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WITHDRAWN: Editor's Forum.

Redox biology

Tsikas D.
PMID: 26746792
Redox Biol. 2015 Aug;5:149. doi: 10.1016/j.redox.2015.01.018. Epub 2015 May 21.

The Publisher regrets that this article is an accidental duplication of an article that has already been published in , http://dx.doi.org/10.1016/j.redox.2015.08.002, http://dx.doi.org/10.1016/j.redox.2015.08.003, http://dx.doi.org/10.1016/j.redox.2015.08.004. The duplicate article has therefore been withdrawn. The full Elsevier Policy on Article Withdrawal can be...

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Tsikas D. WITHDRAWN: Editor's Forum. Redox Biol. 2015;5:149doi: 10.1016/j.redox.2015.01.018.
Tsikas, D. (2015). WITHDRAWN: Editor's Forum. Redox biology, 5149. https://doi.org/10.1016/j.redox.2015.01.018
Tsikas, Dimitrios. "WITHDRAWN: Editor's Forum." Redox biology vol. 5 (2015): 149. doi: https://doi.org/10.1016/j.redox.2015.01.018
Tsikas D. WITHDRAWN: Editor's Forum. Redox Biol. 2015 Aug;5:149. doi: 10.1016/j.redox.2015.01.018. Epub 2015 May 21. PMID: 26746792.
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Corrigendum to "CO-releasing molecules CORM2 attenuates angiotensin II-induced human aortic smooth muscle cell migration through inhibition of ROS/IL-6 generation and matrix metalloproteinases-9 expression" [Redox Biol. 12 (2017) 377-388].

Redox biology

Tsai MH, Lee CW, Hsu LF, Li SY, Chiang YC, Lee MH, Chen CH, Liang HF, How JM, Chang PJ, Wu CM, Lee IT.
PMID: 30262241
Redox Biol. 2020 Jan;28:101005. doi: 10.1016/j.redox.2018.09.012. Epub 2018 Sep 24.

No abstract available.

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Tsai MH, Lee CW, Hsu LF, et al. Corrigendum to "CO-releasing molecules CORM2 attenuates angiotensin II-induced human aortic smooth muscle cell migration through inhibition of ROS/IL-6 generation and matrix metalloproteinases-9 expression" [Redox Biol. 12 (2017) 377-388]. Redox Biol. 2018;28:101005doi: 10.1016/j.redox.2018.09.012.
Tsai, M. H., Lee, C. W., Hsu, L. F., Li, S. Y., Chiang, Y. C., Lee, M. H., Chen, C. H., Liang, H. F., How, J. M., Chang, P. J., Wu, C. M., & Lee, I. T. (2020). Corrigendum to "CO-releasing molecules CORM2 attenuates angiotensin II-induced human aortic smooth muscle cell migration through inhibition of ROS/IL-6 generation and matrix metalloproteinases-9 expression" [Redox Biol. 12 (2017) 377-388]. Redox biology, 28101005. https://doi.org/10.1016/j.redox.2018.09.012
Tsai, Ming-Horng, et al. "Corrigendum to "CO-releasing molecules CORM2 attenuates angiotensin II-induced human aortic smooth muscle cell migration through inhibition of ROS/IL-6 generation and matrix metalloproteinases-9 expression" [Redox Biol. 12 (2017) 377-388]." Redox biology vol. 28 (2020): 101005. doi: https://doi.org/10.1016/j.redox.2018.09.012
Tsai MH, Lee CW, Hsu LF, Li SY, Chiang YC, Lee MH, Chen CH, Liang HF, How JM, Chang PJ, Wu CM, Lee IT. Corrigendum to "CO-releasing molecules CORM2 attenuates angiotensin II-induced human aortic smooth muscle cell migration through inhibition of ROS/IL-6 generation and matrix metalloproteinases-9 expression" [Redox Biol. 12 (2017) 377-388]. Redox Biol. 2020 Jan;28:101005. doi: 10.1016/j.redox.2018.09.012. Epub 2018 Sep 24. PMID: 30262241; PMCID: PMC6920295.
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Corrigendum to 'Protective effect of dioscin against doxorubicin-induced cardiotoxicity via adjusting microRNA-140-5p-mediated myocardial oxidative stress' [Redox Biol.], 2018, 16: 189-198.

Redox biology

Zhao L, Tao X, Qi Y, Xu L, Yin L, Peng J.
PMID: 31466879
Redox Biol. 2019 Sep;26:101303. doi: 10.1016/j.redox.2019.101303. Epub 2019 Aug 26.

No abstract available.

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Zhao L, Tao X, Qi Y, et al. Corrigendum to 'Protective effect of dioscin against doxorubicin-induced cardiotoxicity via adjusting microRNA-140-5p-mediated myocardial oxidative stress' [Redox Biol.], 2018, 16: 189-198. Redox Biol. 2019;26:101303doi: 10.1016/j.redox.2019.101303.
Zhao, L., Tao, X., Qi, Y., Xu, L., Yin, L., & Peng, J. (2019). Corrigendum to 'Protective effect of dioscin against doxorubicin-induced cardiotoxicity via adjusting microRNA-140-5p-mediated myocardial oxidative stress' [Redox Biol.], 2018, 16: 189-198. Redox biology, 26101303. https://doi.org/10.1016/j.redox.2019.101303
Zhao, Lisha, et al. "Corrigendum to 'Protective effect of dioscin against doxorubicin-induced cardiotoxicity via adjusting microRNA-140-5p-mediated myocardial oxidative stress' [Redox Biol.], 2018, 16: 189-198." Redox biology vol. 26 (2019): 101303. doi: https://doi.org/10.1016/j.redox.2019.101303
Zhao L, Tao X, Qi Y, Xu L, Yin L, Peng J. Corrigendum to 'Protective effect of dioscin against doxorubicin-induced cardiotoxicity via adjusting microRNA-140-5p-mediated myocardial oxidative stress' [Redox Biol.], 2018, 16: 189-198. Redox Biol. 2019 Sep;26:101303. doi: 10.1016/j.redox.2019.101303. Epub 2019 Aug 26. PMID: 31466879; PMCID: PMC6831889.
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Corrigendum to "Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress" [Redox Biol. 20 (2019) 296-306].

Redox biology

Bi J, Zhang J, Ren Y, Du Z, Li Q, Wang Y, Wei S, Yang L, Zhang J, Liu C, Lv Y, Wu R.
PMID: 31043340
Redox Biol. 2019 Sep;26:101193. doi: 10.1016/j.redox.2019.101193. Epub 2019 Apr 29.

No abstract available.

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Bi J, Zhang J, Ren Y, et al. Corrigendum to "Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress" [Redox Biol. 20 (2019) 296-306]. Redox Biol. 2019;26:101193doi: 10.1016/j.redox.2019.101193.
Bi, J., Zhang, J., Ren, Y., Du, Z., Li, Q., Wang, Y., Wei, S., Yang, L., Zhang, J., Liu, C., Lv, Y., & Wu, R. (2019). Corrigendum to "Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress" [Redox Biol. 20 (2019) 296-306]. Redox biology, 26101193. https://doi.org/10.1016/j.redox.2019.101193
Bi, Jianbin, et al. "Corrigendum to "Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress" [Redox Biol. 20 (2019) 296-306]." Redox biology vol. 26 (2019): 101193. doi: https://doi.org/10.1016/j.redox.2019.101193
Bi J, Zhang J, Ren Y, Du Z, Li Q, Wang Y, Wei S, Yang L, Zhang J, Liu C, Lv Y, Wu R. Corrigendum to "Irisin alleviates liver ischemia-reperfusion injury by inhibiting excessive mitochondrial fission, promoting mitochondrial biogenesis and decreasing oxidative stress" [Redox Biol. 20 (2019) 296-306]. Redox Biol. 2019 Sep;26:101193. doi: 10.1016/j.redox.2019.101193. Epub 2019 Apr 29. PMID: 31043340; PMCID: PMC6831868.
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Mitofusin1 in oocyte is essential for female fertility.

Redox biology

Hou X, Zhu S, Zhang H, Li C, Qiu D, Ge J, Guo X, Wang Q.
PMID: 30690319
Redox Biol. 2019 Feb;21:101110. doi: 10.1016/j.redox.2019.101110. Epub 2019 Jan 12.

Mitofusins (Mfn) are the important regulators of mitochondrial organization in mammalian cells; however, their roles during oocyte development remain unknown. In the present study, we generated mice with oocyte-specific knockout of Mfn1 or Mfn2 (Mfn1

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Hou X, Zhu S, Zhang H, et al. Mitofusin1 in oocyte is essential for female fertility. Redox Biol. 2019;21:101110doi: 10.1016/j.redox.2019.101110.
Hou, X., Zhu, S., Zhang, H., Li, C., Qiu, D., Ge, J., Guo, X., & Wang, Q. (2019). Mitofusin1 in oocyte is essential for female fertility. Redox biology, 21101110. https://doi.org/10.1016/j.redox.2019.101110
Hou, Xiaojing, et al. "Mitofusin1 in oocyte is essential for female fertility." Redox biology vol. 21 (2019): 101110. doi: https://doi.org/10.1016/j.redox.2019.101110
Hou X, Zhu S, Zhang H, Li C, Qiu D, Ge J, Guo X, Wang Q. Mitofusin1 in oocyte is essential for female fertility. Redox Biol. 2019 Feb;21:101110. doi: 10.1016/j.redox.2019.101110. Epub 2019 Jan 12. PMID: 30690319; PMCID: PMC6351231.
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1,25-Dihydroxyvitamin D.

Redox biology

Nakajo T, Katayoshi T, Kitajima N, Tsuji-Naito K.
PMID: 34872043
Redox Biol. 2021 Dec 01;48:102203. doi: 10.1016/j.redox.2021.102203. Epub 2021 Dec 01.

The nucleotide-binding oligomerization domain-like receptor family pyrin domain-containing protein (NLRP) inflammasome is a key inflammatory signaling pathway activated via a two-step signaling process consisting of priming and activation steps. Several studies have shown that 1,25-dihydroxyvitamin D3 (1,25(OH)

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Nakajo T, Katayoshi T, Kitajima N, et al. 1,25-Dihydroxyvitamin D. Redox Biol. 2021;48:102203doi: 10.1016/j.redox.2021.102203.
Nakajo, T., Katayoshi, T., Kitajima, N., & Tsuji-Naito, K. (2021). 1,25-Dihydroxyvitamin D. Redox biology, 48102203. https://doi.org/10.1016/j.redox.2021.102203
Nakajo, Takahisa, et al. "1,25-Dihydroxyvitamin D." Redox biology vol. 48 (2021): 102203. doi: https://doi.org/10.1016/j.redox.2021.102203
Nakajo T, Katayoshi T, Kitajima N, Tsuji-Naito K. 1,25-Dihydroxyvitamin D. Redox Biol. 2021 Dec 01;48:102203. doi: 10.1016/j.redox.2021.102203. Epub 2021 Dec 01. PMID: 34872043.
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Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins.

Redox biology

Coombs GS, Rios-Monterrosa JL, Lai S, Dai Q, Goll AC, Ketterer MR, Valdes MF, Uche N, Benjamin IJ, Wallrath LL.
PMID: 34872044
Redox Biol. 2021 Nov 25;48:102196. doi: 10.1016/j.redox.2021.102196. Epub 2021 Nov 25.

Mutations in the human LMNA gene cause a collection of diseases called laminopathies, which includes muscular dystrophy and dilated cardiomyopathy. The LMNA gene encodes lamins, filamentous proteins that form a meshwork on the inner side of the nuclear envelope....

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Coombs GS, Rios-Monterrosa JL, Lai S, et al. Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins. Redox Biol. 2021;48:102196doi: 10.1016/j.redox.2021.102196.
Coombs, G. S., Rios-Monterrosa, J. L., Lai, S., Dai, Q., Goll, A. C., Ketterer, M. R., Valdes, M. F., Uche, N., Benjamin, I. J., & Wallrath, L. L. (2021). Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins. Redox biology, 48102196. https://doi.org/10.1016/j.redox.2021.102196
Coombs, Gary S, et al. "Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins." Redox biology vol. 48 (2021): 102196. doi: https://doi.org/10.1016/j.redox.2021.102196
Coombs GS, Rios-Monterrosa JL, Lai S, Dai Q, Goll AC, Ketterer MR, Valdes MF, Uche N, Benjamin IJ, Wallrath LL. Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins. Redox Biol. 2021 Nov 25;48:102196. doi: 10.1016/j.redox.2021.102196. Epub 2021 Nov 25. PMID: 34872044.
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Peroxiredoxin 6 protects irradiated cells from oxidative stress and shapes their senescence-associated cytokine landscape.

Redox biology

Salovska B, Kondelova A, Pimkova K, Liblova Z, Pribyl M, Fabrik I, Bartek J, Vajrychova M, Hodny Z.
PMID: 34923300
Redox Biol. 2021 Dec 11;49:102212. doi: 10.1016/j.redox.2021.102212. Epub 2021 Dec 11.

Cellular senescence is a complex stress response defined as an essentially irreversible cell cycle arrest mediated by the inhibition of cell cycle-specific cyclin dependent kinases. The imbalance in redox homeostasis and oxidative stress have been repeatedly observed as one...

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Salovska B, Kondelova A, Pimkova K, et al. Peroxiredoxin 6 protects irradiated cells from oxidative stress and shapes their senescence-associated cytokine landscape. Redox Biol. 2021;49:102212doi: 10.1016/j.redox.2021.102212.
Salovska, B., Kondelova, A., Pimkova, K., Liblova, Z., Pribyl, M., Fabrik, I., Bartek, J., Vajrychova, M., & Hodny, Z. (2021). Peroxiredoxin 6 protects irradiated cells from oxidative stress and shapes their senescence-associated cytokine landscape. Redox biology, 49102212. https://doi.org/10.1016/j.redox.2021.102212
Salovska, Barbora, et al. "Peroxiredoxin 6 protects irradiated cells from oxidative stress and shapes their senescence-associated cytokine landscape." Redox biology vol. 49 (2021): 102212. doi: https://doi.org/10.1016/j.redox.2021.102212
Salovska B, Kondelova A, Pimkova K, Liblova Z, Pribyl M, Fabrik I, Bartek J, Vajrychova M, Hodny Z. Peroxiredoxin 6 protects irradiated cells from oxidative stress and shapes their senescence-associated cytokine landscape. Redox Biol. 2021 Dec 11;49:102212. doi: 10.1016/j.redox.2021.102212. Epub 2021 Dec 11. PMID: 34923300; PMCID: PMC8688892.
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CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners.

Redox biology

Liu Z, Wang H, Hou Y, Yang Y, Jia J, Wu J, Zuo Z, Gao T, Ren S, Bian Y, Liu S, Fu J, Sun Y, Li J, Yamamoto M, Zhang Q, Xu Y, Pi J.
PMID: 34763297
Redox Biol. 2021 Nov 06;48:102180. doi: 10.1016/j.redox.2021.102180. Epub 2021 Nov 06.

Fine-tuning of osteoclast differentiation (OD) and bone remodeling is crucial for bone homeostasis. Dissecting the mechanisms regulating osteoclastogenesis is fundamental to understanding the pathogenesis of various bone disorders including osteoporosis and arthritis. Nuclear factor erythroid 2-related factor 1 (NFE2L1,...

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Liu Z, Wang H, Hou Y, et al. CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners. Redox Biol. 2021;48:102180doi: 10.1016/j.redox.2021.102180.
Liu, Z., Wang, H., Hou, Y., Yang, Y., Jia, J., Wu, J., Zuo, Z., Gao, T., Ren, S., Bian, Y., Liu, S., Fu, J., Sun, Y., Li, J., Yamamoto, M., Zhang, Q., Xu, Y., & Pi, J. (2021). CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners. Redox biology, 48102180. https://doi.org/10.1016/j.redox.2021.102180
Liu, Zhiyuan, et al. "CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners." Redox biology vol. 48 (2021): 102180. doi: https://doi.org/10.1016/j.redox.2021.102180
Liu Z, Wang H, Hou Y, Yang Y, Jia J, Wu J, Zuo Z, Gao T, Ren S, Bian Y, Liu S, Fu J, Sun Y, Li J, Yamamoto M, Zhang Q, Xu Y, Pi J. CNC-bZIP protein NFE2L1 regulates osteoclast differentiation in antioxidant-dependent and independent manners. Redox Biol. 2021 Nov 06;48:102180. doi: 10.1016/j.redox.2021.102180. Epub 2021 Nov 06. PMID: 34763297; PMCID: PMC8591424.
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Epigallocatechin-3-gallate pretreatment alleviates doxorubicin-induced ferroptosis and cardiotoxicity by upregulating AMPKα2 and activating adaptive autophagy.

Redox biology

He H, Wang L, Qiao Y, Yang B, Yin D, He M.
PMID: 34775319
Redox Biol. 2021 Nov 11;48:102185. doi: 10.1016/j.redox.2021.102185. Epub 2021 Nov 11.

Reports indicate that the mechanism of doxorubicin (Dox)-induced cardiotoxicity is very complex, involving multiple regulatory cell death forms. Furthermore, the clinical intervention effect is not ideal. Iron dependence, abnormal lipid metabolism, and excess reactive oxygen species generation, three characteristics...

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He H, Wang L, Qiao Y, et al. Epigallocatechin-3-gallate pretreatment alleviates doxorubicin-induced ferroptosis and cardiotoxicity by upregulating AMPKα2 and activating adaptive autophagy. Redox Biol. 2021;48:102185doi: 10.1016/j.redox.2021.102185.
He, H., Wang, L., Qiao, Y., Yang, B., Yin, D., & He, M. (2021). Epigallocatechin-3-gallate pretreatment alleviates doxorubicin-induced ferroptosis and cardiotoxicity by upregulating AMPKα2 and activating adaptive autophagy. Redox biology, 48102185. https://doi.org/10.1016/j.redox.2021.102185
He, Huan, et al. "Epigallocatechin-3-gallate pretreatment alleviates doxorubicin-induced ferroptosis and cardiotoxicity by upregulating AMPKα2 and activating adaptive autophagy." Redox biology vol. 48 (2021): 102185. doi: https://doi.org/10.1016/j.redox.2021.102185
He H, Wang L, Qiao Y, Yang B, Yin D, He M. Epigallocatechin-3-gallate pretreatment alleviates doxorubicin-induced ferroptosis and cardiotoxicity by upregulating AMPKα2 and activating adaptive autophagy. Redox Biol. 2021 Nov 11;48:102185. doi: 10.1016/j.redox.2021.102185. Epub 2021 Nov 11. PMID: 34775319; PMCID: PMC8600154.
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The sex steroid precursor dehydroepiandrosterone prevents nonalcoholic steatohepatitis by activating the AMPK pathway mediated by GPR30.

Redox biology

Li L, Wang H, Yao Y, Cao J, Jiang Z, Yan W, Chu X, Li Q, Lu M, Ma H.
PMID: 34781165
Redox Biol. 2021 Nov 12;48:102187. doi: 10.1016/j.redox.2021.102187. Epub 2021 Nov 12.

The prevalence of nonalcoholic steatohepatitis (NASH) caused by estrogen deficiency increased sharply in recent decades and has become a major threat to liver health in postmenopausal women. There is no effective strategy to control the incidence and development of...

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Li L, Wang H, Yao Y, et al. The sex steroid precursor dehydroepiandrosterone prevents nonalcoholic steatohepatitis by activating the AMPK pathway mediated by GPR30. Redox Biol. 2021;48:102187doi: 10.1016/j.redox.2021.102187.
Li, L., Wang, H., Yao, Y., Cao, J., Jiang, Z., Yan, W., Chu, X., Li, Q., Lu, M., & Ma, H. (2021). The sex steroid precursor dehydroepiandrosterone prevents nonalcoholic steatohepatitis by activating the AMPK pathway mediated by GPR30. Redox biology, 48102187. https://doi.org/10.1016/j.redox.2021.102187
Li, Longlong, et al. "The sex steroid precursor dehydroepiandrosterone prevents nonalcoholic steatohepatitis by activating the AMPK pathway mediated by GPR30." Redox biology vol. 48 (2021): 102187. doi: https://doi.org/10.1016/j.redox.2021.102187
Li L, Wang H, Yao Y, Cao J, Jiang Z, Yan W, Chu X, Li Q, Lu M, Ma H. The sex steroid precursor dehydroepiandrosterone prevents nonalcoholic steatohepatitis by activating the AMPK pathway mediated by GPR30. Redox Biol. 2021 Nov 12;48:102187. doi: 10.1016/j.redox.2021.102187. Epub 2021 Nov 12. PMID: 34781165; PMCID: PMC8604675.
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MicroRNA-455-3p improves synaptic, cognitive functions and extends lifespan: Relevance to Alzheimer's disease.

Redox biology

Kumar S, Morton H, Sawant N, Orlov E, Bunquin LE, Pradeepkiran JA, Alvir R, Reddy PH.
PMID: 34781166
Redox Biol. 2021 Nov 09;48:102182. doi: 10.1016/j.redox.2021.102182. Epub 2021 Nov 09.

BACKGROUND: MicroRNA-455-3p is one of the highly conserved miRNAs involved in multiple cellular functions in humans and we explored its relevance to learning and memory functions in Alzheimer's disease (AD). Our recent in vitro studies exhibited the protective role...

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Kumar S, Morton H, Sawant N, et al. MicroRNA-455-3p improves synaptic, cognitive functions and extends lifespan: Relevance to Alzheimer's disease. Redox Biol. 2021;48:102182doi: 10.1016/j.redox.2021.102182.
Kumar, S., Morton, H., Sawant, N., Orlov, E., Bunquin, L. E., Pradeepkiran, J. A., Alvir, R., & Reddy, P. H. (2021). MicroRNA-455-3p improves synaptic, cognitive functions and extends lifespan: Relevance to Alzheimer's disease. Redox biology, 48102182. https://doi.org/10.1016/j.redox.2021.102182
Kumar, Subodh, et al. "MicroRNA-455-3p improves synaptic, cognitive functions and extends lifespan: Relevance to Alzheimer's disease." Redox biology vol. 48 (2021): 102182. doi: https://doi.org/10.1016/j.redox.2021.102182
Kumar S, Morton H, Sawant N, Orlov E, Bunquin LE, Pradeepkiran JA, Alvir R, Reddy PH. MicroRNA-455-3p improves synaptic, cognitive functions and extends lifespan: Relevance to Alzheimer's disease. Redox Biol. 2021 Nov 09;48:102182. doi: 10.1016/j.redox.2021.102182. Epub 2021 Nov 09. PMID: 34781166; PMCID: PMC8604688.
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