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Oocyte aging underlies female reproductive aging: biological mechanisms and therapeutic strategies
Open accessAbstract
In recent years, postponement of marriage and childbearing in women of reproductive age has led to an increase in the incidence of age‐related infertility. The reproductive aging process in women is assumed to occur due to a decrease in both the quantity and quality of the oocytes, with the ultimate result being a decline in fecundity. This age‐related decline in fecundity is strongly dependent on oocyte quality, which is critical for fertilization and subsequent embryo development. Aged oocytes display increased chromosomal abnormality and dysfunction of cellular organelles, both of which factor into oocyte quality. In particular, mitochondrial dysfunction has been suggested as a major contributor to the reduction in oocyte quality as well as to chromosomal abnormalities in aged oocytes and embryos. Participation of oxidative stress in the oocyte aging process has been proposed because oxidative stress has the capacity to induce mitochondrial dysfunction and directly damage many intracellular components of the oocytes such as lipids, protein, and DNA. In an attempt to improve mitochondrial function in aged oocytes, several therapeutic strategies have been investigated using both animal models and assisted reproductive technology. Here, we review the biological mechanisms and present status of therapeutic strategies in the female reproductive aging field and indicate possible future therapeutic strategies.
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“Aging progresses throughout the lifespan can be accentuated at etiologic sites of multiple acute and chronic diseases, including in children6,8–12.”
From Cellular senescence and senolytics: the path to the clinic (2022) · cites this paper as [12]
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“fundamental aging processes can operate even before conception, for example, in the context of aged oocytes linked to Down syndrome12,13.”
From Cellular senescence and senolytics: the path to the clinic (2022) · cites this paper as [12]
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1 retracted
RETRACTED: Contribution of myo-inositol and melatonin to human reproduction
Carlomagno, G., Nordio, M., Chiu, T. T. Y., & Unfer, V. (2011) · European Journal of Obstetrics & Gynecology and Reproductive Biology · doi:10.1016/j.ejogrb.2011.07.038 · Cited by 84
RetractedTherapeutic potential of resveratrol: the in vivo evidence
Baur, J. A., & Sinclair, D. A. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd2060 · Cited by 3,958
Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan
Howitz, K. T., Bitterman, K. J., Cohen, H. Y., Lamming, D. W., Lavu, S., Wood, J. G., Zipkin, R. E., Chung, P., Kisielewski, A., Zhang, L.-L., et al. (2003) · Nature · doi:10.1038/nature01960 · Cited by 3,796
Extending Healthy Life Span—From Yeast to Humans
Fontana, L., Partridge, L., & Longo, V. D. (2010) · Science · doi:10.1126/science.1172539 · Cited by 3,023
Metabolic control through the PGC-1 family of transcription coactivators
Lin, J., Handschin, C., & Spiegelman, B. M. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.05.004 · Cited by 2,130 · cited 1×
“PGC-1a acts as the ‘‘master regulator’’ of mitochondrial biogenesis [65, 72], thermogenesis, and gluconeogenesis [71].”
BackgroundPrice, N. L., Gomes, A. P., Ling, A. J. Y., Duarte, F. V., Martin-Montalvo, A., North, B. J., Agarwal, B., Ye, L., Ramadori, G., Teodoro, J. S., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.04.003 · Cited by 1,602
The variability of female reproductive ageing
te Velde, E. R. (2002) · Human Reproduction Update · doi:10.1093/humupd/8.2.141 · Cited by 1,214
MENKEN, J. A., Trussell, J., & Larsen, U. (1986) · Science · doi:10.1126/science.3755843 · Cited by 705
Blerkom, J. V., Davis, P. W., & Lee, J. A. (1995) · Human Reproduction · doi:10.1093/oxfordjournals.humrep.a135954 · Cited by 671
Mitochondrial function in the human oocyte and embryo and their role in developmental competence
Blerkom, J. V. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.09.012 · Cited by 667
ESHRE Capri Workshop Group (2005) · Human Reproduction Update · doi:10.1093/humupd/dmi006 · Cited by 616
Nyboe Andersen, A., Goossens, V., Bhattacharya, S., Ferraretti, A. P., Kupka, M. S., de Mouzon, J., & Nygren, K. G. (2009) · Human Reproduction · doi:10.1093/humrep/dep035 · Cited by 599
Female age-related fertility decline
(2014) · Fertility and Sterility · doi:10.1016/j.fertnstert.2013.12.032 · Cited by 583
Assisted reproductive technology in Europe, 2004: results generated from European registers by ESHRE
Andersen, A. N., Goossens, V., Ferraretti, A. P., Bhattacharya, S., Felberbaum, R. E., de Mouzon, J., & Nygren, K. G. (2008) · Human Reproduction · doi:10.1093/humrep/den014 · Cited by 565
Mitochondrial DNA content affects the fertilizability of human oocytes
Reynier, P., May‐Panloup, P., Chrétien, M.-F., Morgan, C. J., Jean, M., Savagner, F., Barrière, P., & Malthièry, Y. (2001) · Molecular Human Reproduction · doi:10.1093/molehr/7.5.425 · Cited by 522
Assisted Reproductive Technology Surveillance — United States, 2013
Sunderam, S., Kissin, D. M., Crawford, S. B., Folger, S. G., Jamieson, D. J., Warner, L., & Barfield, W. D. (2015) · MMWR Surveillance Summaries · doi:10.15585/mmwr.ss6411a1 · Cited by 521
Age-associated alteration of gene expression patterns in mouse oocytes
Hamatani, T., Falco, G., Carter, M. G., Akutsu, H., Stagg, C. A., Sharov, A. A., Dudekula, D. B., VanBuren, V., & Ko, M. S. H. (2004) · Human Molecular Genetics · doi:10.1093/hmg/ddh241 · Cited by 516
Assisted reproductive technology
da Silva, S. G., Bertoldi, A. D., da Silveira, M. F., Domingues, M. R., Evenson, K. R., & Santos, I. S. (2019) · Revista de Saúde Pública · doi:10.11606/s1518-8787.2019053000737 · Cited by 513
Guarente, L. (2011) · New England Journal of Medicine · doi:10.1056/nejmra1100831 · Cited by 510
Oocyte aging: cellular and molecular changes, developmental potential and reversal possibility
Miao, Y.-L., Kikuchi, K., Sun, Q. Y., & Schatten, H. (2009) · Human Reproduction Update · doi:10.1093/humupd/dmp014 · Cited by 497
Delaying childbearing: effect of age on fecundity and outcome of pregnancy.
van Noord‐Zaadstra, B. M., Looman, C. W. N., Alsbach, H., Habbema, J. D. F., Velde, E. R. T., & Karbaat, J. (1991) · BMJ · doi:10.1136/bmj.302.6789.1361 · Cited by 446
Female reproductive ageing: current knowledge and future trends
Broekmans, F. J., Knauff, E. A. H., te Velde, E. R., Macklon, N. S., & Fauser, B. C. (2007) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2007.01.004 · Cited by 427
Ferraretti, A. P., Goossens, V., Kupka, M. S., Bhattacharya, S., de Mouzon, J., Castilla, J. A., Erb, K., Корсак, В. С., Andersen, A. N., (EIM), T. E. I.-M., et al. (2013) · Human Reproduction · doi:10.1093/humrep/det278 · Cited by 371
Luzzo, K. M., Wang, Q., Purcell, S. H., Chi, M. M.-Y., Jimenez, P. T., Grindler, N. M., Schedl, T., & Moley, K. H. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049217 · Cited by 356
Ooplasmic transfer in mature human oocytes
Cohen, J. (1998) · Molecular Human Reproduction · doi:10.1093/molehr/4.3.269 · Cited by 340
Mitochondria in human offspring derived from ooplasmic transplantation: Brief communication
Barritt, J. A., Brenner, C. A., Malter, H. E., & Cohen, J. (2001) · Human Reproduction · doi:10.1093/humrep/16.3.513 · Cited by 317
Blerkom, J. V., Davis, P., & Alexander, S. (2000) · Human Reproduction · doi:10.1093/humrep/15.12.2621 · Cited by 309
Regulation of FoxO transcription factors by acetylation and protein–protein interactions
Daitoku, H., Sakamaki, J.-I., & Fukamizu, A. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.03.001 · Cited by 297
Mitochondrial deoxyribonucleic acid deletions in oocytes and reproductive aging in women
Keefe, D. L., Niven‐Fairchild, T., Powell, S., & Buradagunta, S. (1995) · Fertility and Sterility · doi:10.1016/s0015-0282(16)57796-6 · Cited by 297
Resveratrol protects against age-associated infertility in mice
Liu, M., Yin, Y., Ye, X., Zeng, M., Zhao, Q., Keefe, D. L., & Liu, L. (2013) · Human Reproduction · doi:10.1093/humrep/des437 · Cited by 287
Oxidative stress and ageing of the post-ovulatory oocyte
Lord, T., & Aitken, R. J. (2013) · Reproduction · doi:10.1530/rep-13-0111 · Cited by 279
Potential effects of age-associated oxidative stress on mammalian oocytes/embryos
Tarín, J. J. (1996) · Molecular Human Reproduction · doi:10.1093/molehr/2.10.717 · Cited by 274
Melatonin in Human Preovulatory Follicular Fluid*
Brzezinski, A., SEIBEL, M. M., Lynch, H. J., Deng, M., & Wurtman, R. J. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-64-4-865 · Cited by 262
Spindles, mitochondria and redox potential in ageing oocytes
Eichenlaub-Ritter, U., Vogt, E.-J., Yin, H., & Gosden, R. G. (2004) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60497-x · Cited by 255
Assisted reproductive technology surveillance--United States, 2009.
Sunderam, S., Kissin, D. M., Flowers, L. M., Anderson, J. E., Folger, S. G., Jamieson, D. J., & Barfield, W. D. (2012) · PubMed · Cited by 242
Chromosome cohesion decreases in human eggs with advanced maternal age
Duncan, F. E., Hornick, J. E., Lampson, M. A., Schultz, R. M., Shea, L. D., & Woodruff, T. K. (2012) · Aging Cell · doi:10.1111/j.1474-9726.2012.00866.x · Cited by 237
Ca2+ oscillatory pattern in fertilized mouse eggs affects gene expression and development to term
Ozil, J., Banrezes, B., Tóth, S., Pan, H., & Schultz, R. M. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.08.041 · Cited by 236
Activation of rabbit oocytes: the impact of the Ca2+ signal regime on development
Ozil, J., & Huneau, D. (2001) · Development · doi:10.1242/dev.128.6.917 · Cited by 236
Germline Energetics, Aging, and Female Infertility
Tilly, J. L., & Sinclair, D. A. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.05.007 · Cited by 223
PGC-1 coactivators in the control of energy metabolism
Liu, C., & Lin, J. D. (2011) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmr007 · Cited by 219
Acton, B. M. (2003) · Molecular Human Reproduction · doi:10.1093/molehr/gah004 · Cited by 209
Mitochondrial DNA in the Oocyte and the Developing Embryo
May‐Panloup, P., Chrétien, M.-F., Malthièry, Y., & Reynier, P. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(06)77003-x · Cited by 206
Selesniemi, K. L., Lee, H., Muhlhauser, A., & Tilly, J. L. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1018793108 · Cited by 204
Eichenlaub-Ritter, U., Wieczorek, M., Lüke, S., & Seidel, T. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.08.011 · Cited by 204
Mechanisms underlying oocyte activation and postovulatory ageing
Fissore, R. A., Kurokawa, M., Knott, J., Zhang, M., & Smyth, J. T. (2002) · Reproduction · doi:10.1530/rep.0.1240745 · Cited by 200
The contribution of mitochondrial function to reproductive aging
Bentov, Y., Yavorska, T., Esfandiari, N., Jurisicova, A., & Casper, R. F. (2011) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-011-9588-7 · Cited by 196
Reactive oxygen/nitrogen species and their functional correlations in neurodegenerative diseases
Ramalingam, M., & Kim, S. (2012) · Journal of Neural Transmission · doi:10.1007/s00702-011-0758-7 · Cited by 194
Melatonin as a free radical scavenger in the ovarian follicle [Review]
Tamura, H., Takasaki, A., Taketani, T., Tanabe, M., Kizuka, F., Lee, L., Tamura, I., Maekawa, R., Asada, H., Yamagata, Y., et al. (2012) · Endocrine Journal · doi:10.1507/endocrj.ej12-0263 · Cited by 194
Antioxidants for female subfertility
Showell, M. G., Brown, J., Clarke, J., & Hart, R. J. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007807.pub2 · Cited by 188
Mitochondria in early mammalian development
Blerkom, J. V. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.12.005 · Cited by 183
Mitochondrial DNA heteroplasmy after human ooplasmic transplantation
Brenner, C. A., Barritt, J. A., Willadsen, S. M., & Cohen, J. (2000) · Fertility and Sterility · doi:10.1016/s0015-0282(00)00681-6 · Cited by 182
Mitochondria and the death of oocytes
Perez, G. I., Trbovich, A. M., Gosden, R. G., & Tilly, J. L. (2000) · Nature · doi:10.1038/35000651 · Cited by 179
Assisted Reproductive Technology Surveillance—United States, 2017
Sunderam, S., Kissin, D. M., Zhang, Y., Jewett, A., Boulet, S. L., Warner, L., Kroelinger, C. D., & Barfield, W. D. (2020) · MMWR. Surveillance Summaries · doi:10.15585/mmwr.ss6909a1 · Cited by 176
Role of calcium signals in early development
Ducibella, T., SCHULTZ, R., & Ozil, J. (2006) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2006.02.010 · Cited by 175
Impact of oxidative stress in aged mouse oocytes on calcium oscillations at fertilization
Takahashi, T., Takahashi, E., Igarashi, H., Tezuka, N., & Kurachi, H. (2003) · Molecular Reproduction and Development · doi:10.1002/mrd.10341 · Cited by 171
Self-citationSeino, T., Saito, H., Kaneko-Tarui, T., Takahashi, T., Kawachiya, S., & Kurachi, H. (2002) · Fertility and Sterility · doi:10.1016/s0015-0282(02)03103-5 · Cited by 167
Self-citationGordo, A. C., Rodrigues, P. I. D. L., Kurokawa, M., Jellerette, T., Exley, G. E., Warner, C., & Fissore, R. A. (2002) · Biology of Reproduction · doi:10.1095/biolreprod66.6.1828 · Cited by 165
Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection?
Schon, E. A., Kim, S. H., Ferreira, J. C., Magalhães, P. M. R., Grace, M., Warburton, D., & Gross, S. J. (2000) · Human Reproduction · doi:10.1093/humrep/15.suppl_2.160 · Cited by 159
Selesniemi, K. L., Lee, H., & Tilly, J. L. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00409.x · Cited by 158
Miyamoto, K., Sato, E. F., Kasahara, E., Jikumaru, M., Hiramoto, K., Tabata, H., Katsuragi, M., Odo, S., Utsumi, K., & Inoue, M. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.05.025 · Cited by 152
Oocyte ageing and its cellular basis
Eichenlaub-Ritter, U. (2012) · The International Journal of Developmental Biology · doi:10.1387/ijdb.120141ue · Cited by 150
Robb, E. L., Page, M. M., Wiens, B. E., & Stuart, J. A. (2008) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.12.138 · Cited by 147
Woods, D. C., & Tilly, J. L. (2013) · Nature Protocols · doi:10.1038/nprot.2013.047 · Cited by 145
Simsek‐Duran, F., Li, F., Ford, W., Swanson, R. J., Jones, H. W., & Castora, F. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064955 · Cited by 138
Mitochondrial Protection by Resveratrol
Ungvari, Z. I., Sonntag, W. E., de Cabo, R., Baur, J. A., & Csiszár, A. (2011) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e3182141f80 · Cited by 131
SIRT1 metabolic actions: Integrating recent advances from mouse models
Boutant, M., & Cantó, C. (2013) · Molecular Metabolism · doi:10.1016/j.molmet.2013.10.006 · Cited by 122
Toner, J. P., Grainger, D. A., & Frazier, L. M. (2002) · Fertility and Sterility · doi:10.1016/s0015-0282(02)03371-x · Cited by 117
Tarín, J. J., Pérez‐Albalá, S., & Cano, A. (2002) · Molecular Reproduction and Development · doi:10.1002/mrd.10041 · Cited by 115
Mitochondrial DNA point mutation in human oocytes is associated with maternal age
Barritt, J. A., Cohen, J., & Brenner, C. A. (2000) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)61946-3 · Cited by 115
Dougall, K. M., Beyene, Y., & Nachtigall, R. D. (2012) · Human Reproduction · doi:10.1093/humrep/des409 · Cited by 113
Unfer, V., Raffone, E., Rizzo, P., & Buffo, S. (2011) · Gynecological Endocrinology · doi:10.3109/09513590.2011.564687 · Cited by 108
Ollero, M., Powers, R. D., & Álvarez, J. G. (2000) · Molecular Reproduction and Development · doi:10.1002/(sici)1098-2795(200003)55:3 · Cited by 106
Corton, J. C., & Brown-Borg, H. M. (2005) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/60.12.1494 · Cited by 106
Resveratrol Improves the Mitochondrial Function and Fertilization Outcome of Bovine Oocytes
Takeo, S., Sato, D., Kimura, K., Monji, Y., Kuwayama, T., Kawahara‐Miki, R., & Iwata, H. (2013) · Journal of Reproduction and Development · doi:10.1262/jrd.2013-102 · Cited by 99
Aging-related changes in calcium oscillations in fertilized mouse oocytes
Igarashi, H., Takahashi, E., Hiroi, M., & Doi, K. (1997) · Molecular Reproduction and Development · doi:10.1002/(sici)1098-2795(199711)48:3 · Cited by 94
Self-citationRelationship between mitochondrial DNA Copy Number and SIRT1 Expression in Porcine Oocytes
Sato, D., Itami, N., Tasaki, H., Takeo, S., Kuwayama, T., & Iwata, H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094488 · Cited by 92
Alterations of PLCβ1 in mouse eggs change calcium oscillatory behavior following fertilization
Igarashi, H., Knott, J. G., Schultz, R. M., & Williams, C. J. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.09.028 · Cited by 90
Self-citationResveratrol Protects Mouse Oocytes from Methylglyoxal-Induced Oxidative Damage
Liu, Y., He, X.-Q., Huang, X., Ding, L., Xu, L., Shen, Y., Zhang, F., Zhu, M.-B., Xu, B., Qi, Z., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0077960 · Cited by 88
Mitochondria as determinant of nucleotide pools and chromosomal stability
Desler, C., Munch‐Petersen, B., Stevnsner, T., Matsui, S., Kulawiec, M., Singh, K. K., & Rasmussen, L. J. (2007) · Mutation research. Fundamental and molecular mechanisms of mutagenesis · doi:10.1016/j.mrfmmm.2007.06.002 · Cited by 85
Woods, D. C., White, Y. A. R., & Tilly, J. L. (2012) · Reproductive Sciences · doi:10.1177/1933719112462632 · Cited by 83
Molecular mechanism of poor embryo development in postovulatory aged oocytes: Mini review
Takahashi, T., Igarashi, H., Amita, M., Hara, S., Matsuo, K., & Kurachi, H. (2013) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.12111 · Cited by 79
Self-citationOutcome of in vitro fertilization in women 45 years and older who use autologous oocytes
Spandorfer, S. D., Bendikson, K. A., Dragisic, K., Schattman, G. L., Davis, O., & Rosenwaks, Z. (2006) · Fertility and Sterility · doi:10.1016/j.fertnstert.2006.05.081 · Cited by 77
Aged Mouse Oocytes Fail to Readjust Intracellular Adenosine Triphosphates at Fertilization1
Igarashi, H., Takahashi, T., Takahashi, E., Tezuka, N., Nakahara, K., Takahashi, K., & Kurachi, H. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.104.034926 · Cited by 75
Self-citationEffect of Female Age on Mouse Oocyte Developmental Competence Following Mitochondrial Injury1
Thouas, G. A., Trounson, A. O., & Jones, G. M. (2005) · Biology of Reproduction · doi:10.1095/biolreprod.105.040956 · Cited by 75
Thirty years of calcium signals at fertilization
Miyazaki, S. (2006) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2006.02.007 · Cited by 75
Park, S., Mori, R., & Shimokawa, I. (2013) · Molecules and Cells · doi:10.1007/s10059-013-0130-x · Cited by 75
A Comparison of Sperm- and IP3-Induced Ca2+Release in Activated and Aging Mouse Oocytes
Jones, K. T., & Whittingham, D. G. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0214 · Cited by 74
Chromosome Cohesion Decreases in Human Eggs with Advanced Maternal Age.
Duncan, F. E., Hornick, J. E., Lampson, M. A., Schultz, R. M., Shea, L. D., & Woodruff, T. K. (2012) · Biology of Reproduction · doi:10.1093/biolreprod/87.s1.60 · Cited by 54
Assisted reproductive technology surveillance -- United States, 2010.
Sunderam, S., Kissin, D. M., Crawford, S. B., Anderson, J. E., Folger, S. G., Jamieson, D. J., & Barfield, W. D. (2013) · PubMed · Cited by 42
Seko, L. M. D., Moroni, R. M., Leitão, V. M. S., Teixeira, D. M., Nastri, C. O., & Martins, W. P. (2013) · Fertility and Sterility · doi:10.1016/j.fertnstert.2013.09.036 · Cited by 41
Calorie restriction increases primordial follicle reserve in mature female chemotherapy-treated rats
Xiang, Y.-F., Xu, J., Li, L., Lin, X.-H., Chen, X., Zhang, X., Fu, Y., & Luo, L. (2011) · Gene · doi:10.1016/j.gene.2011.11.019 · Cited by 35
Too old for IVF: are we discriminating against older women?
Gleicher, N., Weghofer, A., & Barad, D. H. (2007) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-007-9182-1 · Cited by 32
Ooplasmic Transfer — Proceed with Care
Templeton, A. A. (2002) · New England Journal of Medicine · doi:10.1056/nejm200203073461013 · Cited by 30
Takeshima, K., Saito, H., Nakaza, A., Kuwahara, A., Ishihara, O., Irahara, M., Hirahara, H., Yoshimura, Y., & Sakumoto, T. (2014) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-014-0181-8 · Cited by 17
Intracellular calcium oscillations in mammalian eggs at fertilization
Miyazaki, S. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.144238 · Cited by 17
The Mitochondrial DNA Mutation (ΔmtDNA5286) in Human Oocytes: Correlation with Age and IVF Outcome
Yesodi, V., Yaron, Y., Lessing, J. B., Amit, A., & Ben‐Yosef, D. (2002) · Journal of Assisted Reproduction and Genetics · doi:10.1023/a:1014439529813 · Cited by 12
Clinical significance and management of poor response in IVF
Klinkert, E. R. (2005) · Utrecht University Repository (Utrecht University) · Cited by 12
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Cecchino, G. N., Seli, E. U., Motta, E. L. A., & García-Velasco, J. A. (2018) · Reproductive BioMedicine Online · doi:10.1016/j.rbmo.2018.02.007 · Cited by 110
Metadata
- Authors
- Igarashi, H., Takahashi, T., & Nagase, S.
- Affiliations
- Yamagata University (JP)
- Corresponding author
- Igarashi, Hideki
- Venue
- Reproductive Medicine and Biology
- Publisher
- Wiley
- Published
- 2015-05-09
- Volume
- 14
- Issue
- 4
- Pages
- 159-169
- ISSN
- 1445-5781 (ISSN-L)
- 1447-0578
- PMC
- PMC5715832
- OpenAlex
- W636461026
- Cited by
- 116
- References
- 97
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 12 · 2023: 10 · 2022: 18 · 2021: 18 · 2020: 18 · 2019: 11 · 2018: 1
- FWCI
- 0.05
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Reproductive Medicine and Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (26462474)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Reproductive biology and impacts on aquatic species
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Keywords
- oocyte aging, female reproductive aging, age-related infertility, oocyte quality, mitochondrial dysfunction, oxidative stress, chromosomal abnormalities, fecundity decline, assisted reproduction, treatment options
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