The unfolded protein response and cellular senescence. A Review in the Theme: Cellular Mechanisms of Endoplasmic Reticulum Stress Signaling in Health and Disease

The Hallmarks of Aging

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A biomarker that identifies senescent human cells in culture and in aging skin in vivo.

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Signal integration in the endoplasmic reticulum unfolded protein response

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The limited in vitro lifetime of human diploid cell strains

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Telomeres shorten during ageing of human fibroblasts

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XBP1 mRNA Is Induced by ATF6 and Spliced by IRE1 in Response to ER Stress to Produce a Highly Active Transcription Factor

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Clearance of p16Ink4a-positive senescent cells delays ageing-associated disorders

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An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress

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THE MAMMALIAN UNFOLDED PROTEIN RESPONSE

Schröder, M., & Kaufman, R. J. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.074134 · Cited by 3,099

Temporal Dynamics of Oxidative Stress and Inflammation in Bronchopulmonary Dysplasia

Teng, M., Wu, T.-J., Jing, X., Day, B. W., Pritchard, K. A., Naylor, S., & Teng, R. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms251810145 · Cited by 34

The Connection Between Cell Fate and Telomere

Engin, A. B., & Engin, A. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-49844-3_3 · Cited by 39

The IRE1 and PERK arms of the unfolded protein response promote survival of rhabdomyosarcoma cells

McCarthy, N., Dolgikh, N., Logue, S. E., Patterson, J. B., Zeng, Q., Gorman, A. M., Samali, A., & Fulda, S. (2020) · Cancer Letters · doi:10.1016/j.canlet.2020.07.009 · Cited by 31

Exploring cellular senescence in the musculoskeletal system: Any insights for biomarkers discovery?

Gerosa, L., Malvandi, A. M., Malavolta, M., Provinciali, M., & Lombardi, G. (2023) · Ageing Research Reviews · doi:10.1016/j.arr.2023.101943 · Cited by 33

Regulatory RNA binding proteins contribute to the transcriptome-wide splicing alterations in human cellular senescence

Dong, Q., Wei, L., Zhang, M. Q., & Wang, X. (2018) · Aging · doi:10.18632/aging.101485 · Cited by 31

ATM-associated signalling triggers the unfolded protein response and cell death in response to stress

Hotokezaka, Y., Katayama, I., & Nakamura, T. (2020) · Communications Biology · doi:10.1038/s42003-020-1102-2 · Cited by 33

Shear stress induces human aortic endothelial cell apoptosis via interleukin-1 receptor-associated kinase 2-induced endoplasmic reticulum stress

Pan, L., Hong, Z., Yu, L., Gao, Y., Zhang, R., Feng, H., Su, L., & Wang, G. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.7524 · Cited by 31

A single dose of Ultraviolet-A induces proteome remodeling and senescence in primary human keratinocytes

Valerio, H. P., Ravagnani, F. G., Ronsein, G. E., & Mascio, P. D. (2021) · Scientific Reports · doi:10.1038/s41598-021-02658-5 · Cited by 34

Anti-Aging Effect of Metformin: A Molecular and Therapeutical Perspective

Torres, W., Nava, M., Galbán, N., Gómez, Y., Morillo, V., Rojas, M., Cano, C., Chacín, M., D’Marco, L., Herazo-Beltrán, Y., et al. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200716161610 · Cited by 28

Relevance of endoplasmic reticulum and mitochondria interactions in age-associated diseases

Gil-Hernández, A., & Silva‐Palacios, A. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101193 · Cited by 30

Keap1 governs ageing-induced protein aggregation in endothelial cells

Kopacz, A., Klóska, D., Targosz‐Korecka, M., Zapotoczny, B., Cysewski, D., Personnic, N., Werner, E., Hajduk, K., Józkowicz, A., & Grochot‐Przeczek, A. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101572 · Cited by 28

Stress response proteins NRP1 and NRP2 are pro-survival factors that inhibit cell death during ER stress

Yang, Y., Liu, X., Zhang, W., Qian, Q., Zhou, L., Liu, S., Li, Y., & Hou, X. (2021) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiab335 · Cited by 28

The Endoplasmic Reticulum Stress Response Mediates Shikonin-Induced Apoptosis of 5-Fluorouracil-Resistant Colorectal Cancer Cells

Piao, M. J., Han, X., Kang, K. A., Fernando, P. D. S. M., Herath, H. M. U. L., & Hyun, J. W. (2021) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2021.118 · Cited by 28

The out-of-field dose in radiation therapy induces delayed tumorigenesis by senescence evasion

Goy, E., Tomezak, M., Facchin, C., Martin, N., Bouchaert, E., Benoît, J., de Schutter, C., Nassour, J., Saas, L., Drullion, C., et al. (2022) · eLife · doi:10.7554/elife.67190 · Cited by 29

Towards Age-Related Anti-Inflammatory Therapy: Klotho Suppresses Activation of ER and Golgi Stress Response in Senescent Monocytes

Mytych, J., Sołek, P., Będzińska, A., Rusinek, K., Warzybok, A., Tabecka-Lonczynska, A., & Koziorowski, M. (2020) · Cells · doi:10.3390/cells9020261 · Cited by 27

α-Klotho prevents diabetic retinopathy by reversing the senescence of macrophages

Li, Q., Wang, P., Xu, M., Gong, Y., Wang, M., Luan, R., Liu, J., Li, X., Li, X., & Shao, Y. X. (2024) · Cell Communication and Signaling · doi:10.1186/s12964-024-01838-w · Cited by 31

Respiratory syncytial virus infection accelerates lung fibrosis through the unfolded protein response in a bleomycin-induced pulmonary fibrosis animal model

Wang, L., Cheng, W., & Zhang, Z. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.6558 · Cited by 27

Autophagy activated via GRP78 to alleviate endoplasmic reticulum stress for cell survival in blue light-mediated damage of A2E-laden RPEs

Feng, J., Chen, Y., Lu, B., Sun, X., Zhu, H., & Sun, X. (2019) · BMC Ophthalmology · doi:10.1186/s12886-019-1261-4 · Cited by 28

Pharmacological landscape of endoplasmic reticulum stress: Uncovering therapeutic avenues for metabolic diseases

Alotaibi, G., & Alkhammash, A. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177509 · Cited by 26

Investigating the associations between adiposity, life course overweight trajectories, and telomere length

Wulaningsih, W., Watkins, J. A., Matsuguchi, T., & Hardy, R. (2016) · Aging · doi:10.18632/aging.101036 · Cited by 26

Oxidative and Endoplasmic Reticulum Stress Responses to Chronic High-Altitude Exposure During the Development of High-Altitude Pulmonary Hypertension

Pu, X., Lin, X., Duan, X., Wang, J., Shang, J., Yun, H., & Chen, Z. (2020) · High Altitude Medicine & Biology · doi:10.1089/ham.2019.0143 · Cited by 26

Advances in the interaction between endoplasmic reticulum stress and osteoporosis

Zhong, M., Wu, Z., Chen, Z., Ren, Q., & Zhou, J. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115134 · Cited by 29

Tanshinone IIA ameliorates diabetic cardiomyopathy by inhibiting Grp78 and CHOP expression in STZ‑induced diabetes rats

Tao, S., Chen, L., Song, J., Zhu, N., Song, X., Shi, R., Ge, G.-F., & Zhang, Y. (2019) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2019.7580 · Cited by 26

Inhibition of mitogen-activated protein kinase signaling pathway sensitizes breast cancer cells to endoplasmic reticulum stress-induced apoptosis

Yang, F., TANG, X. Y., Liu, H., & Jiang, Z. W. (2016) · Oncology Reports · doi:10.3892/or.2016.4580 · Cited by 25

Protection of zero-valent iron nanoparticles against sepsis and septic heart failure

Wang, D., Wang, C., Liang, Z., Lei, W., Deng, C., Liu, X., Jiang, S., Zhu, Y., Zhang, S., Yang, W., et al. (2022) · Journal of Nanobiotechnology · doi:10.1186/s12951-022-01589-1 · Cited by 24

Co-activation of Akt, Nrf2, and NF-κB signals under UPRER in torpid Myotis ricketti bats for survival

Huang, W., Liao, C.-C., Han, Y., Lv, J., Lei, M., Li, Y., Lv, Q., Dong, D., Zhang, S., Pan, Y.-H., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-01378-2 · Cited by 26

Heparin-based coacervate of bFGF facilitates peripheral nerve regeneration by inhibiting endoplasmic reticulum stress following sciatic nerve injury

Li, R., Zou, S., Wu, Y., Li, Y., Khor, S., Mao, Y., He, H., Xu, K., Zhang, H., Li, X., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.18256 · Cited by 24

Cellular senescence in the pathogenesis of ovarian dysfunction

Harada, M. (2024) · Journal of obstetrics and gynaecology research · doi:10.1111/jog.15918 · Cited by 23

Shikimic acid protects skin cells from UV-induced senescence through activation of the NAD+-dependent deacetylase SIRT1

Martínez-Gutiérrez, A., Fernández-Duran, I., Marazuela-Duque, A., Simonet, N. G., Yousef, I., Martínez‐Rovira, I., Martínez-Hoyos, J., & Vaquero, A. (2021) · Aging · doi:10.18632/aging.203010 · Cited by 23

Silencing of both ATF4 and PERK inhibits cell cycle progression and promotes the apoptosis of differentiating chondrocytes

Wu, Z., Li, M., Zheng, W., Hu, Q., Cheng, Z., & Guo, F. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.2985 · Cited by 23

Potential mechanisms of uremic muscle wasting and the protective role of the mitochondria-targeted antioxidant Mito-TEMPO

Liu, Y., Elangovan, P., Bi, X., Wang, Y., & Ding, W. Q. (2020) · International Urology and Nephrology · doi:10.1007/s11255-020-02508-9 · Cited by 23

The novel GLP-1/GIP dual agonist DA3-CH is more effective than liraglutide in reducing endoplasmic reticulum stress in diabetic rats with cerebral ischemia-reperfusion injury

Bai, B., Li, D., Xue, G., Feng, P., Wang, M., Han, Y., Wang, Y., & Hölscher, C. (2020) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2020.09.002 · Cited by 22

Modulation of Oxidative Stress-Induced Senescence during Non-Alcoholic Fatty Liver Disease

Pedroza-Díaz, J., Arroyave-Ospina, J. C., Salas, S. S., & Moshage, H. J. (2022) · Antioxidants · doi:10.3390/antiox11050975 · Cited by 27

Cellular Aging and Senescence in Cancer: A Holistic Review of Cellular Fate Determinants

Tufail, M., Huang, Y., Hu, J.-J., Liang, J., He, C., Wan, W., Jiang, C., Wu, H., & Li, N. (2024) · Aging and Disease · doi:10.14336/ad.2024.0421 · Cited by 27

The consequences of ageing, progeroid syndromes and cellular senescence on mechanotransduction and the nucleus

Gilbert, H. T. J., & Swift, J. (2019) · Experimental Cell Research · doi:10.1016/j.yexcr.2019.03.002 · Cited by 22

Real-time tracking of ER turnover during ERLAD by a rhenium complex via lifetime imaging

Liang, H., Ling, Y., Huang, Z.-X., Pan, Z., Tan, C., & Mao, Z. (2021) · National Science Review · doi:10.1093/nsr/nwab194 · Cited by 22

GRP78/BiP determines senescence evasion cell fate after cisplatin-based chemotherapy

Zin, Z., Choochuay, K., Tubsuwan, A., Pinkaew, D., Suksomtip, M., Vinayanuwattikun, C., Pithi Chanvorachote, B., & Chunhacha, P. (2021) · Scientific Reports · doi:10.1038/s41598-021-01540-8 · Cited by 21

ER-Stress and Senescence Coordinately Promote Endothelial Barrier Dysfunction in Diabetes-Induced Atherosclerosis

Fatima, S., Ambreen, S., Mathew, A., Elwakiel, A., Gupta, A., Singh, K. K., Krishnan, S., Rana, R., Khawaja, H., Gupta, D., et al. (2022) · Nutrients · doi:10.3390/nu14142786 · Cited by 21

Routes of Albumin Overload Toxicity in Renal Tubular Epithelial Cells

Eleftheriadis, T., Pissas, G., Golfinopoulos, S., Efthymiadi, M., Poulianiti, C., Konsta, M. A. P., Liakopoulos, V., & Stefanidis, I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119640 · Cited by 21

HRD1-induced TMEM2 ubiquitination promotes ER stress-mediated apoptosis through a non-canonical pathway in intestinal ischemia/reperfusion

Zhao, X., Liu, D., Zhao, Y., Wang, Z., Wang, Y., Chen, Z., Ning, S., Wang, G., Meng, L., Yao, J., et al. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06504-0 · Cited by 21

Renin-angiotensin system activation accelerates atherosclerosis in experimental renal failure by promoting endoplasmic reticulum stress-related inflammation

Yang, J., Zhang, X., Yu, X.-Y., Tang, W., & Gan, H. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.2856 · Cited by 18

Senescence of Alveolar Stem Cells Drives Progressive Pulmonary FibrosisPreprint

Yao, C., Guan, X., Carraro, G., Parimon, T., Liu, X., Huang, G., Soukiasian, H. J., David, G., WEIGT, S. S., Belperio, J. A., et al. (2019) · SSRN Electronic Journal · doi:10.1101/820175 · Cited by 21

Disruption of endoplasmic reticulum homeostasis exacerbates liver injury in clinically ketotic cows

Shi, Z., Song, Y., Gao, X., Loor, J. J., Aboragah, A. A., Yu, H., Fang, Z., Zhu, Y., Du, X., Li, X., et al. (2021) · Journal of Dairy Science · doi:10.3168/jds.2021-20238 · Cited by 20

Cellular Senescence in Cardiovascular Diseases: From Pathogenesis to Therapeutic Challenges

Li, D., Li, Y., Ding, H., Wang, Y., Xie, Y., & Zhang, X. (2023) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd10100439 · Cited by 21

Molecular docking studies of salubrinal and its analogs as inhibitors of the GADD34:PP1 enzyme

Zadorozhnii, P. V., Pokotylo, I. O., Kiselev, V. V., Okhtina, O. V., & Kharchenko, A. V. (2019) · ADMET & DMPK · doi:10.5599/admet.632 · Cited by 20

GSK3 inhibition rescues growth and telomere dysfunction in dyskeratosis congenita iPSC-derived type II alveolar epithelial cells

Fernandez, R. J., Gardner, Z., Slovik, K. J., Liberti, D. C., Estep, K. N., Yang, W., Chen, Q., Santini, G. T., Perez, J. V., Root, S., et al. (2022) · eLife · doi:10.7554/elife.64430 · Cited by 19

Tonsil-derived mesenchymal stem cells incorporated in reactive oxygen species-releasing hydrogel promote bone formation by increasing the translocation of cell surface GRP78

Choi, D. H., Lee, K. E., Oh, S.-Y., Lee, S., Jo, B. S., Lee, J., Park, J., Park, Y. J., Park, K. D., Jo, I., et al. (2021) · Biomaterials · doi:10.1016/j.biomaterials.2021.121156 · Cited by 19

New Trends in Aging Drug Discovery

Benhamú, B., Martín‐Fontecha, M., Vázquez‐Villa, H., López-Rodríguez, M. L., & Ortega‐Gutiérrez, S. (2022) · Biomedicines · doi:10.3390/biomedicines10082006 · Cited by 20

Transcriptional regulation of CDKN2A/p16 by sirtuin 7 in senescence

Rodríguez, S., Bermúdez, L. G., González, D. M., Bernal, C., Cañas, A., Morales‐Ruíz, T., Henríquez, B., & Rojas, A. P. (2022) · Molecular Medicine Reports · doi:10.3892/mmr.2022.12861 · Cited by 20

Differentiated Hepatic Response to Fructose Intake during Adolescence Reveals the Increased Susceptibility to Non‐Alcoholic Fatty Liver Disease of Maternal High‐Fat Diet Male Rat Offspring

Oliveira, L. S. D., Caetano, B., Miranda, R. A., Souza, A. F. P., Cordeiro, A., Woyames, J., de Andrade, C. B. V., Atella, G. C., Takiya, C. M., Fortunato, R. S., et al. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900838 · Cited by 19

Smyd3-PARP16 axis accelerates unfolded protein response and vascular aging

Yang, D., Wang, Q., Wei, G., Wu, J., Zhu, Y. C., Zhu, Q., Ni, T., Liu, X., & Zhu, Y. Z. (2020) · Aging · doi:10.18632/aging.103895 · Cited by 19

To Decipher the Mycoplasma hominis Proteins Targeting into the Endoplasmic Reticulum and Their Implications in Prostate Cancer Etiology Using Next-Generation Sequencing Data

Zakariah, M., Khan, S., Chaudhary, A. A., Rolfo, C. D., Ismail, M. M. B., & Alotaibi, Y. A. (2018) · Molecules · doi:10.3390/molecules23050994 · Cited by 18

Targeting sphingosine kinase 1 (SK1) enhances oncogene-induced senescence through ceramide synthase 2 (CerS2)-mediated generation of very-long-chain ceramides

Trayssac, M., Clarke, C. J., Stith, J. L., Snider, J. M., Newen, N., Gault, C. R., Hannun, Y. A., & Obeid, L. M. (2021) · Cell Death and Disease · doi:10.1038/s41419-020-03281-4 · Cited by 18

Apoptosis Induction by Iron Radiation via Inhibition of Autophagy in Trp53+/- Mouse Testes: Is Chronic Restraint-Induced Stress a Modifying Factor?

Li, H., Wang, B., Zhang, H., Katsube, T., Xie, Y., & Gan, L. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.22805 · Cited by 18

Inhibition of neural stem cell aging through the transient induction of reprogramming factors

Han, M. J., Lee, W. J., Choi, J., Hong, Y. J., Uhm, S. J., Choi, Y., & Tae, J. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24967 · Cited by 19

Oxidised protein metabolism: recent insights

Samardzic, K., & Rodgers, K. J. (2017) · Biological Chemistry · doi:10.1515/hsz-2017-0124 · Cited by 18

The autophagy-senescence axis as a threshold model of aging and therapeutic targeting

Bahar, M. E., Hwang, J. S., Lai, T. H., Akter, K.-M., Maulidi, R. F., & Kim, D. R. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104079 · Cited by 20

Senescent Changes and Endoplasmic Reticulum Stress May Be Involved in the Pathogenesis of Missed Miscarriage

Tang, Y., Zhang, X., Zhang, Y., Feng, H., Gao, J., Liu, H., Guo, F., & Chen, Q. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.656549 · Cited by 17

The role of unfolded protein response-associated miRNAs in immunogenic cell death amplification: A literature review and bioinformatics analysis

Azizi, M., Salehi-Mazandarani, S., Nikpour, P., Andalib, A., & Rezaei, M. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121341 · Cited by 17

Fingolimod sensitizes EGFR wild‑type non‑small cell lung cancer cells to lapatinib or sorafenib and induces cell cycle arrest

Ota, K., Okuma, T., Lorenzo, A. D., Yokota, A., Hino, H., Kazama, H., Moriya, S., Takano, N., Hiramoto, M., & Miyazawa, K. (2019) · Oncology Reports · doi:10.3892/or.2019.7140 · Cited by 18

Neuroprotective Effect of the Inhibitor Salubrinal after Cardiac Arrest in a Rodent Model

Zhang, J., Wang, Y., Ju, M., Song, J., Zheng, Y., Lin, S., Zhu, D., Wen, L., Zhong, M., Pan, S., et al. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/7468738 · Cited by 17

CCAAT/enhancer-binding protein (C/EBP) homologous protein promotes alveolar epithelial cell senescence via the nuclear factor-kappa B pathway in pulmonary fibrosis

Jing, X., Sun, W., Yang, X., Huang, H. F., Wang, P., Luo, Q., Xia, S., Fang, C., Zhang, Q., Guo, J., et al. (2021) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2021.106142 · Cited by 17

Distinct phenotypes and ‘bystander’ effects of senescent tumour cells induced by docetaxel or immunomodulatory cytokines

Sapega, O., Mikyškov�, R., Bieblov�, J., Mrázková, B., Hodn�, Z., & Reiniš, M. (2018) · International Journal of Oncology · doi:10.3892/ijo.2018.4553 · Cited by 18

ER Stress and Micronuclei Cluster: Stress Response Contributes to Genome Chaos in Cancer

Heng, E., Moy, A., Liu, G., Heng, H. H., & Zhang, K. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.673188 · Cited by 16

Salubrinal-mediated activation of eIF2α signaling improves oxidative stress-induced BMSCs senescence and senile osteoporosis

Li, L., Hu, G., Xie, R., Yang, J., Shi, X., Jia, Z., Qu, X., Wang, M., & Wu, Y. (2022) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2022.04.041 · Cited by 16

Endoplasmic Reticulum Stress in Gliomas: Exploiting a Dual-Effect Dysfunction through Chemical Pharmaceutical Compounds and Natural Derivatives for Therapeutical Uses

García-López, D., Zaragoza‐Ojeda, M., Eguía-Aguilar, P., & Arenas‐Huertero, F. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25074078 · Cited by 16

Overexpression of augmenter of liver regeneration (ALR) mitigates the effect of H2O2-induced endoplasmic reticulum stress in renal tubule epithelial cells

Jiang, X., Liao, X., Huang, L., Sun, H., Liu, Q., & Zhang, L. (2019) · APOPTOSIS · doi:10.1007/s10495-019-01517-z · Cited by 16

The role of the MAD2-TLR4-MyD88 axis in paclitaxel resistance in ovarian cancer

Bates, M., Spillane, C. D., Gallagher, M. F., McCann, A. H., Martin, C. M., Blackshields, G., Keegan, H., Gubbins, L., Brooks, R. D., Brooks, D. A., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0243715 · Cited by 16

Using mass spectrometry imaging to visualize age-related subcellular disruption

Hogan, K. A., Zeidler, J. D., Beasley, H. K., Alsaadi, A. I., Alshaheeb, A. A., Chang, Y., Tian, H., Hinton, A. O., Jr., & McReynolds, M. R. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.906606 · Cited by 16

Signalling inhibition by ponatinib disrupts productive alternative lengthening of telomeres (ALT)

Kusuma, F. K., Prabhu, A., Tieo, G., Ahmed, S. M., Dakle, P., Yong, W. K., Pathak, E., Madan, V., Jiang, Y. Y., Tam, W. L., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-37633-3 · Cited by 15

Alleviation of endoplasmic reticulum stress by tauroursodeoxycholic acid delays senescence of mouse ovarian surface epithelium

Vašíčková, K., Moráň, L., Gurín, D., & Vaňhara, P. (2018) · Cell and Tissue Research · doi:10.1007/s00441-018-2888-9 · Cited by 15

Metabolic Vulnerabilities in Multiple Myeloma

Lim, J. S. L., Chong, P. S. Y., & Chng, W. J. (2022) · Cancers · doi:10.3390/cancers14081905 · Cited by 15

Transmissible Endoplasmic Reticulum Stress Mediated by Extracellular Vesicles from Adipocyte Promoting the Senescence of Adipose‐Derived Mesenchymal Stem Cells in Hypertrophic Obesity

Fang, J., Li, L., Cao, X., Yue, H., Fu, W., Chen, Y., Xu, Z., Zhao, Q., Zhao, J., Wang, Y., et al. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/7175027 · Cited by 14

Deficiency of spns1 exacerbates per- and polyfluoroalkyl substances mediated hepatic toxicity and steatosis in zebrafish (Danio rerio)

Gadi, S. V., Niture, S. K., Hoang, H., Qi, Q., Hatcher, C., Huang, X., Haider, J., Norford, D. C., Leung, T., Levine, K. E., et al. (2023) · Toxicology · doi:10.1016/j.tox.2023.153641 · Cited by 15

Crosstalk between protein misfolding and endoplasmic reticulum stress during ageing and their role in age-related disorders

Hemagirri, M., Chen, Y., Gopinath, S. C. B., Sahreen, S., Adnan, M., & Sasidharan, S. (2023) · Biochimie · doi:10.1016/j.biochi.2023.10.019 · Cited by 15

The Inability of the Choroid to Revascularize in Oxygen-Induced Retinopathy Results from Increased p53/miR-Let-7b Activity

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