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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Mitochondrial m-calpain opens the mitochondrial permeability transition pore in ischemia–reperfusion
Kaori Shintani‐Ishida, Kenichi Yoshida
International Journal of Cardiology (2015) Vol. 197, pp. 26-32
Closed Access | Times Cited: 47

Showing 1-25 of 47 citing articles:

Mitochondrial Ca2+ and regulation of the permeability transition pore
Stephen Hurst, Jan B. Hoek, Shey‐Shing Sheu
Journal of Bioenergetics and Biomembranes (2016) Vol. 49, Iss. 1, pp. 27-47
Open Access | Times Cited: 188
The mitochondrial permeability transition pore in AD 2016: An update
Lucia Biasutto, Michele Azzolini, Ildikò Szabó, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2016) Vol. 1863, Iss. 10, pp. 2515-2530
Closed Access | Times Cited: 120
Physiopathology of the Permeability Transition Pore: Molecular Mechanisms in Human Pathology
Massimo Bonora, Simone Patergnani, Daniela Ramaccini, et al.
Biomolecules (2020) Vol. 10, Iss. 7, pp. 998-998
Open Access | Times Cited: 101
Mitochondrial pathways to cardiac recovery: TFAM
G Kunkel, Pankaj Chaturvedi, Suresh C. Tyagi
Heart Failure Reviews (2016) Vol. 21, Iss. 5, pp. 499-517
Open Access | Times Cited: 89
Endoplasmic reticulum stress-mediated mitochondrial dysfunction in aged hearts
Qun Chen, Arun Samidurai, Jeremy Thompson, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2020) Vol. 1866, Iss. 11, pp. 165899-165899
Open Access | Times Cited: 62
Increased calpain-1 in mitochondria induces dilated heart failure in mice: role of mitochondrial superoxide anion
Ting Cao, Shuai Fan, Dong Zheng, et al.
Basic Research in Cardiology (2019) Vol. 114, Iss. 3
Open Access | Times Cited: 58
Inhibition of the ubiquitous calpains protects complex I activity and enables improved mitophagy in the heart following ischemia-reperfusion
Qun Chen, Jeremy Thompson, Ying Hu, et al.
AJP Cell Physiology (2019) Vol. 317, Iss. 5, pp. C910-C921
Open Access | Times Cited: 55
Activation of mitochondrial calpain and increased cardiac injury: beyond AIF release
Jeremy Thompson, Ying Hu, Edward J. Lesnefsky, et al.
AJP Heart and Circulatory Physiology (2015) Vol. 310, Iss. 3, pp. H376-H384
Open Access | Times Cited: 58
Endoplasmic reticulum stress-induced complex I defect: Central role of calcium overload
Ahmed A. Mohsin, Jeremy Thompson, Ying Hu, et al.
Archives of Biochemistry and Biophysics (2020) Vol. 683, pp. 108299-108299
Open Access | Times Cited: 43
Calpain Inhibition Restores Autophagy and Prevents Mitochondrial Fragmentation in a Human iPSC Model of Diabetic Endotheliopathy
Sang‐Bing Ong, Won Hee Lee, Ning-Yi Shao, et al.
Stem Cell Reports (2019) Vol. 12, Iss. 3, pp. 597-610
Open Access | Times Cited: 41
Sevoflurane postconditioning improves myocardial mitochondrial respiratory function and reduces myocardial ischemia-reperfusion injury by up-regulating HIF-1.
Yang Long, Peng Xie, Jianjiang Wu, et al.
PubMed (2016) Vol. 8, Iss. 10, pp. 4415-4424
Closed Access | Times Cited: 40
Calpain-Mediated Mitochondrial Damage: An Emerging Mechanism Contributing to Cardiac Disease
Mengxiao Zhang, Grace Wang, Tianqing Peng
Cells (2021) Vol. 10, Iss. 8, pp. 2024-2024
Open Access | Times Cited: 30
Nitrite and myocardial ischaemia reperfusion injury. Where are we now?
Kayleigh Griffiths, Jordan Lee, Michael Frenneaux, et al.
Pharmacology & Therapeutics (2021) Vol. 223, pp. 107819-107819
Closed Access | Times Cited: 29
ACSS3 regulates the metabolic homeostasis of epithelial cells and alleviates pulmonary fibrosis
Lan Wang, Hongmei Yuan, Wenwen Li, et al.
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2023) Vol. 1870, Iss. 2, pp. 166960-166960
Open Access | Times Cited: 12
The roles of intracellular proteolysis in cardiac ischemia–reperfusion injury
Bridgette Hartley, Wesam Bassiouni, Richard Schulz, et al.
Basic Research in Cardiology (2023) Vol. 118, Iss. 1
Closed Access | Times Cited: 11
Heart mitochondria and calpain 1: Location, function, and targets
Qun Chen, Edward J. Lesnefsky
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2015) Vol. 1852, Iss. 11, pp. 2372-2378
Open Access | Times Cited: 37
Targeted inhibition of calpain in mitochondria alleviates oxidative stress-induced myocardial injury
Dong Zheng, Ting Cao, Lulu Zhang, et al.
Acta Pharmacologica Sinica (2020) Vol. 42, Iss. 6, pp. 909-920
Open Access | Times Cited: 31
Calpain-2 as a therapeutic target for acute neuronal injury
Yubin Wang, Xiaoning Bi, Michel Baudry
Expert Opinion on Therapeutic Targets (2017) Vol. 22, Iss. 1, pp. 19-29
Open Access | Times Cited: 30
Targeting ER stress and calpain activation to reverse age-dependent mitochondrial damage in the heart
Jeremy Thompson, Michael Maceyka, Qun Chen
Mechanisms of Ageing and Development (2020) Vol. 192, pp. 111380-111380
Open Access | Times Cited: 24
Calpain-mediated protein targets in cardiac mitochondria following ischemia–reperfusion
Ling Li, Jeremy Thompson, Ying Hu, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 15
Calpains and Coronary Vascular Disease
Brittany A. Potz, Ashraf A. Sabe, M. Ruhul Abid, et al.
Circulation Journal (2015) Vol. 80, Iss. 1, pp. 4-10
Open Access | Times Cited: 25
Calpain-Inhibitors Protect Frataxin-Deficient Dorsal Root Ganglia Neurons from Loss of Mitochondrial Na+/Ca2+ Exchanger, NCLX, and Apoptosis
Elena Britti, Fabien Delaspre, Jordi Tamarit, et al.
Neurochemical Research (2020) Vol. 46, Iss. 1, pp. 108-119
Closed Access | Times Cited: 21
Reversing mitochondrial defects in aged hearts: role of mitochondrial calpain activation
Qun Chen, Jeremy Thompson, Ying Hu, et al.
AJP Cell Physiology (2022) Vol. 322, Iss. 2, pp. C296-C310
Open Access | Times Cited: 12
Calpain: the regulatory point of myocardial ischemia-reperfusion injury
Guo-Yang Liu, Wanli Xie, Yanting Wang, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 6
Proteomics as a Tool for the Study of Mitochondrial Proteome, Its Dysfunctionality and Pathological Consequences in Cardiovascular Diseases
Miroslava Št́astná
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 5, pp. 4692-4692
Open Access | Times Cited: 6
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