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:
Profound cellular defects attribute to muscular pathogenesis in the rhesus monkey model of Duchenne muscular dystrophy
Shuaiwei Ren, Xin Fu, Wenting Guo, et al.
Cell (2024)
Closed Access | Times Cited: 7
Shuaiwei Ren, Xin Fu, Wenting Guo, et al.
Cell (2024)
Closed Access | Times Cited: 7
Showing 7 citing articles:
Histone deacetylase inhibition with givinostat: a multi-targeted mode of action with the potential to halt the pathological cascade of Duchenne muscular dystrophy
Annemieke Aartsma‐Rus
Frontiers in Cell and Developmental Biology (2025) Vol. 12
Open Access | Times Cited: 1
Annemieke Aartsma‐Rus
Frontiers in Cell and Developmental Biology (2025) Vol. 12
Open Access | Times Cited: 1
Histological and Molecular Manifestations of Cleft Myopathy
Yixuan Huang, Pingping He, Li Jinggui, et al.
The Cleft Palate-Craniofacial Journal (2025)
Closed Access
Yixuan Huang, Pingping He, Li Jinggui, et al.
The Cleft Palate-Craniofacial Journal (2025)
Closed Access
Activation of endogenous full-length utrophin by MyoAAV-UA as a therapeutic approach for Duchenne muscular dystrophy
Ruo Wu, Peng Li, Puhao Xiao, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Ruo Wu, Peng Li, Puhao Xiao, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access
Single-cut gene therapy in a one-step generated rhesus monkey model of Duchenne muscular dystrophy
Raoxian Bai, Wenting Guo, Ting Zhang, et al.
Cell Reports Medicine (2025), pp. 102037-102037
Open Access
Raoxian Bai, Wenting Guo, Ting Zhang, et al.
Cell Reports Medicine (2025), pp. 102037-102037
Open Access
Exploring new therapeutics for Duchenne muscular dystrophy and related cardiomyopathy
Bin Li, Weiyao Xiong, Andrew Chia Hao Chang, et al.
Rare Disease and Orphan Drugs Journal (2025) Vol. 5, Iss. 2
Open Access
Bin Li, Weiyao Xiong, Andrew Chia Hao Chang, et al.
Rare Disease and Orphan Drugs Journal (2025) Vol. 5, Iss. 2
Open Access
First, do no harm: the role of preclinical animal models in predicting adverse events in gene therapy clinical trials for Duchenne muscular dystrophy and X-Linked myotubular myopathy
Joe N. Kornegay, Hansell H. Stedman, Michael W. Lawlor, et al.
Rare Disease and Orphan Drugs Journal (2024) Vol. 3, Iss. 4
Open Access
Joe N. Kornegay, Hansell H. Stedman, Michael W. Lawlor, et al.
Rare Disease and Orphan Drugs Journal (2024) Vol. 3, Iss. 4
Open Access
Cellular pathophysiology of Duchenne muscular dystrophy: insights from a novel rhesus macaque model
Alessandra Moretti, Christian Kupatt, Eckhard Wolf
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access
Alessandra Moretti, Christian Kupatt, Eckhard Wolf
Signal Transduction and Targeted Therapy (2024) Vol. 9, Iss. 1
Open Access
