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1Academic Journal
Συγγραφείς: E. D. Trusova, M. I. Krapivin, D. A. Staroverov, Y. M. Sagurova, E. M. Komarova, O. A. Efimova, A. A. Pendina, Е. Д. Трусова, М. И. Крапивин, Д. А. Староверов, Я. М. Сагурова, Е. М. Комарова, О. А. Ефимова, А. А. Пендина
Συνεισφορές: The study was supported by the Russian Science Foundation, grant No. 24-15-00402 https://rscf.ru/project/24-15-00402/. D.A. Staroverov was personally supported by scholarship from RF President (SPN.2025.00487)., Исследование выполнено за счет гранта Российского научного фонда № 24-15-00402, https://rscf.ru/ project/24-15-00402/. Д.А. Староверов является получателем стипендии Президента Российской Федерации (SPN.2025.00487).
Πηγή: Medical Genetics; Том 24, № 9 (2025); 131-134 ; Медицинская генетика; Том 24, № 9 (2025); 131-134 ; 2073-7998
Θεματικοί όροι: сперматиды, coilin, AZF deletions, azoospermia, spermatogonia, spermatocytes I, spermatocytes II, spermatids, коилин, делеции AZF, азооспермия, сперматогонии, сперматоциты I, сперматоциты II
Περιγραφή αρχείου: application/pdf
Relation: https://www.medgen-journal.ru/jour/article/view/3198/2058; Cox C.M., Thoma M.E., Tchangalova N., et al. Infertility prevalence and the methods of estimation from 1990 to 2021: a systematic review and meta-analysis. Hum Reprod Open. 2022; 2022(4):hoac051. doi:10.1093/hropen/hoac051.; Deng C.Y., Zhang Z., Tang W.H., et al. Microdeletions and vertical transmission of the Y-chromosome azoospermia factor region. Asian J Androl. 2023; 25(1):5–12. doi:10.4103/aja2021130.; Machyna M., Neugebauer K.M., Staněk D. Coilin: The first 25 years. RNA Biol. 2015; 12(6):590–596. doi:10.1080/15476286.2015.1034923.; Vangompel M.J., Xu E.Y. The roles of the DAZ family in spermatogenesis: More than just translation? Spermatogenesis. 2011; 1(1):36–46. doi:10.4161/spmg.1.1.14659.; Efimova O.A., Pendina A.A., Tikhonov A.V., et al. Genome-wide 5-hydroxymethylcytosine patterns in human spermatogenesis are associated with semen quality. Oncotarget. 2017; 8(51):88294. doi:10.18632/oncotarget.18331.; Fefilova A.S., Antifeeva I.A., Gavrilova A.A., et al. Reorganization of cell compartmentalization induced by stress. Biomolecules. 2022; 12(10):1441. doi:10.3390/biom12101441.
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2Academic Journal
Συγγραφείς: Y. M. Sagurova, A. A. Pendina, T. V. Chugunova, M. I. Krapivin, E. M. Komarova, O. A. Efimova, Я. М. Сагурова, А. А. Пендина, Т. В. Чугунова, М. И. Крапивин, Е. М Комарова, О. А. Ефимова
Συνεισφορές: This research was funded by Russian Science Foundation, grant number 24-15-00402, https://rscf.ru/project/24-15-00402/., Исследование выполнено за счет гранта Российского научного фонда № 24-15-00402, https://rscf.ru/ project/24-15-00402/.
Πηγή: Medical Genetics; Том 24, № 9 (2025); 107-110 ; Медицинская генетика; Том 24, № 9 (2025); 107-110 ; 2073-7998
Θεματικοί όροι: сперматоциты II, spermatogenesis, azoospermia, spermatogonia, spermatocytes I, spermatocytes II, сперматогенез, азооспермия, сперматогонии, сперматоциты I
Περιγραφή αρχείου: application/pdf
Relation: https://www.medgen-journal.ru/jour/article/view/3190/2050; Turner K.J., Vasu V., Griffin D.K. Telomere Biology and Human Phenotype. Cells. 2019;8(1):73. doi:10.3390/cells8010073; Lindsey J., McGill N.I., Lindsey L.A., et al. In vivo loss of telomeric repeats with age in humans. Mutation Research. 1991; 256:45–48. doi:10.1016/0921-8734(91)90032-7.; Takubo K., Nakamura K.I., Izumiyama N., et al. Telomere shortening with aging in human liver. The journals of gerontology. Series A, Biological sciences and medical sciences. 2000; 55:B533– B536. doi:10.1093/gerona/55.11.B533.; Kimura M., Cherkas L.F., Kato B.S., et al. Offspring’s leukocyte telomere length, paternal age, and telomere elongation in sperm. PLoS Genetics. 2008; 4(2):e37. doi:10.1371/journal.pgen.0040037.; Aston K.I., Hunt S.C., Susser E., et al. Divergence of sperm and leukocyte age-dependent telomere dynamics: implications for maledriven evolution of telomere length in humans. Molecular human reproduction. 2012; 18(10):517–522. doi:10.1093/molehr/gas028.; Pendina A.A., Krapivin M.I., Sagurova Y.M., et al. Telomere Length in Human Spermatogenic Cells as a New Potential Predictor of Clinical Outcomes in ART Treatment with Intracytoplasmic Injection of Testicular Spermatozoa. International journal of molecular sciences. 2023; 24(13): 10427. doi:10.3390/ijms241310427; Temura K., Ogura A., Cheong C., et al. Dynamic rearrangement of telomeres during spermatogenesis in mice. Developmental biology. 2005; 281(2):196–207. doi:10.1016/j.ydbio.2005.02.025; Achi M.V., Ravindranath N., Dym M. Telomere length in male germ cells is inversely correlated with telomerase activity. Biology of Reproduction. 2000; 63(2):591-598.; Pendina A.A., Krapivin M.I., Efimova O.A., et al. Telomere Length in Metaphase Chromosomes of Human Triploid Zygotes. International journal of molecular sciences. 2021; 22(11):5579. doi:10.3390/ijms22115579; Tire B., Ozturk S. Potential effects of assisted reproductive technology on telomere length and telomerase activity in human oocytes and early embryos. Journal of Ovarian Research. 2023; 16(1):130. https://doi.org/10.1186/s13048-023-01211-4; Antunes D.M., Kalmbach K.H., Wang F., et al. A single-cell assay for telomere DNA content shows increasing telomere length heterogeneity, as well as increasing mean telomere length in human spermatozoa with advancing age. Journal of Assisted Reproduction and Genetics. 2015; 32:1685–1690. doi:10.1007/s10815-015-0574-3.