| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1126/SCIENCE.270.5237.755 |
| P698 | PubMed publication ID | 7481760 |
| P2093 | author name string | Worton R | |
| P433 | issue | 5237 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 755-756 | |
| P577 | publication date | 1995-11-01 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Muscular dystrophies: diseases of the dystrophin-glycoprotein complex | |
| P478 | volume | 270 |
| Q35434715 | A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families |
| Q24517965 | A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies |
| Q28281749 | A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B |
| Q28477344 | A high throughput screen identifies chemical modulators of the laminin-induced clustering of dystroglycan and aquaporin-4 in primary astrocytes |
| Q36237662 | A new model for the interaction of dystrophin with F-actin |
| Q71668561 | Adhalin (alpha-sarcoglycan) is not required for anchoring of nitric oxide synthase I (NOS I) to the sarcolemma in non-mammalian skeletal (striated) muscle fibers |
| Q24321436 | Agrin binds to the nerve-muscle basal lamina via laminin |
| Q24317041 | Agrin is a high-affinity binding protein of dystroglycan in non-muscle tissue |
| Q28574863 | Alternative splicing of agrin regulates its binding to heparin alpha-dystroglycan, and the cell surface |
| Q24320265 | An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy |
| Q24311859 | Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene |
| Q93384433 | Cardiac MRI biomarkers for Duchenne muscular dystrophy |
| Q28114838 | Characterization of DRP2, a novel human dystrophin homologue |
| Q74545362 | Comparative analysis of PCR-deletion detection and immunohistochemistry in Brazilian Duchenne and Becker muscular dystrophy patients |
| Q28298796 | Distinct alpha 7A beta 1 and alpha 7B beta 1 integrin expression patterns during mouse development: alpha 7A is restricted to skeletal muscle but alpha 7B is expressed in striated muscle, vasculature, and nervous system |
| Q36294055 | Distinct regions in the 3' untranslated region are responsible for targeting and stabilizing utrophin transcripts in skeletal muscle cells |
| Q51757419 | Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach. |
| Q33840935 | Dystrophin and utrophin: genetic analyses of their role in skeletal muscle |
| Q41160185 | Dystrophin-associated proteins and the muscular dystrophies: a glossary |
| Q82296972 | Early detection of cardiomyopathy in Duchenne muscular dystrophy, is there a role for MRI? |
| Q35813381 | Effects of aging, exercise, and disease on force transfer in skeletal muscle |
| Q36642389 | Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle |
| Q28344242 | Expression of agrin, dystroglycan, and utrophin in normal renal tissue and in experimental glomerulopathies |
| Q39728926 | Expression of the utrophin gene during myogenic differentiation |
| Q35763916 | Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle |
| Q41625113 | Gene therapy of Duchenne muscular dystrophy. |
| Q37370555 | Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells. |
| Q47950276 | Genetic modelling of muscular dystrophies |
| Q44062960 | Improvement of dy/dy dystrophic diaphragm by 3,4-diaminopyridine |
| Q36155766 | In situ molecular association of dystrophin with actin revealed by sensitized emission immuno-resonance energy transfer |
| Q35069765 | Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein |
| Q42439794 | Laminin-alpha2 but not -alpha1-mediated adhesion of human (Duchenne) and murine (mdx) dystrophic myotubes is seriously defective. |
| Q44927815 | Laminin-induced aggregation of the inwardly rectifying potassium channel, Kir4.1, and the water-permeable channel, AQP4, via a dystroglycan-containing complex in astrocytes |
| Q36254531 | Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering. |
| Q34071975 | Laminins and human disease |
| Q52606781 | Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats. |
| Q33701932 | Making sense of the limb-girdle muscular dystrophies |
| Q28238601 | Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain |
| Q58830814 | Modulation of Splicing in theDMDGene by Antisense Oligoribonucleotides |
| Q41735698 | Molecular basis of genetic heterogeneity: role of the clinical neurologist |
| Q77131893 | Molecular mechanisms and putative signalling events controlling utrophin expression in mammalian skeletal muscle fibres |
| Q34470065 | Multiple regulatory events controlling the expression and localization of utrophin in skeletal muscle fibers: insights into a therapeutic strategy for Duchenne muscular dystrophy |
| Q33599802 | Muscle as a collagen fiber reinforced composite: a review of force transmission in muscle and whole limb |
| Q50525829 | Muscle fibers of mdx mice are more vulnerable to exercise than those of normal mice. |
| Q64068599 | Mutation-Based Therapeutic Strategies for Duchenne Muscular Dystrophy: From Genetic Diagnosis to Therapy |
| Q77601951 | PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness |
| Q92421314 | Pericytes in Muscular Dystrophies |
| Q41456452 | Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse |
| Q29040531 | Presence of Laminin 5 Chain and Lack of Laminin 1 Chain during Human Muscle Development and in Muscular Dystrophies |
| Q41857185 | Purification of native p94, a muscle-specific calpain, and characterization of its autolysis |
| Q47360059 | Regenerative capacity of the dystrophic (mdx) diaphragm after induced injury |
| Q33887124 | Regulation and functional significance of utrophin expression at the mammalian neuromuscular synapse |
| Q37354969 | Role of aquaporin-4 in cerebral edema and stroke |
| Q42101673 | Simultaneous dystrophin and dysferlin deficiencies associated with high-level expression of the coxsackie and adenovirus receptor in transgenic mice |
| Q46303843 | Sparing of mdx extraocular muscles from dystrophic pathology is not attributable to normalized concentration or distribution of neuronal nitric oxide synthase |
| Q43783192 | Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vector |
| Q28296180 | Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy |
| Q35882763 | Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein. |
| Q24555081 | Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein |
| Q61828712 | Tenascin-C expression correlates with macrophage invasion in Duchenne muscular dystrophy and in myositis |
| Q48789968 | The dystrophy of Duchenne |
| Q33904974 | The emergence of modern neuroscience: some implications for neurology and psychiatry |
| Q74418249 | The expression of dystrophin and alpha1-syntrophin during skeletal muscle regeneration |
| Q41363131 | The functions of laminins: lessons from in vivo studies |
| Q41681470 | The membrane-cytoskeleton interface: the role of dystrophin and utrophin |
| Q41738877 | The molecular basis of activity-induced muscle injury in Duchenne muscular dystrophy |
| Q34284711 | The molecular basis of water transport in the brain |
| Q34807150 | The role of utrophin in the potential therapy of Duchenne muscular dystrophy |
| Q24678868 | The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12 |
| Q48634703 | Tissue-specific heterogeneity in alpha-dystroglycan sialoglycosylation. Skeletal muscle alpha-dystroglycan is a latent receptor for Vicia villosa agglutinin b4 masked by sialic acid modification |
| Q45281544 | Utrophin is lacking at the neuromuscular junctions in the extraocular muscles of normal cat: artefact or true? |
| Q41160197 | Utrophin: a structural and functional comparison to dystrophin |
| Q39456232 | WHOLE-BODY VIBRATION EXERCISE IS WELL TOLERATED IN PATIENTS WITH DUCHENNE MUSCULAR DYSTROPHY: A SYSTEMATIC REVIEW. |
| Q36256527 | alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability. |
| Q40831877 | alpha-dystroglycan isoforms are differentially distributed in adult rat retina |
Search more.