Nitric oxide release combined with nonsteroidal antiinflammatory activity prevents muscular dystrophy pathology and enhances stem cell therapy.
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Syntaxin 4 is required for acid sphingomyelinase activity and apoptotic functionAutomated drug screening with contractile muscle tissue engineered from dystrophic myoblastsMitochondrial biogenesis: regulation by endogenous gases during inflammation and organ stressNutraceuticals and Their Potential to Treat Duchenne Muscular Dystrophy: Separating the Credible from the ConjectureTreatment with a nitric oxide-donating NSAID alleviates functional muscle ischemia in the mouse model of Duchenne muscular dystrophyGlucocorticoid-induced leucine zipper (GILZ) and long GILZ inhibit myogenic differentiation and mediate anti-myogenic effects of glucocorticoidsAmelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptorFunctional deficits in nNOSmu-deficient skeletal muscle: myopathy in nNOS knockout miceAttempting to Compensate for Reduced Neuronal Nitric Oxide Synthase Protein with Nitrate Supplementation Cannot Overcome Metabolic Dysfunction but Rather Has Detrimental Effects in Dystrophin-Deficient mdx Muscle.Combined isosorbide dinitrate and ibuprofen as a novel therapy for muscular dystrophies: evidence from Phase I studies in healthy volunteers.Long-term treatment with naproxcinod significantly improves skeletal and cardiac disease phenotype in the mdx mouse model of dystrophyGolgi and sarcolemmal neuronal NOS differentially regulate contraction-induced fatigue and vasoconstriction in exercising mouse skeletal muscleSildenafil increases muscle protein synthesis and reduces muscle fatigue.Preclinical drug trials in the mdx mouse: assessment of reliable and sensitive outcome measures.Co-administration of ibuprofen and nitric oxide is an effective experimental therapy for muscular dystrophy, with immediate applicability to humans.Deficient nitric oxide signalling impairs skeletal muscle growth and performance: involvement of mitochondrial dysregulation.Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice.Nordihydroguaiaretic acid and aspirin increase lifespan of genetically heterogeneous male miceStem cell transplantation for treating Duchenne muscular dystrophy: A Web of Science-based literature analysisNitrosative stress elicited by nNOSµ delocalization inhibits muscle force in dystrophin-null miceA dual acting compound releasing nitric oxide (NO) and ibuprofen, NCX 320, shows significant therapeutic effects in a mouse model of muscular dystrophy.Modulation of Acid Sphingomyelinase in Melanoma Reprogrammes the Tumour Immune MicroenvironmentRegenerative potential of human muscle stem cells in chronic inflammation.Naproxcinod shows significant advantages over naproxen in the mdx model of Duchenne Muscular Dystrophy.Nitric oxide sustains long-term skeletal muscle regeneration by regulating fate of satellite cells via signaling pathways requiring Vangl2 and cyclic GMP.uPA deficiency exacerbates muscular dystrophy in MDX mice.Nitric Oxide Donor Molsidomine Positively Modulates Myogenic Differentiation of Embryonic Endothelial Progenitors.Co-administration of aspirin and allogeneic adipose-derived stromal cells attenuates bone loss in ovariectomized rats through the anti-inflammatory and chemotactic abilities of aspirinEmerging drugs for Duchenne muscular dystrophyNitric oxide in skeletal muscle: role on mitochondrial biogenesis and function.Requirement of inducible nitric oxide synthase for skeletal muscle regeneration after acute damage.Towards developing standard operating procedures for pre-clinical testing in the mdx mouse model of Duchenne muscular dystrophyPreclinical studies in the mdx mouse model of duchenne muscular dystrophy with the histone deacetylase inhibitor givinostatDesign of aging intervention studies: the NIA interventions testing program.HDAC2 blockade by nitric oxide and histone deacetylase inhibitors reveals a common target in Duchenne muscular dystrophy treatment.Regenerative pharmacology in the treatment of genetic diseases: the paradigm of muscular dystrophyMicro-dystrophin and follistatin co-delivery restores muscle function in aged DMD model.Mesenchymal stem cells: emerging therapy for Duchenne muscular dystrophyMatrix Metalloproteinases and Tissue Inhibitor of Metalloproteinases in Inflammation and Fibrosis of Skeletal MusclesTadalafil alleviates muscle ischemia in patients with Becker muscular dystrophy.
P2860
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P2860
Nitric oxide release combined with nonsteroidal antiinflammatory activity prevents muscular dystrophy pathology and enhances stem cell therapy.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Nitric oxide release combined ...... nd enhances stem cell therapy.
@ast
Nitric oxide release combined ...... nd enhances stem cell therapy.
@en
type
label
Nitric oxide release combined ...... nd enhances stem cell therapy.
@ast
Nitric oxide release combined ...... nd enhances stem cell therapy.
@en
prefLabel
Nitric oxide release combined ...... nd enhances stem cell therapy.
@ast
Nitric oxide release combined ...... nd enhances stem cell therapy.
@en
P2093
P2860
P50
P356
P1476
Nitric oxide release combined ...... nd enhances stem cell therapy.
@en
P2093
Angela Monopoli
Anna Innocenzi
Diego Covarello
Ennio Ongini
Francesca Sanvito
Giulio Cossu
Roberto Bottinelli
P2860
P304
P356
10.1073/PNAS.0608277104
P407
P577
2006-12-20T00:00:00Z