Function and genetics of dystrophin and dystrophin-related proteins in muscle.
about
Interventions to prevent steroid-induced osteoporosis and osteoporotic fractures in Duchenne muscular dystrophyBinding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated musclesDystrophin Dp71: the smallest but multifunctional product of the Duchenne muscular dystrophy geneSarcoglycan subcomplex expression in normal human smooth muscleDysbindin-1 is a synaptic and microtubular protein that binds brain snapinHypernitrosylated ryanodine receptor calcium release channels are leaky in dystrophic muscleChanges in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patientsReinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding proteinMolecular and cell-based therapies for muscle degenerations: a road under constructionBiglycan binds to alpha- and gamma-sarcoglycan and regulates their expression during developmentHermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)Investigation of Debio 025, a cyclophilin inhibitor, in the dystrophic mdx mouse, a model for Duchenne muscular dystrophySildenafil and cardiomyocyte-specific cGMP signaling prevent cardiomyopathic changes associated with dystrophin deficiencyMechanosensitive channel properties and membrane mechanics in mouse dystrophic myotubesCritical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and DiseaseStem cells: An insight into the therapeutic aspects from medical and dental perspectivesCardiac involvement in Duchenne and Becker muscular dystrophyOveractive bone morphogenetic protein signaling in heterotopic ossification and Duchenne muscular dystrophyClinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD geneA TALEN-Exon Skipping Design for a Bethlem Myopathy Model in ZebrafishEarly pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells.Low intensity, high frequency vibration training to improve musculoskeletal function in a mouse model of Duchenne muscular dystrophyThe Rap1 guanine nucleotide exchange factor C3G is required for preservation of larval muscle integrity in Drosophila melanogasterInteractions between connected half-sarcomeres produce emergent mechanical behavior in a mathematical model of muscleThe Crystal Structures of Dystrophin and Utrophin Spectrin Repeats: Implications for Domain BoundariesPerturbation of the Monomer–Monomer Interfaces of the Benzoylformate Decarboxylase TetramerCurrent understanding of molecular pathology and treatment of cardiomyopathy in duchenne muscular dystrophyAnimal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapyIncreased expression of cSHMT, Tbx3 and utrophin in plasma of ovarian and breast cancer patientsDiverse roles of the actin cytoskeleton in striated muscleCytoplasmic gamma-actin expression in diverse animal models of muscular dystrophyAge-related alterations in the sarcolemmal environment are attenuated by lifelong caloric restriction and voluntary exerciseInterplay between exonic splicing enhancers, mRNA processing, and mRNA surveillance in the dystrophic Mdx mouseUtrophin up-regulation by an artificial transcription factor in transgenic miceDestabilization of the dystrophin-glycoprotein complex without functional deficits in alpha-dystrobrevin null muscleThe effect of 6-thioguanine on alternative splicing and antisense-mediated exon skipping treatment for duchenne muscular dystrophyTreatment with a nitric oxide-donating NSAID alleviates functional muscle ischemia in the mouse model of Duchenne muscular dystrophyDeregulated protein kinase A signaling and myospryn expression in muscular dystrophyInduction of dystrophin Dp71 expression during neuronal differentiation: opposite roles of Sp1 and AP2alpha in Dp71 promoter activityExpression of utrophin A mRNA correlates with the oxidative capacity of skeletal muscle fiber types and is regulated by calcineurin/NFAT signaling
P2860
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P2860
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
description
2002 nî lūn-bûn
@nan
2002 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@ast
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@en
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@nl
type
label
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@ast
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@en
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@nl
prefLabel
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@ast
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@en
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@nl
P2093
P1476
Function and genetics of dystrophin and dystrophin-related proteins in muscle.
@en
P2093
Andrew Weir
Derek J Blake
Kay E Davies
Sarah E Newey
P304
P356
10.1152/PHYSREV.00028.2001
P577
2002-04-01T00:00:00Z