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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:

Mitochondrial dysfunction induces muscle atrophy during prolonged inactivity: A review of the causes and effects
Hayden W. Hyatt, Rafael Deminice, Toshinori Yoshihara, et al.
Archives of Biochemistry and Biophysics (2018) Vol. 662, pp. 49-60
Open Access | Times Cited: 167

Showing 1-25 of 167 citing articles:

Skeletal muscle atrophy: From mechanisms to treatments
Lin Yin, Na Li, Weihua Jia, et al.
Pharmacological Research (2021) Vol. 172, pp. 105807-105807
Closed Access | Times Cited: 221
Skeletal muscle alterations in patients with acute Covid‐19 and post‐acute sequelae of Covid‐19
M Soares, Moritz Eggelbusch, Elie Naddaf, et al.
Journal of Cachexia Sarcopenia and Muscle (2022) Vol. 13, Iss. 1, pp. 11-22
Open Access | Times Cited: 197
Mitochondrial dysfunction: roles in skeletal muscle atrophy
Xin Chen, Yanan Ji, Ruiqi Liu, et al.
Journal of Translational Medicine (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 110
The Role of Diet as a Modulator of the Inflammatory Process in the Neurological Diseases
Antonina Kurowska, Wojciech Ziemichód, Mariola Herbet, et al.
Nutrients (2023) Vol. 15, Iss. 6, pp. 1436-1436
Open Access | Times Cited: 67
Mitochondrial dysfunction and skeletal muscle atrophy: Causes, mechanisms, and treatment strategies
Gökhan Burçin Kubat, Esmaa Bouhamida, Oner Ulger, et al.
Mitochondrion (2023) Vol. 72, pp. 33-58
Closed Access | Times Cited: 47
Uremic metabolites impair skeletal muscle mitochondrial energetics through disruption of the electron transport system and matrix dehydrogenase activity
Trace Thome, Zachary R. Salyers, Ravi A. Kumar, et al.
AJP Cell Physiology (2019) Vol. 317, Iss. 4, pp. C701-C713
Open Access | Times Cited: 80
Polyphenols and Their Effects on Muscle Atrophy and Muscle Health
Takeshi Nikawa, Anayt Ulla, Iori Sakakibara
Molecules (2021) Vol. 26, Iss. 16, pp. 4887-4887
Open Access | Times Cited: 80
Mitochondrial Dysfunction Is a Common Denominator Linking Skeletal Muscle Wasting Due to Disease, Aging, and Prolonged Inactivity
Hayden W. Hyatt, Scott K. Powers
Antioxidants (2021) Vol. 10, Iss. 4, pp. 588-588
Open Access | Times Cited: 67
Muscle-to-tumor crosstalk: The effect of exercise-induced myokine on cancer progression
Qianrui Huang, Meng‐Ling Wu, Xuyi Wu, et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2022) Vol. 1877, Iss. 5, pp. 188761-188761
Closed Access | Times Cited: 53
Chronic kidney disease-induced muscle atrophy: Molecular mechanisms and promising therapies
Kexin Wang, Liu Qing-yuan, Mingyu Tang, et al.
Biochemical Pharmacology (2022) Vol. 208, pp. 115407-115407
Open Access | Times Cited: 47
Exercise as an anti-inflammatory therapy for cancer cachexia: a focus on interleukin-6 regulation
Hélène N. Daou
AJP Regulatory Integrative and Comparative Physiology (2019) Vol. 318, Iss. 2, pp. R296-R310
Open Access | Times Cited: 64
Isoquercitrin Delays Denervated Soleus Muscle Atrophy by Inhibiting Oxidative Stress and Inflammation
Yuntian Shen, Qiuyu Zhang, Ziwei Huang, et al.
Frontiers in Physiology (2020) Vol. 11
Open Access | Times Cited: 64
The Role of Calpains in Skeletal Muscle Remodeling with Exercise and Inactivity-induced Atrophy
Hayden W. Hyatt, Scott K. Powers
International Journal of Sports Medicine (2020) Vol. 41, Iss. 14, pp. 994-1008
Open Access | Times Cited: 57
Effect of Quercetin on Dexamethasone-Induced C2C12 Skeletal Muscle Cell Injury
Chun Chen, Jai‐Sing Yang, Chi‐Cheng Lu, et al.
Molecules (2020) Vol. 25, Iss. 14, pp. 3267-3267
Open Access | Times Cited: 55
Energy metabolism design of the striated muscle cell
Brian Glancy, Robert S. Balaban
Physiological Reviews (2021) Vol. 101, Iss. 4, pp. 1561-1607
Open Access | Times Cited: 53
Ultra-processed diet, systemic oxidative stress, and breach of immunologic tolerance
Edwin E. Martínez Leo, Abigail Meza Peñafiel, Victor M. Hernandez-Escalante, et al.
Nutrition (2021) Vol. 91-92, pp. 111419-111419
Closed Access | Times Cited: 43
Redox signaling regulates skeletal muscle remodeling in response to exercise and prolonged inactivity
Scott K. Powers, Matthew A. Schrager
Redox Biology (2022) Vol. 54, pp. 102374-102374
Open Access | Times Cited: 36
Pathogenesis of sarcopenia in chronic obstructive pulmonary disease
Kai Ma, Fengxiang Huang, Ruiping Qiao, et al.
Frontiers in Physiology (2022) Vol. 13
Open Access | Times Cited: 31
Regulatory networks coordinating mitochondrial quality control in skeletal muscle
Mikhaela Slavin, Jonathan M. Memme, Ashley N. Oliveira, et al.
AJP Cell Physiology (2022) Vol. 322, Iss. 5, pp. C913-C926
Closed Access | Times Cited: 29
The Link between Mitochondrial Dysfunction and Sarcopenia: An Update Focusing on the Role of Pyruvate Dehydrogenase Kinase 4
Min‐Ji Kim, Ibotombi Singh Sinam, Zerwa Siddique, et al.
Diabetes & Metabolism Journal (2023) Vol. 47, Iss. 2, pp. 153-163
Open Access | Times Cited: 22
Elevated phospholipid hydroperoxide glutathione peroxidase (GPX4) expression modulates oxylipin formation and inhibits age-related skeletal muscle atrophy and weakness
Agnieszka Czyżowska, Jacob L. Brown, Hongyang Xu, et al.
Redox Biology (2023) Vol. 64, pp. 102761-102761
Open Access | Times Cited: 22
Mitochondrial dynamics define muscle fiber type by modulating cellular metabolic pathways
Tatsuki Yasuda, Takaya Ishihara, Ayaka Ichimura, et al.
Cell Reports (2023) Vol. 42, Iss. 5, pp. 112434-112434
Open Access | Times Cited: 20
Increased mitochondrial Ca2+ contributes to health decline with age and Duchene muscular dystrophy in C. elegans
Atsushi Higashitani, Mika Teranishi, Yui Nakagawa, et al.
The FASEB Journal (2023) Vol. 37, Iss. 4
Open Access | Times Cited: 16
Redox Control of Proteolysis During Inactivity-Induced Skeletal Muscle Atrophy
Scott K. Powers, Mustafa Ozdemir, Hayden W. Hyatt
Antioxidants and Redox Signaling (2020) Vol. 33, Iss. 8, pp. 559-569
Open Access | Times Cited: 46
Evaluation of an Antioxidant and Anti-inflammatory Cocktail Against Human Hypoactivity-Induced Skeletal Muscle Deconditioning
Coralie Arc‐Chagnaud, Guillaume Py, Théo Fovet, et al.
Frontiers in Physiology (2020) Vol. 11
Open Access | Times Cited: 45
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