Cargando…

A reporter mouse for optical imaging of inflammation in mdx muscles

BACKGROUND: Duchenne muscular dystrophy (DMD) is due to mutations in the gene coding for human DMD; DMD is characterized by progressive muscle degeneration, inflammation, fat accumulation, and fibrosis. The mdx mouse model of DMD lacks dystrophin protein and undergoes a predictable disease course. W...

Descripción completa

Detalles Bibliográficos
Autores principales:	Martinez, Leonel, Ermolova, Natalia V, Ishikawa, Tomo-O, Stout, David B, Herschman, Harvey R, Spencer, Melissa J
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Methodology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4422315/ https://www.ncbi.nlm.nih.gov/pubmed/25949789 http://dx.doi.org/10.1186/s13395-015-0042-x

Ejemplares similares

Whole-body clearing, staining and screening of calcium deposits in the mdx mouse model of Duchenne muscular dystrophy
por: Bozycki, Lukasz, et al.
Publicado: (2018)

Conditional Bicistronic Cre Reporter Line Expressing Both Firefly Luciferase and β-galactosidase
por: Ishikawa, Tomo-o, et al.
Publicado: (2010)

In Vivo Mouse Bioluminescence Tomography with Radionuclide-Based Imaging Validation
por: Lu, Yujie, et al.
Publicado: (2010)

IL-6 signaling blockade increases inflammation but does not affect muscle function in the mdx mouse
por: Kostek, Matthew C, et al.
Publicado: (2012)

Temporal changes in magnetic resonance imaging in the mdx mouse
por: Pratt, Stephen JP, et al.
Publicado: (2013)

Non-invasive Optical Imaging of Muscle Pathology in mdx Mice Using Cathepsin Caged Near-Infrared Imaging
por: Baudy, Andreas R., et al.
Publicado: (2010)

Reduction in mdx mouse muscle degeneration by low-intensity endurance exercise: a proteomic analysis in quadriceps muscle of exercised compared with sedentary mdx mice
por: Fontana, Simona, et al.
Publicado: (2015)

Quantitative T2 Combined with Texture Analysis of Nuclear Magnetic Resonance Images Identify Different Degrees of Muscle Involvement in Three Mouse Models of Muscle Dystrophy: mdx, Large(myd) and mdx/Large(myd)
por: Martins-Bach, Aurea B., et al.
Publicado: (2015)

New pathobiochemical insights into dystrophinopathy from the proteomics of senescent mdx mouse muscle
por: Holland, Ashling, et al.
Publicado: (2014)

A Mathematical Model of Skeletal Muscle Disease and Immune Response in the mdx Mouse
por: Jarrah, Abdul Salam, et al.
Publicado: (2014)

An accelerated mouse model for atherosclerosis and adipose tissue inflammation
por: Neuhofer, Angelika, et al.
Publicado: (2014)

Modified protocol for in vivo imaging of wild-type mouse retina with customized miniature spectral domain optical coherence tomography (SD-OCT) device
por: Ferguson, Lee R, et al.
Publicado: (2012)

Skeletal Muscle NADPH Oxidase Is Increased and Triggers Stretch-Induced Damage in the mdx Mouse
por: Whitehead, Nicholas P., et al.
Publicado: (2010)

Aquaporin 4 Expression in the mdx Mouse Diaphragm
por: Hara, Hajime, et al.
Publicado: (2011)

Decrease in Prosaposin in the Dystrophic mdx Mouse Brain
por: Gao, Hui-ling, et al.
Publicado: (2013)

Cognitive impairment appears progressive in the mdx mouse
por: Bagdatlioglu, Emine, et al.
Publicado: (2020)

A comparison of the bone and growth phenotype of mdx, mdx:Cmah(−/−) and mdx:Utrn(+/−) murine models with the C57BL/10 wild-type mouse
por: Wood, Claire L., et al.
Publicado: (2020)

Live imaging of developing mouse retinal slices
por: Barrasso, Anthony P., et al.
Publicado: (2018)

Growth hormone secretagogues modulate inflammation and fibrosis in mdx mouse model of Duchenne muscular dystrophy
por: Boccanegra, Brigida, et al.
Publicado: (2023)

The panniculus carnosus muscle: A novel model of striated muscle regeneration that exhibits sex differences in the mdx mouse
por: Bahri, Ola A., et al.
Publicado: (2019)

Inducible Cre transgenic mouse strain for skeletal muscle-specific gene targeting
por: McCarthy, John J, et al.
Publicado: (2012)

Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers
por: Vandebrouck, Clarisse, et al.
Publicado: (2002)

Profiling of Age-Related Changes in the Tibialis Anterior Muscle Proteome of the mdx Mouse Model of Dystrophinopathy
por: Carberry, Steven, et al.
Publicado: (2012)

The Effect of Vitamin D Supplementation on Skeletal Muscle in the mdx Mouse Model of Duchenne Muscular Dystrophy
por: Debruin, Danielle A., et al.
Publicado: (2019)

Lipocalin 2 Influences Bone and Muscle Phenotype in the MDX Mouse Model of Duchenne Muscular Dystrophy
por: Ponzetti, Marco, et al.
Publicado: (2022)

Early Developmental Changes of Muscle Acetylcholine Receptors Are Little Influenced by Dystrophin Absence in mdx Mouse
por: Morotti, Marta, et al.
Publicado: (2022)

Treatment with rGDF11 does not improve the dystrophic muscle pathology of mdx mice
por: Rinaldi, Fabrizio, et al.
Publicado: (2016)

Hormonal Receptors in Skeletal Muscles of Dystrophic Mdx Mice
por: Feder, David, et al.
Publicado: (2013)

Muscle Structure Influences Utrophin Expression in mdx Mice
por: Banks, Glen B., et al.
Publicado: (2014)

Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
por: Hastings, Robert Louis, et al.
Publicado: (2020)

Cardiomyocyte Regeneration in the mdx Mouse Model of Nonischemic Cardiomyopathy
por: Richardson, Gavin David, et al.
Publicado: (2015)

Humanizing the mdx mouse model of DMD: the long and the short of it
por: Yucel, Nora, et al.
Publicado: (2018)

A nitric oxide synthase transgene ameliorates muscular dystrophy in mdx mice
por: Wehling, Michelle, et al.
Publicado: (2001)

Myostatin genetic inactivation inhibits myogenesis by muscle-derived stem cells in vitro but not when implanted in the mdx mouse muscle
por: Tsao, James, et al.
Publicado: (2013)

A novel tetracycline-responsive transgenic mouse strain for skeletal muscle-specific gene expression
por: Iwata, Masahiro, et al.
Publicado: (2018)

Normal myogenic cells from newborn mice restore normal histology to degenerating muscles of the mdx mouse
Publicado: (1990)

Increased plasma lipid levels exacerbate muscle pathology in the mdx mouse model of Duchenne muscular dystrophy
por: Milad, Nadia, et al.
Publicado: (2017)

A Reduction in Selenoprotein S Amplifies the Inflammatory Profile of Fast-Twitch Skeletal Muscle in the mdx Dystrophic Mouse
por: Wright, Craig Robert, et al.
Publicado: (2017)

MuscleJ: a high-content analysis method to study skeletal muscle with a new Fiji tool
por: Mayeuf-Louchart, Alicia, et al.
Publicado: (2018)

Visualization of PAX7 protein dynamics in muscle satellite cells in a YFP knock-in-mouse line
por: Kitajima, Yasuo, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_bbs9p9ckhokavnnd6psuf6nmc5