Cited by CrossRef (13)

  1. Sanjay Kumar, Rahail Ashraf, Aparna C.K.. Mitochondrial dynamics regulators: implications for therapeutic intervention in cancer. Cell Biol Toxicol 2021
    https://doi.org/10.1007/s10565-021-09662-5
  2. Wenyan Fu, Yang Liu, Hang Yin. Mitochondrial Dynamics: Biogenesis, Fission, Fusion, and Mitophagy in the Regulation of Stem Cell Behaviors. Stem Cells International 2019;2019:1
    https://doi.org/10.1155/2019/9757201
  3. Akiyuki Nishimura, Tsukasa Shimauchi, Tomohiro Tanaka, Kakeru Shimoda, Takashi Toyama, Naoyuki Kitajima, Tatsuya Ishikawa, Naoya Shindo, Takuro Numaga-Tomita, Satoshi Yasuda, Yoji Sato, Koichiro Kuwahara, Yoshito Kumagai, Takaaki Akaike, Tomomi Ide, Akio Ojida, Yasuo Mori, Motohiro Nishida. Hypoxia-induced interaction of filamin with Drp1 causes mitochondrial hyperfission–associated myocardial senescence. Sci. Signal. 2018;11
    https://doi.org/10.1126/scisignal.aat5185
  4. Lingling Si, Weiwei Liu, Toshihiko Hayashi, Yachao Ji, Jianing Fu, Yuheng Nie, Kazunori Mizuno, Shunji Hattori, Satoshi Onodera, Takashi Ikejima. Silibinin-induced apoptosis of breast cancer cells involves mitochondrial impairment. Archives of Biochemistry and Biophysics 2019;671:42
    https://doi.org/10.1016/j.abb.2019.05.009
  5. Kaori Saito, Qi Zhang, Haeun Yang, Kotoko Yamatani, Tomohiko Ai, Vivian Ruvolo, Natalia Baran, Tianyu Cai, Helen Ma, Rodrigo Jacamo, Vinitha Kuruvilla, Junichi Imoto, Sonoko Kinjo, Kazuho Ikeo, Kaori Moriya, Koya Suzuki, Takashi Miida, Yong-Mi Kim, Christopher P. Vellano, Michael Andreeff, Joseph R. Marszalek, Yoko Tabe, Marina Konopleva. Exogenous mitochondrial transfer and endogenous mitochondrial fission facilitate AML resistance to OxPhos inhibition. 2021;5:4233
    https://doi.org/10.1182/bloodadvances.2020003661
  6. Dan Zhao, Chen‑Yi Yin, Xian‑Wei Ye, Zi‑Fen Wan, De‑Gang Zhao, Xiang‑Yan Zhang. Mitochondrial separation protein inhibitor inhibits cell apoptosis in rat lungs during�intermittent hypoxia . Exp Ther Med 2019
    https://doi.org/10.3892/etm.2019.7201
  7. Zachary A. Bacigalupa, W. Kimryn Rathmell. Beyond glycolysis: Hypoxia signaling as a master regulator of alternative metabolic pathways and the implications in clear cell renal cell carcinoma. Cancer Letters 2020;489:19
    https://doi.org/10.1016/j.canlet.2020.05.034
  8. Francesco Ciccarese, Elisabetta Zulato, Stefano Indraccolo. LKB1/AMPK Pathway and Drug Response in Cancer: A Therapeutic Perspective. Oxidative Medicine and Cellular Longevity 2019;2019:1
    https://doi.org/10.1155/2019/8730816
  9. Hyunsook Lee, Kyu-Tae Kang. Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis. Korean J Physiol Pharmacol 2018;22:705
    https://doi.org/10.4196/kjpp.2018.22.6.705
  10. Walaa Fakih, Ali Mroueh, Houssein Salah, Ali H. Eid, Makram Obeid, Firas Kobeissy, Hala Darwish, Ahmed F. El-Yazbi. Dysfunctional cerebrovascular tone contributes to cognitive impairment in a non-obese rat model of prediabetic challenge: Role of suppression of autophagy and modulation by anti-diabetic drugs. Biochemical Pharmacology 2020;178:114041
    https://doi.org/10.1016/j.bcp.2020.114041
  11. Yi Zhu, Xi-Qiong Han, Xue-Jiao Sun, Rui Yang, Wen-Qi Ma, Nai-Feng Liu. Lactate accelerates vascular calcification through NR4A1-regulated mitochondrial fission and BNIP3-related mitophagy. Apoptosis 2020;25:321
    https://doi.org/10.1007/s10495-020-01592-7
  12. Chalita Kingnate, Kittipat Charoenkwan, Sirinart Kumfu, Nipon Chattipakorn, Siriporn C. Chattipakorn. Possible Roles of Mitochondrial Dynamics and the Effects of Pharmacological Interventions in Chemoresistant Ovarian Cancer. EBioMedicine 2018;34:256
    https://doi.org/10.1016/j.ebiom.2018.07.026
  13. Shenglong Ding, Ji Xu, Qichen Zhang, Fangyi Chen, Jihong Zhang, Keke Gui, Min Xiong, Bing Li, Zhiyong Ruan, Mingdong Zhao. OGR1 mediates the inhibitory effects of acidic environment on proliferation and angiogenesis of endothelial progenitor cells. Cell Biol Int 2019;43:1307
    https://doi.org/10.1002/cbin.11179