Academic literature on the topic 'Duchenne, animal models, DMD'
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Journal articles on the topic "Duchenne, animal models, DMD"
Lim, Kenji Rowel Q., Quynh Nguyen, Kasia Dzierlega, Yiqing Huang, and Toshifumi Yokota. "CRISPR-Generated Animal Models of Duchenne Muscular Dystrophy." Genes 11, no. 3 (March 24, 2020): 342. http://dx.doi.org/10.3390/genes11030342.
Full textNakamura, Akinori, and Shin'ichi Takeda. "Mammalian Models of Duchenne Muscular Dystrophy: Pathological Characteristics and Therapeutic Applications." Journal of Biomedicine and Biotechnology 2011 (2011): 1–8. http://dx.doi.org/10.1155/2011/184393.
Full textDonandt, Tina, Stefan Hintze, Sabine Krause, Eckhard Wolf, Benedikt Schoser, Maggie C. Walter, and Peter Meinke. "Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular Dystrophy." Life 12, no. 10 (October 21, 2022): 1668. http://dx.doi.org/10.3390/life12101668.
Full textWilson, Kristin, Crystal Faelan, Janet C. Patterson-Kane, Daniel G. Rudmann, Steven A. Moore, Diane Frank, Jay Charleston, Jon Tinsley, G. David Young, and Anthony J. Milici. "Duchenne and Becker Muscular Dystrophies: A Review of Animal Models, Clinical End Points, and Biomarker Quantification." Toxicologic Pathology 45, no. 7 (October 2017): 961–76. http://dx.doi.org/10.1177/0192623317734823.
Full textSayers, Stephen P. "The Role of Exercise as a Therapy for Children with Duchenne Muscular Dystrophy." Pediatric Exercise Science 12, no. 1 (February 2000): 23–33. http://dx.doi.org/10.1123/pes.12.1.23.
Full textEnglish, Katherine G., Andrea L. Reid, Adrienne Samani, Gerald J. F. Coulis, S. Armando Villalta, Christopher J. Walker, Sharon Tamir, and Matthew S. Alexander. "Next-Generation SINE Compound KPT−8602 Ameliorates Dystrophic Pathology in Zebrafish and Mouse Models of DMD." Biomedicines 10, no. 10 (September 26, 2022): 2400. http://dx.doi.org/10.3390/biomedicines10102400.
Full textWong, Tatianna Wai Ying, Abdalla Ahmed, Grace Yang, Eleonora Maino, Sydney Steiman, Elzbieta Hyatt, Parry Chan, et al. "A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy." Disease Models & Mechanisms 13, no. 9 (September 1, 2020): dmm045369. http://dx.doi.org/10.1242/dmm.045369.
Full textWells, Dominic J. "Tracking progress: an update on animal models for Duchenne muscular dystrophy." Disease Models & Mechanisms 11, no. 6 (June 1, 2018): dmm035774. http://dx.doi.org/10.1242/dmm.035774.
Full textEchigoya, Yusuke, Nhu Trieu, William Duddy, Hong M. Moulton, HaiFang Yin, Terence A. Partridge, Eric P. Hoffman, et al. "A Dystrophin Exon-52 Deleted Miniature Pig Model of Duchenne Muscular Dystrophy and Evaluation of Exon Skipping." International Journal of Molecular Sciences 22, no. 23 (December 2, 2021): 13065. http://dx.doi.org/10.3390/ijms222313065.
Full textHughes, K. J., A. Rodriguez, K. M. Flatt, S. Ray, A. Schuler, B. Rodemoyer, V. Veerappan, et al. "Physical exertion exacerbates decline in the musculature of an animal model of Duchenne muscular dystrophy." Proceedings of the National Academy of Sciences 116, no. 9 (February 12, 2019): 3508–17. http://dx.doi.org/10.1073/pnas.1811379116.
Full textDissertations / Theses on the topic "Duchenne, animal models, DMD"
Barthélémy, Inès. "Développement d'outils d'évaluation d'un modèle pré-clinique de dystrophie musculaire de Duchenne, le chien GRMD." Phd thesis, Université Paris-Est, 2010. http://tel.archives-ouvertes.fr/tel-00630718.
Full textZatti, Susi. "Micro-engineered skeletal and cardiac muscle for Duchenne muscular dystrophy in vitro models." Doctoral thesis, Università degli studi di Padova, 2012. http://hdl.handle.net/11577/3422953.
Full textLa distrofia muscolare di Duchenne è una delle più frequenti e severe patologie genetiche neuromuscolari che affliggono la funzionalità del muscolo scheletrico e cardiaco. Il gene codificante la distrofina, proteina la cui mutazione è alla base della patologia, è stato scoperto più di vent’anni fa. Da allora, notevoli progressi sono stati compiuti nella comprensione della patogenesi di questa malattia e diverse strategie sperimentali volte al suo trattamento sono state testate, sia in vitro su convenzionali colture cellulari che in vivo su diversi animali modello. Tuttavia, eccezione fatta per alcuni promettenti risultati recentemente ottenuti in trials clinici, ad oggi non vi è ancora una cura efficace e definitiva in grado di alterare o rallentare la progressione di questa patologia, il cui tasso di mortalità è pari al 100%. In tale contesto, lo scopo di questa tesi di dottorato è quello di sviluppare dei modelli in vitro micro-ingegnerizzati di muscolo scheletrico e cardiaco umano, che siano rappresentativi dei tessuti distrofici e dunque utili per testare approcci terapeutici volti al ripristino dell’espressione di distrofina. La strategia applicata per l’ottenimento di tali modelli si basa sull’applicazione di tecnologie su microscala per riprodurre in vitro i principali stimoli che guidano il differenziamento e consentono la funzionalità del muscolo scheletrico e cardiaco in vivo. In particolare, le proprietà meccaniche del micro-ambiente e l’organizzazione topologica della coltura cellulare sono stati ottimizzati sia per il muscolo scheletrico che cardiaco. Tali tecnologie su micro-scala sono state accoppiate con un’appropriata fonte cellulare umana. Per l’ingegnerizzazione del muscolo scheletrico sono stati utilizzati mioblasti umani primari derivanti da biopsie di pazienti DMD mentre, per la modellazione del muscolo cardiaco, cellule umane pluripotenti indotte (iPS) sono state differenziate in cardiomiociti paziente-specifici. Entrambi i modelli in vitro di muscolo distrofico ottenuti sono stati validati testando l’abilità di diversi approcci terapeutici nel ripristinarne l’espressione di distrofina. In particolare, tre diversi tipi cellulari miogenici sono stati testati nel muscolo scheletrico distrofico ingegnerizzato. Inoltre, nei cardiomiociti distrofici derivanti da cellule iPS è stato testato il ripristino dell’espressione di distrofina per mezzo di un cromosoma artificiale portante la sua completa sequenza genomica. Da tali risultati emerge come i modelli umani in vitro sviluppati in questo lavoro possano rappresentare un’utile piattaforma su cui effettuare test pre-clinici preliminari di diverse strategie terapeutiche. Inoltre, essi posso potenzialmente essere utilizzati come strumento complementare durante i trials clinici, per testare, ad esempio, diverse preparazioni di cellule destinate al paziente.
Childers, Martin K. "Contraction-induced muscle damage in dogs with golden retriever muscular dystrophy." free to MU campus, others may purchase free online, 2002. http://wwwlib.umi.com/cr/mo/preview?3074385.
Full textCardone, Nastasia. "Myopathologic readouts identification in dystrophinopathies trough comparative analyses of human and animal models muscles." Doctoral thesis, 2022. http://hdl.handle.net/2158/1279908.
Full textBooks on the topic "Duchenne, animal models, DMD"
1932-, Kakulas Byron A., Howell J. McC, and Roses Allen D, eds. Duchenne muscular dystrophy: Animal models and genetic manipulation. New York: Raven Press, 1992.
Find full textMcChowell, John. Duchenne Muscular Dystrophy: Animal Models and Genetic Manipulation. Raven Press Ltd, 1992.
Find full textBook chapters on the topic "Duchenne, animal models, DMD"
Lu-Nguyen, Ngoc, Alberto Malerba, and Linda Popplewell. "Use of Small Animal Models for Duchenne and Parameters to Assess Efficiency upon Antisense Treatment." In Methods in Molecular Biology, 301–13. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_20.
Full textSrivastava, Niraj Kumar, Ramakant Yadav, and Deepak Sharma. "Aging: Influence on Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD)." In Models, Molecules and Mechanisms in Biogerontology, 149–76. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-3585-3_8.
Full textLópez-Martínez, Andrea, Patricia Soblechero-Martín, and Virginia Arechavala-Gomeza. "Evaluation of Exon Skipping and Dystrophin Restoration in In Vitro Models of Duchenne Muscular Dystrophy." In Methods in Molecular Biology, 217–33. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_14.
Full textYin, HaiFang, Hong Moulton, Corinne Betts, and Matthew Wood. "CPP-Directed Oligonucleotide Exon Skipping in Animal Models of Duchenne Muscular Dystrophy." In Methods in Molecular Biology, 321–38. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-919-2_23.
Full textLu, Qi Long, and Bo Wu. "Systemic Delivery of Antisense Oligomer in Animal Models and Its Implications for Treating DMD." In Methods in Molecular Biology, 393–405. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-767-5_25.
Full textV. Egorova, Tatiana, Ivan I. Galkin, Yulia V. Ivanova, and Anna V. Polikarpova. "Duchenne Muscular Dystrophy Animal Models." In Animal Models in Medicine and Biology [Working Title]. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96738.
Full textHoffman, Eric P., and Jose Rafael M. Gorospe. "Chapter 8 The Animal Models of Duchenne Muscular Dystrophy: Windows on the Pathophysiological Consequences of Dystrophin Deficiency." In Ordering the Membrane-Cytoskeleton Trilayer, 113–54. Elsevier, 1991. http://dx.doi.org/10.1016/s0070-2161(08)60785-6.
Full textElhussieny, Ahmed, Ken’ichiro Nogami, Fusako Sakai-Takemura, Yusuke Maruyama, AbdElraouf Omar Abdelbakey, Wael Abou El-kheir, Shin’ichi Takeda, and Yuko Miyagoe-Suzuki. "Mesenchymal Stem Cells for Regenerative Medicine for Duchenne Muscular Dystrophy." In Muscular Dystrophy - Research Updates and Therapeutic Strategies. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.92824.
Full textConference papers on the topic "Duchenne, animal models, DMD"
Andersen, Bret, and Nathan Angerhofer. "An Improved and Adjustable Vest System for the Support of Gravity-Counterbalancing Exoskeleton Arms." In 2017 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/dmd2017-3361.
Full textRizzuto, E., A. Musarò, A. Catizone, and Z. Del Prete. "Morpho-Functional Interaction Between Muscle and Tendon in Hypertrophic MLC/mIGF-1 Mice." In ASME 2010 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2010. http://dx.doi.org/10.1115/sbc2010-19332.
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