Pages that link to "Q47314000"
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The following pages link to Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy (Q47314000):
Displaying 50 items.
- Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling (Q24815340) (← links)
- Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation (Q27309883) (← links)
- Gene expression profiling in the type 1 diabetes rat diaphragm (Q30886004) (← links)
- Transcriptome-scale similarities between mouse and human skeletal muscles with normal and myopathic phenotypes (Q33235717) (← links)
- Blastocyst injection of wild type embryonic stem cells induces global corrections in mdx mice (Q33416809) (← links)
- Evaluation of skeletal and cardiac muscle function after chronic administration of thymosin beta-4 in the dystrophin deficient mouse (Q33529003) (← links)
- Differential expression of lipid and carbohydrate metabolism genes in upper airway versus diaphragm muscle (Q33700774) (← links)
- Therapeutic targeting of signaling pathways in muscular dystrophy (Q33707964) (← links)
- Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients. (Q33894799) (← links)
- RNA expression analysis of passive transfer myasthenia supports extraocular muscle as a unique immunological environment. (Q33915924) (← links)
- Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm. (Q33946757) (← links)
- Alterations in the expression of leukemia inhibitory factor following exercise: comparisons between wild-type and mdx muscles (Q34106079) (← links)
- Pharmacologic management of Duchenne muscular dystrophy: target identification and preclinical trials (Q34152280) (← links)
- Skeletal muscle repair in a mouse model of nemaline myopathy (Q34552514) (← links)
- Phospholipase D1 facilitates second-phase myoblast fusion and skeletal muscle regeneration (Q35027582) (← links)
- A multidisciplinary evaluation of the effectiveness of cyclosporine a in dystrophic mdx mice. (Q35083651) (← links)
- ACE2 is augmented in dystrophic skeletal muscle and plays a role in decreasing associated fibrosis. (Q35138448) (← links)
- Biological organization of the extraocular muscles (Q36284737) (← links)
- Bex1 knock out mice show altered skeletal muscle regeneration (Q36491989) (← links)
- Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1. (Q37035048) (← links)
- MicroRNA-206: the skeletal muscle-specific myomiR. (Q37125050) (← links)
- Wasting mechanisms in muscular dystrophy. (Q37138490) (← links)
- OPN-a induces muscle inflammation by increasing recruitment and activation of pro-inflammatory macrophages. (Q37394133) (← links)
- Heterogeneity in the muscle satellite cell population (Q37789857) (← links)
- Role of proteoglycans in the regulation of the skeletal muscle fibrotic response. (Q38096495) (← links)
- Wnt signaling in skeletal muscle dynamics: myogenesis, neuromuscular synapse and fibrosis (Q38135328) (← links)
- Gene expression profiling of diaphragm muscle in alpha2-laminin (merosin)-deficient dy/dy dystrophic mice (Q38317471) (← links)
- Quantitative proteome profiling of dystrophic dog skeletal muscle reveals a stabilized muscular architecture and protection against oxidative stress after systemic delivery of MuStem cells. (Q38391853) (← links)
- Alterations in lung gene expression in streptozotocin-induced diabetic rats (Q38481002) (← links)
- Lack of dystrophin in mdx mice modulates the expression of genes involved in neuron survival and differentiation. (Q38498496) (← links)
- Oxidoreductase, morphogenesis, extracellular matrix, and calcium ion-binding gene expression in streptozotocin-induced diabetic rat heart (Q38516040) (← links)
- Progressive muscle proteome changes in a clinically relevant pig model of Duchenne muscular dystrophy (Q38820669) (← links)
- Transforming growth factor type-β inhibits Mas receptor expression in fibroblasts but not in myoblasts or differentiated myotubes; Relevance to fibrosis associated to muscular dystrophies. (Q38895037) (← links)
- CTGF/CCN-2 over-expression can directly induce features of skeletal muscle dystrophy (Q39493006) (← links)
- Degenerative and regenerative features of myofibers differ among skeletal muscles in a murine model of muscular dystrophy. (Q39545041) (← links)
- Diversity in transcriptional start site selection and alternative splicing affects the 5'-UTR of mouse striated muscle myosin transcripts. (Q40259328) (← links)
- Distinctive morphological and gene/protein expression signatures during myogenesis in novel cell lines from extraocular and hindlimb muscle (Q40350595) (← links)
- Treatment with human immunoglobulin G improves the early disease course in a mouse model of Duchenne muscular dystrophy (Q41527279) (← links)
- Comparative transcriptome analysis of muscular dystrophy models Large(myd), Dmd(mdx)/Large(myd) and Dmd(mdx): what makes them different? (Q41691404) (← links)
- Endotoxin triggers nuclear factor-kappaB-dependent up-regulation of multiple proinflammatory genes in the diaphragm (Q42496888) (← links)
- Is oxidative stress a cause or consequence of disuse muscle atrophy in mice? A proteomic approach in hindlimb-unloaded mice (Q43263806) (← links)
- Muscle genome-wide expression profiling during disease evolution in mdx mice. (Q44471658) (← links)
- Connective tissue cells expressing fibro/adipogenic progenitor markers increase under chronic damage: relevance in fibroblast-myofibroblast differentiation and skeletal muscle fibrosis (Q44783314) (← links)
- Regulation of cell proliferation by fast Myosin light chain 1 in myoblasts derived from extraocular muscle, diaphragm and gastrocnemius (Q46288810) (← links)
- Therapeutic gene transfer to dystrophic diaphragm by an adenoviral vector deleted of all viral genes (Q47449775) (← links)
- Expression and regulation of CC class chemokines in the dystrophic (mdx) diaphragm (Q47806024) (← links)
- The pro-fibrotic connective tissue growth factor (CTGF/CCN2) correlates with the number of necrotic-regenerative foci in dystrophic muscle (Q48100107) (← links)
- Role of tumour necrosis factor alpha, but not of cyclo-oxygenase-2-derived eicosanoids, on functional and morphological indices of dystrophic progression in mdx mice: a pharmacological approach (Q51007790) (← links)
- Expression profiling of disease progression in canine model of Duchenne muscular dystrophy. (Q52648781) (← links)
- Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis. (Q53198376) (← links)