Evidence for the presence of calsequestrin in both peripheral and interior regions of sheep Purkinje fibers.

PubWeight™: 0.85‹?›

🔗 View Article (PMID 6378421)

Published in Circ Res on August 01, 1984

Authors

A O Jorgensen, A G McLeod, K P Campbell, G H Denney

Articles by these authors

Membrane organization of the dystrophin-glycoprotein complex. Cell (1991) 6.64

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature (1992) 6.37

Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle. J Cell Biol (1988) 6.30

Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus. Science (1998) 5.83

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol (1993) 5.73

Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum. J Gen Physiol (1988) 4.56

Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit. Nature (1994) 4.34

The naming of voltage-gated calcium channels. Neuron (1994) 4.31

Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature (1990) 4.23

Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells. J Exp Med (2000) 3.50

Sequence and expression of mRNAs encoding the alpha 1 and alpha 2 subunits of a DHP-sensitive calcium channel. Science (1988) 3.38

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J Cell Biol (1997) 3.32

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit. Nat Genet (1998) 3.31

Structure and development of E-C coupling units in skeletal muscle. Annu Rev Physiol (1994) 3.28

Purified ryanodine receptor from skeletal muscle sarcoplasmic reticulum is the Ca2+-permeable pore of the calcium release channel. J Biol Chem (1987) 3.25

Nomenclature of voltage-gated calcium channels. Neuron (2000) 3.09

Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle. Nature (1992) 2.76

G-protein-mediated Ca2+ sensitization of smooth muscle contraction through myosin light chain phosphorylation. J Biol Chem (1991) 2.69

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. Hum Mol Genet (1997) 2.69

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice. J Cell Biol (1991) 2.68

Molecular basis of muscular dystrophies. Muscle Nerve (2000) 2.65

Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature (1993) 2.63

Direct binding of G-protein betagamma complex to voltage-dependent calcium channels. Nature (1997) 2.60

Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell (1999) 2.57

Ryanodine receptor of skeletal muscle is a gap junction-type channel. Science (1988) 2.56

Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy. Nat Med (1999) 2.50

The ryanodine receptor/Ca2+ release channel. J Biol Chem (1993) 2.50

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice. J Cell Biol (1998) 2.44

Staining of the Ca2+-binding proteins, calsequestrin, calmodulin, troponin C, and S-100, with the cationic carbocyanine dye "Stains-all". J Biol Chem (1983) 2.40

A role for dystroglycan in basement membrane assembly. Cell (1998) 2.36

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy. Lancet (1993) 2.33

Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle. Neuron (1991) 2.30

Congenital muscular dystrophy with merosin deficiency. C R Acad Sci III (1994) 2.22

The Ca2+-release channel/ryanodine receptor is localized in junctional and corbular sarcoplasmic reticulum in cardiac muscle. J Cell Biol (1993) 2.18

Localization of the neurofilament protein in neuroblastoma cells by immunofluorescent staining. Proc Natl Acad Sci U S A (1976) 2.17

Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol (1997) 2.13

Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. J Cell Biol (1991) 2.10

Purification, primary structure, and immunological characterization of the 26-kDa calsequestrin binding protein (junctin) from cardiac junctional sarcoplasmic reticulum. J Biol Chem (1995) 2.08

The brain ryanodine receptor: a caffeine-sensitive calcium release channel. Neuron (1991) 2.05

Isolation, characterization, and localization of the inositol 1,4,5-trisphosphate receptor protein in Xenopus laevis oocytes. J Biol Chem (1992) 2.05

Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction. Neuron (1996) 2.04

Induction of calcium currents by the expression of the alpha 1-subunit of the dihydropyridine receptor from skeletal muscle. Nature (1989) 2.04

Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex. Neuron (2000) 2.04

Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan. J Cell Biol (2001) 2.03

Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae. Science (1998) 2.02

The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel. Trends Neurosci (1988) 1.98

Further characterization of light and heavy sarcoplasmic reticulum vesicles. Identification of the 'sarcoplasmic reticulum feet' associated with heavy sarcoplasmic reticulum vesicles. Biochim Biophys Acta (1980) 1.96

Ca2+ channel regulation by a conserved beta subunit domain. Neuron (1994) 1.92

Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. J Cell Biol (2000) 1.92

Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulum. J Biol Chem (1995) 1.86

Differences in affinity of binding of lymphocytic choriomeningitis virus strains to the cellular receptor alpha-dystroglycan correlate with viral tropism and disease kinetics. J Virol (2001) 1.85

Subcellular fractionation of dystrophin to the triads of skeletal muscle. Nature (1988) 1.81

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering. Cell (1994) 1.80

Identification and characterization of the high affinity [3H]ryanodine receptor of the junctional sarcoplasmic reticulum Ca2+ release channel. J Biol Chem (1987) 1.80

Forced expression of dystrophin deletion constructs reveals structure-function correlations. J Cell Biol (1996) 1.79

Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Muscle Nerve (1994) 1.78

Distribution of dystroglycan in normal adult mouse tissues. J Histochem Cytochem (1998) 1.77

Differential immunohistochemical localization of inositol 1,4,5-trisphosphate- and ryanodine-sensitive Ca2+ release channels in rat brain. J Neurosci (1993) 1.76

Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study. Ann Neurol (2000) 1.75

Localization of sarcoplasmic reticulum proteins in rat skeletal muscle by immunofluorescence. J Cell Biol (1979) 1.72

A beta 4 isoform-specific interaction site in the carboxyl-terminal region of the voltage-dependent Ca2+ channel alpha 1A subunit. J Biol Chem (1998) 1.71

Cloning and tissue-specific expression of the brain calcium channel beta-subunit. FEBS Lett (1991) 1.70

Dystroglycan inside and out. Curr Opin Cell Biol (1999) 1.70

Structural characterization of the 1,4-dihydropyridine receptor of the voltage-dependent Ca2+ channel from rabbit skeletal muscle. Evidence for two distinct high molecular weight subunits. J Biol Chem (1987) 1.70

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature (1992) 1.70

Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. Nat Genet (1994) 1.70

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan. J Biol Chem (1995) 1.67

Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E. Mol Cell (2000) 1.66

Subunit regulation of the neuronal alpha 1A Ca2+ channel expressed in Xenopus oocytes. J Physiol (1995) 1.63

Structural characterization of the dihydropyridine-sensitive calcium channel alpha 2-subunit and the associated delta peptides. J Biol Chem (1991) 1.63

Primary structure of the gamma subunit of the DHP-sensitive calcium channel from skeletal muscle. Science (1990) 1.62

SH3 domain-mediated interaction of dystroglycan and Grb2. J Biol Chem (1995) 1.61

Purification and characterization of calsequestrin from canine cardiac sarcoplasmic reticulum and identification of the 53,000 dalton glycoprotein. J Biol Chem (1983) 1.60

Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. J Virol (1999) 1.58

Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. N Engl J Med (1996) 1.57

Subcellular distribution of the 1,4-dihydropyridine receptor in rabbit skeletal muscle in situ: an immunofluorescence and immunocolloidal gold-labeling study. J Cell Biol (1989) 1.57

Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem (1994) 1.56

The effects of ryanodine on passive calcium fluxes across sarcoplasmic reticulum membranes. J Biol Chem (1987) 1.53

Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology (1993) 1.52

Dissection of functional domains of the voltage-dependent Ca2+ channel alpha2delta subunit. J Neurosci (1997) 1.52

Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Hum Mol Genet (1993) 1.50

Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton. Curr Opin Cell Biol (1996) 1.49

Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice. Hum Mol Genet (1995) 1.49

Expression of human full-length and minidystrophin in transgenic mdx mice: implications for gene therapy of Duchenne muscular dystrophy. Hum Mol Genet (1995) 1.49

Attenuated pain responses in mice lacking Ca(V)3.2 T-type channels. Genes Brain Behav (2006) 1.49

Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice. Nat Genet (1994) 1.48

Subunit stoichiometry of human muscle chloride channels. J Gen Physiol (1997) 1.47

Dystrophin and the membrane skeleton. Curr Opin Cell Biol (1993) 1.47

Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis. J Biol Chem (1989) 1.44

Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex. J Clin Invest (2001) 1.41

Purification of dystrophin from skeletal muscle. J Biol Chem (1991) 1.41

Dystroglycan in the cerebellum is a laminin alpha 2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells. Eur J Neurosci (1996) 1.40

Primary structure and topological analysis of a skeletal muscle-specific junctional sarcoplasmic reticulum glycoprotein (triadin). J Biol Chem (1993) 1.39

Distinct roles for dystroglycan, beta1 integrin and perlecan in cell surface laminin organization. J Cell Sci (2001) 1.39

A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock. Nature (1998) 1.39

Biosynthesis of dystroglycan: processing of a precursor propeptide. FEBS Lett (2000) 1.38

In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Ther (1996) 1.37

Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex. Neuron (1995) 1.35