Artykuły w czasopismach na temat „D2-mdx”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „D2-mdx”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.
De Giorgio, Daria, Deborah Novelli, Francesca Motta, Marianna Cerrato, Davide Olivari, Annasimon Salama, Francesca Fumagalli i in. "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, nr 14 (22.07.2023): 11805. http://dx.doi.org/10.3390/ijms241411805.
Pełny tekst źródłaHassani, Medhi, Dylan Moutachi, Mégane Lemaitre, Alexis Boulinguiez, Denis Furling, Onnik Agbulut i 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, nr 3 (8.03.2024): e0295700. http://dx.doi.org/10.1371/journal.pone.0295700.
Pełny tekst źródłaHayes, Holly M., Julie Angerosa, Adam T. Piers, Jason D. White, Jane Koleff, Madeline Thurgood, Jessica Moody, Michael M. Cheung i 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 (16.03.2022): 1–19. http://dx.doi.org/10.1155/2022/5362115.
Pełny tekst źródłaKrishna, Swathy, Tiffany Quindry, Matthew B. Hudson, John C. Quindry i Joshua T. Selsby. "Defective Autophagic Degradation in Aged D2‐mdx Diaphragms". FASEB Journal 34, S1 (kwiecień 2020): 1. http://dx.doi.org/10.1096/fasebj.2020.34.s1.04955.
Pełny tekst źródłaYarlagadda, Sai, Christina Kulis, Peter G. Noakes i Mark L. Smythe. "Hematopoietic Prostaglandin D Synthase Inhibitor PK007 Decreases Muscle Necrosis in DMD mdx Model Mice". Life 11, nr 9 (21.09.2021): 994. http://dx.doi.org/10.3390/life11090994.
Pełny tekst źródłaSpaulding, Hannah R., Tiffany Quindry, Kayleen Hammer, John C. Quindry i 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, nr 4 (1.10.2019): 1058–66. http://dx.doi.org/10.1152/japplphysiol.00162.2019.
Pełny tekst źródłaMartins-Bach, A., E. Araujo, B. Matot, Y. Fromes, P. Baudin, I. Richard i P. Carlier. "Nuclear magnetic resonance relaxometry characterization of D2-mdx mice". Neuromuscular Disorders 27 (październik 2017): S124. http://dx.doi.org/10.1016/j.nmd.2017.06.120.
Pełny tekst źródłaWard, Christopher W., Frederick Sachs, Ernest D. Bush i Thomas M. Suchyna. "GsMTx4-D provides protection to the D2.mdx mouse". Neuromuscular Disorders 28, nr 10 (październik 2018): 868–77. http://dx.doi.org/10.1016/j.nmd.2018.07.005.
Pełny tekst źródłaPandeya, Sarbesh R., Janice A. Nagy, Daniela Riveros, Carson Semple, Rebecca S. Taylor, Benjamin Sanchez i 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, nr 10 (29.10.2021): e0259071. http://dx.doi.org/10.1371/journal.pone.0259071.
Pełny tekst źródłaEnglish, Katherine G., Andrea L. Reid, Adrienne Samani, Gerald J. F. Coulis, S. Armando Villalta, Christopher J. Walker, Sharon Tamir i Matthew S. Alexander. "Next-Generation SINE Compound KPT−8602 Ameliorates Dystrophic Pathology in Zebrafish and Mouse Models of DMD". Biomedicines 10, nr 10 (26.09.2022): 2400. http://dx.doi.org/10.3390/biomedicines10102400.
Pełny tekst źródłaPutten, Maaike, Kayleigh Putker, Maurice Overzier, W. A. Adamzek, Svetlana Pasteuning-Vuhman, Jaap J. Plomp i Annemieke Aartsma-Rus. "Natural disease history of the D2‐mdx mouse model for Duchenne muscular dystrophy". FASEB Journal 33, nr 7 (kwiecień 2019): 8110–24. http://dx.doi.org/10.1096/fj.201802488r.
Pełny tekst źródłaKennedy, Tahnee L., Simon Guiraud, Ben Edwards, Sarah Squire, Lee Moir, Arran Babbs, Guy Odom i in. "Micro-utrophin Improves Cardiac and Skeletal Muscle Function of Severely Affected D2/mdx Mice". Molecular Therapy - Methods & Clinical Development 11 (grudzień 2018): 92–105. http://dx.doi.org/10.1016/j.omtm.2018.10.005.
Pełny tekst źródłaSpaulding, H. R., T. Quindry, J. C. Quindry i J. T. Selsby. "Nutraceutical and pharmaceutical cocktails did not preserve diaphragm muscle function or reduce muscle damage in D2‐mdx mice". Experimental Physiology 105, nr 6 (19.05.2020): 989–99. http://dx.doi.org/10.1113/ep087887.
Pełny tekst źródłaPandeya, Sarbesh R., Janice A. Nagy, Daniela Riveros, Carson Semple, Rebecca S. Taylor, Marie Mortreux, Benjamin Sanchez, Kush Kapur i 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, nr 6 (7.04.2021): 941–50. http://dx.doi.org/10.1002/mus.27240.
Pełny tekst źródłaRamos, Sofhia V., Meghan C. Hughes, Luca J. Delfinis, Catherine A. Bellissimo i 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, nr 10 (1.10.2020): e0237138. http://dx.doi.org/10.1371/journal.pone.0237138.
Pełny tekst źródłaHamamura, Kengo, Yuya Yoshida, Kosuke Oyama, Junhao Li, Shimpei Kawano, Kimiko Inoue, Keiko Toyooka i in. "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, nr 3 (3.02.2024): 1846. http://dx.doi.org/10.3390/ijms25031846.
Pełny tekst źródłaBush, E., C. Ward, T. Suchyna, F. Sacks, M. Blaustein i 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 (październik 2017): S192. http://dx.doi.org/10.1016/j.nmd.2017.06.358.
Pełny tekst źródłaMenuet, A., S. Buono, A. Robé, S. Chhor, L. Eyler, J. Becker, S. Colombo i 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 (październik 2022): S99. http://dx.doi.org/10.1016/j.nmd.2022.07.237.
Pełny tekst źródłaCernisova, Viktorija, Ngoc Lu-Nguyen, Jessica Trundle, Shan Herath, Alberto Malerba i 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, nr 9 (3.05.2023): 8174. http://dx.doi.org/10.3390/ijms24098174.
Pełny tekst źródłaMázala, Davi A. G., Ravi Hindupur, Young Jae Moon, Fatima Shaikh, Iteoluwakishi H. Gamu, Dhruv Alladi, Georgiana Panci i in. "Altered muscle niche contributes to myogenic deficit in the D2-mdx model of severe DMD". Cell Death Discovery 9, nr 1 (4.07.2023). http://dx.doi.org/10.1038/s41420-023-01503-0.
Pełny tekst źródłaRosen, Grace, Kennedy Whitley, Alexander ReyesNegron, Nicolas Berger, Jared Lourie, Riley Cleverdon, Val Fajardo i Kai Zou. "Impaired mitochondrial quality control in skeletal muscles from C57 and D2 mdx model of Duchenne Muscular Dystrophy". Physiology 38, S1 (maj 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5732496.
Pełny tekst źródłaRosen, H. Grace, Nicolas Berger, Shantel Hodge, Atsutaro Fujishiro, Jared Lourie, Vrusti Kapadia i Kai Zou. "Inhibiting Mitochondrial Fission Protein Drp1 Enhances Mitochondrial Structure, Attenuates Lipid Peroxidation, and Improves Muscle Strength in D2-mdx Mice". Physiology 39, S1 (maj 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.2399.
Pełny tekst źródłaBellissimo, Catherine A., Luca J. Delfinis, Meghan C. Hughes, Patrick C. Turnbull, Shivam Gandhi, Sara N. DiBenedetto, Fasih A. Rahman i in. "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, 23.01.2023. http://dx.doi.org/10.1152/ajpcell.00377.2022.
Pełny tekst źródłaMarcella, Bianca, Briana Hockey, Luc Wasilewicz, Sophie Hamstra, Mia Geromella, Rebecca MacPherson i 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 (maj 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5731889.
Pełny tekst źródłaGeromella, Mia, Bianca Marcella, Briana Hockey, Rene Vandenboom i Val Fajardo. "Voluntary wheel running and lithium supplementation improves muscle force production without altering SERCA function in the D2 mdx mouse". Physiology 38, S1 (maj 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5730580.
Pełny tekst źródłaKrishna, Swathy, Hannah R. Spaulding, Tiffany S. Quindry, Matthew B. Hudson, John C. Quindry i Joshua T. Selsby. "Indices of Defective Autophagy in Whole Muscle and Lysosome Enriched Fractions From Aged D2-mdx Mice". Frontiers in Physiology 12 (9.07.2021). http://dx.doi.org/10.3389/fphys.2021.691245.
Pełny tekst źródłaBellissimo, Catherine A., Shivam Gandhi, Laura N. Castellani, Mayoorey Murugathasan, Luca J. Delfinis, Arshdeep Thuhan, Madison C. Garibotti i in. "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, 25.12.2023. http://dx.doi.org/10.1152/ajpcell.00638.2023.
Pełny tekst źródłaLicandro, Simonetta Andrea, Luca Crippa, Roberta Pomarico, Raffaella Perego, Gianluca Fossati, Flavio Leoni i 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, nr 1 (22.07.2021). http://dx.doi.org/10.1186/s13395-021-00273-6.
Pełny tekst źródłaYoung, Laura V., William Morrison, Craig Campbell, Emma C. Moore, Michel G. Arsenault, Athan G. Dial, Sean Ng i in. "Loss of dystrophin expression in skeletal muscle is associated with senescence of macrophages and endothelial cells." American Journal of Physiology-Cell Physiology, 12.05.2021. http://dx.doi.org/10.1152/ajpcell.00397.2020.
Pełny tekst źródłaAartsma-Rus, Annemieke, Maaike van Putten, Paola Mantuano i 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, 31.10.2022, 1–4. http://dx.doi.org/10.3233/jnd-221547.
Pełny tekst źródłaPandeya, Sarbesh, Benjamin Sanchez, Janice A. Nagy i Seward B. Rutkove. "Combining electromyographic and electrical impedance data sets through machine learning: A study in D2‐mdx and wild‐type mice". Muscle & Nerve, 2.09.2023. http://dx.doi.org/10.1002/mus.27963.
Pełny tekst źródłaDonen, Graham, Nadia Milad i Pascal Bernatchez. "Humanization of the mdx Mouse Phenotype for Duchenne Muscular Dystrophy Modeling: A Metabolic Perspective". Journal of Neuromuscular Diseases, 10.08.2023, 1–10. http://dx.doi.org/10.3233/jnd-230126.
Pełny tekst źródłaDonen, Graham, Nadia Milad i Pascal Bernatchez. "Humanization of the mdx Mouse Phenotype for Duchenne Muscular Dystrophy Modeling: A Metabolic Perspective". Journal of Neuromuscular Diseases, 10.08.2023, 1–10. http://dx.doi.org/10.3233/jnd-230126.
Pełny tekst źródłaStec, Michael J., Qi Su, Christina Adler, Lance Zhang, David R. Golann, Naveen P. Khan, Lampros Panagis i in. "A cellular and molecular spatial atlas of dystrophic muscle". Proceedings of the National Academy of Sciences 120, nr 29 (6.07.2023). http://dx.doi.org/10.1073/pnas.2221249120.
Pełny tekst źródłaCopeland, Emily, Bianca Marcella, Bradley Baranowski, Ahmad Mohammad, Shawn Beaudette, Rebecca MacPherson i Val Fajardo. "Combined effects of lithium supplementation and exercise on memory in the D2 mdx mouse". Physiology 38, S1 (maj 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5731878.
Pełny tekst źródłaKrishna, Swathy, Hannah R. Spaulding, James E. Koltes, John C. Quindry, Rudy J. Valentine i Joshua T. Selsby. "Indicators of increased ER stress and UPR in aged D2-mdx and human dystrophic skeletal muscles". Frontiers in Physiology 14 (25.04.2023). http://dx.doi.org/10.3389/fphys.2023.1152576.
Pełny tekst źródłaWasilewicz, Luc, Sophie Hamstra, Briana Hockey, Jessica Braun, Bianca Marcella, Ryan Baranowski, Rebecca MacPherson i Val Fajardo. "Investigating the effects of thermoneutral housing on skeletal and cardiac muscle function in D2 mdx mice". Physiology 38, S1 (maj 2023). http://dx.doi.org/10.1152/physiol.2023.38.s1.5792468.
Pełny tekst źródłaDort, Junio, Zakaria Orfi, Melissa Fiscaletti, Philippe M. Campeau i 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 (14.08.2023). http://dx.doi.org/10.3389/fcell.2023.1187253.
Pełny tekst źródłaBoccanegra, Brigida, Paola Mantuano, Elena Conte, Alessandro Giovanni Cerchiara, Lisamaura Tulimiero, Raffaella Quarta, Erika Caputo i in. "LKB1 signaling is altered in skeletal muscle of a Duchenne muscular dystrophy mouse model". Disease Models & Mechanisms 16, nr 7 (1.07.2023). http://dx.doi.org/10.1242/dmm.049930.
Pełny tekst źródłaQuindry, John C., Tiffany S. Quindry, Kathryn Tiemessen i Joshua T. Selsby. "Cardiac, respiratory, and physical activity profiles in young D2‐mdx dystrophic mice". FASEB Journal 32, S1 (kwiecień 2018). http://dx.doi.org/10.1096/fasebj.2018.32.1_supplement.583.3.
Pełny tekst źródłaCopeland, Emily, Kennedy Whitley, Riley Cleverdon, Bradley Baranowski, Daniel Marko, Rebecca MacPherson, David Allison i Val Fajardo. "Kynurenine Metabolism in the D2 mdx Mouse: A Muscle‐to‐Brain Connection". FASEB Journal 35, S1 (maj 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02762.
Pełny tekst źródłaChrzanowski, Stephen Mark, Janice A. Nagy, Sarbesh Pandeya i 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, 25.11.2022, 1–10. http://dx.doi.org/10.3233/jnd-210787.
Pełny tekst źródłaKendra, Jacob, Alexandra Naman, Richard Brow, Steven Segal i Aaron Morton. "TRIM Enhances Dystrophic Muscle Function 70 Days Post Treatment". Physiology 39, S1 (maj 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.937.
Pełny tekst źródłaNaman, Alexandra, Jacob Kendra, Richard Brow, Steven Segal i Aaron Morton. "TRIM Enhances Angiogenesis in Dystrophic Muscle 140 Days Post Treatment". Physiology 39, S1 (maj 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.947.
Pełny tekst źródłaWohlgemuth, Ross, Sathvik Sriram, Kyle Henricson, Daryl Dinh, Sarah Brashear i Lucas Smith. "Collagen fibers within skeletal muscle extracellular matrix dynamically change their alignment in a stretch-dependent fashion". Physiology 39, S1 (maj 2024). http://dx.doi.org/10.1152/physiol.2024.39.s1.809.
Pełny tekst źródłaHayward, Grant, M. Caceres, Emily Copeland, Bradley Baranowski, Ahmad Mohammad, Kennedy Whitley, Val Fajardo i Rebecca MacPherson. "Characterization of Alzheimer's Disease‐like Neuropathology in Duchenne Muscular Dystrophy Using the D2 mdx Mouse Model". FASEB Journal 35, S1 (maj 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02834.
Pełny tekst źródłaCleverdon, Riley, Kennedy Whitley, Daniel Marko, Rebecca MacPherson i Val Fajardo. "Sarcoplasmic Reticulum Ca 2+ Handling in Gastrocnemius Muscles from 10‐week‐old C57 and D2‐ mdx Mice". FASEB Journal 35, S1 (maj 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.03200.
Pełny tekst źródłaHeezen, L. G. M., T. Abdelaal, M. van Putten, A. Aartsma-Rus, A. Mahfouz i P. Spitali. "Spatial transcriptomics reveal markers of histopathological changes in Duchenne muscular dystrophy mouse models". Nature Communications 14, nr 1 (15.08.2023). http://dx.doi.org/10.1038/s41467-023-40555-9.
Pełny tekst źródłaWhitley, Kennedy, Sophie Hamstra, Sebastian Silvera i Val Fajardo. "Tideglusib inhibition of GSK3 promotes the oxidative muscle phenotype and reduces serum creatine kinase in D2 mdx mice". FASEB Journal 35, S1 (maj 2021). http://dx.doi.org/10.1096/fasebj.2021.35.s1.02597.
Pełny tekst źródłaHammers, David W., Cora C. Hart, Michael K. Matheny, Lillian A. Wright, Megan Armellini, Elisabeth R. Barton i H. Lee Sweeney. "The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy". Scientific Reports 10, nr 1 (21.08.2020). http://dx.doi.org/10.1038/s41598-020-70987-y.
Pełny tekst źródła