Expression Of Utrophin At Dystrophin-deficient Neuromuscular Synapses Of Mdx Mice: A Study Of Protected And Affected Muscles.

dc.creatorFerretti, Renato
dc.creatorNeto, Humberto Santo
dc.creatorMarques, Maria Julia
dc.date2011-Feb
dc.date2015-11-27T13:22:18Z
dc.date2015-11-27T13:22:18Z
dc.date.accessioned2018-03-29T01:14:35Z
dc.date.available2018-03-29T01:14:35Z
dc.identifierAnatomical Record (hoboken, N.j. : 2007). v. 294, n. 2, p. 283-6, 2011-Feb.
dc.identifier1932-8494
dc.identifier10.1002/ar.21297
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/21235003
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/199811
dc.identifier21235003
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1300044
dc.descriptionIn mdx mice, intrinsic laryngeal muscles are spared and sternomastoid muscles are affected, showing cycles of muscle regeneration. We observed that utrophin and acetylcholine receptors are fragmented only in affected muscles, providing further evidence that changes in the overall distribution of molecules at dystrophic neuromuscular junctions may be correlated with muscle regeneration.
dc.description294
dc.description283-6
dc.languageeng
dc.relationAnatomical Record (hoboken, N.j. : 2007)
dc.relationAnat Rec (Hoboken)
dc.rightsfechado
dc.rights2010 Wiley-Liss, Inc.
dc.sourcePubMed
dc.subjectAnimals
dc.subjectDisease Models, Animal
dc.subjectDystrophin
dc.subjectLaryngeal Muscles
dc.subjectMale
dc.subjectMice
dc.subjectMice, Inbred C57bl
dc.subjectMice, Inbred Mdx
dc.subjectMuscle, Skeletal
dc.subjectMuscular Dystrophy, Duchenne
dc.subjectNeck Muscles
dc.subjectNeuromuscular Junction
dc.subjectReceptors, Cholinergic
dc.subjectRegeneration
dc.subjectSynapses
dc.subjectUtrophin
dc.titleExpression Of Utrophin At Dystrophin-deficient Neuromuscular Synapses Of Mdx Mice: A Study Of Protected And Affected Muscles.
dc.typeArtículos de revistas


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