Unraveling the Clinical Relevance of Ferroptosis-Related Genes in Human Ovarian Aging
Author:
Funder
Ministry of Science Technology
Kaohsiung Veterans General Hospital
Publisher
Springer Science and Business Media LLC
Subject
Obstetrics and Gynecology
Link
https://link.springer.com/content/pdf/10.1007/s43032-023-01310-z.pdf
Reference32 articles.
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2. Giorgi C, Marchi S, Simoes ICM, Ren Z, Morciano G, Perrone M, Patalas-Krawczyk P, Borchard S, Jedrak P, Pierzynowska K, Szymanski J, Wang DQ, Portincasa P, Wegrzyn G, Zischka H, Dobrzyn P, Bonora M, Duszynski J, Rimessi A, Karkucinska-Wieckowska A, Dobrzyn A, Szabadkai G, Zavan B, Oliveira PJ, Sardao VA, Pinton P, Wieckowski MR. Mitochondria and reactive oxygen species in aging and age-related diseases. Int Rev Cell Mol Biol. 2018;340:209–344.
3. Li CJ, Lin LT, Tsai HW, Chern CU, Wen ZH, Wang PH, Tsui KH. The molecular regulation in the pathophysiology in ovarian aging. Aging Dis. 2021;12(3):934–49.
4. de Vet A, Laven JS, de Jong FH, Themmen AP, Fauser BC. Antimullerian hormone serum levels: a putative marker for ovarian aging. Fertil Steril. 2002;77(2):357–62.
5. Chen X, Yu C, Kang R, Tang D. Iron metabolism in ferroptosis. Front Cell Dev Biol. 2020;8:590226.
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1. The effect of norepinephrine on ovarian dysfunction by mediating ferroptosis in mice model;2024-07-31
2. Iron accumulation in ovarian microenvironment damages the local redox balance and oocyte quality in aging mice;Redox Biology;2024-07
3. Correction: Unraveling the Clinical Relevance of Ferroptosis-Related Genes in Human Ovarian Aging;Reproductive Sciences;2024-06-12
4. Cuproptosis-Related Gene FDX1 Identified as a Potential Target for Human Ovarian Aging;Reproductive Sciences;2024-04-30
5. Iron Accumulation in Ovarian Microenvironment Damages the Local Redox Balance and Oocyte Quality in Aging Mice;2024
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