# References

> References — Longevity & Cellular Health peptide literature — yolopeptide — The full citation list behind the yolopeptide digest of Longevity & Cellular Health research peptides: peer-reviewed sources on epitalon and MOTS-c, with journal, year and source links.

**SOURCES**

Every bracketed number on this site resolves to an entry below.

## References

The twelve sources below are the whole evidentiary basis of this site. Entries 1 to 5 concern MOTS-c; entries 6 to 12 concern epitalon. Where a page states a quantity, a sample size or a duration, the bracketed number beside it points here.

## References

[1] Kumagai H, Kim SJ, Miller B, et al. MOTS-c modulates skeletal muscle function by directly binding and activating CK2. iScience. 2024;27(11):111212. https://pubmed.ncbi.nlm.nih.gov/39559755/
[2] Bolignano D, Greco M, Presta P, Duni A, et al. The Mitochondrial-Derived Peptide MOTS-c May Refine Mortality and Cardiovascular Risk Prediction in Chronic Hemodialysis Patients: A Multicenter Cohort Study. Blood Purification. 2024;53(10):824-837. https://pubmed.ncbi.nlm.nih.gov/39111290/
[3] Wan W, Zhang L, Lin Y, Rao X, Wang X, Hua F, Ying J. Mitochondria-derived peptide MOTS-c: effects and mechanisms related to stress, metabolism and aging. Journal of Translational Medicine. 2023;21(1):36. https://pubmed.ncbi.nlm.nih.gov/36670507/
[4] Reynolds JC, Lai RW, Woodhead JST, Joly JH, Mitchell CJ, Cameron-Smith D, Lu R, Cohen P, Graham NA, Benayoun BA, Merry TL, Lee C. MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis. Nature Communications. 2021;12(1):470. https://pubmed.ncbi.nlm.nih.gov/33473109/
[5] Kim KH, Son JM, Benayoun BA, Lee C. The Mitochondrial-Encoded Peptide MOTS-c Translocates to the Nucleus to Regulate Nuclear Gene Expression in Response to Metabolic Stress. Cell Metabolism. 2018;28(3):516-524.e7. https://pubmed.ncbi.nlm.nih.gov/29983246/
[6] Araj SK, Brzezik J, Mądra-Gackowska K, Szeleszczuk Ł. Overview of Epitalon-Highly Bioactive Pineal Tetrapeptide with Promising Properties. Int J Mol Sci. 2025;26(6):2691. https://pubmed.ncbi.nlm.nih.gov/40141333/
[7] Al-Dulaimi S, Thomas R, Matta S, Roberts T. Epitalon increases telomere length in human cell lines through telomerase upregulation or ALT activity. Biogerontology. 2025;26(5):178. https://pubmed.ncbi.nlm.nih.gov/40908429/
[8] Khavinson VKh, Linkova NS, Kvetnoy IM, et al. Molecular cellular mechanisms of peptide regulation of melatonin synthesis in pinealocyte culture. Bull Exp Biol Med. 2012;153(2):255-258. https://pubmed.ncbi.nlm.nih.gov/22816096/
[9] Khavinson VK, Bondarev IE, Butyugov AA. Epithalon peptide induces telomerase activity and telomere elongation in human somatic cells. Bull Exp Biol Med. 2003;135(6):590-592. https://pubmed.ncbi.nlm.nih.gov/12937682/
[10] Khavinson VKh, Morozov VG. Peptides of pineal gland and thymus prolong human life. Neuro Endocrinol Lett. 2003;24(3-4):233-240. https://pubmed.ncbi.nlm.nih.gov/14523363/
[11] Anisimov VN, Khavinson VKh, Provinciali M, et al. Effect of Epitalon on biomarkers of aging, life span and spontaneous tumor incidence in female Swiss-derived SHR mice. Biogerontology. 2003;4(4):193-202. https://pubmed.ncbi.nlm.nih.gov/14501183/
[12] Various. Epitalon protects against post-ovulatory aging-related damage of mouse oocytes in vitro. Aging (Albany NY). 2022;14(8):3551-3565. https://pubmed.ncbi.nlm.nih.gov/35413689/

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A reference desk for the ageing-and-cellular-health literature: every figure here traces to a listed study, and none of it is a clinic, a vendor, or a protocol.