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OpenAlex Citation Counts

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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:

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

Showing 1-25 of 58 citing articles:

Mitochondrial Dysfunction and Myocardial Ischemia-Reperfusion: Implications for Novel Therapies
Edward J. Lesnefsky, Qun Chen, Bernard Tandler, et al.
The Annual Review of Pharmacology and Toxicology (2016) Vol. 57, Iss. 1, pp. 535-565
Closed Access | Times Cited: 359
Calpain research for drug discovery: challenges and potential
Yasuko Ono, Takaomi C. Saido, Hiroyuki Sorimachi
Nature Reviews Drug Discovery (2016) Vol. 15, Iss. 12, pp. 854-876
Closed Access | Times Cited: 254
Stress-induced dynamic regulation of mitochondrial STAT3 and its association with cyclophilin D reduce mitochondrial ROS production
Jeremy A. Meier, Moonjung Hyun, Marc Cantwell, et al.
Science Signaling (2017) Vol. 10, Iss. 472
Open Access | Times Cited: 94
Involvement of calpain in the neuropathogenesis of Alzheimer’s disease
Yacoubou Abdoul Razak Mahaman, Fang Huang, Henok Kessete Afewerky, et al.
Medicinal Research Reviews (2018) Vol. 39, Iss. 2, pp. 608-630
Open Access | Times Cited: 94
Fisetin Confers Cardioprotection against Myocardial Ischemia Reperfusion Injury by Suppressing Mitochondrial Oxidative Stress and Mitochondrial Dysfunction and Inhibiting Glycogen Synthase Kinase 3β Activity
Karthi Shanmugam, Sriram Ravindran, Gino A. Kurian, et al.
Oxidative Medicine and Cellular Longevity (2018) Vol. 2018, Iss. 1
Open Access | Times Cited: 78
Metformin attenuates ER stress–induced mitochondrial dysfunction
Qun Chen, Jeremy Thompson, Ying Hu, et al.
Translational research (2017) Vol. 190, pp. 40-50
Open Access | Times Cited: 73
Calpain silencing alleviates myocardial ischemia-reperfusion injury through the NLRP3/ASC/Caspase-1 axis in mice
Rongchuan Yue, Shengzhong Lu, Yu Luo, et al.
Life Sciences (2019) Vol. 233, pp. 116631-116631
Closed Access | Times Cited: 70
Heat shock protein 70: A promising therapeutic target for myocardial ischemia–reperfusion injury
Yanjun Song, Chongbin Zhong, Xianbao Wang
Journal of Cellular Physiology (2018) Vol. 234, Iss. 2, pp. 1190-1207
Closed Access | Times Cited: 65
Mitochondria in Structural and Functional Cardiac Remodeling
Natalia Torrealba, Pablo Aránguiz, Camila Alonso, et al.
Advances in experimental medicine and biology (2017), pp. 277-306
Closed Access | Times Cited: 63
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
Calcium phosphate precipitation inhibits mitochondrial energy metabolism
Sathyavani Malyala, Yizhu Zhang, Jasiel O. Strubbe, et al.
PLoS Computational Biology (2019) Vol. 15, Iss. 1, pp. e1006719-e1006719
Open Access | Times Cited: 56
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
Apoptosis inducing factor and mitochondrial NADH dehydrogenases: redox-controlled gear boxes to switch between mitochondrial biogenesis and cell death
Johannes M. Herrmann, Jan Riemer
Biological Chemistry (2020) Vol. 402, Iss. 3, pp. 289-297
Open Access | Times Cited: 46
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
p53 contributes to cardiovascular diseases via mitochondria dysfunction: A new paradigm
Hao Wang, Wei Yu, Yibo Wang, et al.
Free Radical Biology and Medicine (2023) Vol. 208, pp. 846-858
Open Access | Times Cited: 15
Mitochondrial LON protease-dependent degradation of cytochrome c oxidase subunits under hypoxia and myocardial ischemia
Naresh Babu V. Sepuri, Rajesh Angireddy, Satish Srinivasan, et al.
Biochimica et Biophysica Acta (BBA) - Bioenergetics (2017) Vol. 1858, Iss. 7, pp. 519-528
Open Access | Times Cited: 41
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
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
Cell death in acute lung injury: caspase-regulated apoptosis, pyroptosis, necroptosis, and PANoptosis
Jun Xiao, Lichuan Wang, Bohan Zhang, et al.
Frontiers in Pharmacology (2025) Vol. 16
Open Access
Mitochondrial calpain-1 truncates ATP synthase beta subunit
Yusaku Chukai, N. FURUKAWA, On Kosegawa, et al.
Biochemical and Biophysical Research Communications (2025) Vol. 765, pp. 151829-151829
Closed Access
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
Modeling the Effects of Calcium Overload on Mitochondrial Ultrastructural Remodeling
Jasiel O. Strubbe, Jiahui Chen, Benjamin West, et al.
Applied Sciences (2021) Vol. 11, Iss. 5, pp. 2071-2071
Open Access | Times Cited: 26
Iron deficiency in myocardial ischaemia: molecular mechanisms and therapeutic perspectives
Francesco Corradi, G Masini, Tonino Bucciarelli, et al.
Cardiovascular Research (2023) Vol. 119, Iss. 14, pp. 2405-2420
Closed Access | Times Cited: 9
Cardiac Specific Knockout of p53 Decreases ER Stress-Induced Mitochondrial Damage
Qun Chen, Jeremy Thompson, Ying Hu, et al.
Frontiers in Cardiovascular Medicine (2019) Vol. 6
Open Access | Times Cited: 26
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