PubRank

K P Campbell

Author PubWeight™ 366.53‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Membrane organization of the dystrophin-glycoprotein complex. Cell 1991 6.64
2 Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. Nature 1992 6.37
3 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
4 Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus. Science 1998 5.83
5 A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin. J Cell Biol 1993 5.73
6 Purified ryanodine receptor from rabbit skeletal muscle is the calcium-release channel of sarcoplasmic reticulum. J Gen Physiol 1988 4.56
7 Calcium channel beta-subunit binds to a conserved motif in the I-II cytoplasmic linker of the alpha 1-subunit. Nature 1994 4.34
8 The naming of voltage-gated calcium channels. Neuron 1994 4.31
9 Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle. Nature 1990 4.23
10 Immunosuppression and resultant viral persistence by specific viral targeting of dendritic cells. J Exp Med 2000 3.50
11 Sequence and expression of mRNAs encoding the alpha 1 and alpha 2 subunits of a DHP-sensitive calcium channel. Science 1988 3.38
12 Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J Cell Biol 1997 3.32
13 The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit. Nat Genet 1998 3.31
14 Purified ryanodine receptor from skeletal muscle sarcoplasmic reticulum is the Ca2+-permeable pore of the calcium release channel. J Biol Chem 1987 3.25
15 Nomenclature of voltage-gated calcium channels. Neuron 2000 3.09
16 Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle. Nature 1992 2.76
17 Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. Hum Mol Genet 1997 2.69
18 Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice. J Cell Biol 1991 2.68
19 Molecular basis of muscular dystrophies. Muscle Nerve 2000 2.65
20 Overexpression of dystrophin in transgenic mdx mice eliminates dystrophic symptoms without toxicity. Nature 1993 2.63
21 Direct binding of G-protein betagamma complex to voltage-dependent calcium channels. Nature 1997 2.60
22 Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell 1999 2.57
23 Ryanodine receptor of skeletal muscle is a gap junction-type channel. Science 1988 2.56
24 Enteroviral protease 2A cleaves dystrophin: evidence of cytoskeletal disruption in an acquired cardiomyopathy. Nat Med 1999 2.50
25 The ryanodine receptor/Ca2+ release channel. J Biol Chem 1993 2.50
26 Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice. J Cell Biol 1998 2.44
27 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
28 A role for dystroglycan in basement membrane assembly. Cell 1998 2.36
29 Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy. Lancet 1993 2.33
30 Dystrophin-related protein is localized to neuromuscular junctions of adult skeletal muscle. Neuron 1991 2.30
31 Congenital muscular dystrophy with merosin deficiency. C R Acad Sci III 1994 2.22
32 The Ca2+-release channel/ryanodine receptor is localized in junctional and corbular sarcoplasmic reticulum in cardiac muscle. J Cell Biol 1993 2.18
33 Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol 1997 2.13
34 Dystrophin-glycoprotein complex is highly enriched in isolated skeletal muscle sarcolemma. J Cell Biol 1991 2.10
35 The brain ryanodine receptor: a caffeine-sensitive calcium release channel. Neuron 1991 2.05
36 Isolation, characterization, and localization of the inositol 1,4,5-trisphosphate receptor protein in Xenopus laevis oocytes. J Biol Chem 1992 2.05
37 Dual function of the voltage-dependent Ca2+ channel alpha 2 delta subunit in current stimulation and subunit interaction. Neuron 1996 2.04
38 Induction of calcium currents by the expression of the alpha 1-subunit of the dihydropyridine receptor from skeletal muscle. Nature 1989 2.04
39 Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex. Neuron 2000 2.04
40 Molecular analysis of the interaction of LCMV with its cellular receptor [alpha]-dystroglycan. J Cell Biol 2001 2.03
41 Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae. Science 1998 2.02
42 The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel. Trends Neurosci 1988 1.98
43 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
44 Ca2+ channel regulation by a conserved beta subunit domain. Neuron 1994 1.92
45 Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. J Cell Biol 2000 1.92
46 Association of triadin with the ryanodine receptor and calsequestrin in the lumen of the sarcoplasmic reticulum. J Biol Chem 1995 1.86
47 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
48 Subcellular fractionation of dystrophin to the triads of skeletal muscle. Nature 1988 1.81
49 A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering. Cell 1994 1.80
50 Identification and characterization of the high affinity [3H]ryanodine receptor of the junctional sarcoplasmic reticulum Ca2+ release channel. J Biol Chem 1987 1.80
51 Forced expression of dystrophin deletion constructs reveals structure-function correlations. J Cell Biol 1996 1.79
52 Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies. Muscle Nerve 1994 1.78
53 Distribution of dystroglycan in normal adult mouse tissues. J Histochem Cytochem 1998 1.77
54 Differential immunohistochemical localization of inositol 1,4,5-trisphosphate- and ryanodine-sensitive Ca2+ release channels in rat brain. J Neurosci 1993 1.76
55 Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study. Ann Neurol 2000 1.75
56 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
57 Cloning and tissue-specific expression of the brain calcium channel beta-subunit. FEBS Lett 1991 1.70
58 Dystroglycan inside and out. Curr Opin Cell Biol 1999 1.70
59 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
60 Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy. Nature 1992 1.70
61 Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophy. Nat Genet 1994 1.70
62 Identification and characterization of the dystrophin anchoring site on beta-dystroglycan. J Biol Chem 1995 1.67
63 Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E. Mol Cell 2000 1.66
64 Subunit regulation of the neuronal alpha 1A Ca2+ channel expressed in Xenopus oocytes. J Physiol 1995 1.63
65 Structural characterization of the dihydropyridine-sensitive calcium channel alpha 2-subunit and the associated delta peptides. J Biol Chem 1991 1.63
66 Primary structure of the gamma subunit of the DHP-sensitive calcium channel from skeletal muscle. Science 1990 1.62
67 SH3 domain-mediated interaction of dystroglycan and Grb2. J Biol Chem 1995 1.61
68 Purification and characterization of calsequestrin from canine cardiac sarcoplasmic reticulum and identification of the 53,000 dalton glycoprotein. J Biol Chem 1983 1.60
69 Minimum requirements for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. J Virol 1999 1.58
70 Brief report: deficiency of a dystrophin-associated glycoprotein (adhalin) in a patient with muscular dystrophy and cardiomyopathy. N Engl J Med 1996 1.57
71 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
72 Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem 1994 1.56
73 The effects of ryanodine on passive calcium fluxes across sarcoplasmic reticulum membranes. J Biol Chem 1987 1.53
74 Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma. Neurology 1993 1.52
75 Dissection of functional domains of the voltage-dependent Ca2+ channel alpha2delta subunit. J Neurosci 1997 1.52
76 Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. Hum Mol Genet 1993 1.50
77 Dystroglycan: an extracellular matrix receptor linked to the cytoskeleton. Curr Opin Cell Biol 1996 1.49
78 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
79 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
80 Attenuated pain responses in mice lacking Ca(V)3.2 T-type channels. Genes Brain Behav 2006 1.49
81 Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx mice. Nat Genet 1994 1.48
82 Subunit stoichiometry of human muscle chloride channels. J Gen Physiol 1997 1.47
83 Dystrophin and the membrane skeleton. Curr Opin Cell Biol 1993 1.47
84 Specific absence of the alpha 1 subunit of the dihydropyridine receptor in mice with muscular dysgenesis. J Biol Chem 1989 1.44
85 Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex. J Clin Invest 2001 1.41
86 Purification of dystrophin from skeletal muscle. J Biol Chem 1991 1.41
87 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
88 Primary structure and topological analysis of a skeletal muscle-specific junctional sarcoplasmic reticulum glycoprotein (triadin). J Biol Chem 1993 1.39
89 A neuronal ryanodine receptor mediates light-induced phase delays of the circadian clock. Nature 1998 1.39
90 Distinct roles for dystroglycan, beta1 integrin and perlecan in cell surface laminin organization. J Cell Sci 2001 1.39
91 Biosynthesis of dystroglycan: processing of a precursor propeptide. FEBS Lett 2000 1.38
92 In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Ther 1996 1.37
93 Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex. Neuron 1995 1.35
94 Properties of the alpha 1-beta anchoring site in voltage-dependent Ca2+ channels. J Biol Chem 1995 1.35
95 Non-muscle alpha-dystroglycan is involved in epithelial development. J Cell Biol 1995 1.34
96 Heterogeneity of the 59-kDa dystrophin-associated protein revealed by cDNA cloning and expression. J Biol Chem 1994 1.34
97 Biochemical characterization and molecular cloning of cardiac triadin. J Biol Chem 1996 1.33
98 mdx muscle pathology is independent of nNOS perturbation. Hum Mol Genet 1998 1.32
99 Identification and characterization of the dihydropyridine-binding subunit of the skeletal muscle dihydropyridine receptor. J Biol Chem 1987 1.32
100 Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform. Hum Mol Genet 1994 1.32
101 Common pathological mechanisms in mouse models for muscular dystrophies. FASEB J 2005 1.31
102 Ultrastructural localization of calsequestrin in adult rat atrial and ventricular muscle cells. J Cell Biol 1985 1.31
103 Ultrastructural localization of calsequestrin in rat skeletal muscle by immunoferritin labeling of ultrathin frozen sections. J Cell Biol 1983 1.30
104 Biochemical and ultrastructural characterization of the 1,4-dihydropyridine receptor from rabbit skeletal muscle. Evidence for a 52,000 Da subunit. J Biol Chem 1988 1.30
105 A beta-subunit normalizes the electrophysiological properties of a cloned N-type Ca2+ channel alpha 1-subunit. Neuropharmacology 1993 1.29
106 The sarcoglycan complex in limb-girdle muscular dystrophy. Curr Opin Neurol 1998 1.28
107 Subunit identification and reconstitution of the N-type Ca2+ channel complex purified from brain. Science 1993 1.27
108 Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin. J Biol Chem 1995 1.26
109 Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin). J Biol Chem 1993 1.26
110 Identification of critical amino acids involved in alpha1-beta interaction in voltage-dependent Ca2+ channels. FEBS Lett 1996 1.24
111 Dystroglycan is a binding protein of laminin and merosin in peripheral nerve. FEBS Lett 1994 1.24
112 Biochemical characterization of the epithelial dystroglycan complex. J Biol Chem 1999 1.24
113 POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG. Neurology 2004 1.22
114 Solubilization and biochemical characterization of the high affinity [3H]ryanodine receptor from rabbit brain membranes. J Biol Chem 1990 1.22
115 Dystroglycan in development and disease. Curr Opin Cell Biol 1998 1.21
116 Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy. Neurology 1997 1.21
117 epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex. J Biol Chem 1999 1.20
118 Localization of the high affinity calcium binding protein and an intrinsic glycoprotein in sarcoplasmic reticulum membranes. J Biol Chem 1980 1.19
119 Beta subunit heterogeneity in N-type Ca2+ channels. J Biol Chem 1996 1.19
120 Association of native Ca2+ channel beta subunits with the alpha 1 subunit interaction domain. J Biol Chem 1995 1.18
121 Intracellular accumulation and reduced sarcolemmal expression of dysferlin in limb--girdle muscular dystrophies. Ann Neurol 2000 1.18
122 Evidence for the presence of calsequestrin in two structurally different regions of myocardial sarcoplasmic reticulum. J Cell Biol 1984 1.18
123 Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex. J Biol Chem 1997 1.17
124 Biochemical and biophysical evidence for gamma 2 subunit association with neuronal voltage-activated Ca2+ channels. J Biol Chem 2001 1.16
125 Photoaffinity labeling of the ryanodine receptor/Ca2+ release channel with an azido derivative of ryanodine. J Biol Chem 1994 1.16
126 Evidence for the association of dystrophin with the transverse tubular system in skeletal muscle. J Biol Chem 1988 1.16
127 Identification of novel proteins unique to either transverse tubules (TS28) or the sarcolemma (SL50) in rabbit skeletal muscle. J Cell Biol 1990 1.15
128 Characterization of dp6troglycan-laminin interaction in peripheral nerve. J Neurochem 1996 1.15
129 Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain. Hum Mol Genet 1997 1.15
130 Characterization of the 1,4-dihydropyridine receptor using subunit-specific polyclonal antibodies. Evidence for a 32,000-Da subunit. J Biol Chem 1989 1.15
131 Characterization of the major brain form of the ryanodine receptor/Ca2+ release channel. J Biol Chem 1993 1.14
132 Extracellular interaction of the voltage-dependent Ca2+ channel alpha2delta and alpha1 subunits. J Biol Chem 1997 1.14
133 Animal models for muscular dystrophy: valuable tools for the development of therapies. Hum Mol Genet 2000 1.13
134 Specific association of calmodulin-dependent protein kinase and related substrates with the junctional sarcoplasmic reticulum of skeletal muscle. Biochemistry 1990 1.13
135 beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain. Mol Cell Neurosci 1999 1.12
136 Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster. Am J Pathol 1998 1.12
137 Expression and subunit interaction of voltage-dependent Ca2+ channels in PC12 cells. J Neurosci 1996 1.12
138 Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). J Med Genet 1997 1.11
139 Intramembrane charge movements and excitation- contraction coupling expressed by two-domain fragments of the Ca2+ channel. Proc Natl Acad Sci U S A 2001 1.11
140 Assembly of the sarcoglycan complex. Insights for muscular dystrophy. J Biol Chem 1998 1.10
141 Absence of the skeletal muscle sarcolemma chloride channel ClC-1 in myotonic mice. J Biol Chem 1995 1.10
142 Dystrophin constitutes 5% of membrane cytoskeleton in skeletal muscle. FEBS Lett 1991 1.10
143 A founder mutation in the gamma-sarcoglycan gene of gypsies possibly predating their migration out of India. Hum Mol Genet 1996 1.10
144 Identification of three subunits of the high affinity omega-conotoxin MVIIC-sensitive Ca2+ channel. J Biol Chem 1996 1.09
145 A calmodulin-dependent protein kinase system from skeletal muscle sarcoplasmic reticulum. Phosphorylation of a 60,000-dalton protein. J Biol Chem 1982 1.09
146 Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster. J Biol Chem 1993 1.08
147 Purification and characterization of the 53,000-dalton glycoprotein from the sarcoplasmic reticulum. J Biol Chem 1981 1.08
148 Membrane targeting and stabilization of sarcospan is mediated by the sarcoglycan subcomplex. J Cell Biol 1999 1.08
149 Biochemical characterization of ultrastructural localization of a major junctional sarcoplasmic reticulum glycoprotein (triadin). J Biol Chem 1993 1.08
150 Reduced expression of dystroglycan in breast and prostate cancer. Hum Pathol 2001 1.06
151 Cortical localization of a calcium release channel in sea urchin eggs. J Cell Biol 1992 1.06
152 Functional rescue of the sarcoglycan complex in the BIO 14.6 hamster using delta-sarcoglycan gene transfer. Mol Cell 1998 1.05
153 Transmembrane auxiliary subunits of voltage-dependent ion channels. J Biol Chem 1996 1.05
154 The calcium signal and neutrophil activation. Clin Biochem 1990 1.04
155 Dystrophin-associated glycoproteins: their possible roles in the pathogenesis of Duchenne muscular dystrophy. Mol Cell Biol Hum Dis Ser 1993 1.04
156 Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycan-laminin interaction. J Cell Sci 1999 1.03
157 Plant cells contain calsequestrin. J Biol Chem 1989 1.02
158 Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy. J Biol Chem 1996 1.01
159 Structural and functional diversity of voltage-activated calcium channels. Ion Channels 1996 1.01
160 A role of dystroglycan in schwannoma cell adhesion to laminin. J Biol Chem 1997 1.01
161 A monoclonal antibody to the Ca2+-ATPase of cardiac sarcoplasmic reticulum cross-reacts with slow type I but not with fast type II canine skeletal muscle fibers: an immunocytochemical and immunochemical study. Cell Motil Cytoskeleton 1988 0.99
162 Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle. Circ Res 1993 0.99
163 Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex. J Biol Chem 2000 0.99
164 Presence of inositol 1,4,5-trisphosphate receptor, calreticulin, and calsequestrin in eggs of sea urchins and Xenopus laevis. Dev Biol 1994 0.98
165 A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Ann Neurol 1997 0.98
166 Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscle. BMC Physiol 2001 0.98
167 Direct photoaffinity labeling of the high affinity nitrendipine-binding site in subcellular membrane fractions isolated from canine myocardium. J Biol Chem 1984 0.98
168 Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy. Neuromuscul Disord 1994 0.98
169 Clustering and immobilization of acetylcholine receptors by the 43-kD protein: a possible role for dystrophin-related protein. J Cell Biol 1993 0.98
170 Sarcospan-deficient mice maintain normal muscle function. Mol Cell Biol 2000 0.98
171 Evidence for a 95 kDa short form of the alpha1A subunit associated with the omega-conotoxin MVIIC receptor of the P/Q-type Ca2+ channels. J Neurosci 1998 0.97
172 Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis. Hum Mol Genet 1993 0.96
173 Purification, calcium binding properties, and ultrastructural localization of the 53,000- and 160,000 (sarcalumenin)-dalton glycoproteins of the sarcoplasmic reticulum. J Biol Chem 1990 0.96
174 Dystroglycan binding to laminin alpha1LG4 module influences epithelial morphogenesis of salivary gland and lung in vitro. Differentiation 2001 0.95
175 Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscle. Curr Opin Neurol 1995 0.95
176 Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis. J Cell Biol 1995 0.95
177 Phosphorylation of heavy sarcoplasmic reticulum vesicles: identification and characterization of three phosphorylated proteins. J Membr Biol 1980 0.95
178 Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Hum Mol Genet 2000 0.95
179 Neural regulation of alpha-dystroglycan biosynthesis and glycosylation in skeletal muscle. J Neurochem 2000 0.95
180 Deficiency of dystrophin-associated proteins: a common mechanism leading to muscle cell necrosis in severe childhood muscular dystrophies. Neuromuscul Disord 1993 0.95
181 Caveolin-3 is not an integral component of the dystrophin glycoprotein complex. FEBS Lett 1998 0.94
182 Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve. FEBS Lett 1993 0.94
183 Sequence similarity of calreticulin with a Ca2(+)-binding protein that co-purifies with an Ins(1,4,5)P3-sensitive Ca2+ store in HL-60 cells. Biochem J 1990 0.94
184 Labeling of high affinity ATP binding sites on the 53,000- and 160,000-dalton glycoproteins of the sarcoplasmic reticulum with the photoaffinity probe 8-N3-[alpha-32P]ATP. J Biol Chem 1983 0.94
185 Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities. Neurology 1995 0.93
186 Dystroglycan expression in the wild type and mdx mouse neural retina: synaptic colocalization with dystrophin, dystrophin-related protein but not laminin. J Neurosci Res 1995 0.92
187 Chloride-induced release of actively loaded calcium from light and heavy sarcoplasmic reticulum vesicles. J Membr Biol 1980 0.91
188 Characterization and ultrastructural localization of a novel 90-kDa protein unique to skeletal muscle junctional sarcoplasmic reticulum. J Biol Chem 1994 0.90
189 A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Hum Mol Genet 1995 0.90
190 Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries. C R Acad Sci III 1993 0.89
191 A monoclonal antibody to the beta subunit of the skeletal muscle dihydropyridine receptor immunoprecipitates the brain omega-conotoxin GVIA receptor. J Biol Chem 1991 0.88
192 Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy. Magn Reson Med 2000 0.88
193 Newly synthesized calsequestrin, destined for the sarcoplasmic reticulum, is contained in early/intermediate Golgi-derived clathrin-coated vesicles. J Biol Chem 1989 0.88
194 Triadin, a linker for calsequestrin and the ryanodine receptor. Soc Gen Physiol Ser 1996 0.87
195 The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophies. Neuromuscul Disord 1994 0.86
196 Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12. FEBS Lett 1996 0.86
197 Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. C R Acad Sci III 1994 0.86
198 Ion pathways in proteins of the sarcoplasmic reticulum. Ann N Y Acad Sci 1980 0.86
199 Characterization of the purified N-type Ca2+ channel and the cation sensitivity of omega-conotoxin GVIA binding. Neuropharmacology 1993 0.86
200 Quercetin inhibits Ca2+ uptake but not Ca2+ release by sarcoplasmic reticulum in skinned muscle fibers. Proc Natl Acad Sci U S A 1980 0.86
201 Evidence that platelet and skeletal sarcoplasmic reticulum Ca2+-ATPase are structurally distinct. J Biol Chem 1985 0.86
202 Reactive oxygen species deglycosilate glomerular alpha-dystroglycan. Kidney Int 2006 0.86
203 Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscul Disord 1998 0.86
204 An investigation of functional similarities between the sarcoplasmic reticulum and platelet calcium-dependent adenosinetriphosphatases with the inhibitors quercetin and calmidazolium. Biochemistry 1987 0.85
205 Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice. Gene Ther 2000 0.85
206 Analysis of excitation-contraction-coupling components in chronically stimulated canine skeletal muscle. Eur J Biochem 1991 0.85
207 Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I. Neurology 2011 0.85
208 Evidence for the presence of calsequestrin in both peripheral and interior regions of sheep Purkinje fibers. Circ Res 1984 0.85
209 Albumin is a major protein component of transverse tubule vesicles isolated from skeletal muscle. J Biol Chem 1989 0.85
210 Phosphorylation of the 1,4-dihydropyridine receptor of the voltage-dependent Ca2+ channel by an intrinsic protein kinase in isolated triads from rabbit skeletal muscle. J Biol Chem 1987 0.85
211 DIDS inhibition of sarcoplasmic reticulum anion efflux and calcium transport. Ann N Y Acad Sci 1980 0.84
212 Mechanism of action of "ruthenium red" compounds on Ca2+ ionophore from sarcoplasmic reticulum (Ca2+ + Mg2+)- adenosine triphosphatase and lipid bilayer. J Biol Chem 1975 0.84
213 Restoration of dystrophin-associated proteins in skeletal muscle of mdx mice transgenic for dystrophin gene. FEBS Lett 1993 0.84
214 Role of the ryanodine receptor of skeletal muscle in excitation-contraction coupling. Ann N Y Acad Sci 1989 0.83
215 A 5' dystrophin duplication mutation causes membrane deficiency of alpha-dystroglycan in a family with X-linked cardiomyopathy. J Mol Cell Cardiol 1997 0.83
216 Alpha-dystroglycan deficiency correlates with elevated serum creatine kinase and decreased muscle contraction tension in golden retriever muscular dystrophy. FEBS Lett 1994 0.83
217 Functional properties of the purified N-type Ca2+ channel from rabbit brain. J Biol Chem 1994 0.83
218 Purification and reconstitution of N-type calcium channel complex from rabbit brain. Methods Enzymol 1994 0.82
219 Analysis of the role of dystroglycan in early postimplantation mouse development. Ann N Y Acad Sci 1998 0.82
220 Dystroglycan overexpression in vivo alters acetylcholine receptor aggregation at the neuromuscular junction. Dev Biol 2000 0.82
221 Identification and characterization of proteins in sarcoplasmic reticulum from normal and failing human left ventricles. J Mol Cell Cardiol 1990 0.82
222 Antibodies against the Calcium-Binding Protein: Calsequestrin from Streptanthus tortuosus (Brassicaceae). Plant Physiol 1989 0.82
223 Distinct immunopeptide maps of the sarcoplasmic reticulum Ca2+ release channel in malignant hyperthermia. J Biol Chem 1990 0.82
224 Muscular dystrophy. Utrophin to the rescue. Nature 1996 0.81
225 Mild deficiency of dystrophin-associated proteins in Becker muscular dystrophy patients having in-frame deletions in the rod domain of dystrophin. Am J Hum Genet 1993 0.81
226 Frog cardiac calsequestrin. Identification, characterization, and subcellular distribution in two structurally distinct regions of peripheral sarcoplasmic reticulum in frog ventricular myocardium. Circ Res 1991 0.81
227 Assessment of the 50-kDa dystrophin-associated glycoprotein in Brazilian patients with severe childhood autosomal recessive muscular dystrophy. J Neurol Sci 1994 0.81
228 114th ENMC International Workshop on Congenital Muscular Dystrophy (CMD) 17-19 January 2003, Naarden, The Netherlands: (8th Workshop of the International Consortium on CMD; 3rd Workshop of the MYO-CLUSTER project GENRE). Neuromuscul Disord 2003 0.81
229 Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome? Neuropediatrics 1996 0.81
230 Ultrastructural localization of adhalin, alpha-dystroglycan and merosin in normal and dystrophic muscle. Neuropathol Appl Neurobiol 1996 0.81
231 Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. J Clin Invest 1994 0.80
232 Partial deficiency of dystrophin-associated proteins in a young girl with sporadic myopathy and normal karyotype. Neurology 1993 0.80
233 Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy. Ann Neurol 1995 0.79
234 A calmodulin-dependent protein kinase system from skeletal muscle sarcoplasmic reticulum. Adv Cyclic Nucleotide Protein Phosphorylation Res 1984 0.79
235 Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies. Neuromuscul Disord 1996 0.78
236 Muscular dystrophy associated with beta-Dystroglycan deficiency. Ann Neurol 1996 0.78
237 Expression of dystrophin-associated glycoproteins and utrophin in carriers of Duchenne muscular dystrophy. Neuromuscul Disord 1995 0.78
238 Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical study. Neuromuscul Disord 1994 0.78
239 Transient expression of Dp140, a product of the Duchenne muscular dystrophy locus, during kidney tubulogenesis. Dev Biol 1997 0.78
240 Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy. Neuromuscul Disord 1994 0.78
241 Clinical and molecular pathological features of severe childhood autosomal recessive muscular dystrophy in Saudi Arabia. Dev Med Child Neurol 1996 0.78
242 Clinical heterogeneity of adhalin deficiency. Ann Neurol 1996 0.77
243 Calcium transport by sarcoplasmic reticulum of skeletal muscle is inhibited by antibodies against the 53-kilodalton glycoprotein of the sarcoplasmic reticulum membrane. Biochemistry 1989 0.77
244 The expression of dystrophin-associated glycoproteins during skeletal muscle degeneration and regeneration. An immunofluorescence study. J Neuropathol Exp Neurol 1995 0.77
245 From adhalinopathies to alpha-sarcoglycanopathies: an overview. Neuromuscul Disord 1996 0.77
246 Expression of deletion-containing dystrophins in mdx muscle: implications for gene therapy and dystrophin function. Pediatr Res 1995 0.77
247 Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells. FEBS Lett 1993 0.77
248 Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster. FEBS Lett 1995 0.77
249 A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics 1998 0.77
250 Biosynthesis of intrinsic sarcoplasmic reticulum proteins during differentiation of the myogenic cell line L6. J Biol Chem 1983 0.76
251 The identification of sarcoplasmic reticulum terminal cisternae proteins in platelets. Biochem J 1989 0.75
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