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Electrical Stimuli Are Anti-Apoptotic in Skeletal Muscle via Extracellular ATP. Alteration of This Signal in Mdx Mice Is a Likely Cause of Dystrophy
(2013-11)
ATP signaling has been shown to regulate gene expression in skeletal muscle and to be altered in models of muscular
dystrophy. We have previously shown that in normal muscle fibers, ATP released through Pannexin1 (Panx1) ...
Criação de um questionário de conhecimento em Distrofia Muscular de Duchenne (Muscular Dystrophy Knowledge Questionnaire) - DDMKQ
(Universidade Federal de São Paulo (UNIFESP), 2012)
Introdução: Pacientes com distrofia muscular de Duchenne (DMD) apresentam durante a evolucao natural da doenca dificuldades fisicas e funcionais progressivas. Ha dependencia de um cuidador, que geralmente e um familiar ...
Body composition of duchenne muscular dystrophy patients supplemented with zinc: a clinical trial
(Universidade Federal do Rio Grande do NorteBrasilUFRNPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE, 2022)
Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy ROLE OF THE C2a SPLICE VARIANT
(AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC, 2010)
Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI. Although the majority of the recessive UCMD ...
Transcriptional regulation differs in affected facioscapulohumeral muscular dystrophy patients compared to asymptomatic related carriers
(NATL ACAD SCIENCES, 2009)
Facioscapulohumeral muscular dystrophy (FSHD) is a progressive muscle disorder that has been associated with a contraction of 3.3-kb repeats on chromosome 4q35. FSHD is characterized by a wide clinical inter- and intrafamilial ...