Conservation of components of the dystrophin complex in Drosophila 1

[1]  Xin Huang,et al.  Structure of a WW domain containing fragment of dystrophin in complex with β-dystroglycan , 2000, Nature Structural Biology.

[2]  P. Tonali,et al.  γ1- and γ2-Syntrophins, Two Novel Dystrophin-binding Proteins Localized in Neuronal Cells* , 2000, The Journal of Biological Chemistry.

[3]  S. Winder,et al.  Adhesion-dependent tyrosine phosphorylation of (beta)-dystroglycan regulates its interaction with utrophin. , 2000, Journal of cell science.

[4]  H. Hama,et al.  Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy. , 2000, Human molecular genetics.

[5]  Stephen M. Mount,et al.  The genome sequence of Drosophila melanogaster. , 2000, Science.

[6]  K. Campbell,et al.  Sarcospan-Deficient Mice Maintain Normal Muscle Function , 2000, Molecular and Cellular Biology.

[7]  J. Fallon,et al.  The Small Leucine-Rich Repeat Proteoglycan Biglycan Binds to α-Dystroglycan and Is Upregulated in Dystrophic Muscle , 2000, The Journal of cell biology.

[8]  L. Ségalat,et al.  Mutations in the dystrophin‐like dys‐1 gene of Caenorhabditis elegans result in reduced acetylcholinesterase activity , 1999, FEBS letters.

[9]  L. Ségalat,et al.  In vitro interactions of Caenorhabditis elegans dystrophin with dystrobrevin and syntrophin , 1999, FEBS letters.

[10]  J. Sanes,et al.  ε-Sarcoglycan Replaces α-Sarcoglycan in Smooth Muscle to Form a Unique Dystrophin-Glycoprotein Complex* , 1999, The Journal of Biological Chemistry.

[11]  J. Campanelli,et al.  WW and EF hand domains of dystrophin-family proteins mediate dystroglycan binding. , 1999, Molecular cell biology research communications : MCBRC.

[12]  D. Bredt Knocking signalling out of the dystrophin complex , 1999, Nature Cell Biology.

[13]  Harry Hines Boulevard,et al.  Role for α-dystrobrevin in the pathogenesis of dystrophin-dependent muscular dystrophies , 1999, Nature Cell Biology.

[14]  K. Bushby,et al.  Making sense of the limb-girdle muscular dystrophies. , 1999, Brain : a journal of neurology.

[15]  H. Peng,et al.  Acetylcholinesterase Clustering at the Neuromuscular Junction Involves Perlecan and Dystroglycan , 1999, The Journal of cell biology.

[16]  J. Sanes,et al.  Membrane Targeting and Stabilization of Sarcospan Is Mediated by the Sarcoglycan Subcomplex , 1999, The Journal of cell biology.

[17]  K. Deininger,et al.  The WW Domain of Dystrophin Requires EF-Hands Region to Interact with β-Dystroglycan , 1999, Biological chemistry.

[18]  L. Ségalat,et al.  Dystrobrevin- and dystrophin-like mutants display similar phenotypes in the nematode Caenorhabditis elegans , 1999, Neurogenetics.

[19]  L. Ségalat,et al.  Mutations in the Caenorhabditis elegans dystrophin-like gene dys-1 lead to hyperactivity and suggest a link with cholinergic transmission , 1998, Neurogenetics.

[20]  J. Ervasti,et al.  A Cluster of Basic Repeats in the Dystrophin Rod Domain Binds F-actin through an Electrostatic Interaction* , 1998, The Journal of Biological Chemistry.

[21]  M. Bobrow,et al.  Dystrophins in vertebrates and invertebrates. , 1998, Human molecular genetics.

[22]  J. Caldwell,et al.  Interaction of Muscle and Brain Sodium Channels with Multiple Members of the Syntrophin Family of Dystrophin-Associated Proteins , 1998, The Journal of Neuroscience.

[23]  Jens Schneider-Mergener,et al.  Journal speciation , 1998, Nature Structural Biology.

[24]  K. Campbell,et al.  Sarcospan, the 25-kDa Transmembrane Component of the Dystrophin-Glycoprotein Complex* , 1997, The Journal of Biological Chemistry.

[25]  L. Kunkel,et al.  Dystrobrevin and dystrophin: an interaction through coiled-coil motifs. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[26]  K. Daniels,et al.  Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice. , 1997, Human molecular genetics.

[27]  M. Ruegg,et al.  Dystroglycan Is a Dual Receptor for Agrin and Laminin-2 in Schwann Cell Membrane* , 1996, The Journal of Biological Chemistry.

[28]  D. Bredt,et al.  Interaction of Nitric Oxide Synthase with the Postsynaptic Density Protein PSD-95 and α1-Syntrophin Mediated by PDZ Domains , 1996, Cell.

[29]  L. Kunkel,et al.  The Three Human Syntrophin Genes Are Expressed in Diverse Tissues, Have Distinct Chromosomal Locations, and Each Bind to Dystrophin and Its Relatives (*) , 1996, The Journal of Biological Chemistry.

[30]  R. Durbin,et al.  A dot-matrix program with dynamic threshold control suited for genomic DNA and protein sequence analysis. , 1995, Gene.

[31]  K. Campbell,et al.  Identification and Characterization of the Dystrophin Anchoring Site on β-Dystroglycan (*) , 1995, The Journal of Biological Chemistry.

[32]  T. Gibson,et al.  Dystrophin and utrophin: the missing links! , 1995, FEBS letters.

[33]  K. Campbell,et al.  Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex , 1995, Neuron.

[34]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[35]  K. Campbell,et al.  Dystrophin–glycoprotein complex: Its role in the molecular pathogenesis of muscular dystrophies , 1994, Muscle & nerve.

[36]  L. Kunkel,et al.  The structural and functional diversity of dystrophin , 1993, Nature Genetics.

[37]  O. Ibraghimov-Beskrovnaya,et al.  Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix , 1992, Nature.

[38]  K. Davies,et al.  Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines , 1991, The Journal of cell biology.

[39]  Simon C Watkins,et al.  Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons , 1990, Nature.

[40]  A. Monaco,et al.  The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein , 1988, Cell.