Regulated cell death and adaptive stress responses

Hallmarks of Cancer: The Next Generation

Hanahan, D., & Weinberg, R. A. (2011) · Cell · doi:10.1016/j.cell.2011.02.013 · Cited by 66,590

AMPK: a nutrient and energy sensor that maintains energy homeostasis

Hardie, D. G., Ross, F. A., & Hawley, S. A. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3311 · Cited by 4,602

The unfolded protein response: controlling cell fate decisions under ER stress and beyond

Hetz, C. A. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3270 · Cited by 4,223

Autophagy and the Integrated Stress Response

Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506

Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009

Kroemer, G., Galluzzi, L., Vandenabeele, P., Abrams, J., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., El-Deiry, W. S., Golstein, P., Green, D. R., et al. (2009) · Cell Death & Differentiation · doi:10.1038/cdd.2008.150 · Cited by 3,399

Protein translation and folding are coupled by an endoplasmic-reticulum-resident kinase

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Immunogenic Cell Death in Cancer Therapy

Kroemer, G., Galluzzi, L., Kepp, O., & Zitvogel, L. (2013) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-100008 · Cited by 3,303

Immunogenic cell death and DAMPs in cancer therapy

Krysko, D. V., Garg, A. D., Kaczmarek, A., Krysko, O., Agostinis, P., & Vandenabeele, P. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3380 · Cited by 3,223

Type I interferons in infectious disease

McNab, F., Mayer-Barber, K., Sher, A., Wack, A., & O'Garra, A. (2015) · Nature Reviews Immunology · doi:10.1038/nri3787 · Cited by 2,780

Molecular definitions of cell death subroutines: recommendations of the Nomenclature Committee on Cell Death 2012

Galluzzi, L., Vitale, I., Abrams, J. M., Alnemri, E. S., Baehrecke, E. H., Blagosklonny, M. V., Dawson, T. M., Dawson, V. L., El-Deiry, W. S., Fulda, S., et al. (2012) · Cell Death & Differentiation · doi:10.1038/cdd.2011.96 · Cited by 2,421

Molecular Mechanisms of Cell Death

Lemasters, J. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-802761-5.00001-8 · Cited by 14

Targeted inhibition of protein synthesis renders cancer cells vulnerable to apoptosis by unfolded protein response

Gsottberger, F., Meier, C., Ammon, A., Parker, S., Wendland, K., George, R., Petkovic, S., Mellenthin, L., Emmerich, C., Lutzny‐Geier, G., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06055-w · Cited by 14

Signaling pathways in glioblastoma

Gomes, I., Oliveira, R. J. D. S., & Girol, A. P. (2025) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2025.104647 · Cited by 13

Do photosynthetic cells communicate with each other during cell death? From cyanobacteria to vascular plants

Aguilera, A., Distéfano, A. M., Jauzein, C., Correa‐Aragunde, N., Martínez, D. E., Martin, M. V., & Sueldo, D. J. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac363 · Cited by 13

Yeast Cells Exposed to Exogenous Palmitoleic Acid Either Adapt to Stress and Survive or Commit to Regulated Liponecrosis and Die

Mohammad, K., Dakik, P., Medkour, Y., McAuley, M., Mitrofanova, D., & Titorenko, V. I. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/3074769 · Cited by 13

Applications of nanotechnology in remodeling the tumour microenvironment for glioblastoma treatment

Mu, Y., Zhang, Z., Zhou, H., Ma, L., & Wang, D. (2024) · Biomaterials Science · doi:10.1039/d4bm00665h · Cited by 12

Cylindrospermopsin impairs tubular transport function in kidney cells LLC-PK1

de Moraes, A. C. N., Freire, D. S., Habibi, H. R., Lowe, J., & de Magalhães, V. F. (2021) · Toxicology Letters · doi:10.1016/j.toxlet.2021.03.002 · Cited by 12

Approaches of Single-Cell Analysis in Crop Improvement

Srivastava, U., & Singh, S. (2022) · Springer protocols handbooks/Springer protocols · doi:10.1007/978-1-0716-2533-0_14 · Cited by 12

Classification and Immune Function of Coelomocytes in Echinoderms

Xue, Z., Peng, T., & Wang, W. (2023) · Current Chinese Science · doi:10.2174/0122102981266814231016051712 · Cited by 11

Advances in non-apoptotic regulated cell death: implications for malignant tumor treatment

Zhang, Y., Yi, S., & Luan, M. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1519119 · Cited by 16

Role of the Redox System in Initiation of a Regenerative Response of Neural Eye Tissues in Vertebrates

Markitantova, Y. V., & Simirskii, V. N. (2020) · Russian Journal of Developmental Biology · doi:10.1134/s106236042001004x · Cited by 10

The role of regulated necrosis in diabetes and its complications

Pang, H., Huang, G., Xie, Z., & Zhou, Z. (2024) · Journal of Molecular Medicine · doi:10.1007/s00109-024-02421-z · Cited by 10

Evaluating the Remote Control of Programmed Cell Death, with or without a Compensatory Cell Proliferation

Dou, X., Chen, L., Lei, M., Zellmer, L., Jia, Q., Ling, P., He, Y., Yang, W., & Liao, D. J. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.26962 · Cited by 10

Measuring Apoptosis and Necrosis in Cholestatic Liver Injury

Woolbright, B. L., & Jaeschke, H. (2019) · Methods in molecular biology · doi:10.1007/978-1-4939-9420-5_9 · Cited by 10

The Dual Role of Necroptosis in Pancreatic Ductal Adenocarcinoma

Giansante, V., Stati, G., Sancilio, S., Guerra, E., Alberti, S., & Pietro, R. D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612633 · Cited by 10

The AP-1-like transcription factor ChAP1 balances tolerance and cell death in the response of the maize pathogen Cochliobolus heterostrophus to a plant phenolic

Simaan, H., Shalaby, S., Hatoel, M., Karinski, O., Goldshmidt‐Tran, O., & Horwitz, B. A. (2019) · Current Genetics · doi:10.1007/s00294-019-01012-7 · Cited by 9

Redefining the concept of erythrocyte senescence: is eryptosis fundamentally different from erythrocyte senescence

Tkachenko, A. S., Havránek, O., Lang, F. J. W., Lang, K. S., & Wieder, T. (2025) · GeroScience · doi:10.1007/s11357-025-02010-z · Cited by 10

Autophagy inhibitors regulate TRAIL sensitivity in human malignant cells by targeting the mitochondrial network and calcium dynamics

Onoe‐Takahashi, A., Suzuki‐Karasaki, M., Suzuki‐Karasaki, M., Ochiai, T., & Suzuki‐Karasaki, Y. (2019) · International Journal of Oncology · doi:10.3892/ijo.2019.4760 · Cited by 8

The interplay between autophagy and programmed cell death in osteoarthritis: insights into mechanisms and therapeutic targets

Wang, H., Zhou, J., Lu, Y., Gao, H., Ning, E., Yang, X. H., Hao, Y., & Hu, D. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05279-y · Cited by 9

Revolutionizing breast cancer treatment: Harnessing the related mechanisms and drugs for regulated cell death (Review)

Ai, L., Yi, N., Qiu, C., Huang, W., Zhang, K., Hou, Q., Jia, L., Li, H., & Liu, L. (2024) · International Journal of Oncology · doi:10.3892/ijo.2024.5634 · Cited by 9

Hormesis Through Low-Dose Radiation

Vaiserman, A. M., Koliada, A. K., & Socol, Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814253-0.00011-5 · Cited by 7

Acute stress reduces population-level metabolic and proteomic variation

Steward, K. F., Refai, M., Dyer, W. E., Copié, V., Lachowiec, J., & Bothner, B. B. (2023) · BMC Bioinformatics · doi:10.1186/s12859-023-05185-4 · Cited by 6

Cellular and Molecular Triggers of Retinal Regeneration in Amphibians

Markitantova, Y. V., & Grigoryan, E. N. (2023) · Life · doi:10.3390/life13101981 · Cited by 6

Regulated Cell Death of Lymphoma Cells after Graded Mitochondrial Damage is Differentially Affected by Drugs Targeting Cell Stress Responses

Lombardo, T., Folgar, M. L. G., Salaverry, L. S., Rey-Roldán, E. B., Álvarez, É., Carreras, M. C., Kornblihtt, L. I., & Blanco, G. A. C. (2017) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.12945 · Cited by 7

Hypertonic stress modulates eNOS function through O-GlcNAc modification at Thr-866

Li, C., He, A., Guo, Y., Yang, X., Luo, M., Cheng, Z., Huang, L., Xia, Y., & Luo, S. (2021) · Scientific Reports · doi:10.1038/s41598-021-90321-4 · Cited by 6

Apoptosis and Efferocytosis in Inflammatory Diseases

Purnama, C. A., Meiliana, A., Barliana, M. I., Dandan, K. L., & Wijaya, A. (2021) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v13i3.1608 · Cited by 5

Effects and mechanisms of Salmonella plasmid virulence gene spv on host-regulated cell death

Li, K., You, J., Li, Y., Huang, R., & Wu, S. (2024) · Current Microbiology · doi:10.1007/s00284-024-03612-0 · Cited by 6

Identification of PSMD11 as a novel cuproptosis‐ and immune‐related prognostic biomarker promoting lung adenocarcinoma progression

Huang, Q., Tian, R., Yu, J., & Du, W. (2024) · Cancer Medicine · doi:10.1002/cam4.7379 · Cited by 5

Pathophysiology of Cancer Cell Death

Galluzzi, L., Linkermann, A., Kepp, O., & Kroemer, G. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-47674-4.00005-0 · Cited by 6

Recombinant Humanized Collagen Enhances Secreted Protein Levels of Fibroblasts and Facilitates Rats’ Skin Basement Membrane Reinforcement

Ye, S., Chen, B., Jeevithan, L., Yang, H., Kong, Y., Diao, X., & Wu, W. (2025) · Journal of Functional Biomaterials · doi:10.3390/jfb16020047 · Cited by 4

Iron and Cell Death

Federico, G., Moccia, M., & Carlomagno, F. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-92033-2_5 · Cited by 4

Programmed cell death of keratinocytes: an active driver in psoriasis

Yuwen, T., Tian, J., Chen, Y., Zhou, Z., Lian, N., & Chen, X. (2026) · APOPTOSIS · doi:10.1007/s10495-025-02207-9 · Cited by 4

Programming regulated cell death to engineer whole-tumor-cell vaccines for cancer immunotherapy

Guan, Y., Bai, D., Bu, N., Hao, W., & Maimaitiyiming, Y. (2026) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2026.189640 · Cited by 4

A companion to the preclinical common data elements and case report forms for neuropathology studies in epilepsy research. A report of the TASK3 WG2 Neuropathology Working Group of the ILAE / AES Joint Translational Task Force

Aronica, E., Binder, D. K., Drexel, M., Ikonomidou, C., Kadam, S. D., Sperk, G., & Steinhäuser, C. (2022) · Epilepsia Open · doi:10.1002/epi4.12638 · Cited by 4

The influence of nitric oxide delivery on the processes of apoptosis, necroptosis and pyroptosis in the renal parenchyma after simulating cardiopulmonary bypass: an experimental study

Tyo, M. A., Олегович, К. Н., Podoksenov, Y. K., Mukhomedzyanov, А. V., Маслов, Л. Н., Kravchenko, I. V., Александровна, Ч. Е., & Kozlov, B. N. (2024) · Messenger of Anesthesiology and Resuscitation · doi:10.24884/2078-5658-2024-21-3-26-33 · Cited by 4

Pharmacologic Inhibition of SIRT1 Limits the Growth of Tumoral and Metastatic Granulosa Cells by Affecting mTOR, Myc, and E2F Pathways

Cluzet, V., Airaud, É., Tête, A., Devillers, M. M., Petit, F., Leary, A. F., Pierre, A., Li, H., Day, C., Weyemi, U., et al. (2025) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-24-0957 · Cited by 4

Epi-Regulation of Cell Death in Cancer

Beato, A., Torre, L. D., Capone, V., Carannante, D., Favale, G., Verrilli, G., Altucci, L., & Carafa, V. (2023) · Biochemistry · doi:10.5772/intechopen.108919 · Cited by 4

Combinational treatment of TPEN and TPGS induces apoptosis in acute lymphoblastic and chronic myeloid leukemia cells in vitro and ex vivo

Mendivil‐Perez, M., Jiménez-Del-Río, M., & Velez‐Pardo, C. (2022) · Medical Oncology · doi:10.1007/s12032-022-01697-w · Cited by 4

Electro‐Responsive Nanotherapeutics for Tumor Therapy by Manipulating Accidental and Regulated Cell Death Pathway

Qu, C. F., Shao, X., Li, Y., Jia, R., Wang, J., & An, H. (2024) · Advanced Therapeutics · doi:10.1002/adtp.202400160 · Cited by 3

When to Die Is the Question: Need and Manipulation of Cell Death by Mycobacterium

Mittal, E., Deore, S., Kumar, M., & Krishnasastry, M. V. (2020) · Current Molecular Biology Reports · doi:10.1007/s40610-020-00137-w · Cited by 3

The glycolysis-related AMPK/ULK signaling pathway mediates the inhibitory effect of adiponectin in prostate cancer cells

Yang, S., Sun, Y., Guo, Y., Zhao, Z., Hu, F., & Cong, L. (2024) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2024.112338 · Cited by 3

Effect of ONC201 Antitumor Drug on the Number of Mitochondrial Nucleoids in BT474 Breast Cancer Cells in Culture

Mishukov, A. A., Berezhnov, A. V., Kobyakova, M. I., Евстратова, Я. В., Mndlyan, E., & Holmuhamedov, E. (2021) · Moscow University Biological Sciences Bulletin · doi:10.3103/s0096392521030111 · Cited by 3

Cytofluorometric assessment of acute cell death responses driven by radiation therapy

Álvarez-Abril, B., Bloy, N., Galassi, C., Sato, A., Jiménez‐Cortegana, C., Klapp, V., Aretz, A., Guilbaud, E., Buqué, A., Galluzzi, L., et al. (2022) · Methods in cell biology · doi:10.1016/bs.mcb.2022.05.002 · Cited by 2

Polyphenol galangin induces the ROS and ER stress-mediated intrinsic and extrinsic apoptotic pathways towards human colon carcinoma HCT-116 cells

Wang, B., Fu, X., Liu, L., Wu, F., & Zhao, X. (2023) · Emirates Journal of Food and Agriculture · doi:10.9755/ejfa.2023.3204 · Cited by 2

The Relationship between Basic Cell Death Pathways and Diseases

Usta, A. (2025) · Biochemistry · doi:10.5772/intechopen.1010600 · Cited by 1

Interplay between survival and regulated cell death mechanisms during periodontitis progression: a systematic review

Torres, A., Díaz, L., Muñoz, J. A. O., Michea, M. A., Xu, X., Salazar‐Onfray, F., & González, F. E. (2025) · Japanese Dental Science Review · doi:10.1016/j.jdsr.2025.08.001 · Cited by 1

RCDRank: a web server to prioritize regulated cell death modalities

Zhou, N., Yin, T., Sun, H., Luo, Q., Zhang, Y., Shi, X., Bao, J., Peng, L., & Yuan, X. (2026) · BMC Bioinformatics · doi:10.1186/s12859-026-06428-w · Cited by 1

Photodynamic therapy mediates antitumor effects through multiple non‑apoptotic cell death pathways

Liao, K., Lin, X., Liang, H., Lin, Y., Liu, S., Yan, X., Liu, X., Zhu, M., Gan, J., Yan, X., et al. (2026) · Journal of Biomedical Science · doi:10.1186/s12929-026-01222-5 · Cited by 1

Cell Death: Many Causes and Many Effects

Cokkinos, D. V. (2019) · Springer eBooks · doi:10.1007/978-3-319-98186-4_7 · Cited by 1

A drug potency signature links progression of chronic lymphocytic leukemia to mitochondria-related stress responses and metabolic reprogramming under hypoxia

Kornblihtt, L. I., Lorenzo, M. C. C., Folgar, M. L. G., Minissale, C., Malusardi, C., Rojas, F., Lombardo, T., & Blanco, G. A. C. (2020) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2020.115016 · Cited by 1

Advances in Micro-Bioreactor Design for Organ Cell Studies

Mandenius, C. (2018) · MDPI eBooks · doi:10.3390/books978-3-03897-232-7 · Cited by 1

Transcription-independent hold of the G1/S transition is exploited to cope with DNA replication stressPreprint

Jin, Y., lan, G., Zhang, J., Sun, H., Li, X., Cao, Q., Tang, C., Yang, X., Lou, H., & Hou, W. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.11.10.515958 · Cited by 1

Editorial: Ferroptosis in cancer and beyond

Wang, X., Chen, G., Pan, C., & Liu, Y. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.1115974 · Cited by 1

Morir para vivir. La muerte celular como proceso regulador

Campero, M. B., Favre, C., & Saborido, C. (2019) · THEORIA An International Journal for Theory History and Foundations of Science · doi:10.1387/theoria.20514

Indicators of cellular metabolism alterationsin patients with traumatic disease due to hypoxia, depending on a management regimen of intensive care

Matvieienko, M. S., Volkova, Y. V., Belozorov, I. V., Shamoun, K. E., Riabov, O. V., & Pronin, V. (2021) · Zaporozhye Medical Journal · doi:10.14739/2310-1210.2021.6.224373

Medicinal plant derived drugs and their treatment for human diseases like cancer: A review

Chanu, M. T., & Singh, A. S. (2022) · World Journal of Advanced Research and Reviews · doi:10.30574/wjarr.2022.16.2.1128 · Cited by 1

The Cell Death and Signal Transduction Mechanisms in Colorectal Carcinogenesis: Recent Advances

Kashyap, M. K., Ved, A., Yadav, R. R. S., Singh, A. P., Kushwaha, M., & Shukla, K. S. (2023) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520623666230328144748

Exploring the mechanisms of age-related osteoarthritis associated with ferroptosis and autophagy using transcriptomics-based integrated analysisPreprint

Yan, F., Yin, R., Qin, C., Qin, R., Chen, T., Wang, C., Jiang, Y., & Gui, J. (2023) · Research Square · doi:10.21203/rs.3.rs-3049076/v1

Estudo da atividade biológica de inibidores de cisteíno catepsinas antineoplásicos em linhagens celulares de câncer de pâncreas (MIA PaCa-2 e BxPC-3)

Laroca, B. A. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.82.2022.tde-10102023-093131

A novel defined cuproptosis-related signature for predicting prognosis and immunotherapy efficacy in pancreatic cancerPreprint

Ge, W. (2023) · Research Square · doi:10.21203/rs.3.rs-3488284/v1

Multifaceted Functions of RNA m6A Modification in Modulating Regulated Cell Death

Zhan, G., Liu, J., Lin, J., Chen, J., Sun, S., Maimaitiyiming, Y., & Hsu, C.-H. (2023) · RNA technologies · doi:10.1007/978-3-031-36390-0_24

Polyphenol galangin induces the ROS and ER stress-mediated intrinsic and extrinsic apoptotic pathways towards human colon carcinoma HCT-116 cells

Wang, B., Fu, X., Liu, L., Wu, F., & Zhao, X. (2023) · Emirates Journal of Food and Agriculture · doi:10.9755/ejfa.2023.v35.i12.3204

Preclinical evaluation of pharmacological inhibition of SIRT1 on the growth of tumoral and metastatic granulosa cellsPreprint

Cluzet, V., Airaud, É., Devillers, M. M., Petit, F., Leary, A. F., Pierre, A., Li, H., Day, C., Weyemi, U., Chauvin, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.02.601506

Resilience and challenges: Evaluating the impact of stress conditions on mesenchymal stem cells across different passages

Ding, Y., Lin, F., & Liang, X. (2024) · World Journal of Stem Cells · doi:10.4252/wjsc.v16.i11.974

Cell Death in Atherosclerosis: Apoptosis? Or Necrosis? Or More?

Watanabe, T., & Fan, J. (2025) · Springer eBooks · doi:10.1007/978-981-96-3675-4_8

Cell Injury: Causes, Mechanisms and Response to Injury

Mulay, K., Goyal, S., & Vemuganti, G. K. (2025) · Springer eBooks · doi:10.1007/978-981-96-8614-8_2

Additional file 2 of Acute stress reduces population-level metabolic and proteomic variation

Steward, K. F., Refai, M., Dyer, W. E., Copié, V., Lachowiec, J., & Bothner, B. B. (2024) · Figshare · doi:10.6084/m9.figshare.26573455

Additional file 1 of Acute stress reduces population-level metabolic and proteomic variation

Steward, K. F., Refai, M., Dyer, W. E., Copié, V., Lachowiec, J., & Bothner, B. B. (2024) · Figshare · doi:10.6084/m9.figshare.26573452

Anticancer Effects of Combined Blue Light and Ionizing Irradiation

Kitano, K., YOSHINO, H., Kawanami, K., Kajimoto, R., & Tsuruga, E. (2025) · Current Issues in Molecular Biology · doi:10.3390/cimb48010045

Integrated Multi-Omics Profiling Maps Ferroptosis–Cuproptosis Diversity in Cervical Cancer and Identifies a PDGFRB-Driven Monocyte Fibrotic Program Targeted by SorafenibPreprint

Li, S., Wu, M., Meng, Y., Liang, C., Huang, X., Li, C., Yang, C., Wang, Z., & Dai, M. (2026) · Research Square · doi:10.21203/rs.3.rs-8811979/v1

the Role of the immunogenetic Profile of patients in response to chemotherapy

Baracco, E. E. (2018) · theses.fr (ABES) · doi:10.70675/26c1db27za511z4c6fza617z433f0d0d141d

New roles of the Lyn tyrosine kinase in psoriasis development and cell death

Diaz, L. E. A. (2018) · theses.fr (ABES) · doi:10.70675/3deccde8zd3dez40abzbda2ze9b04bfdfd62

Échapper à la mort cellulaire dans le cancer : mitophagie et régulation de la mort indépendante des caspases

Villa, E. (2017) · theses.fr (ABES) · doi:10.70675/f0d1579dzdd47z4ac8z82abz4e3b85a0100b

Role of p27/Kip1 in auphagy under metabolic stress conditions

Nowosad, A. (2018) · theses.fr (ABES) · doi:10.70675/11eb36d1zc3baz4d74z8d00zc049667c5976

Transfert de mitochondries des cellules souches mésenchymateuses aux cellules souches de glioblastome : effets sur le métabolisme et la résistance à la chimiothérapie

Nakhle, J. (2020) · theses.fr (ABES) · doi:10.70675/f6e90ca8z49b6z4381z867czff86a692ef33

Contribution of the DNA sensing pathway STING in neutrophilic allergic asthma exacerbation

Messaoud-Nacer, Y. (2023) · theses.fr (ABES) · doi:10.70675/0a513877zf132z4f96zbdd6z1e714da5c991

Adenosine Triphosphate Nanoparticles with Blood–Brain Barrier Permeability for Prevention of Cerebral Ischemic Injury via Mitochondrial Homeostasis

Ju, J., Kim, Y., Seo, S. J., Jin, Y., Ahn, J.-Y., & Shin, M. (2026) · ACS Nano · doi:10.1021/acsnano.6c05982

Discovering ferroptosis in biliary epithelium during liver fibrosis

Mancinelli, R., Casini, A., Leone, S., Ceci, L., Vaccaro, R., Sotto, A. D., Vivacqua, G., Heyn, R., Garro, L., Tagliafierro, M., et al. (2026) · European Journal of Histochemistry · doi:10.4081/ejh.2026.4615

Prologue: Innate Immune Tools to Defend Against Stressful Injury: Success and Failure

Land, W. G. (2018) · Springer eBooks · doi:10.1007/978-3-319-78655-1_17

The Growing Clinical Relevance of Cellular Stress Responses and Regulated Cell Death

Land, W. G. (2020) · Springer eBooks · doi:10.1007/978-3-030-53868-2_4 · Cited by 1

Cellular Stress, Survival Mechanism and Adaptation

Singh, S., & Nandave, M. (2023) · Springer eBooks · doi:10.1007/978-981-99-7652-2_16 · Cited by 4

Organelle autoregulation and crosstalk under stress condition

He, Y. (. (2017) · University of Southern California Digital Library · doi:10.25549/usctheses-c40-406335

Introduction to Cell Toxicity: A Perspective on Intracellular Targets

Chipman, J. K. (1997) · Advances in molecular and cell biology · doi:10.1016/s1569-2558(08)60269-6