
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:
Acute conversion of patient-derived Duchenne muscular dystrophy iPSC into myotubes reveals constitutive and inducible over-activation of TGFβ-dependent pro-fibrotic signaling
Luca Caputo, Alice Granados, Jessica Lenzi, et al.
Skeletal Muscle (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 31
Luca Caputo, Alice Granados, Jessica Lenzi, et al.
Skeletal Muscle (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 31
Showing 1-25 of 31 citing articles:
HDAC inhibitors as pharmacological treatment for Duchenne muscular dystrophy: a discovery journey from bench to patients
Chiara Mozzetta, Vittorio Sartorelli, Prem Puri
Trends in Molecular Medicine (2024) Vol. 30, Iss. 3, pp. 278-294
Closed Access | Times Cited: 17
Chiara Mozzetta, Vittorio Sartorelli, Prem Puri
Trends in Molecular Medicine (2024) Vol. 30, Iss. 3, pp. 278-294
Closed Access | Times Cited: 17
Advanced Cellular Models for Rare Disease Study: Exploring Neural, Muscle and Skeletal Organoids
Cristina Bombieri, Andrea Corsi, Elisabetta Trabetti, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1014-1014
Open Access | Times Cited: 11
Cristina Bombieri, Andrea Corsi, Elisabetta Trabetti, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 2, pp. 1014-1014
Open Access | Times Cited: 11
Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset
Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont, et al.
Journal of Cachexia Sarcopenia and Muscle (2021) Vol. 12, Iss. 1, pp. 209-232
Open Access | Times Cited: 48
Virginie Mournetas, Emmanuelle Massouridès, Jean‐Baptiste Dupont, et al.
Journal of Cachexia Sarcopenia and Muscle (2021) Vol. 12, Iss. 1, pp. 209-232
Open Access | Times Cited: 48
Advanced models of human skeletal muscle differentiation, development and disease: Three-dimensional cultures, organoids and beyond
Salma Jalal, Sumitava Dastidar, Francesco Saverio Tedesco
Current Opinion in Cell Biology (2021) Vol. 73, pp. 92-104
Open Access | Times Cited: 38
Salma Jalal, Sumitava Dastidar, Francesco Saverio Tedesco
Current Opinion in Cell Biology (2021) Vol. 73, pp. 92-104
Open Access | Times Cited: 38
Expression of Endogenous Angiotensin-Converting Enzyme 2 in Human Induced Pluripotent Stem Cell-Derived Retinal Organoids
Henkie Isahwan Ahmad Mulyadi Lai, Shih‐Jie Chou, Yueh Chien, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 3, pp. 1320-1320
Open Access | Times Cited: 33
Henkie Isahwan Ahmad Mulyadi Lai, Shih‐Jie Chou, Yueh Chien, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 3, pp. 1320-1320
Open Access | Times Cited: 33
Disease exacerbation in MYOrganoids derived from Duchenne Muscular Dystrophy iPSC reveals limitations of microdystrophin therapeutic efficacy
Sonia Albini, Laura Palmieri, Louna Pili, et al.
Research Square (Research Square) (2025)
Closed Access
Sonia Albini, Laura Palmieri, Louna Pili, et al.
Research Square (Research Square) (2025)
Closed Access
Conditional Dystrophin ablation causes profound effects on muscle development, neurobehavior, and extracellular matrix pathways
Muthukumar Karuppasamy, Katherine G. English, James R. Conner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Muthukumar Karuppasamy, Katherine G. English, James R. Conner, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Gene therapy with secreted acid alpha-glucosidase rescues Pompe disease in a novel mouse model with early-onset spinal cord and respiratory defects
Pasqualina Colella, Pauline Sellier, Manuel J. Gómez, et al.
EBioMedicine (2020) Vol. 61, pp. 103052-103052
Open Access | Times Cited: 23
Pasqualina Colella, Pauline Sellier, Manuel J. Gómez, et al.
EBioMedicine (2020) Vol. 61, pp. 103052-103052
Open Access | Times Cited: 23
Bioengineering human skeletal muscle models: Recent advances, current challenges and future perspectives
Yunsong Jiang, Tugce Torun, Sara M. Maffioletti, et al.
Experimental Cell Research (2022) Vol. 416, Iss. 2, pp. 113133-113133
Open Access | Times Cited: 14
Yunsong Jiang, Tugce Torun, Sara M. Maffioletti, et al.
Experimental Cell Research (2022) Vol. 416, Iss. 2, pp. 113133-113133
Open Access | Times Cited: 14
Advancements in 2D and 3D In Vitro Models for Studying Neuromuscular Diseases
Ha‐Neul Kim, Gon Sup Kim, Sang‐Hwan Hyun, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17006-17006
Open Access | Times Cited: 8
Ha‐Neul Kim, Gon Sup Kim, Sang‐Hwan Hyun, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 23, pp. 17006-17006
Open Access | Times Cited: 8
Engineering cell fate: Applying synthetic biology to cellular reprogramming
Nathan Wang, Adam M. Beitz, Kate E. Galloway
Current Opinion in Systems Biology (2020) Vol. 24, pp. 18-31
Open Access | Times Cited: 19
Nathan Wang, Adam M. Beitz, Kate E. Galloway
Current Opinion in Systems Biology (2020) Vol. 24, pp. 18-31
Open Access | Times Cited: 19
MyoD-Induced Trans-Differentiation: A Paradigm for Dissecting the Molecular Mechanisms of Cell Commitment, Differentiation and Reprogramming
Cecilia Battistelli, Sabrina Garbo, Rossella Maione
Cells (2022) Vol. 11, Iss. 21, pp. 3435-3435
Open Access | Times Cited: 12
Cecilia Battistelli, Sabrina Garbo, Rossella Maione
Cells (2022) Vol. 11, Iss. 21, pp. 3435-3435
Open Access | Times Cited: 12
Human muscle production in vitro from pluripotent stem cells: Basic and clinical applications
Lu Yan, Alejandra Rodríguez‐delaRosa, Olivier Pourquié
Seminars in Cell and Developmental Biology (2021) Vol. 119, pp. 39-48
Open Access | Times Cited: 16
Lu Yan, Alejandra Rodríguez‐delaRosa, Olivier Pourquié
Seminars in Cell and Developmental Biology (2021) Vol. 119, pp. 39-48
Open Access | Times Cited: 16
The Evolution of Complex Muscle Cell In Vitro Models to Study Pathomechanisms and Drug Development of Neuromuscular Disease
Jana Zschüntzsch, Stefanie Meyer, Mina Shahriyari, et al.
Cells (2022) Vol. 11, Iss. 7, pp. 1233-1233
Open Access | Times Cited: 11
Jana Zschüntzsch, Stefanie Meyer, Mina Shahriyari, et al.
Cells (2022) Vol. 11, Iss. 7, pp. 1233-1233
Open Access | Times Cited: 11
Induced Pluripotent Stem Cells for Modeling Physiological and Pathological Striated Muscle Complexity
Leslie Caron, Stefano Testa, Frédérique Magdinier
Journal of Neuromuscular Diseases (2023) Vol. 10, Iss. 5, pp. 761-776
Open Access | Times Cited: 5
Leslie Caron, Stefano Testa, Frédérique Magdinier
Journal of Neuromuscular Diseases (2023) Vol. 10, Iss. 5, pp. 761-776
Open Access | Times Cited: 5
Treating Duchenne Muscular Dystrophy: The Promise of Stem Cells, Artificial Intelligence, and Multi-Omics
Carlos Vera, Angela Zhang, Paul Pang, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 8
Carlos Vera, Angela Zhang, Paul Pang, et al.
Frontiers in Cardiovascular Medicine (2022) Vol. 9
Open Access | Times Cited: 8
hERG-deficient human embryonic stem cell-derived cardiomyocytes for modelling QT prolongation
Yun Chang, Yanan Li, Rui Bai, et al.
Stem Cell Research & Therapy (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 10
Yun Chang, Yanan Li, Rui Bai, et al.
Stem Cell Research & Therapy (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 10
SETDB1 modulates the TGFβ response in Duchenne muscular dystrophy myotubes
Alice Granados, Maeva Zamperoni, Roberta Rapone, et al.
Science Advances (2024) Vol. 10, Iss. 18
Open Access | Times Cited: 1
Alice Granados, Maeva Zamperoni, Roberta Rapone, et al.
Science Advances (2024) Vol. 10, Iss. 18
Open Access | Times Cited: 1
The Potential of Induced Pluripotent Stem Cells to Test Gene Therapy Approaches for Neuromuscular and Motor Neuron Disorders
M Cappella, Sahar Elouej, Maria Grazia Biferi
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 8
M Cappella, Sahar Elouej, Maria Grazia Biferi
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 8
Modeling Patient-Specific Muscular Dystrophy Phenotypes and Therapeutic Responses in Reprogrammed Myotubes Engineered on Micromolded Gelatin Hydrogels
Florian Barthélémy, Jeffrey W. Santoso, Laura Rabichow, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Florian Barthélémy, Jeffrey W. Santoso, Laura Rabichow, et al.
Frontiers in Cell and Developmental Biology (2022) Vol. 10
Open Access | Times Cited: 6
Multiomic Approaches to Uncover the Complexities of Dystrophin-Associated Cardiomyopathy
Aoife Gowran, Maura Brioschi, Davide Rovina, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8954-8954
Open Access | Times Cited: 4
Aoife Gowran, Maura Brioschi, Davide Rovina, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 16, pp. 8954-8954
Open Access | Times Cited: 4
COX6A2 deficiency leads to cardiac remodeling in human pluripotent stem cell-derived cardiomyocytes
Mengqi Jiang, Yuanxiu Song, Xi Chen, et al.
Stem Cell Research & Therapy (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Mengqi Jiang, Yuanxiu Song, Xi Chen, et al.
Stem Cell Research & Therapy (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Functional Characterization of a Novel Genetic Variant in Desmin (p.Glu353dup) Causing Myofibrillar Myopathy and Generation of Patient-Derived Induced Pluripotent Stem Cells for Disease Modeling
Sheila Castañeda, Guadalupe Amín, Federico Zabalegui, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
Sheila Castañeda, Guadalupe Amín, Federico Zabalegui, et al.
Research Square (Research Square) (2023)
Open Access | Times Cited: 1
Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy
Philip Barrett, Ke’ale Louie, Jean‐Baptiste Dupont, et al.
WIREs Mechanisms of Disease (2024)
Closed Access
Philip Barrett, Ke’ale Louie, Jean‐Baptiste Dupont, et al.
WIREs Mechanisms of Disease (2024)
Closed Access
HuD impairs neuromuscular junctions and induces apoptosis in human iPSC and Drosophila ALS models
Beatrice Silvestri, Michela Mochi, Darilang Mawrie, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Beatrice Silvestri, Michela Mochi, Darilang Mawrie, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access