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Proteomic analysis of a developmentally regulated secretory vesicle
PROTEOMICS
Dystrophin and muscular dystrophy: Past, present, and future
MOLECULAR GENETICS AND METABOLISM
Cellular and molecular properties of alpha-dystrobrevin in skeletal muscle
FRONTIERS IN BIOSCIENCE
Regulation of laminin 1-induced pancreatic beta-cell differentiation by alpha(6) integrin and alpha-dystroglycan
MOLECULAR MEDICINE
Risks and benefits of glycoprotein IIb/IIIa antagonists in acute coronary syndrome
ANNALS OF PHARMACOTHERAPY
Role of nitric oxide in the pathogenesis of muscular dystrophies: A "two hit" hypothesis, of the cause of muscle necrosis
MICROSCOPY RESEARCH AND TECHNIQUE
Localization of sarcoglycan, neuronal nitric oxide synthase, beta-dystroglycan, and dystrophin molecules in normal skeletal myofiber: Triple immunogold labeling electron microscopy
MICROSCOPY RESEARCH AND TECHNIQUE
Association of neuronal nitric oxide synthase (nNOS) with alpha 1-syntrophin at the sarcolemma
MICROSCOPY RESEARCH AND TECHNIQUE
Just in time and place: NOS/NO system assembly in neuromuscular junction formation
MICROSCOPY RESEARCH AND TECHNIQUE
Apical transport of osteopontin is independent of N-glycosylation and sialylation
MOLECULAR MEMBRANE BIOLOGY
The complexities of dystroglycan
TRENDS IN BIOCHEMICAL SCIENCES
Processing of beta-dystroglycan by matrix metalloproteinase disrupts the link between the extracellular matrix and cell membrane via the dystroglycancomplex
HUMAN MOLECULAR GENETICS
Non-toxic ubiquitous over-expression of utrophin in the mdx mouse
NEUROMUSCULAR DISORDERS
Identification of altered gene expression in skeletal muscles from Duchenne muscular dystrophy patients
NEUROMUSCULAR DISORDERS
Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice
NEUROMUSCULAR DISORDERS
Cationic channels in normal and dystrophic human myotubes
NEUROMUSCULAR DISORDERS
Differential targeting of components of the dystrophin complex to the postsynaptic membrane
EUROPEAN JOURNAL OF NEUROSCIENCE
Muc4/sialomucin complex, an intramembrane modulator of ErbB2/HER2/Neu, potentiates primary tumor growth and suppresses apoptosis in a xenotransplanted tumor
ONCOGENE
Most apoptotic cells in mdx diaphragm muscle contain accumulated lipofuscin
HISTOCHEMISTRY AND CELL BIOLOGY
Specific disruption of a Schwann cell dystrophin-related protein complex in a demyelinating neuropathy
NEURON
GP120: Biologic aspects of structural features
ANNUAL REVIEW OF IMMUNOLOGY
The PlA1/A2 polymorphism of platelet glycoprotein IIIa is not associated with deep venous thrombosis
INTERNATIONAL ANGIOLOGY
The dystrophin/utrophin homologues in Drosophila and in sea urchin
GENE
Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations
ANNALS OF NEUROLOGY
Increased expression of utrophin in a slow vs. a fast muscle involves posttranscriptional events
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Stretch-activated cation channels in skeletal muscle myotubes from sarcoglycan-deficient hamsters
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
CD63 associates with the alpha(IIb)beta(3) integrin-CD9 complex on the surface of activated platelets
THROMBOSIS AND HAEMOSTASIS
Characteristics of rodent intestinal mucin Muc3 and alterations in a mousemodel of human cystic fibrosis
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY
Isolation of a mouse brain cDNA expressed in developing neuroblasts and mature neurons
MOLECULAR BRAIN RESEARCH
Coordinated Muc2 and Muc3 mucin gene expression in Trichinella spiralis infection in wild-type and cytokine-deficient mice
DIGESTIVE DISEASES AND SCIENCES
Confocal analysis of the dystrophin protein complex in muscular dystrophy
MUSCLE & NERVE
Dynamic restoration of dystrophin to dystrophin deficient myotubes
MUSCLE & NERVE
Production and localization of Muc4/sialomucin complex and its receptor tyrosine kinase ErbB2 in the rat lacrimal gland
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
The expression of dystrophin and alpha 1-syntrophin during skeletal muscleregeneration
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY
Urine excretion of protein HC in proteinuric glomerular diseases correlates to urine IgG but not to albuminuria
KIDNEY INTERNATIONAL
Expression and localization of immunoreactive-sialomucin complex (Muc4) insalivary glands
TISSUE & CELL
Stretch-induced cell damage in sarcoglycan-deficient myotubes
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Angiographic evaluation of middle cerebral artery reperfusion caused by platelet glycoprotein IIb/IIIa receptor complex antagonist murine 7E3 F(ab ')(2) in a model of focal cerebral ischemia in rats
JOURNAL OF NEUROSURGERY
Dystroglycan contributes to the formation of multiple dystrophin-like complexes in brain
JOURNAL OF NEUROCHEMISTRY
Molecular, genetic and physiological characterisation of dystrobrevin-like(dyb-1) mutants of Caenorhabditis elegans
JOURNAL OF MOLECULAR BIOLOGY
Ischemic loss of sarcolemmal dystrophin and spectrin: Correlation with myocardial injury
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
Distribution of iodine 125-labeled alpha(1)-microglobulin in rats after intravenous injection
JOURNAL OF LABORATORY AND CLINICAL MEDICINE
Variations in dystrophin complex in red and white caudal muscles from Torpedo marmorata
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
delta- and gamma-sarcoglycan localization in the sarcoplasmic reticulum ofskeletal muscle
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY
Varicella-zoster virus gH : gL contains a structure reactive with the anti-human gamma chain of IgG near the glycosylation site
JOURNAL OF GENERAL VIROLOGY
Human immunodeficiency virus 1 envelope glycoprotein complex-induced apoptosis involves mammalian target. of rapamycin/FKBP12-rapamycin-associated protein-mediated p53 phosphorylation
JOURNAL OF EXPERIMENTAL MEDICINE
Sialomucin complex (rat Muc4) transmembrane subunit binds the differentiation marker peanut lectin in the normal rat mammary gland
JOURNAL OF CELLULAR PHYSIOLOGY
Molecular analysis of the interaction of LCMV with its cellular receptor alpha-dystroglycan
JOURNAL OF CELL BIOLOGY
Distinct regions in the 3 ' untranslated region are responsible for targeting and stabilizing utrophin transcripts in skeletal muscle cells
JOURNAL OF CELL BIOLOGY
A stoichiometric complex of neurexins and dystroglycan in brain
JOURNAL OF CELL BIOLOGY
Agrin-induced phosphorylation of the acetylcholine receptor regulates cytoskeletal anchoring and clustering
JOURNAL OF CELL BIOLOGY
Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle
JOURNAL OF BIOLOGICAL CHEMISTRY
Differential Vicia villosa agglutinin reactivity identifies three distinctdystroglycan complexes in skeletal
JOURNAL OF BIOLOGICAL CHEMISTRY
Interactions of the rapsyn RING-H2 domain with dystroglycan
JOURNAL OF BIOLOGICAL CHEMISTRY
The GPIIIa (beta(3) integrin) P1(A) polymorphism in the early development of coronary atherosclerosis
ATHEROSCLEROSIS
Dystrophin-associated proteins in obliquely striated muscle of the leech Pontobdella muricata (Annelida, hirudinea)
HISTOCHEMICAL JOURNAL
Multiple receptors mediate apoJ-dependent clearance of cellular debris into nonprofessional phagocytes
EXPERIMENTAL CELL RESEARCH
Protein targeting to the plasma membrane of adult skeletal muscle fiber: An organized mosaic of functional domains
EXPERIMENTAL CELL RESEARCH
Identification of myogenesis-dependent transcriptional enhancers in promoter region of mouse gamma-sarcoglycan gene
EUROPEAN JOURNAL OF BIOCHEMISTRY
Identification of the beta-dystroglycan binding epitope within the C-terminal region of alpha-dystroglycan
EUROPEAN JOURNAL OF BIOCHEMISTRY
gamma-sarcoglycanopathy in two Palestinian-American siblings
CLINICAL PEDIATRICS
Dystrophin-deficient myocardium is vulnerable to pressure overload in vivo
CARDIOVASCULAR RESEARCH
Effect of glycosylation on structure and dynamics of MHC class I glycoprotein: A molecular dynamics study
BIOPOLYMERS
Mouse alpha 1-syntrophin binding to Grb2: Further evidence of a role for syntrophin in cell signaling
BIOCHEMISTRY
Dystrophin in adult zebrafish muscle
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Expression of dystroglycan complex in satellite cells of dorsal root ganglia
ACTA NEUROPATHOLOGICA
Limb-girdle muscular dystrophy: one gene with different phenotypes, one phenotype with different genes
CURRENT OPINION IN NEUROLOGY
The cellulose-binding activity of the PsB multiprotein complex is requiredfor proper assembly of the spore coat and spore viability in Dictyosteliumdiscoideum
MICROBIOLOGY-UK
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity oflimb-girdle muscular dystrophy type 2E
MOLECULAR CELL
Clinical and histopathological study of merosin-deficient and merosin-positive congenital muscular dystrophy
PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
Coagulation tests and anti-phospholipid antibodies in patients positive for lupus anticoagulant
CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
The Torpedo electrocyte: A model system to study membrane-cytoskeleton interactions at the postsynaptic membrane
MICROSCOPY RESEARCH AND TECHNIQUE
Plasma membrane cytoskeleton of muscle: A fine structural analysis
MICROSCOPY RESEARCH AND TECHNIQUE
Dystrophin and utrophin: Genetic analyses of their role in skeletal muscle
MICROSCOPY RESEARCH AND TECHNIQUE
Sarcoglycans in muscular dystrophy
MICROSCOPY RESEARCH AND TECHNIQUE
Eye muscle sparing by the muscular dystrophies: Lessons to be learned?
MICROSCOPY RESEARCH AND TECHNIQUE
Developments in gene therapy for muscular dystrophy
MICROSCOPY RESEARCH AND TECHNIQUE
Syntrophin isoforms at the neuromuscular junction: Developmental time course and differential localization
MOLECULAR AND CELLULAR NEUROSCIENCE
Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice
GENE THERAPY
The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy
STRUCTURE WITH FOLDING & DESIGN
Dystrophin and utrophin influence fiber type composition and post-synapticmembrane structure
HUMAN MOLECULAR GENETICS
Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy
HUMAN MOLECULAR GENETICS
A sarcoglycan-dystroglycan complex anchors Dp116 and utrophin in the peripheral nervous system
HUMAN MOLECULAR GENETICS
Animal models for muscular dystrophy: valuable tools for the development of therapies
HUMAN MOLECULAR GENETICS
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy
HUMAN MOLECULAR GENETICS
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions
HUMAN MOLECULAR GENETICS
Crossing the finish line of development: regulated secretion of Dictyostelium proteins
TRENDS IN CELL BIOLOGY
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
NEUROMUSCULAR DISORDERS
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F
NEUROMUSCULAR DISORDERS
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain
NEUROMUSCULAR DISORDERS
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
NEUROMUSCULAR DISORDERS
Integrin and dystrophin associated adhesion protein complexes during regeneration of shearing-type muscle injury
NEUROMUSCULAR DISORDERS
Carbohydrate groups of alpha(1)-microglobulin are important for secretion and tissue localization but not for immunological properties
GLYCOBIOLOGY
Extracellular regulated kinase (ERK)-dependent regulation of sialomucin complex/rat Muc4 in mammary epithelial cells
ONCOGENE
A practical approach to the diagnosis and management of thrombocytopenia associated with glycoprotein IIb/IIIa receptor inhibitors
JOURNAL OF THROMBOSIS AND THROMBOLYSIS
Antiplatelet medications and their indications in preventing and treating coronary thrombosis
ANNALS OF MEDICINE
Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy
MAGNETIC RESONANCE IN MEDICINE
Intracellular accumulation and reduced sarcolemmal expression of dysferlinin limb-girdle muscular dystrophies
ANNALS OF NEUROLOGY
150-kDa oxygen-regulated protein (ORP150) functions as a novel molecular chaperone in MDCK cells
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Altered membrane proteins and permeability correlate with cardiac dysfunction in cardiomyopathic hamsters
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY