Show source-provided references
1. Fucic, A., Duca, R.C., Galea, K.S., Maric, T., Garcia, K., Bloom, M.S., Andersen, H.R., and Vena, J.E. (2021). Reproductive health risks associated with occupational and environmental exposure to pesticides. Int. J. Environ. Res. Public. Health, 18.
10.3390/ijerph18126576 ↗3. Lindane may modulate the female reproductive development through the interaction with er-β: An in vivo-in vitro approach
10.1016/j.cbi.2007.04.008 ↗4. Detection of Lindane and 7,12-Dimethylbenz[a]Anthracene toxicity at low concentrations in a three-dimensional ovarian follicle culture system
10.1016/j.reprotox.2018.04.010 ↗7. Bretveld, R.W., Thomas, C.M., Scheepers, P.T., Zielhuis, G.A., and Roeleveld, N. (2006). Pesticide exposure: The hormonal function of the female reproductive system disrupted?. Reprod. Biol. Endocrinol., 4.
10.1186/1477-7827-4-30 ↗8. Exposure to endocrine disruptors during adulthood: Consequences for female fertility
10.1530/JOE-17-0023 ↗12. Endocrine and reproductive function in ewes exposed to the organochlorine pesticides lindane or pentachlorophenol
10.1080/009841099158213 ↗13. Thyroid function and effects on reproduction in ewes exposed to the organochlorine pesticides Lindane or Pentachlorophenol (PCP) from conception
10.1080/009841099157124 ↗15. Organochlorine pesticide exposures, metabolic enzyme genetic polymorphisms and semen quality parameters among men attending an infertility clinic
10.1016/j.chemosphere.2022.135010 ↗16. In vivo and in vitro effects of the organochlorine pesticides DDT, TCPM, Methoxychlor, and Lindane on the female reproductive tract of mammals: A review
10.1016/j.reprotox.2008.03.002 ↗17. Pesticides and Breast Cancer Risk: A review of DDT, DDE, and Dieldrin
18. Qi, S.-Y., Xu, X.-L., Ma, W.-Z., Deng, S.-L., Lian, Z.-X., and Yu, K. (2022). Effects of organochlorine pesticide residues in maternal body on infants. Front. Endocrinol., 13.
10.3389/fendo.2022.890307 ↗19. Levels of certain metals, organochlorine pesticides and dioxins in cord blood, maternal blood, human milk and some commonly used nutrients in the surroundings of the Aral sea (Karakalpakstan, Republic of Uzbekistan)
10.1111/j.1651-2227.2001.tb02808.x ↗23. The toxicity of Lindane in the female reproductive system: A review on the Aral sea
25. Plasma gamma-Hexachlorocyclohexane concentrations in forestry workers exposed to lindane
10.1136/oem.45.7.493 ↗26. Effect of prenatal exposure of lindane on alterations in the expression of cerebral cytochrome p450s and neurotransmitter receptors in brain regions
10.1016/j.fct.2014.12.010 ↗27. (2025, May 28). Stockholm Convention on Persistent Organic Pollutants (POPs). Available online: https://chm.pops.int/Countries/StatusofRatifications/PartiesandSignatoires/tabid/4500/Default.aspx.
28. HCH and Lindane contaminated sites: European and global need for a permanent solution for a long-time neglected issue
10.1016/j.envpol.2019.02.029 ↗29. Zhang, W., Lin, Z., Pang, S., Bhatt, P., and Chen, S. (2020). Insights Into the biodegradation of Lindane (γ-Hexachlorocyclohexane) using a microbial system. Front. Microbiol., 11.
10.3389/fmicb.2020.00522 ↗30. Evaluation of Hexachlorocyclohexane contamination from the last Lindane production plant operating in India
10.1007/s11356-010-0401-4 ↗32. Differential estrogenic effects of the persistent organochlorine pesticides dieldrin, endosulfan, and lindane in primary neuronal cultures
10.1093/toxsci/kfr019 ↗33. Lindane, a gap junction blocker, suppresses FSH and Transforming Growth Factor Β1-Induced Connexin43 gap junction formation and steroidogenesis in rat granulosa cells
10.1677/joe.1.05776 ↗34. Lindane, an inhibitor of gap junction formation, abolishes oocyte directed follicle organizing activity in vitro
10.1210/endo.138.10.5567 ↗35. Divergent roles for glutathione in lindane-induced acute and delayed-onset inhibition of rat myometrial gap junctions
10.1093/toxsci/kfi123 ↗42. Gatti, M., Belli, M., De Rubeis, M., Tokita, S., Ikema, H., Yamashiro, H., Fujishima, Y., Anderson, D., Goh, V.S.T., and Shinoda, H. (2024). Ultrastructural analysis of large japanese field mouse (Apodemus speciosus) testes exposed to low-dose-rate (ldr) radiation after the Fukushima Nuclear Power Plant accident. Biology, 13.
10.3390/biology13040239 ↗43. Gatti, M., Belli, M., De Rubeis, M., Khalili, M.A., Familiari, G., Nottola, S.A., Macchiarelli, G., Hajderi, E., and Palmerini, M.G. (2023). Ultrastructural evaluation of mouse oocytes exposed in vitro to different concentrations of the fungicide mancozeb. Biology, 12.
10.3390/biology12050698 ↗47. Antioxidants prevent γ-hexachlorocyclohexane-induced inhibition of rat myometrial gap junctions and contractions1
10.1095/biolreprod64.2.537 ↗48. Morphological reproductive characteristics of testes and fertilization capacity of cryopreserved sperm after the Fukushima accident in raccoon ( Procyon lotor)
10.1111/rda.13887 ↗49. Mancozeb impairs the ultrastructure of mouse granulosa cells in a dose-dependent manner
10.1262/jrd.2017-143 ↗51. Belli, M., Palmerini, M.G., Bianchi, S., Bernardi, S., Khalili, M.A., Nottola, S.A., and Macchiarelli, G. (2021). Ultrastructure of mitochondria of human oocytes in different clinical conditions during assisted reproduction. Arch. Biochem. Biophys., 703.
10.1016/j.abb.2021.108854 ↗52. The impact of endocrine disruptor chemicals on oocyte/embryo and clinical outcomes in ivf
10.1530/EC-20-0135 ↗53. Dutta, S., Sengupta, P., Bagchi, S., Chhikara, B.S., Pavlík, A., Sláma, P., and Roychoudhury, S. (2023). Reproductive toxicity of combined effects of endocrine disruptors on human reproduction. Front. Cell Dev. Biol., 11.
10.3389/fcell.2023.1162015 ↗54. Effects of Hexachlorocyclohexane (HCH-γ-Isomer, Lindane) on the reproductive system of zebrafish (danio rerio)
10.4194/1303-2712-v16_4_19 ↗55. Effect of low dose chronic exposure to deltamethrin and lindaneon reproductive system of male mice
56. Aziz, S.A., and Mehta, R. (2016). Immunohistochemistry and female reproductive toxicology: The ovary and mammary glands. Technical Aspects of Toxicological Immunohistochemistry, Springer.
10.1007/978-1-4939-1516-3 ↗61. Chen, M.-W., Santos, H.M., Que, D.E., Gou, Y.-Y., Tayo, L.L., Hsu, Y.-C., Chen, Y.-B., Chen, F.-A., Chao, H.-R., and Huang, K.-L. (2018). Association between organochlorine pesticide levels in breast milk and their effects on female reproduction in a taiwanese population. Int. J. Environ. Res. Public. Health, 15.
10.3390/ijerph15050931 ↗65. Methoxychlor exposure induces oxidative stress and affects mouse oocyte meiotic maturation: Methoxychlor affects mouse oocyte maturation
10.1002/mrd.22683 ↗69. Belli, M., Rinaudo, P., Palmerini, M.G., Ruggeri, E., Antonouli, S., Nottola, S.A., and Macchiarelli, G. (2020). Pre-implantation mouse embryos cultured in vitro under different oxygen concentrations show altered ultrastructures. Int. J. Environ. Res. Public. Health, 17.
10.3390/ijerph17103384 ↗73. Chang, T., Zhao, J., Li, Q., Meng, A., Xia, Q., Li, Y., Xiang, W., and Yao, Z. (2023). Nuclear-cytoplasmic asynchrony in oocyte maturation caused by TUBB8 variants via impairing microtubule function: A novel pathogenic mechanism. Reprod. Biol. Endocrinol., 21.
10.1186/s12958-023-01161-y ↗74. Ghadially, F.N. (1997). Ultrastructural Pathology of the Cell and Matrix, Butterworths. [3rd ed.].
75. Xavier, V.J., and Martinou, J.-C. (2021). RNA granules in the mitochondria and their organization under mitochondrial stresses. Int. J. Mol. Sci., 22.
10.3390/ijms22179502 ↗78. Thiamethoxam exposure induces endoplasmic reticulum stress and affects ovarian function and oocyte development in mice
10.1021/acs.jafc.0c06340 ↗80. Qualitative and morphometric analysis of the ultrastructure of human oocytes cryopreserved by two alternative slow cooling protocols
10.1007/s10815-010-9394-7 ↗82. Freeze/thaw stress induces organelle remodeling and membrane recycling in cryopreserved human mature oocytes
10.1007/s10815-016-0798-x ↗83. Ghadially, F.N. (1997). Ultrastructural Pathology of the Cell and Matrix, Butterworths. [3rd ed.].
84. Immunohistochemical and ultrastructural visualization of different routes of oocyte elimination in adult rats
10.4081/ejh.2012.17 ↗87. Liu, M. (2011). The biology and dynamics of mammalian cortical granules. Reprod. Biol. Endocrinol., 9.
10.1186/1477-7827-9-149 ↗88. Impaired maturation, fertilization, and embryonic development of porcine oocytes following exposure to an environmentally relevant organochlorine mixture1
10.1095/biolreprod65.2.554 ↗89. An environmentally-relevant mixture of organochlorines and its vehicle control, dimethylsulfoxide, induce ultrastructural alterations in porcine oocytes
10.1002/mrd.20365 ↗94. The Beneficial Effects of cumulus cells and oocyte-cumulus cell gap junctions depends on oocyte maturation and fertilization methods in mice
10.7717/peerj.1761 ↗95. Xie, J., Xu, X., and Liu, S. (2023). Intercellular communication in the cumulus-oocyte complex during folliculogenesis: A review. Front. Cell Dev. Biol., 11.
10.3389/fcell.2023.1087612 ↗96. A protective role of cumulus cells after short-term exposure of rat cumulus cell-oocyte complexes to lifestyle or environmental contaminants
10.1016/j.reprotox.2017.01.003 ↗98. Disruption of gap junctional intercellular communication by Lindane is associated with aberrant localization of connexin43 and zonula occludens-1 in 42gpa9 Sertoli cells
10.1093/carcin/22.9.1537 ↗99. Pratticò, D., Laganà, F., Oliva, G., Fiorillo, A.S., Pullano, S.A., Calcagno, S., De Carlo, D., and La Foresta, F. (2025). Integration of lstm and u-net models for monitoring electrical absorption with a system of sensors and electronic circuits. IEEE Trans. Instrum. Meas., 74.
10.1109/TIM.2025.3573363 ↗