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Reduced expression of dystroglycan in breast and prostate cancer
HUMAN PATHOLOGY
Intramembrane charge movements and excitation-contraction coupling expressed by two-domain fragments of the Ca2+ channel
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Differences in affinity of binding of lymphocytic choriomeningitis virus strains to the cellular receptor alpha-dystroglycan correlate with viral tropism and disease kinetics
JOURNAL OF VIROLOGY
Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex
JOURNAL OF CLINICAL INVESTIGATION
Distinct roles for dystroglycan, beta 1 integrin and perlecan in cell surface laminin organization
JOURNAL OF CELL SCIENCE
Molecular analysis of the interaction of LCMV with its cellular receptor alpha-dystroglycan
JOURNAL OF CELL BIOLOGY
Biochemical and biophysical evidence for gamma(2) subunit association withneuronal voltage-activated Ca2+ channels
JOURNAL OF BIOLOGICAL CHEMISTRY
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity oflimb-girdle muscular dystrophy type 2E
MOLECULAR CELL
Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice
GENE THERAPY
Animal models for muscular dystrophy: valuable tools for the development of therapies
HUMAN MOLECULAR GENETICS
Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions
HUMAN MOLECULAR GENETICS
Nomenclature of voltage-gated calcium channels
NEURON
Maturation and maintenance of the neuromuscular synapse: Genetic evidence for roles of the dystrophin-glycoprotein complex
NEURON
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
Congenital muscular dystrophy with rigid spine syndrome: A clinical, pathological, radiological, and genetic study
ANNALS OF NEUROLOGY
Sarcospan-deficient mice maintain normal muscle function
MOLECULAR AND CELLULAR BIOLOGY
Molecular basis of muscular dystrophies
MUSCLE & NERVE
Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle
JOURNAL OF NEUROCHEMISTRY
Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells
JOURNAL OF EXPERIMENTAL MEDICINE
Assembly of the dystrophin-associated protein complex does not require thedystrophin COOH-terminal domain
JOURNAL OF CELL BIOLOGY
Expression of gamma-sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex
JOURNAL OF BIOLOGICAL CHEMISTRY
Biosynthesis of dystroglycan: processing of a precursor propeptide
FEBS LETTERS
Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction
DEVELOPMENTAL BIOLOGY
Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy
NATURE MEDICINE
beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain
MOLECULAR AND CELLULAR NEUROSCIENCE
Dystroglycan inside and out
CURRENT OPINION IN CELL BIOLOGY
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle:A novel mechanism for cardiomyopathy and muscular dystrophy
CELL
Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors
JOURNAL OF VIROLOGY
Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction
JOURNAL OF CELL SCIENCE
Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction (vol 112, pg 209, 1999)
JOURNAL OF CELL SCIENCE
Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex
JOURNAL OF CELL BIOLOGY
epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex
JOURNAL OF BIOLOGICAL CHEMISTRY
Biochemical characterization of the epithelial dystroglycan complex
JOURNAL OF BIOLOGICAL CHEMISTRY
THE SARCOGLYCAN COMPLEX IN LIMB-GIRDLE MUSCULAR-DYSTROPHY
Current opinion in neurology
FUNCTIONAL RESCUE OF THE SARCOGLYCAN COMPLEX IN THE BIO-14.6 HAMSTER USING DELTA-SARCOGLYCAN GENE-TRANSFER
MOLECULAR CELL
THE MOUSE STARGAZER GENE ENCODES A NEURONAL CA2-CHANNEL GAMMA-SUBUNIT()
Nature genetics
A ROLE FOR DYSTROGLYCAN IN THE FORMATION OF BASEMENT-MEMBRANES
Molecular biology of the cell
MDX MUSCLE PATHOLOGY IS INDEPENDENT OF NNOS PERTURBATION
Human molecular genetics
BETA-SARCOGLYCAN - GENOMIC ANALYSIS AND IDENTIFICATION OF A NOVEL MISSENSE MUTATION IN THE LGMD2E AMISH ISOLATE
Neuromuscular disorders
DYSTROGLYCAN IN DEVELOPMENT AND DISEASE
Current opinion in cell biology
EVIDENCE FOR A 95 KDA SHORT-FORM OF THE ALPHA(1A) SUBUNIT ASSOCIATED WITH THE OMEGA-CONOTOXIN MVIIC RECEPTOR OF THE P Q-TYPE CA2+ CHANNELS/
The Journal of neuroscience
A novel form of familial congenital muscular dystrophy in two adolescents
NEUROPEDIATRICS
A role for dystroglycan in basement membrane assembly
CELL
Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae
SCIENCE
Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and lassa fever virus
SCIENCE
Characterisation of antibody models of the ryanodine receptor for use in high-throughput screening
PESTICIDE SCIENCE
LATE-ONSET MEROSIN DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY
Neurology
EVANS BLUE UPTAKE DEMONSTRATES SARCOLEMMAL DISRUPTION IN THE MYODYSTROPHY MOUSE
Neurology
A NEURONAL RYANODINE RECEPTOR MEDIATES LIGHT-INDUCED PHASE DELAYS OF THE CIRCADIAN CLOCK
Nature
DISTRIBUTION OF DYSTROGLYCAN IN NORMAL ADULT-MOUSE TISSUES
The Journal of histochemistry and cytochemistry
PROGRESSIVE MUSCULAR-DYSTROPHY IN ALPHA-SARCOGLYCAN-DEFICIENT MICE
The Journal of cell biology
A BETA(4) ISOFORM-SPECIFIC INTERACTION SITE IN THE CARBOXYL-TERMINAL REGION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(1A) SUBUNIT
The Journal of biological chemistry
Assembly of the sarcoglycan complex - Insights for muscular dystrophy
JOURNAL OF BIOLOGICAL CHEMISTRY
CAVEOLIN-3 IS NOT AN INTEGRAL COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX
FEBS letters
MOLECULAR PATHOGENESIS OF MUSCLE DEGENERATION IN THE DELTA-SARCOGLYCAN-DEFICIENT HAMSTER
The American journal of pathology
MUSCULAR-DYSTROPHIES AND THE DYSTROPHIN-GLYCOPROTEIN COMPLEX
Current opinion in neurology
DYSTROGLYCAN IS ESSENTIAL FOR EARLY EMBRYONIC-DEVELOPMENT - DISRUPTION OF REICHERTS-MEMBRANE IN DAG1-NULL MICE
Human molecular genetics
MILD CONGENITAL MUSCULAR-DYSTROPHY IN 2 PATIENTS WITH AN INTERNALLY DELETED LAMININ ALPHA-2-CHAIN
Human molecular genetics
MOLECULAR PATHOGENESIS OF MUSCULAR-DYSTROPHY
The FASEB journal
DYSTROPHIN AND NNOS DOUBLE KNOCKOUT MICE MAINTAIN DYSTROPHIC PHENOTYPE
The FASEB journal
HOT PAPERS - GENETICS - BETA-SARCOGLYCAN - CHARACTERIZATION AND ROLE IN LIMB-GIRDLE MUSCULAR-DYSTROPHY LINKED TO 4Q12 BY LIM,L.E., DUCLOS,F., BROUX,O., BOURG,N., SUNADA,Y., ALLAMAND,V., MEYER,J., RICHARD,I., MOOMAW,C., SLAUGHTER,C., TOME,F.M.S., FARDEAU,M., JACKSON,C.E., BECKMANN,J.S., CAMPBELL,K.P. - COMMENTS
The Scientist
A BIOCHEMICAL, GENETIC, AND CLINICAL SURVEY OF AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES IN TURKEY
Annals of neurology
DISSECTION OF FUNCTIONAL DOMAINS OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA SUBUNIT
The Journal of neuroscience
PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY
Neurology
IMMUNOHISTOCHEMICAL ANALYSIS OF MYODYSTROPHY MOUSE MUSCLE
Neurology
DIRECT BINDING OF G-PROTEIN BETA-GAMMA COMPLEX TO VOLTAGE-DEPENDENT CALCIUM CHANNELS
Nature
A 5'-DYSTROPHIN DUPLICATION MUTATION CAUSES MEMBRANE DEFICIENCY OF ALPHA-DYSTROGLYCAN IN A FAMILY WITH X-LINKED CARDIOMYOPATHY
Journal of Molecular and Cellular Cardiology
MUTATIONAL DIVERSITY AND HOT-SPOTS IN THE ALPHA-SARCOGLYCAN GENE IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY (LGMD2D)
Journal of Medical Genetics
SUBUNIT STOICHIOMETRY OF HUMAN MUSCLE CHLORIDE CHANNELS
The Journal of general physiology
ANIMAL-MODELS FOR MUSCULAR-DYSTROPHY SHOW DIFFERENT PATTERNS OF SARCOLEMMAL DISRUPTION
The Journal of cell biology
SARCOSPAN, THE 25-KDA TRANSMEMBRANE COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX
The Journal of biological chemistry
EXTRACELLULAR INTERACTION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA AND ALPHA(1) SUBUNITS
The Journal of biological chemistry
A ROLE OF DYSTROGLYCAN IN SCHWANNOMA CELL-ADHESION TO LAMININ
The Journal of biological chemistry
TRANSIENT EXPRESSION OF DP140, A PRODUCT OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS, DURING KIDNEY TUBULOGENESIS
Developmental biology
DIRECT INTERACTION BETWEEN VOLTAGE-DEPENDENT CA2-PROTEIN BETA-GAMMA COMPLEX( CHANNELS AND G)
Biophysical journal
CHARACTERIZATION OF INTERACTION DOMAINS BETWEEN THE VOLTAGE-DEPENDENTCALCIUM-CHANNEL ALPHA(2)DELTA AND ALPHA(1) SUBUNITS
Biophysical journal
SARCOSPAN - A NOVEL 25KDA COMPONENT OF THE DYSTROPHIN-GLYCOPROTEIN COMPLEX MAPS TO HUMAN-CHROMOSOME 12P11.2
American journal of human genetics
FUNCTIONAL RESTORATION OF THE SARCOGLYCAN AND DYSTROGLYCAN COMPLEXES IN THE CARDIOMYOPATHIC HAMSTER
American journal of human genetics
ANIMAL-MODELS FOR MUSCULAR-DYSTROPHY SHOW DIFFERENT PATTERNS OF SARCOLEMMAL DISRUPTION
Molecular biology of the cell
IN-VIVO MUSCLE GENE-TRANSFER OF FULL-LENGTH DYSTROPHIN WITH AN ADENOVIRAL VECTOR THAT LACKS ALL VIRAL GENES
Gene therapy
A FOUNDER MUTATION IN THE GAMMA-SARCOGLYCAN GENE OF GYPSIES POSSIBLY PREDATING THEIR MIGRATION OUT OF INDIA
Human molecular genetics
IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES
Neuromuscular disorders
FROM ADHALINOPATHIES TO ALPHA-SARCOGLYCANOPATHIES - AN OVERVIEW
Neuromuscular disorders
DYSTROGLYCAN - AN EXTRACELLULAR-MATRIX RECEPTOR-LINKED TO THE CYTOSKELETON
Current opinion in cell biology
DYSTROGLYCAN IN THE CEREBELLUM IS A LAMININ ALPHA-2-CHAIN BINDING-PROTEIN AT THE GLIAL-VASCULAR INTERFACE AND IS EXPRESSED IN PURKINJE-CELLS
European journal of neuroscience
DUAL FUNCTION OF THE VOLTAGE-DEPENDENT CA2+ CHANNEL ALPHA(2)DELTA SUBUNIT IN CURRENT STIMULATION AND SUBUNIT INTERACTION
Neuron
MUSCULAR-DYSTROPHY ASSOCIATED WITH BETA-DYSTROGLYCAN DEFICIENCY
Annals of neurology
CLINICAL HETEROGENEITY OF ADHALIN DEFICIENCY
Annals of neurology
ULTRASTRUCTURAL-LOCALIZATION OF ADHALIN, ALPHA-DYSTROGLYCAN AND MEROSIN IN NORMAL AND DYSTROPHIC MUSCLE
Neuropathology and applied neurobiology
EXPRESSION AND SUBUNIT INTERACTION OF VOLTAGE-DEPENDENT CA2+ CHANNELSIN PC12 CELLS
The Journal of neuroscience
LETHAL CONGENITAL MUSCULAR-DYSTROPHY IN 2 SIBS WITH ARTHROGRYPOSIS MULTIPLEX - NEW ENTITY OR VARIANT OF COBBLESTONE LISSENCEPHALY SYNDROME
Neuropediatrics
NEUROSENSORY HEARING-LOSS IN SECONDARY ADHALINOPATHY
Neuropediatrics
CHARACTERIZATION OF DYSTROGLYCAN-LAMININ INTERACTION IN PERIPHERAL-NERVE
Journal of muscle research and cell motility
IMMUNOGOLD LOCALIZATION OF ADHALIN AND ALPHA-DYSTROGLYCAN IN NORMAL AND DYSTROPHIC SKELETAL-MUSCLE
Journal of muscle research and cell motility
BRIEF REPORT - DEFICIENCY OF A DYSTROPHIN-ASSOCIATED GLYCOPROTEIN (ADHALIN) IN A PATIENT WITH MUSCULAR-DYSTROPHY AND CARDIOMYOPATHY
The New England journal of medicine
CLINICAL PHENOTYPES IN ADHALIN DEFICIENCY
Neurology
ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS
Neurology
MUSCULAR-DYSTROPHY - UTROPHIN TO THE RESCUE
Nature
CHARACTERIZATION OF DYSTROGLYCAN - LAMININ INTERACTION IN PERIPHERAL-NERVE
Journal of neurochemistry