Mitochondrial dynamics and apoptosis

Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade

Li, P., Nijhawan, D., Budihardjo, I., Srinivasula, S. M., Ahmad, M., Alnemri, E. S., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80434-1 · Cited by 7,289

Induction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c

Liu, X., Kim, C. N., Yang, J., Jemmerson, R., & Wang, X. (1996) · Cell · doi:10.1016/s0092-8674(00)80085-9 · Cited by 5,167

Prevention of Apoptosis by Bcl-2: Release of Cytochrome c from Mitochondria Blocked

Yang, J., Liu, X., Bhalla, K. N., Kim, C. N., Ibrado, A. M., Cai, J., Peng, T.-I., Jones, D. P., & Wang, X. (1997) · Science · doi:10.1126/science.275.5303.1129 · Cited by 4,913

The BCL-2 protein family: opposing activities that mediate cell death

Youle, R. J., & Strasser, A. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2308 · Cited by 4,806

The Release of Cytochrome c from Mitochondria: A Primary Site for Bcl-2 Regulation of Apoptosis

Kluck, R. M., Bossy‐Wetzel, E., Green, D. R., & Newmeyer, D. D. (1997) · Science · doi:10.1126/science.275.5303.1132 · Cited by 4,715

Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells

Vaux, D., Cory, S., & Adams, J. (1988) · Nature · doi:10.1038/335440a0 · Cited by 3,355

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

Chen, H., Detmer, S. A., Ewald, A. J., Griffin, E. E., Fraser, S. E., & Chan, D. C. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211046 · Cited by 2,601

The Bcl-2 apoptotic switch in cancer development and therapy

Adams, J. M., & Cory, S. (2007) · Oncogene · doi:10.1038/sj.onc.1210220 · Cited by 2,256

The Role of Mitochondria in Apoptosis

Wang, C., & Youle, R. J. (2009) · Annual Review of Genetics · doi:10.1146/annurev-genet-102108-134850 · Cited by 1,987

In vitro cultured calculus bovis attenuates cerebral ischaemia-reperfusion injury by inhibiting neuronal apoptosis and protecting mitochondrial function in rats

Lu, F., Wang, L., Chen, Y., Zhong, X., & Huang, Z. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113168 · Cited by 16

Chronic Pharmacological Modulation of Mitochondrial Dynamics Alleviates Prediabetes-Induced Myocardial Ischemia–Reperfusion Injury by Preventing Mitochondrial Dysfunction and Programmed Apoptosis

Maneechote, C., Kerdphoo, S., Jaiwongkam, T., Chattipakorn, S. C., & Chattipakorn, N. (2021) · Cardiovascular Drugs and Therapy · doi:10.1007/s10557-021-07250-7 · Cited by 16

DRP1 Inhibition Enhances Venetoclax-Induced Mitochondrial Apoptosis in TP53-Mutated Acute Myeloid Leukemia Cells through BAX/BAK Activation

Jang, J. E., Hwang, D. Y., Eom, J.-I., Cheong, J., Jeung, H.-K., Cho, H., Chung, H., Kim, J. S., & Min, Y. H. (2023) · Cancers · doi:10.3390/cancers15030745 · Cited by 17

Fish Models for Exploring Mitochondrial Dysfunction Affecting Neurodegenerative Disorders

Otsuka, T., & Matsui, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24087079 · Cited by 17

Annexin II receptor induces apoptosis independent of Annexin II

Xiong, Y., Fan, C., Kong, L., Lin, D., Zhu, N., Zhang, J., Wang, L., Qin, T., Shen, Y., & Chen, M. (2013) · APOPTOSIS · doi:10.1007/s10495-013-0846-2 · Cited by 16

Protection of carboxymethylated chitosan on chondrocytes from nitric oxide-induced apoptosis by regulating phosphatidylinositol 3-kinase/Akt signaling pathway

He, B., Tao, H., Wei, A., Liu, S., Li, X., & Chen, R. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.09.084 · Cited by 16

Two-photon deep-tissue spatially resolved mitochondrial imaging using membrane potential fluorescence fluctuations

Tehrani, K. F., Pendleton, E. G., Southern, W. M., Call, J. A., & Mortensen, L. J. (2017) · Biomedical Optics Express · doi:10.1364/boe.9.000254 · Cited by 16

Contacts in Death: The Role of the ER–Mitochondria Axis in Acetic Acid-Induced Apoptosis in Yeast

Martins, V. M., Fernandes, T. R., Lopes, D., Afonso, C. B., Domingues, M. R., Côrte‐Real, M., & Sousa, M. J. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.11.002 · Cited by 17

Endothelial mitochondrial senescence accelerates cardiovascular disease in antiretroviral-receiving HIV patients

Chen, Y.-F., & Dugas, T. R. (2019) · Toxicology Letters · doi:10.1016/j.toxlet.2019.09.018 · Cited by 17

Bleomycin A5 suppresses Drp1‑mediated mitochondrial fission and induces apoptosis in human nasal polyp‑derived fibroblasts

Wu, F., Ma, Y., Wang, J., Ou, H., Dang, H., Zheng, Y., Tian, P., & Zou, H. (2020) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2020.4797 · Cited by 16

Players in Mitochondrial Dynamics and Female Reproduction

Zou, W., Ji, D., Zhang, Z., Yang, L., & Cao, Y. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.717328 · Cited by 18

Control of mitochondrial dynamics and apoptotic pathways by peroxisomes

Jiang, C., & Okazaki, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.938177 · Cited by 17

Ethanol and Vitamin D Receptor in T Cell Apoptosis

Rehman, S., Chandel, N., Salhan, D., Rai, P., Sharma, B., Singh, T., Husain, M., Malhotra, A., & Singhal, P. C. (2012) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-012-9393-9 · Cited by 17

Mitofusin 1 inhibits an apoptosis-associated amino-terminal conformational change in Bax, but not its mitochondrial translocation, in a GTPase-dependent manner

Ryu, S., Choi, K., Park, J., Park, Y., Kim, S., & Choi, C. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.03.038 · Cited by 16

Novel triterpenoids isolated from raisins exert potent antiproliferative activities by targeting mitochondrial and Ras/Raf/ERK signaling in human breast cancer cells

Liu, J., Wang, Y., Liu, R. H., & He, X. (2016) · Food & Function · doi:10.1039/c6fo00768f · Cited by 16

Mitochondrial dynamics in diabetic peripheral neuropathy: Pathogenesis, progression, and therapeutic approaches

Yu, H., Yang, C., Wang, G., & Wang, X. (2025) · Medicine · doi:10.1097/md.0000000000042748 · Cited by 16

Mitochondrial transport, partitioning, and quality control at the heart of cell proliferation and fate acquisition

Sharma, R. K., Chafik, A., & Bertolin, G. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00256.2021 · Cited by 16

Glutathione-depleted cyclodextrin pseudo-polyrotaxane nanoparticles for anti-inflammatory oxaliplatin (IV) prodrug delivery and enhanced colorectal cancer therapy

Wang, W., He, X., Wang, X., Zhao, T., Muraoka, O., Tanabe, G., Xie, W., Zhou, T., Xing, L., Jin, Q., et al. (2023) · Chinese Chemical Letters · doi:10.1016/j.cclet.2023.108656 · Cited by 15

Val-Leu-Leu-Tyr (VLLY) Alleviates Ethanol-Induced Gastric Mucosal Cell Impairment by Improving Mitochondrial Fission

Zheng, Z., Sun, N., Mao, C., Tang, Y., & Lin, S. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c01764 · Cited by 15

Mitochondrial fission enhances IL ‐6‐induced metastatic potential in ovarian cancer via ERK1 /2 activation

Lee, J., Han, Y., Kim, S., Jo, H., Wang, W., Cho, U., Kim, S. I., Kim, B., & Song, Y. S. (2024) · Cancer Science · doi:10.1111/cas.16064 · Cited by 15

Sex-Specific Effects of Estradiol and Progesterone in Ischemic Kidney Injury

Andrianova, N. V., Brezgunova, A. A., Buyan, M. I., Makievskaya, C. I., Buyan, A., Cherkesova, K. S., Pevzner, I. B., Zorova, L. D., Zorov, D. B., Plotnikov, E. Y., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25063155 · Cited by 15

Bacteria–organelle communication in physiology and disease

Lee, Y.-T., Şentürk, M., Guan, Y., & Wang, M. C. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202310134 · Cited by 15

Reactive Oxygen Species and Extracellular Signal-Regulated Kinase 1/2 Mediate Hexachlorobenzene-Induced Cell Death in FRTL-5 Rat Thyroid Cells

Chiappini, F., Pontillo, C. A., Randi, A. S., Álvarez, L., & de Pisarev, D. L. K. (2013) · Toxicological Sciences · doi:10.1093/toxsci/kft117 · Cited by 15

Src-family kinase signaling, actin-mediated membrane trafficking and organellar dynamics in the control of cell fate: Lessons to be learned from the adenovirus E4orf4 death factor

Lavoie, J. N., Landry, M.-C., Faure, R. L., & Champagne, C. (2010) · Cellular Signalling · doi:10.1016/j.cellsig.2010.04.007 · Cited by 15

Increased sensitivity of African American triple negative breast cancer cells to nitric oxide-induced mitochondria-mediated apoptosis

Martinez, L., Thames, E. C., Kim, J., Chaudhuri, G., Singh, R., & Pervin, S. (2016) · BMC Cancer · doi:10.1186/s12885-016-2547-z · Cited by 15

Identification of Mitochondrial Genome-Encoded Small RNAs Related to Egg Deterioration Caused by Postovulatory Aging in Rainbow Trout

Ma, H., Weber, G. M., Wei, H., & Yao, J. (2016) · Marine Biotechnology · doi:10.1007/s10126-016-9719-3 · Cited by 15

Regulation of mitochondrial dynamics in 2-methoxyestradiol-mediated osteosarcoma cell death

Górska‐Ponikowska, M., Bastian, P., Zauszkiewicz–Pawlak, A., Płoska, A., Zubrzycki, A., Kuban‐Jankowska, A., Nußberger, S., Kalinowski, L., & Kmieć, Z. (2021) · Scientific Reports · doi:10.1038/s41598-020-80816-x · Cited by 14

Autophagy and mitochondrial dynamics contribute to the protective effect of diosgenin against 3-MCPD induced kidney injury

Zhong, Y., Sun, D., Yao, Y., Liu, Q., Guo, T., Wang, X., & Peng, X. (2022) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2022.109850 · Cited by 15

Synthetic racemates of abyssinone I and II induces apoptosis through mitochondrial pathway in human cervix carcinoma cells

Samaga, K. K. L., Rao, G. V., Reddy, G. C., Kush, A. K., & Diwakar, L. (2014) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2014.06.004 · Cited by 15

Involvement of apoptosis and autophagy in the death of RPMI 8226 multiple myeloma cells by two enantiomeric sigma receptor ligands

Korpis, K., Weber, F., Brune, S., Wünsch, B., & Bednarski, P. J. (2013) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2013.11.033 · Cited by 15

PE-induced apoptosis in SMMC-7721 cells: Involvement of Erk and Stat signalling pathways

Li, X., Li, M., Chen, T., Sun, H., Zhu, J., Li, X., WU, F., Wang, B., Li, J., & Chen, Y. (2014) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2014.1777 · Cited by 15

Alterations of mitochondrial dynamics allow retrograde propagation of locally initiated axonal insults

Lassus, B., Magnifico, S., Pignon, S., Belenguer, P., Miquel, M., & Peyrin, J. (2016) · Scientific Reports · doi:10.1038/srep32777 · Cited by 16

DAP3 Is Involved in Modulation of Cellular Radiation Response by RIG-I-Like Receptor Agonist in Human Lung Adenocarcinoma Cells

Sato, Y., Yoshino, H., Kashiwakura, I., & Tsuruga, E. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22010420 · Cited by 15

Metabolic reprogramming nanomedicine potentiates colon cancer sonodynamic immunotherapy by inhibiting the CD39/CD73/ADO pathway

Zhang, Y., Jin, W., Deng, Z., Gao, B., Zhu, Y., Fu, J., Xu, C., Wang, W., Bai, T., Jiao, L., et al. (2025) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2025.03.046 · Cited by 15

The Use of Chinese Yang/Qi-Invigorating Tonic Botanical Drugs/Herbal Formulations in Ameliorating Chronic Kidney Disease by Enhancing Mitochondrial Function

Tian, J., Huang, Y., Wu, T., Huang, H., Ko, K. M., Zhu, B. T., & Chen, J. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.622498 · Cited by 14

Ginsenoside Re blocks Bay k-8644-induced neurotoxicity via attenuating mitochondrial dysfunction and PKCδ activation in the hippocampus of mice: Involvement of antioxidant potential

Tran, N. K. C., Jeong, J. H., Sharma, N., Nguyen, Y. N. D., Tran, H.-Y. P., Dang, D., Park, J. H., Byun, J. K., Jin, D., Xiaoyan, Z., et al. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113869 · Cited by 14

Photobiomodulation therapy with light-emitting diode in stimulating adipose tissue mitochondria

Modena, D. A. O., Ferro, A. P., Guirro, E. C. D. O., Cazzo, E., & Chaim, É. A. (2023) · Lasers in Medical Science · doi:10.1007/s10103-023-03906-y · Cited by 14

Mitochondria as integrators of signal transduction and energy production in cardiac physiology and disease

Frohman, M. A. (2010) · Journal of Molecular Medicine · doi:10.1007/s00109-010-0662-x · Cited by 15

The intrinsically kinase-inactive EPHB6 receptor predisposes cancer cells to DR5-induced apoptosis by promoting mitochondrial fragmentation

Zawily, A. M. E., Toosi, B. M., Freywald, T., Indukuri, V., Vizeacoumar, F. J., Leary, S. C., & Freywald, A. (2016) · Oncotarget · doi:10.18632/oncotarget.12838 · Cited by 14

Protective Effects of Ginsenosides on 17α-Ethynyelstradiol-Induced Intrahepatic Cholestasis via Anti-Oxidative and Anti-Inflammatory Mechanisms in Rats

Xu, Y., Yu, Z., Zhang, C., Li, X.-P., Feng, C.-Y., Lei, K., He, W., & Liu, D. (2017) · The American Journal of Chinese Medicine · doi:10.1142/s0192415x17500872 · Cited by 14

Methylmalonic aciduria cblB type: characterization of two novel mutations and mitochondrial dysfunction studies

Brasil, S., Richard, E., Jorge‐Finnigan, A., Leal, F., Merinero, B., Banerjee, R. V., Desviat, L. R., Ugarte, M., & Pérez, B. (2014) · Clinical Genetics · doi:10.1111/cge.12426 · Cited by 14

Total saponins of Tupistra chinensis induces apoptosis in A549 cells

Huang, W., Zhang, H., ZOU, K., Chen, J., Li, X., LIU, C., & Huang, N. (2012) · Neoplasma · doi:10.4149/neo_2012_078 · Cited by 14

A novel chenodeoxycholic acid-verticinone ester induces apoptosis and cell cycle arrest in HepG2 cells

Dong, L., Zhou, Q., Zhang, J., Gong, W., Xu, C., Li, B., Wang, Y., & Li, J. (2012) · Steroids · doi:10.1016/j.steroids.2012.08.013 · Cited by 14

Increased vulnerability with aging to MPTP: the mechanisms underlying mitochondrial dynamics

Jiang, N., Hai, B., Song, C., Guo, J., Zhao, F., Feng, H., Ding, H., Ji, L., & Zhang, Y. (2013) · Neurological Research · doi:10.1179/1743132813y.0000000296 · Cited by 16

Effects of biphasic and monophasic electrical stimulation on mitochondrial dynamics, cell apoptosis, and cell proliferation

Love, M. R., Sripetchwandee, J., Palee, S., Chattipakorn, S. C., Mower, M. M., & Chattipakorn, N. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26897 · Cited by 16

High TRIAP1 expression in penile carcinoma is associated with high risk of recurrence and poor survival

Zhang, J., Cong, R., Zhao, K., Wang, Y., Song, N., & Gu, M. (2019) · Annals of Translational Medicine · doi:10.21037/atm.2019.06.47 · Cited by 14

Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells

Lee, D. G., Kim, K., Lee, H., Bae, Y. C., Huh, J., Lee, S., & Lee, D. (2019) · NeuroToxicology · doi:10.1016/j.neuro.2019.08.003 · Cited by 14

Inhibition of invasive pancreatic cancer: restoring cell apoptosis by activating mitochondrial p53.

Cheng, J., Okolotowicz, K. J., Ryan, D., Mose, E. S., Lowy, A. M., & Cashman, J. R. (2019) · Europe PMC (PubMed Central) · Cited by 13

Sinapic Acid Ameliorates REV-ERB α Modulated Mitochondrial Fission against MPTP-Induced Parkinson's Disease Model

Sang-Bin, L. E. E., & Yang, H. O. (2022) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2022.020 · Cited by 15

MitoQ alleviates prion-induced neurodegeneration by modulating DRP1- and OPA1-mediated mitochondrial dynamics

Wu, W., Zhang, X., Xing, J., Kong, S., Jiang, M., Zhou, M., Liao, Y., Liao, B., & Ma, N. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.07.017 · Cited by 13

Brain Mitochondria as a Therapeutic Target for Carnosic Acid

Infantino, V., Pappalardo, I., Santarsiero, A., Tripathi, S., Singh, G., & de Oliveira, M. R. (2024) · Journal of Integrative Neuroscience · doi:10.31083/j.jin2303053 · Cited by 13

Antioxidants as a preventive therapeutic option for age related neurodegenerative diseases

(2015) · Therapeutic Targets for Neurological Diseases · doi:10.14800/ttnd.592 · Cited by 13

Modeling the mitochondrial dysfunction in neurogenerative diseases due to high H+ concentration

Alexiou, A. T., Rekkas, J., & Vlamos, P. (2011) · Bioinformation · doi:10.6026/97320630006173 · Cited by 13

Interactions Among Regulatory Non-coding RNAs Involved in Cardiovascular Diseases

Gabriel, A. F., Costa, M. C., & Enguita, F. J. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-1671-9_4 · Cited by 13

Mitochondrial Fusion Potentially Regulates a Metabolic Change in Tibetan Chicken Embryonic Brain During Hypoxia

Tang, Q., Ding, C., Xu, Q., Bai, Y., Qiao, X., Wang, K., & Fang, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.585166 · Cited by 14

Cardiac effects of renal ischemia

Dominguez, J. H., Xie, D., & Kelly, K. J. (2022) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00183.2022 · Cited by 13

Carboxyl-terminal modulator protein induces apoptosis by regulating mitochondrial function in lung cancer cells

Cho, M. (2011) · International Journal of Oncology · doi:10.3892/ijo.2011.1319 · Cited by 13

Translocation and oligomerization of Bax is regulated independently by activation of p38 MAPK and caspase-2 during MN9D dopaminergic neurodegeneration

Oh, C.-K., Han, B.-S., Choi, W.-S., Youdim, M. B. H., & Oh, Y. J. (2011) · APOPTOSIS · doi:10.1007/s10495-011-0627-8 · Cited by 13

Principles of control over formation of structures responsible for respiratory functions of mitochondria

Luzikov, V. N. (2009) · Biochemistry (Moscow) · doi:10.1134/s0006297909130021 · Cited by 13

Bcl-2 homologue Debcl enhances α-synuclein -induced phenotypes in Drosophila

M'angale, P. G., & Staveley, B. E. (2016) · PeerJ · doi:10.7717/peerj.2461 · Cited by 13

Tat-DJ-1 enhances cell survival by inhibition of oxidative stress, NF-κB and MAPK activation in HepG2 cells

Jo, H. S., Yeo, E. J., Shin, M. J., Choi, Y. J., Yeo, H. J., Cho, S. B., Park, J. H., Lee, C. H., Eum, W. S., & Choi, S. Y. (2017) · Biotechnology Letters · doi:10.1007/s10529-017-2286-5 · Cited by 13

COX assembly factor ccdc56 regulates mitochondrial morphology by affecting mitochondrial recruitment of Drp1

Ban-Ishihara, R., Tomohiro-Takamiya, S., Tani, M., Baudier, J., Ishihara, N., & Kuge, O. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.08.039 · Cited by 13

Novel Nile Blue Analogue Stains Yeast Vacuolar Membrane, Endoplasmic Reticulum, and Lipid Droplets, Inducing Cell Death through Vacuole Membrane Permeabilization

Ferreira, J. C. C., Lopes, C., Preto, A., Gonçalves, M. S. T., & Sousa, M. J. (2021) · Journal of Fungi · doi:10.3390/jof7110971 · Cited by 11

Ubiquitination of Ku70 by Parkin promotes apoptosis of lens epithelial cells

Zhang, W., Wu, A., Zhang, G., Ding, X., Kang, L., Zhou, T., Ji, M. J., & Guan, H. (2023) · FEBS Journal · doi:10.1111/febs.16784 · Cited by 12

Therapeutic Targeting of Mitochondrial Plasticity and Redox Control to Overcome Cancer Chemoresistance

Mani, S., Ralph, S. J., Swargiary, G., Rani, M., Wasnik, S., Singh, M., & Devi, A. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0379 · Cited by 12

Mitochondrial Quality Control in Ovarian Function: From Mechanisms to Therapeutic Strategies

Wang, X., Liu, Y., Wang, J., Lu, X., Guo, Z., Lv, S., Sun, Z., Gao, T., Gao, F., & Yuan, J. (2024) · Reproductive Sciences · doi:10.1007/s43032-024-01634-4 · Cited by 12

Mitochondrial dynamics: Molecular mechanism and implications in endometriosis

Marino, Y., Inferrera, F., Genovese, T., Cuzzocrea, S., Fusco, R., & Paola, R. D. (2025) · Biochimie · doi:10.1016/j.biochi.2025.01.012 · Cited by 15

Knockdown of TWIST1 enhances arsenic trioxide- and ionizing radiation-induced cell death in lung cancer cells by promoting mitochondrial dysfunction

Seo, S., Kim, J., Choi, H.-N., Choe, T., Hong, S., Yi, J.-Y., Hwang, S., Lee, H.-G., Lee, Y., & Park, I. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.05.030 · Cited by 15

Epigenetics of Subcellular Structure Functioning in the Origin of Risk or Resilience to Comorbidity of Neuropsychiatric and Cardiometabolic Disorders

del Campo, C. M. Z.-M., Rosas, M., & Guarner‐Lans, V. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051456 · Cited by 12

Galectin-7 promotes cisplatin efficacy by facilitating apoptosis and G3BP1 degradation in cervical cancer

Liu, C., Zhou, L., Chen, J., Yang, Z., Chen, S., Wang, X., Liu, X., Li, Y., Zhang, C., Wang, Y., et al. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115834 · Cited by 12

New roles for OMA1 metalloprotease

Quirós, P. M., Ramsay, A. J., & López-Otı́n, C. (2012) · Adipocyte · doi:10.4161/adip.21999 · Cited by 12

Mitochondrial‐morphology‐targeted breeding of industrial yeast strains for alcohol fermentation

Kitagaki, H. (2009) · Biotechnology and Applied Biochemistry · doi:10.1042/ba20090032 · Cited by 12

The NFL-TBS.40-63 Anti-Glioblastoma Peptide Disrupts Microtubule and Mitochondrial Networks in the T98G Glioma Cell Line

Rivalin, R., Lépinoux-Chambaud, C., Eyer, J., & Savagner, F. (2014) · PLoS ONE · doi:10.1371/journal.pone.0098473 · Cited by 12

Changes in mitochondrial dynamics during amyloid β-induced PC12 cell apoptosis

Liu, X., Feng, L., Yan, M., Xu, K., Yu, Y., & Zheng, X. (2010) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0552-0 · Cited by 12

Function and regulation of mitofusin 2 in cardiovascular physiology and pathology

Yu, F., Xu, T., Wang, M., Chang, W., Li, P., & Wang, J. (2018) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2018.07.003 · Cited by 12

Oxidatively stressed mitochondria-mimicking membranes: A molecular insight into their organization during apoptosis

Dingeldein, A., Sparrman, T., & Gröbner, G. (2018) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2018.10.007 · Cited by 13

Extract from Zanthoxylum piperitum Induces Apoptosis of AGS Gastric Cancer Cells Through Akt/MDM2/p53 Signaling Pathway

Park, Y. S., Nam, G. H., Jo, K. J., Kawk, H. W., Kim, S. Y., & Kim, Y. M. (2021) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-021-3486-8 · Cited by 12

Opa1 Prevents Apoptosis and Cisplatin-Induced Ototoxicity in Murine Cochleae

Dong, T., Zhang, X., Liu, Y., Xu, S., Chang, H., Chen, F., Pan, L., Hu, S., Wang, M., & Lu, M. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.744838 · Cited by 12

Cytotoxicity of Mahanimbine from Curry Leaves in Human Breast Cancer Cells (MCF-7) via Mitochondrial Apoptosis and Anti-Angiogenesis

Hobani, Y. H. (2022) · Molecules · doi:10.3390/molecules27030971 · Cited by 12

Detection of mitochondrial fission with orientation‐dependent optical Fourier filters

Pasternack, R. M., Zheng, J., & Boustany, N. N. (2011) · Cytometry Part A · doi:10.1002/cyto.a.21011 · Cited by 12

The serine protease inhibitor TLCK attenuates intrinsic death pathways in neurons upstream of mitochondrial demise

Reuther, C., Ganjam, G. K., Dolga, A. M., & Culmsee, C. (2014) · APOPTOSIS · doi:10.1007/s10495-014-1027-7 · Cited by 12

Heat shock protein 72 suppresses apoptosis by increasing the stability of X-linked inhibitor of apoptosis protein in renal ischemia/reperfusion injury

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