Artigos de revistas sobre o tema "D2-mdx"
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De Giorgio, Daria, Deborah Novelli, Francesca Motta, Marianna Cerrato, Davide Olivari, Annasimon Salama, Francesca Fumagalli et al. "Characterization of the Cardiac Structure and Function of Conscious D2.B10-Dmdmdx/J (D2-mdx) mice from 16–17 to 24–25 Weeks of Age". International Journal of Molecular Sciences 24, n.º 14 (22 de julho de 2023): 11805. http://dx.doi.org/10.3390/ijms241411805.
Texto completo da fonteHassani, Medhi, Dylan Moutachi, Mégane Lemaitre, Alexis Boulinguiez, Denis Furling, Onnik Agbulut e Arnaud Ferry. "Beneficial effects of resistance training on both mild and severe mouse dystrophic muscle function as a preclinical option for Duchenne muscular dystrophy". PLOS ONE 19, n.º 3 (8 de março de 2024): e0295700. http://dx.doi.org/10.1371/journal.pone.0295700.
Texto completo da fonteHayes, Holly M., Julie Angerosa, Adam T. Piers, Jason D. White, Jane Koleff, Madeline Thurgood, Jessica Moody, Michael M. Cheung e Salvatore Pepe. "Preserved Left Ventricular Function despite Myocardial Fibrosis and Myopathy in the Dystrophin-Deficient D2.B10-Dmdmdx/J Mouse". Oxidative Medicine and Cellular Longevity 2022 (16 de março de 2022): 1–19. http://dx.doi.org/10.1155/2022/5362115.
Texto completo da fonteKrishna, Swathy, Tiffany Quindry, Matthew B. Hudson, John C. Quindry e Joshua T. Selsby. "Defective Autophagic Degradation in Aged D2‐mdx Diaphragms". FASEB Journal 34, S1 (abril de 2020): 1. http://dx.doi.org/10.1096/fasebj.2020.34.s1.04955.
Texto completo da fonteYarlagadda, Sai, Christina Kulis, Peter G. Noakes e Mark L. Smythe. "Hematopoietic Prostaglandin D Synthase Inhibitor PK007 Decreases Muscle Necrosis in DMD mdx Model Mice". Life 11, n.º 9 (21 de setembro de 2021): 994. http://dx.doi.org/10.3390/life11090994.
Texto completo da fonteSpaulding, Hannah R., Tiffany Quindry, Kayleen Hammer, John C. Quindry e Joshua T. Selsby. "Nutraceutical and pharmaceutical cocktails did not improve muscle function or reduce histological damage in D2-mdx mice". Journal of Applied Physiology 127, n.º 4 (1 de outubro de 2019): 1058–66. http://dx.doi.org/10.1152/japplphysiol.00162.2019.
Texto completo da fonteMartins-Bach, A., E. Araujo, B. Matot, Y. Fromes, P. Baudin, I. Richard e P. Carlier. "Nuclear magnetic resonance relaxometry characterization of D2-mdx mice". Neuromuscular Disorders 27 (outubro de 2017): S124. http://dx.doi.org/10.1016/j.nmd.2017.06.120.
Texto completo da fonteWard, Christopher W., Frederick Sachs, Ernest D. Bush e Thomas M. Suchyna. "GsMTx4-D provides protection to the D2.mdx mouse". Neuromuscular Disorders 28, n.º 10 (outubro de 2018): 868–77. http://dx.doi.org/10.1016/j.nmd.2018.07.005.
Texto completo da fontePandeya, Sarbesh R., Janice A. Nagy, Daniela Riveros, Carson Semple, Rebecca S. Taylor, Benjamin Sanchez e Seward B. Rutkove. "Relationships between in vivo surface and ex vivo electrical impedance myography measurements in three different neuromuscular disorder mouse models". PLOS ONE 16, n.º 10 (29 de outubro de 2021): e0259071. http://dx.doi.org/10.1371/journal.pone.0259071.
Texto completo da fonteEnglish, Katherine G., Andrea L. Reid, Adrienne Samani, Gerald J. F. Coulis, S. Armando Villalta, Christopher J. Walker, Sharon Tamir e Matthew S. Alexander. "Next-Generation SINE Compound KPT−8602 Ameliorates Dystrophic Pathology in Zebrafish and Mouse Models of DMD". Biomedicines 10, n.º 10 (26 de setembro de 2022): 2400. http://dx.doi.org/10.3390/biomedicines10102400.
Texto completo da fontePutten, Maaike, Kayleigh Putker, Maurice Overzier, W. A. Adamzek, Svetlana Pasteuning-Vuhman, Jaap J. Plomp e Annemieke Aartsma-Rus. "Natural disease history of the D2‐mdx mouse model for Duchenne muscular dystrophy". FASEB Journal 33, n.º 7 (abril de 2019): 8110–24. http://dx.doi.org/10.1096/fj.201802488r.
Texto completo da fonteKennedy, Tahnee L., Simon Guiraud, Ben Edwards, Sarah Squire, Lee Moir, Arran Babbs, Guy Odom et al. "Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice". Molecular Therapy - Methods & Clinical Development 11 (dezembro de 2018): 92–105. http://dx.doi.org/10.1016/j.omtm.2018.10.005.
Texto completo da fonteSpaulding, H. R., T. Quindry, J. C. Quindry e J. T. Selsby. "Nutraceutical and pharmaceutical cocktails did not preserve diaphragm muscle function or reduce muscle damage in D2‐mdx mice". Experimental Physiology 105, n.º 6 (19 de maio de 2020): 989–99. http://dx.doi.org/10.1113/ep087887.
Texto completo da fontePandeya, Sarbesh R., Janice A. Nagy, Daniela Riveros, Carson Semple, Rebecca S. Taylor, Marie Mortreux, Benjamin Sanchez, Kush Kapur e Seward B. Rutkove. "Estimating myofiber cross‐sectional area and connective tissue deposition with electrical impedance myography: A study in D2 ‐ mdx mice". Muscle & Nerve 63, n.º 6 (7 de abril de 2021): 941–50. http://dx.doi.org/10.1002/mus.27240.
Texto completo da fonteRamos, Sofhia V., Meghan C. Hughes, Luca J. Delfinis, Catherine A. Bellissimo e Christopher G. R. Perry. "Mitochondrial bioenergetic dysfunction in the D2.mdx model of Duchenne muscular dystrophy is associated with microtubule disorganization in skeletal muscle". PLOS ONE 15, n.º 10 (1 de outubro de 2020): e0237138. http://dx.doi.org/10.1371/journal.pone.0237138.
Texto completo da fonteHamamura, Kengo, Yuya Yoshida, Kosuke Oyama, Junhao Li, Shimpei Kawano, Kimiko Inoue, Keiko Toyooka et al. "Hematopoietic Prostaglandin D Synthase Is Increased in Mast Cells and Pericytes in Autopsy Myocardial Specimens from Patients with Duchenne Muscular Dystrophy". International Journal of Molecular Sciences 25, n.º 3 (3 de fevereiro de 2024): 1846. http://dx.doi.org/10.3390/ijms25031846.
Texto completo da fonteBush, E., C. Ward, T. Suchyna, F. Sacks, M. Blaustein e D. Escolar. "AT-300, a calcium modulator, improves muscle force production and decreases muscle degeneration in D2-mdx model of Duchenne muscular dystrophy". Neuromuscular Disorders 27 (outubro de 2017): S192. http://dx.doi.org/10.1016/j.nmd.2017.06.358.
Texto completo da fonteMenuet, A., S. Buono, A. Robé, S. Chhor, L. Eyler, J. Becker, S. Colombo e B. Cowling. "P.121 Dnm2 reduction combined with dystrophin re-expression ameliorates the myopathic phenotype observed in the D2-mdx model of Duchenne muscular dystrophy". Neuromuscular Disorders 32 (outubro de 2022): S99. http://dx.doi.org/10.1016/j.nmd.2022.07.237.
Texto completo da fonteCernisova, Viktorija, Ngoc Lu-Nguyen, Jessica Trundle, Shan Herath, Alberto Malerba e Linda Popplewell. "Microdystrophin Gene Addition Significantly Improves Muscle Functionality and Diaphragm Muscle Histopathology in a Fibrotic Mouse Model of Duchenne Muscular Dystrophy". International Journal of Molecular Sciences 24, n.º 9 (3 de maio de 2023): 8174. http://dx.doi.org/10.3390/ijms24098174.
Texto completo da fonteMázala, Davi A. G., Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H. Gamu, Dhruv Alladi, Georgiana Panci et al. "Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD". Cell Death Discovery 9, n.º 1 (4 de julho de 2023). http://dx.doi.org/10.1038/s41420-023-01503-0.
Texto completo da fonteRosen, Grace, Kennedy Whitley, Alexander ReyesNegron, Nicolas Berger, Jared Lourie, Riley Cleverdon, Val Fajardo e Kai Zou. "Impaired mitochondrial quality control in skeletal muscles from C57 and D2 mdx model of Duchenne Muscular Dystrophy". Physiology 38, S1 (maio de 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5732496.
Texto completo da fonteRosen, H. Grace, Nicolas Berger, Shantel Hodge, Atsutaro Fujishiro, Jared Lourie, Vrusti Kapadia e Kai Zou. "Inhibiting Mitochondrial Fission Protein Drp1 Enhances Mitochondrial Structure, Attenuates Lipid Peroxidation, and Improves Muscle Strength in D2-mdx Mice". Physiology 39, S1 (maio de 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.2399.
Texto completo da fonteBellissimo, Catherine A., Luca J. Delfinis, Meghan C. Hughes, Patrick C. Turnbull, Shivam Gandhi, Sara N. DiBenedetto, Fasih A. Rahman et al. "Mitochondrial creatine sensitivity is lost in the D2.mdx model of Duchenne muscular dystrophy and rescued by the mitochondrial-enhancing compound Olesoxime". American Journal of Physiology-Cell Physiology, 23 de janeiro de 2023. http://dx.doi.org/10.1152/ajpcell.00377.2022.
Texto completo da fonteMarcella, Bianca, Briana Hockey, Luc Wasilewicz, Sophie Hamstra, Mia Geromella, Rebecca MacPherson e Val Andrew Fajardo. "Voluntary wheel running and lithium supplementation promotes fatigue resistance, fat oxidation, and improves insulin tolerance in D2 mdx mice". Physiology 38, S1 (maio de 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5731889.
Texto completo da fonteGeromella, Mia, Bianca Marcella, Briana Hockey, Rene Vandenboom e Val Fajardo. "Voluntary wheel running and lithium supplementation improves muscle force production without altering SERCA function in the D2 mdx mouse". Physiology 38, S1 (maio de 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5730580.
Texto completo da fonteKrishna, Swathy, Hannah R. Spaulding, Tiffany S. Quindry, Matthew B. Hudson, John C. Quindry e Joshua T. Selsby. "Indices of Defective Autophagy in Whole Muscle and Lysosome Enriched Fractions From Aged D2-mdx Mice". Frontiers in Physiology 12 (9 de julho de 2021). http://dx.doi.org/10.3389/fphys.2021.691245.
Texto completo da fonteBellissimo, Catherine A., Shivam Gandhi, Laura N. Castellani, Mayoorey Murugathasan, Luca J. Delfinis, Arshdeep Thuhan, Madison C. Garibotti et al. "The slow-release adiponectin analogue ALY688-SR modifies early-stage disease development in the D2.mdx mouse model of Duchenne muscular dystrophy". American Journal of Physiology-Cell Physiology, 25 de dezembro de 2023. http://dx.doi.org/10.1152/ajpcell.00638.2023.
Texto completo da fonteLicandro, Simonetta Andrea, Luca Crippa, Roberta Pomarico, Raffaella Perego, Gianluca Fossati, Flavio Leoni e Christian Steinkühler. "The pan HDAC inhibitor Givinostat improves muscle function and histological parameters in two Duchenne muscular dystrophy murine models expressing different haplotypes of the LTBP4 gene". Skeletal Muscle 11, n.º 1 (22 de julho de 2021). http://dx.doi.org/10.1186/s13395-021-00273-6.
Texto completo da fonteYoung, Laura V., William Morrison, Craig Campbell, Emma C. Moore, Michel G. Arsenault, Athan G. Dial, Sean Ng et al. "Loss of dystrophin expression in skeletal muscle is associated with senescence of macrophages and endothelial cells." American Journal of Physiology-Cell Physiology, 12 de maio de 2021. http://dx.doi.org/10.1152/ajpcell.00397.2020.
Texto completo da fonteAartsma-Rus, Annemieke, Maaike van Putten, Paola Mantuano e Annamaria De Luca. "On the use of D2.B10-Dmdmdx/J (D2.mdx) Versus C57BL/10ScSn-Dmdmdx/J (mdx) Mouse Models for Preclinical Studies on Duchenne Muscular Dystrophy: A Cautionary Note from Members of the TREAT-NMD Advisory Committee on Therapeutics". Journal of Neuromuscular Diseases, 31 de outubro de 2022, 1–4. http://dx.doi.org/10.3233/jnd-221547.
Texto completo da fontePandeya, Sarbesh, Benjamin Sanchez, Janice A. Nagy e Seward B. Rutkove. "Combining electromyographic and electrical impedance data sets through machine learning: A study in D2‐mdx and wild‐type mice". Muscle & Nerve, 2 de setembro de 2023. http://dx.doi.org/10.1002/mus.27963.
Texto completo da fonteDonen, Graham, Nadia Milad e Pascal Bernatchez. "Humanization of the mdx Mouse Phenotype for Duchenne Muscular Dystrophy Modeling: A Metabolic Perspective". Journal of Neuromuscular Diseases, 10 de agosto de 2023, 1–10. http://dx.doi.org/10.3233/jnd-230126.
Texto completo da fonteDonen, Graham, Nadia Milad e Pascal Bernatchez. "Humanization of the mdx Mouse Phenotype for Duchenne Muscular Dystrophy Modeling: A Metabolic Perspective". Journal of Neuromuscular Diseases, 10 de agosto de 2023, 1–10. http://dx.doi.org/10.3233/jnd-230126.
Texto completo da fonteStec, Michael J., Qi Su, Christina Adler, Lance Zhang, David R. Golann, Naveen P. Khan, Lampros Panagis et al. "A cellular and molecular spatial atlas of dystrophic muscle". Proceedings of the National Academy of Sciences 120, n.º 29 (6 de julho de 2023). http://dx.doi.org/10.1073/pnas.2221249120.
Texto completo da fonteCopeland, Emily, Bianca Marcella, Bradley Baranowski, Ahmad Mohammad, Shawn Beaudette, Rebecca MacPherson e Val Fajardo. "Combined effects of lithium supplementation and exercise on memory in the D2 mdx mouse". Physiology 38, S1 (maio de 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5731878.
Texto completo da fonteKrishna, Swathy, Hannah R. Spaulding, James E. Koltes, John C. Quindry, Rudy J. Valentine e Joshua T. Selsby. "Indicators of increased ER stress and UPR in aged D2-mdx and human dystrophic skeletal muscles". Frontiers in Physiology 14 (25 de abril de 2023). http://dx.doi.org/10.3389/fphys.2023.1152576.
Texto completo da fonteWasilewicz, Luc, Sophie Hamstra, Briana Hockey, Jessica Braun, Bianca Marcella, Ryan Baranowski, Rebecca MacPherson e Val Fajardo. "Investigating the effects of thermoneutral housing on skeletal and cardiac muscle function in D2 mdx mice". Physiology 38, S1 (maio de 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5792468.
Texto completo da fonteDort, Junio, Zakaria Orfi, Melissa Fiscaletti, Philippe M. Campeau e Nicolas A. Dumont. "Gpr18 agonist dampens inflammation, enhances myogenesis, and restores muscle function in models of Duchenne muscular dystrophy". Frontiers in Cell and Developmental Biology 11 (14 de agosto de 2023). http://dx.doi.org/10.3389/fcell.2023.1187253.
Texto completo da fonteBoccanegra, Brigida, Paola Mantuano, Elena Conte, Alessandro Giovanni Cerchiara, Lisamaura Tulimiero, Raffaella Quarta, Erika Caputo et al. "LKB1 signaling is altered in skeletal muscle of a Duchenne muscular dystrophy mouse model". Disease Models & Mechanisms 16, n.º 7 (1 de julho de 2023). http://dx.doi.org/10.1242/dmm.049930.
Texto completo da fonteQuindry, John C., Tiffany S. Quindry, Kathryn Tiemessen e Joshua T. Selsby. "Cardiac, respiratory, and physical activity profiles in young D2‐mdx dystrophic mice". FASEB Journal 32, S1 (abril de 2018). http://dx.doi.org/10.1096/fasebj.2018.32.1_supplement.583.3.
Texto completo da fonteCopeland, Emily, Kennedy Whitley, Riley Cleverdon, Bradley Baranowski, Daniel Marko, Rebecca MacPherson, David Allison e Val Fajardo. "Kynurenine Metabolism in the D2 mdx Mouse: A Muscle‐to‐Brain Connection". FASEB Journal 35, S1 (maio de 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02762.
Texto completo da fonteChrzanowski, Stephen Mark, Janice A. Nagy, Sarbesh Pandeya e Seward B. Rutkove. "Electrical Impedance Myography Correlates with Functional Measures of Disease Progression in D2-mdx Mice and Boys with Duchenne Muscular Dystrophy". Journal of Neuromuscular Diseases, 25 de novembro de 2022, 1–10. http://dx.doi.org/10.3233/jnd-210787.
Texto completo da fonteKendra, Jacob, Alexandra Naman, Richard Brow, Steven Segal e Aaron Morton. "TRIM Enhances Dystrophic Muscle Function 70 Days Post Treatment". Physiology 39, S1 (maio de 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.937.
Texto completo da fonteNaman, Alexandra, Jacob Kendra, Richard Brow, Steven Segal e Aaron Morton. "TRIM Enhances Angiogenesis in Dystrophic Muscle 140 Days Post Treatment". Physiology 39, S1 (maio de 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.947.
Texto completo da fonteWohlgemuth, Ross, Sathvik Sriram, Kyle Henricson, Daryl Dinh, Sarah Brashear e Lucas Smith. "Collagen fibers within skeletal muscle extracellular matrix dynamically change their alignment in a stretch-dependent fashion". Physiology 39, S1 (maio de 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.809.
Texto completo da fonteHayward, Grant, M. Caceres, Emily Copeland, Bradley Baranowski, Ahmad Mohammad, Kennedy Whitley, Val Fajardo e Rebecca MacPherson. "Characterization of Alzheimer's Disease‐like Neuropathology in Duchenne Muscular Dystrophy Using the D2 mdx Mouse Model". FASEB Journal 35, S1 (maio de 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02834.
Texto completo da fonteCleverdon, Riley, Kennedy Whitley, Daniel Marko, Rebecca MacPherson e Val Fajardo. "Sarcoplasmic Reticulum Ca 2+ Handling in Gastrocnemius Muscles from 10‐week‐old C57 and D2‐ mdx Mice". FASEB Journal 35, S1 (maio de 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.03200.
Texto completo da fonteHeezen, L. G. M., T. Abdelaal, M. van Putten, A. Aartsma-Rus, A. Mahfouz e P. Spitali. "Spatial transcriptomics reveal markers of histopathological changes in Duchenne muscular dystrophy mouse models". Nature Communications 14, n.º 1 (15 de agosto de 2023). http://dx.doi.org/10.1038/s41467-023-40555-9.
Texto completo da fonteWhitley, Kennedy, Sophie Hamstra, Sebastian Silvera e Val Fajardo. "Tideglusib inhibition of GSK3 promotes the oxidative muscle phenotype and reduces serum creatine kinase in D2 mdx mice". FASEB Journal 35, S1 (maio de 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02597.
Texto completo da fonteHammers, David W., Cora C. Hart, Michael K. Matheny, Lillian A. Wright, Megan Armellini, Elisabeth R. Barton e H. Lee Sweeney. "The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy". Scientific Reports 10, n.º 1 (21 de agosto de 2020). http://dx.doi.org/10.1038/s41598-020-70987-y.
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