Up-regulation of utrophin alleviates the dystrophic phenotype in the mdx mouse heart

Up-regulation of utrophin alleviates the dystrophic phenotype in the mdx mouse heart

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Sang, E, Bia, B, Tinsley, J, Davies, K, Clarke, K
التنسيق:	Journal article
منشور في:	2000

مواد مشابهة

Non-toxic ubiquitous overexpression of utrophin in the mdx mouse.
حسب: Fisher, R, وآخرون
منشور في: (2000)

Non-toxic ubiquitous over-expression of utrophin in the mdx mouse.
حسب: Fisher, R, وآخرون
منشور في: (2001)

Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene.
حسب: Wakefield, P, وآخرون
منشور في: (2000)

Daily treatment with SMTC1100, a novel small molecule utrophin upregulator, dramatically reduces the dystrophic symptoms in the mdx mouse.
حسب: Tinsley, J, وآخرون
منشور في: (2011)

A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration.
حسب: Weir, A, وآخرون
منشور في: (2004)

Increased susceptibility of the dystrophic mdx mouse heart to ischemic and hypoxic injuries
حسب: Zhang, W, وآخرون
منشور في: (2005)

Daily treatment with SMTC1100, a novel small molecule utrophin upregulator, dramatically reduces the dystrophic symptoms in the mdx mouse.
حسب: Jonathon M Tinsley, وآخرون
منشور في: (2011-05-01)

Chronic Dosing with Membrane Sealant Poloxamer 188 NF Improves Respiratory Dysfunction in Dystrophic Mdx and Mdx/Utrophin-/- Mice.
حسب: Bruce E Markham, وآخرون
منشور في: (2015-01-01)

A- and B-utrophin have different expression patterns and are differentially up-regulated in mdx muscle.
حسب: Weir, A, وآخرون
منشور في: (2002)

Abnormal cardiac morphology, function and energy metabolism in the dystrophic mdx mouse: an MRI and MRS study.
حسب: Zhang, W, وآخرون
منشور في: (2008)

Prevention of pathology in mdx mice by expression of utrophin: analysis using an inducible transgenic expression system.
حسب: Squire, S, وآخرون
منشور في: (2002)

Heregulin ameliorates the dystrophic phenotype in mdx mice.
حسب: Krag, T, وآخرون
منشور في: (2004)

T-cell-dependent fibrosis in the mdx dystrophic mouse.
حسب: Morrison, J, وآخرون
منشور في: (2000)

Decrease in prosaposin in the Dystrophic mdx mouse brain.
حسب: Hui-Ling Gao, وآخرون
منشور في: (2013-01-01)

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle
حسب: Kennedy, T, وآخرون
منشور في: (2017)

l-arginine improves dystrophic phenotype in mdx mice
حسب: Vincent Voisin, وآخرون
منشور في: (2005-10-01)

Muscle structure influences utrophin expression in mdx mice.
حسب: Glen B Banks, وآخرون
منشور في: (2014-06-01)

Dystrophic phenotype improvement in the diaphragm muscle of mdx mice by diacerhein.
حسب: Rafael Dias Mâncio, وآخرون
منشور في: (2017-01-01)

Utrophin influences mitochondrial pathology and oxidative stress in dystrophic muscle
حسب: Tahnee L. Kennedy, وآخرون
منشور في: (2017-10-01)

Microarray analysis of mdx mice expressing high levels of utrophin: therapeutic implications for dystrophin deficiency.
حسب: Baban, D, وآخرون
منشور في: (2008)

Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer.
حسب: Cerletti, M, وآخرون
منشور في: (2003)

Regulation of utrophin in transgenic mice.
حسب: Davies, K
منشور في: (2005)

Metabolic profiles of dystrophin and utrophin expression in mouse models of Duchenne muscular dystrophy.
حسب: Griffin, J, وآخرون
منشور في: (2002)

Cardioprotective Effect of Whole Body Periodic Acceleration in Dystrophic Phenotype mdx Rodent
حسب: Arkady Uryash, وآخرون
منشور في: (2021-05-01)

Functional amounts of dystrophin produced by skipping the mutated exon in the mdx dystrophic mouse.
حسب: Lu, Q, وآخرون
منشور في: (2003)

Functional improvement of dystrophic muscle by repression of utrophin: let-7c interaction.
حسب: Manoj K Mishra, وآخرون
منشور في: (2017-01-01)

Utrophin luciferase knock-in mouse model for in vivo assessment of drug efficacy in preclinical trials for utrophin upregulation
حسب: Fairclough, R, وآخرون
منشور في: (2010)

Increased mitochondrial uncoupling protein 3 is associated with the cardiomyopathy in the dystrophic mouse heart
حسب: Zhang, W, وآخرون
منشور في: (2006)

Micro-utrophin improves cardiac and skeletal muscle function of severely affected D2/mdx mice
حسب: Kennedy, T, وآخرون
منشور في: (2018)

Utrophin in the therapy of Duchenne Muscular Dystrophy
حسب: Potter, A, وآخرون
منشور في: (2006)

Choline administration attenuates aspects of the dystrophic pathology in mdx mice
حسب: Francesca M. Alves, وآخرون
منشور في: (2019-04-01)

Use of antisense-mediated exon skipping to generate dystrophin in muscles of the mdx dystrophic mouse
حسب: Lu, Q, وآخرون
منشور في: (2004)

Confirmation by immunogold labeling that utrophin is localised to the normal position of dystrophin in dystrophin-negative transgenic mouse muscle
حسب: Cullen, M, وآخرون
منشور في: (2001)

Erythropoietin reduces the expression of myostatin in mdx dystrophic mice
حسب: D. Feder, وآخرون
منشور في: (2014-11-01)

Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping.
حسب: Goyenvalle, A, وآخرون
منشور في: (2010)

Utrophin up-regulation by an artificial transcription factor in transgenic mice
حسب: Mattei, E, وآخرون
منشور في: (2007)

Testing of SHIRPA, a mouse phenotypic assessment protocol, on Dmd(mdx) and Dmd(mdx3cv) dystrophin-deficient mice.
حسب: Rafael, J, وآخرون
منشور في: (2000)

Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice.
حسب: Yusuke Echigoya, وآخرون
منشور في: (2013-01-01)

Proteome Profiling of the Dystrophic <i>mdx</i> Mice Diaphragm
حسب: Olga Mucha, وآخرون
منشور في: (2023-11-01)

Dysfunctional muscle and liver glycogen metabolism in mdx dystrophic mice.
حسب: David I Stapleton, وآخرون
منشور في: (2014-01-01)