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:
From diagnosis to therapy in Duchenne muscular dystrophy
Arran Babbs, Maria Chatzopoulou, Ben Edwards, et al.
Biochemical Society Transactions (2020) Vol. 48, Iss. 3, pp. 813-821
Open Access | Times Cited: 25
Arran Babbs, Maria Chatzopoulou, Ben Edwards, et al.
Biochemical Society Transactions (2020) Vol. 48, Iss. 3, pp. 813-821
Open Access | Times Cited: 25
Showing 25 citing articles:
Regenerative medicine: postnatal approaches
Paul Kwong Hang Tam, Kenneth Kak Yuen Wong, Anthony Atala, et al.
The Lancet Child & Adolescent Health (2022) Vol. 6, Iss. 9, pp. 654-666
Open Access | Times Cited: 25
Paul Kwong Hang Tam, Kenneth Kak Yuen Wong, Anthony Atala, et al.
The Lancet Child & Adolescent Health (2022) Vol. 6, Iss. 9, pp. 654-666
Open Access | Times Cited: 25
Utrophin modulator drugs as potential therapies for Duchenne and Becker muscular dystrophies
Patricia Soblechero‐Martín, Andrea López‐Martínez, Laura de la Puente Ovejero, et al.
Neuropathology and Applied Neurobiology (2021) Vol. 47, Iss. 6, pp. 711-723
Open Access | Times Cited: 30
Patricia Soblechero‐Martín, Andrea López‐Martínez, Laura de la Puente Ovejero, et al.
Neuropathology and Applied Neurobiology (2021) Vol. 47, Iss. 6, pp. 711-723
Open Access | Times Cited: 30
Spatial compartmentalization of signaling imparts source-specific functions on secreted factors
Elena Groppa, Paolo Martini, Nima Derakhshan, et al.
Cell Reports (2023) Vol. 42, Iss. 2, pp. 112051-112051
Open Access | Times Cited: 10
Elena Groppa, Paolo Martini, Nima Derakhshan, et al.
Cell Reports (2023) Vol. 42, Iss. 2, pp. 112051-112051
Open Access | Times Cited: 10
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
Molecular Insights into Determinants of Translational Readthrough and Implications for Nonsense Suppression Approaches
Silvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 24, pp. 9449-9449
Open Access | Times Cited: 24
Silvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
International Journal of Molecular Sciences (2020) Vol. 21, Iss. 24, pp. 9449-9449
Open Access | Times Cited: 24
Muscle: to the neuromuscular disease phenotype in spinal muscular atrophy
Narendra Nath Jha, Jeong-Ki Kim, Yoon-Ra Her, et al.
JCI Insight (2023) Vol. 8, Iss. 18
Open Access | Times Cited: 9
Narendra Nath Jha, Jeong-Ki Kim, Yoon-Ra Her, et al.
JCI Insight (2023) Vol. 8, Iss. 18
Open Access | Times Cited: 9
A review on mechanistic insights into structure and function of dystrophin protein in pathophysiology and therapeutic targeting of Duchenne muscular dystrophy
Abdelbaset Mohamed Elasbali, Waleed Abu Al‐Soud, Saleha Anwar, et al.
International Journal of Biological Macromolecules (2024) Vol. 264, pp. 130544-130544
Closed Access | Times Cited: 3
Abdelbaset Mohamed Elasbali, Waleed Abu Al‐Soud, Saleha Anwar, et al.
International Journal of Biological Macromolecules (2024) Vol. 264, pp. 130544-130544
Closed Access | Times Cited: 3
Nutraceutical Screening in a Zebrafish Model of Muscular Dystrophy: Gingerol as a Possible Food Aid
Rosario Licitra, Maria Marchese, Letizia Brogi, et al.
Nutrients (2021) Vol. 13, Iss. 3, pp. 998-998
Open Access | Times Cited: 14
Rosario Licitra, Maria Marchese, Letizia Brogi, et al.
Nutrients (2021) Vol. 13, Iss. 3, pp. 998-998
Open Access | Times Cited: 14
β-Glucans as Dietary Supplement to Improve Locomotion and Mitochondrial Respiration in a Model of Duchenne Muscular Dystrophy
Letizia Brogi, Maria Marchese, Alessandro Cellerino, et al.
Nutrients (2021) Vol. 13, Iss. 5, pp. 1619-1619
Open Access | Times Cited: 14
Letizia Brogi, Maria Marchese, Alessandro Cellerino, et al.
Nutrients (2021) Vol. 13, Iss. 5, pp. 1619-1619
Open Access | Times Cited: 14
MiRNAs, Myostatin, and Muscle MRI Imaging as Biomarkers of Clinical Features in Becker Muscular Dystrophy
Roberta Marozzo, Valentina Pegoraro, C. Angelini
Diagnostics (2020) Vol. 10, Iss. 9, pp. 713-713
Open Access | Times Cited: 13
Roberta Marozzo, Valentina Pegoraro, C. Angelini
Diagnostics (2020) Vol. 10, Iss. 9, pp. 713-713
Open Access | Times Cited: 13
Translation termination codons in protein synthesis and disease
Silvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
Advances in protein chemistry and structural biology (2022), pp. 1-48
Closed Access | Times Cited: 7
Silvia Lombardi, Maria Francesca Testa, Mirko Pinotti, et al.
Advances in protein chemistry and structural biology (2022), pp. 1-48
Closed Access | Times Cited: 7
Correction of exon 2, exon 2–9 and exons 8–9 duplications in DMD patient myogenic cells by a single CRISPR/Cas9 system
Juliette Lemoine, Auriane Dubois, Alan R.L. Dorval, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Juliette Lemoine, Auriane Dubois, Alan R.L. Dorval, et al.
Scientific Reports (2024) Vol. 14, Iss. 1
Open Access | Times Cited: 1
Matrilineal analysis of mutations in the DMD gene in a multigenerational South Indian cohort using DMD gene panel sequencing
Arun Shastry, Sankaramoorthy Aravind, Meeta Sunil, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 5
Open Access | Times Cited: 6
Arun Shastry, Sankaramoorthy Aravind, Meeta Sunil, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 5
Open Access | Times Cited: 6
The raft cytoskeleton binding protein complexes personate functional regulators in cell behaviors
Jinxin Han, Hangyu Zhang, Na Li, et al.
Acta Histochemica (2022) Vol. 124, Iss. 2, pp. 151859-151859
Closed Access | Times Cited: 3
Jinxin Han, Hangyu Zhang, Na Li, et al.
Acta Histochemica (2022) Vol. 124, Iss. 2, pp. 151859-151859
Closed Access | Times Cited: 3
Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy
Tina Donandt, Stefan Hintze, Sabine Krause, et al.
Life (2022) Vol. 12, Iss. 10, pp. 1668-1668
Open Access | Times Cited: 3
Tina Donandt, Stefan Hintze, Sabine Krause, et al.
Life (2022) Vol. 12, Iss. 10, pp. 1668-1668
Open Access | Times Cited: 3
Distrofia muscular de Duchenne
Marcus Vinicius Menezes Portela, Felipe Lima Weksler, Yuri Vasconcellos Vallim, et al.
Revista Eletrônica Acervo Saúde (2023) Vol. 23, Iss. 7, pp. e12912-e12912
Open Access | Times Cited: 1
Marcus Vinicius Menezes Portela, Felipe Lima Weksler, Yuri Vasconcellos Vallim, et al.
Revista Eletrônica Acervo Saúde (2023) Vol. 23, Iss. 7, pp. e12912-e12912
Open Access | Times Cited: 1
Basic notions about gene therapy from the nucleic acid perspective and applications in a pediatric disease: Duchenne muscular dystrophy
Isabelle Richard
Archives de Pédiatrie (2023) Vol. 30, Iss. 8, pp. 8S2-8S11
Closed Access | Times Cited: 1
Isabelle Richard
Archives de Pédiatrie (2023) Vol. 30, Iss. 8, pp. 8S2-8S11
Closed Access | Times Cited: 1
Exploring the Nexus of Food and Medicine: Boundaries, Synergies, Unraveling the Role of Food in Shaping Future Health
Shambhu Swarnakar, Papan Chowhan, Sumi Paul, et al.
(2024), pp. 551-569
Closed Access
Shambhu Swarnakar, Papan Chowhan, Sumi Paul, et al.
(2024), pp. 551-569
Closed Access
Iranian Registry of Duchenne and Becker Muscular Dystrophies: Characterization and Preliminary Data
Farhad Bayat, Isis G. Sarmiento, Negar Poor Ahmadian, et al.
Journal of Neuromuscular Diseases (2020) Vol. 8, Iss. 2, pp. 251-259
Closed Access | Times Cited: 2
Farhad Bayat, Isis G. Sarmiento, Negar Poor Ahmadian, et al.
Journal of Neuromuscular Diseases (2020) Vol. 8, Iss. 2, pp. 251-259
Closed Access | Times Cited: 2
Recent advances in the treatment of Duchenne muscular dystrophy
Tracey Willis
Paediatrics and Child Health (2021) Vol. 31, Iss. 9, pp. 359-363
Closed Access | Times Cited: 1
Tracey Willis
Paediatrics and Child Health (2021) Vol. 31, Iss. 9, pp. 359-363
Closed Access | Times Cited: 1
Validity and Reliability of Quick Motor Function Test in Ambulatory Duchenne Muscular Dystrophy Patients
Sena İmamoğlu, Özge Kenis‐Coskun, Mehmet Deveci, et al.
Journal of Pediatric Neurology (2022) Vol. 20, Iss. 06, pp. 380-385
Closed Access
Sena İmamoğlu, Özge Kenis‐Coskun, Mehmet Deveci, et al.
Journal of Pediatric Neurology (2022) Vol. 20, Iss. 06, pp. 380-385
Closed Access
>b<Efeito da associação da terapia celular e do treino de baixa intensidade no músculo distrófico de camundongo >i<mdx>/i<>/b<
Priscilla Avelino Ferreira Pinto
(2022)
Open Access
Priscilla Avelino Ferreira Pinto
(2022)
Open Access
Spatial compartmentalization of signalling imparts source-specific functions on secreted factors
Elena Groppa, Paolo Martini, Nima Derakhshan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Elena Groppa, Paolo Martini, Nima Derakhshan, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access
Duchenne muscular dystrophy diagnosed in infancy – a case report
Martyna Śliwińska, Anna Rakuś-Kwiatosz, Katarzyna Wojciechowska
Pediatria i Medycyna Rodzinna (2022) Vol. 18, Iss. 3, pp. 285-289
Open Access
Martyna Śliwińska, Anna Rakuś-Kwiatosz, Katarzyna Wojciechowska
Pediatria i Medycyna Rodzinna (2022) Vol. 18, Iss. 3, pp. 285-289
Open Access
