physiology and Reproduction in Fish: A Literature Review

Faheem, M., & Bhandari, R. K. (2020) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2020.103497 · Cited by 113 · see citing works

Prenatal maternal and childhood bisphenol a exposure and brain structure and behavior of young children

the APrON Study Team, Grohs, M. N., Reynolds, J. E., Liu, J., Martin, J. W., Pollock, T., Lebel, C. A., & Dewey, D. (2019) · Environmental Health · doi:10.1186/s12940-019-0528-9 · Cited by 100 · see citing works

Neuroprotective effects of Withania somnifera in BPA induced-cognitive dysfunction and oxidative stress in mice

Birla, H., Keswani, C., Nand, S., Singh, S. S., Zahra, W., Dilnashin, H., Rathore, A. S., & Singh, S. P. (2019) · Behavioral and Brain Functions · doi:10.1186/s12993-019-0160-4 · Cited by 101 · see citing works

Gestational and lactational exposure to bisphenol-A affects anxiety- and depression-like behaviors in mice

Xu, X., Hong, X., Xie, L., Li, T., Yang, Y., Zhang, Q., Zhang, G., & Liu, X. (2012) · Hormones and Behavior · doi:10.1016/j.yhbeh.2012.08.005 · Cited by 95 · see citing works

A Review of Recent Studies on Bisphenol A and Phthalate Exposures and Child Neurodevelopment

Minatoya, M., & Kishi, R. (2021) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph18073585 · Cited by 97 · see citing works

Exposure to bisphenol A appears to impair hippocampal neurogenesis and spatial learning and memory

Kim, M. E., Park, H. R., Gong, E. J., Choi, S. Y., Kim, H. S., & Lee, J. (2011) · Food and Chemical Toxicology · doi:10.1016/j.fct.2011.09.017 · Cited by 95 · see citing works

17α-Ethinyl estradiol affects anxiety and shoaling behavior in adult male zebra fish (Danio rerio)

Reyhanian, N., Volkova, K., Hallgren, S., Bollner, T., Olsson, P.-E., Olsén, H., & Hällström, I. P. (2011) · Aquatic Toxicology · doi:10.1016/j.aquatox.2011.05.009 · Cited by 93 · see citing works

Opening the black box of endocrine disruption of brain development: Lessons from the characterization of Bisphenol A

Nesan, D., Sewell, L., & Kurrasch, D. M. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.12.001 · Cited by 92 · see citing works

Exposure to Microplastics during Early Developmental Stage: Review of Current Evidence

Amran, N. H., Zaid, S. S. M., Mokhtar, M. H., Manaf, L. A., & Othman, S. (2022) · Toxics · doi:10.3390/toxics10100597 · Cited by 92 · see citing works

Sex-specific influence of exposure to bisphenol-A between adolescence and young adulthood on mouse behaviors

Xu, X., Dong, T., Hong, X., Chen, L., & Xie, L. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.027 · Cited by 88 · see citing works

Neurotoxicity of low bisphenol A (BPA) exposure for young male mice: Implications for children exposed to environmental levels of BPA

Zhou, Y., Wang, Z., Xia, M., Zhuang, S., Gong, X., Pan, J., Li, C., Fan, R., Pang, Q., & Lu, S. (2017) · Environmental Pollution · doi:10.1016/j.envpol.2017.05.043 · Cited by 87 · see citing works

Bisphenol A Impairs Synaptic Plasticity by Both Pre‐ and Postsynaptic Mechanisms

Hu, F., Li, T., Gong, H., Chen, Z., Jin, Y., Xu, G., & Wang, M. (2017) · Advanced Science · doi:10.1002/advs.201600493 · Cited by 87 · see citing works

The impact of neonatal bisphenol-A exposure on sexually dimorphic hypothalamic nuclei in the female rat

Adewale, H. B., Todd, K. L., Mickens, J. A., & Patisaul, H. B. (2011) · NeuroToxicology · doi:10.1016/j.neuro.2010.07.008 · Cited by 86 · see citing works

Impairment of object recognition memory by maternal bisphenol A exposure is associated with inhibition of Akt and ERK/CREB/BDNF pathway in the male offspring hippocampus

Wang, C., Li, Z., Han, H., Luo, G., Zhou, B., Wang, S., & Wang, J. (2016) · Toxicology · doi:10.1016/j.tox.2016.01.010 · Cited by 86 · see citing works

Effects of uterine and lactational exposure to di-(2-ethylhexyl) phthalate on spatial memory and NMDA receptor of hippocampus in mice

Dai, Y., Yang, Y., Xu, X., & Hu, Y. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.03.008 · Cited by 81 · see citing works

Exposure to bisphenol A and behavior in school-age children

Pérez‐Lobato, R., Mustieles, V., Calvente, I., Jiménez-Díaz, I., Ramos, R., Caballero‐Casero, N., López-Jiménez, F. J., Rubio, S., Olea, N., & Fernández, M. F. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.12.001 · Cited by 84 · see citing works

Protective effect of N-acetylcysteine on bisphenol A-induced cognitive dysfunction and oxidative stress in rats

Jain, S., Kumar, C. H., Suranagi, U. D., & Mediratta, P. K. (2011) · Food and Chemical Toxicology · doi:10.1016/j.fct.2011.03.032 · Cited by 79 · see citing works

The detrimental effect of microplastics on critical periods of development in the neuroendocrine system

Solleiro-Villavicencio, H., de León, C. T. G., Río‐Araiza, V. H. D., & Morales‐Montor, J. (2020) · Birth Defects Research · doi:10.1002/bdr2.1776 · Cited by 80 · see citing works

Prenatal and postnatal bisphenol A exposure and social impairment in 4-year-old children

Lim, Y.-H., Bae, S., Kim, B.-N., Shin, C. H., Lee, Y. A., Kim, J. I., & Hong, Y. (2017) · Environmental Health · doi:10.1186/s12940-017-0289-2 · Cited by 77 · see citing works

The ENDpoiNTs Project: Novel Testing Strategies for Endocrine Disruptors Linked to Developmental Neurotoxicity

Lupu, D., Andersson, P. L., Bornehag, C., DEMENEIX, B. A., Fritsche, E., Gennings, C., LICHTENSTEIGER, W., Leist, M., Leonards, P. E. G., Ponsonby, A., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21113978 · Cited by 75 · see citing works

Effect of Bisphenol A on Rat Metabolic Profiling Studied by Using Capillary Electrophoresis Time-of-Flight Mass Spectrometry

Zeng, J., Kuang, H., Hu, C., Shi, X., Yan, M., Xu, L., Wang, L., Xu, C., & Xu, G. (2013) · Environmental Science & Technology · doi:10.1021/es400490f · Cited by 74 · see citing works

Gestational Exposure to Common Endocrine Disrupting Chemicals and Their Impact on Neurodevelopment and Behavior

Nesan, D., & Kurrasch, D. M. (2019) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021119-034555 · Cited by 73 · see citing works

Does Bisphenol A Confer Risk of Neurodevelopmental Disorders? What We Have Learned from Developmental Neurotoxicity Studies in Animal Models

Welch, C. J., & Mulligan, K. A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052894 · Cited by 74 · see citing works

Adolescent exposure to Bisphenol-A increases anxiety and sucrose preference but impairs spatial memory in rats independent of sex

Diaz Weinstein, S., Villafane, J. J., Juliano, N., & Bowman, R. E. (2013) · Brain Research · doi:10.1016/j.brainres.2013.07.018 · Cited by 73 · see citing works

Bisphenol A Inhibits Voltage-Activated Ca2+ Channels in Vitro: Mechanisms and Structural Requirements

Deutschmann, A. U., Hans, M., Meyer, R., Häberlein, H., & Swandulla, D. (2012) · Molecular Pharmacology · doi:10.1124/mol.112.081372 · Cited by 74 · see citing works

Prenatal phthalate, triclosan, and bisphenol A exposures and child visual-spatial abilities

Braun, J. M., Bellinger, D. C., Hauser, R. B., Wright, R. O., Chen, A., Calafat, A. M., Yolton, K. A., & Lanphear, B. P. (2016) · NeuroToxicology · doi:10.1016/j.neuro.2016.11.009 · Cited by 70 · see citing works

Assessment of dietary exposure to bisphenol A in the French population with a special focus on risk characterisation for pregnant French women

Bemrah, N., Jean, J., Rivière, G., Sanaa, M., Leconte, S., Bachelot, M., Deceuninck, Y., Bizec, B. L., Dauchy, X., Roudot, A., et al. (2014) · Food and Chemical Toxicology · doi:10.1016/j.fct.2014.07.005 · Cited by 70 · see citing works

Changes in memory and synaptic plasticity induced in male rats after maternal exposure to bisphenol A

Wang, C., Niu, R., Zhu, Y., Han, H., Luo, G., Zhou, B., & Wang, J. (2014) · Toxicology · doi:10.1016/j.tox.2014.05.001 · Cited by 70 · see citing works

Developmental exposure of zebrafish (Danio rerio) to 17α-ethinylestradiol affects non-reproductive behavior and fertility as adults, and increases anxiety in unexposed progeny

Volkova, K., Caspillo, N. R., Porseryd, T., Hallgren, S., Dinnétz, P., & Porsch-Hällström, I. (2015) · Hormones and Behavior · doi:10.1016/j.yhbeh.2015.05.014 · Cited by 69 · see citing works

Sex-specific effects of bisphenol-A on memory and synaptic structural modification in hippocampus of adult mice

Xu, X., Liu, X., Zhang, Q., Zhang, G., Lu, Y., Ruan, Q., Dong, F., & Yang, Y. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.03.004 · Cited by 69 · see citing works

Perinatal exposure to bisphenol-A inhibits synaptogenesis and affects the synaptic morphological development in offspring male mice

Xu, X., Xie, L., Hong, X., Ruan, Q., Lü, H., Zhang, Q., Zhang, G., & Liu, X. (2013) · Chemosphere · doi:10.1016/j.chemosphere.2012.12.065 · Cited by 68 · see citing works

Sex Differences in the Effects of Prenatal Bisphenol A Exposure on Genes Associated with Autism Spectrum Disorder in the Hippocampus

Thongkorn, S., Kanlayaprasit, S., Jindatip, D., Tencomnao, T., Hu, V. W., & Sarachana, T. (2019) · Scientific Reports · doi:10.1038/s41598-019-39386-w · Cited by 66 · see citing works

Sex differences in the effects of prenatal bisphenol A exposure on autism-related genes and their relationships with the hippocampus functions

Thongkorn, S., Kanlayaprasit, S., Panjabud, P., Saeliw, T., Jantheang, T., Kasitipradit, K., Sarobol, S., Jindatip, D., Hu, V. W., Tencomnao, T., et al. (2021) · Scientific Reports · doi:10.1038/s41598-020-80390-2 · Cited by 64 · see citing works

Bisphenol-A exposure during adolescence leads to enduring alterations in cognition and dendritic spine density in adult male and female rats

Bowman, R. E., Luine, V. N., Weinstein, S. D., Khandaker, H., DeWolf, S., & Frankfurt, M. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.12.007 · Cited by 64 · see citing works

Prenatal bisphenol A exposure, fetal thyroid hormones and neurobehavioral development in children at 2 and 4 years: A prospective cohort study

Li, F., Yang, F., Li, D., Tian, Y., Miao, M., Zhang, Y., Ji, H., Yuan, W., & Liang, H. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.137887 · Cited by 63 · see citing works

Prenatal bisphenol A exposure is linked to epigenetic changes in glutamate receptor subunit gene Grin2b in female rats and humans

Alavian-Ghavanini, A., Lin, P.-I., Lind, P. M., Risén Rimfors, S., Halin Lejonklou, M., Dunder, L., Tang, M., Lindh, C., Bornehag, C.-G., & Rüegg, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-29732-9 · Cited by 61 · see citing works

Data integration, analysis, and interpretation of eight academic CLARITY-BPA studies

Heindel, J. J., Belcher, S. M., Flaws, J. A., Prins, G. S., Ho, S., Mao, J., Patisaul, H. B., Ricke, W. A., Rosenfeld, C. S., Soto, A. M., et al. (2020) · Reproductive Toxicology · doi:10.1016/j.reprotox.2020.05.014 · Cited by 61 · see citing works

Sex-biased impact of endocrine disrupting chemicals on behavioral development and vulnerability to disease: Of mice and children

Palanza, P., Paterlini, S., Brambilla, M., Ramundo, G., Caviola, G., Gioiosa, L., Parmigiani, S., Saal, F. S. V., & Ponzi, D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.11.015 · Cited by 59 · see citing works

Protective effects of lycopene on hippocampal neurotoxicity and memory impairment induced by bisphenol A in rats

Morsy, E. M. E., & Ahmed, M. (2020) · Human & Experimental Toxicology · doi:10.1177/0960327120909882 · Cited by 58 · see citing works

In utero exposure to endocrine disruptors and developmental neurotoxicity: Implications for behavioural and neurological disorders in adult life

Arul, G. L. R., Subhashree, K. D., & Kantayya, K. E. (2021) · Environmental Research · doi:10.1016/j.envres.2021.111829 · Cited by 57 · see citing works

An effect-directed strategy for characterizing emerging chemicals in food contact materials made from paper and board

Rosenmai, A. K., Bengtström, L., Taxvig, C., Trier, X., Petersen, J. H., Svingen, T., Binderup, M., Alice, V. V.-L. B. M., Dybdahl, M., Granby, K., et al. (2017) · Food and Chemical Toxicology · doi:10.1016/j.fct.2017.05.061 · Cited by 56 · see citing works

Impairment of learning and memory induced by perinatal exposure to BPA is associated with ERα-mediated alterations of synaptic plasticity and PKC/ERK/CREB signaling pathway in offspring rats

Wu, D., Wu, F., Lin, R., Meng, Y., Wei, W., Sun, Q., & Jia, L. (2020) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2020.04.023 · Cited by 55 · see citing works

Prenatal exposure to bisphenol A alters the transcriptome-interactome profiles of genes associated with Alzheimer’s disease in the offspring hippocampus

Sukjamnong, S., Thongkorn, S., Kanlayaprasit, S., Saeliw, T., Hussem, K., Warayanon, W., Hu, V. W., Tencomnao, T., & Sarachana, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-65229-0 · Cited by 56 · see citing works

Milestones on Steroids and the Nervous System: 10 Years of Basic and Translational Research

Panzica, G., Balthazart, J., Frye, C. A., García‐Segura, L. M., Herbison, A. E., Mensah‐Nyagan, A. G., McCarthy, M. M., & Melcangi, R. C. (2011) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2011.02265.x · Cited by 55 · see citing works

Maternal Bisphenol A Diet Induces Anxiety-Like Behavior in Female Juvenile with Neuroimmune Activation

Luo, G., Wang, S., Li, Z., Wei, R., Zhang, L., Liu, H., Wang, C., Niu, R., & Wang, J. (2014) · Toxicological Sciences · doi:10.1093/toxsci/kfu085 · Cited by 53 · see citing works

Perinatal Exposure to Low-Dose Bisphenol A Impairs Spatial Learning and Memory in Male Rats

Kuwahara, R., Kawaguchi, S., Kohara, Y., Cui, H., & Yamashita, K. (2013) · Journal of Pharmacological Sciences · doi:10.1254/jphs.13093fp · Cited by 52 · see citing works

Bisphenol-A rapidly promotes dynamic changes in hippocampal dendritic morphology through estrogen receptor-mediated pathway by concomitant phosphorylation of NMDA receptor subunit NR2B

Xu, X., Ye, Y., Li, T., Chen, L., Dong, T., Luo, Q., & Lü, M. (2010) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2010.09.007 · Cited by 52 · see citing works

The influence of study design and sex-differences on results from developmental neurotoxicity studies of bisphenol A, implications for toxicity testing

Beronius, A., Johansson, N., Rudén, C., & Hanberg, A. (2013) · Toxicology · doi:10.1016/j.tox.2013.02.012 · Cited by 50 · see citing works

Bisphenol A promotes dendritic morphogenesis of hippocampal neurons through estrogen receptor-mediated ERK1/2 signal pathway

Xu, X., Lu, Y., Zhang, G., Chen, L., Tian, D., Shen, X., Yang, Y., & Dong, F. (2014) · Chemosphere · doi:10.1016/j.chemosphere.2013.09.063 · Cited by 49 · see citing works

Bisphenol-A rapidly enhanced passive avoidance memory and phosphorylation of NMDA receptor subunits in hippocampus of young rats

Xu, X., Li, T., Luo, Q., Hong, X., Xie, L., & Tian, D. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.06.022 · Cited by 49 · see citing works

Effects of maternal exposure to bisphenol AF on emotional behaviors in adolescent mice offspring

Gong, M., Huai, Z., Song, H. S., Cui, L., Guo, Q., Shao, J., Gao, Y., & Shi, H. (2017) · Chemosphere · doi:10.1016/j.chemosphere.2017.08.119 · Cited by 49 · see citing works

Perinatal exposure to bisphenol A enhances contextual fear memory and affects the serotoninergic system in juvenile female mice

Matsuda, S., Matsuzawa, D., Ishii, D., Tomizawa, H., Sajiki, J., & Shimizu, E. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.03.016 · Cited by 47 · see citing works

Bisphenol A-induced apoptosis, oxidative stress and DNA damage in cultured rhesus monkey embryo renal epithelial Marc-145 cells

Yuan, J., Kong, Y., Ommati, M. M., Tang, Z., Li, H., Li, L., Zhao, C., Shi, Z., & Wang, J. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.06.125 · Cited by 47 · see citing works

Combinatory effects of low concentrations of 17α-etinylestradiol and citalopram on non-reproductive behavior in adult zebrafish (Danio rerio)

Porseryd, T., Kellner, M., Caspillo, N. R., Volkova, K., Elabbas, L. E., Ullah, S., Olsén, H., Dinnétz, P., & Hällström, I. P. (2017) · Aquatic Toxicology · doi:10.1016/j.aquatox.2017.10.001 · Cited by 46 · see citing works

Impairment of learning and memory performances induced by BPA: Evidences from the literature of a MoA mediated through an ED

Mhaouty‐Kodja, S., Belzunces, L., Lavier, M.-C. C., Schroeder, H., Chevrier, C., & Pasquier, E. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.03.017 · Cited by 47 · see citing works

Bisphenol A (BPA) and neurological disorders: An overview

Hyun, S., & Ka, M. (2024) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2024.106614 · Cited by 45 · see citing works

Adolescent bisphenol‐A exposure decreases dendritic spine density: Role of sex and age

Bowman, R. E., Luine, V. N., Khandaker, H., Villafane, J. J., & Frankfurt, M. (2014) · Synapse · doi:10.1002/syn.21758 · Cited by 45 · see citing works

Does preconception paternal exposure to a physiologically relevant level of bisphenol A alter spatial memory in an adult rat?

Fan, Y., Ding, S., Ye, X., Manyande, A., Dong-liang, H., Zhao, N., Yang, H., Jin, X., Liu, J., Tian, C., et al. (2013) · Hormones and Behavior · doi:10.1016/j.yhbeh.2013.08.014 · Cited by 43 · see citing works

Prenatal bisphenol-A exposure altered exploratory and anxiety-like behaviour and induced non-monotonic, sex-specific changes in the cortical expression of CYP19A1, BDNF and intracellular signaling proteins in F1 rats

Arul, G. L. R., Lite, C., Subhashree, K. D., Santosh, W., & Seetharaman, B. (2020) · Food and Chemical Toxicology · doi:10.1016/j.fct.2020.111442 · Cited by 42 · see citing works

Early-Life Environment Influence on Late-Onset Alzheimer’s Disease

Gauvrit, T., Benderradji, H., Buée, L., Blum, D. L., & Vieau, D. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.834661 · Cited by 42 · see citing works

Effects of Bisphenol A on ion channels: Experimental evidence and molecular mechanisms

Soriano, S., Ripoll, C., Alonso‐Magdalena, P., Fuentes, E., Quesada, I., Nadal, Á., & Martínez‐Pinna, J. (2016) · Steroids · doi:10.1016/j.steroids.2016.02.020 · Cited by 41 · see citing works

Impact of endocrine disrupting chemicals on neurodevelopment: the need for better testing strategies for endocrine disruption-induced developmental neurotoxicity

Cediel-Ulloa, A., Lupu, D. L., Johansson, Y., Hinojosa, M. G., Özel, F., & Rüegg, J. (2022) · Expert Review of Endocrinology & Metabolism · doi:10.1080/17446651.2022.2044788 · Cited by 41 · see citing works

Accelerated reduction of serum thyroxine and hippocampal histone acetylation links to exacerbation of spatial memory impairment in aged CD-1 mice pubertally exposed to bisphenol-a

Jiang, W., Cao, L., Wang, F., Ge, H., Wu, P.-C., Li, X.-W., & Chen, G.-H. (2016) · AGE · doi:10.1007/s11357-016-9947-5 · Cited by 38 · see citing works

Concerns related to ED-mediated effects of Bisphenol A and their regulatory consideration

Pouzaud, F., Thierry-Mieg, M., Pérez, K. F. B., Vérines-Jouin, L., Fiore, K., Beausoleil, C., Michel, C., Rousselle, C., & Pasquier, E. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.02.002 · Cited by 39 · see citing works

Sex-specific Effects of Endocrine-disrupting Chemicals on Brain Monoamines and Cognitive Behavior

Hilz, E. N., & Gore, A. C. (2022) · Endocrinology · doi:10.1210/endocr/bqac128 · Cited by 38 · see citing works

Differential gene expression patterns in developing sexually dimorphic rat brain regions exposed to antiandrogenic, estrogenic, or complex endocrine disruptor mixtures: glutamatergic synapses as target.

Lichtensteiger, W., Bassetti-Gaille, C., Faass, O., Axelstad, M., Boberg, J., Christiansen, S., Rehrauer, H., Georgijevic, J. K., Hass, U., Kortenkamp, A., et al. (2015) · Endocrinology · doi:10.1210/en.2014-1504 · Cited by 38 · see citing works

Inhalation Toxicity of Bisphenol A and Its Effect on Estrous Cycle, Spatial Learning, and Memory in Rats upon Whole-Body Exposure

Chung, Y. H., Han, J. H., Lee, S.-B., & Lee, Y.-H. (2017) · Toxicological Research · doi:10.5487/tr.2017.33.2.165 · Cited by 38 · see citing works

EFFECTS OF PERINATAL EXPOSURE TO BISPHENOL-A ON DEVELOPMENT OF THE N-METHYL-D-ASPARTATE RECEPTOR OF THE MALE OFFSPRING RAT'S BRAIN

Ye, Y. (2009) · Acta Biophysica Sinica

Perinatal exposure to bisphenol-A changes <i>N</i>-methyl-<i>D</i>-aspartate receptor expression in the hippocampus of male rat offspring

Xu, X.-H., Wang, Y.-M., Zhang, J., Luo, Q.-Q., Ye, Y.-P., & Ruan, Q. (2010) · Environmental Toxicology and Chemistry · doi:10.1002/etc.18 · Cited by 53 · see citing works

Prenatal bisphenol A exposure impairs the aversive and spatial memory reduces the level of NMDA receptor subunits in the hippocampus of male Sprague Dawley rats

Nayan, N. M., Husin, A., Kadir, S. H. S. A., Aziz, C. B. A., Mazlan, M., & Siran, R. (2022) · Brain Science Advances · doi:10.26599/bsa.2022.9050009 · Cited by 11 · see citing works

Bisphenol-A rapidly enhanced passive avoidance memory and phosphorylation of NMDA receptor subunits in hippocampus of young rats

Xu, X., Li, T., Luo, Q., Hong, X., Xie, L., & Tian, D. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.06.022 · Cited by 49 · see citing works

The effects of prenatal bisphenol a exposure on the expression of MIRNA and NMDA receptor subunits in learning and memory function

Nayan, N. M. (2024) · UiTM Institutional Repositories (Universiti Teknologi MARA)