Specific Disruption of a Schwann Cell Dystrophin-Related Protein Complex in a Demyelinating Neuropathy

[1]  T. Milner,et al.  Axonal Regulation of Schwann Cell Integrin Expression Suggests a Role for ct 6 4 in Myelination , 2002 .

[2]  A. Mégarbané,et al.  A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease. , 2001, Human molecular genetics.

[3]  P. Stankiewicz,et al.  Periaxin mutations cause recessive Dejerine-Sottas neuropathy. , 2001, American journal of human genetics.

[4]  S. Noguchi,et al.  A sarcoglycan-dystroglycan complex anchors Dp116 and utrophin in the peripheral nervous system. , 2000, Human molecular genetics.

[5]  S. Hall,et al.  Influence of laminin‐2 on Schwann cell–axon interactions , 2000, Glia.

[6]  M. Sheng,et al.  Association of Dystrophin-Related Protein 2 (DRP2) with Postsynaptic Densities in Rat Brain , 2000, Molecular and Cellular Neuroscience.

[7]  C. Montell,et al.  TRP and the PDZ Protein, Inad, Form the Core Complex Required for Retention of the Signalplex in Drosophila Photoreceptor Cells , 2000, The Journal of cell biology.

[8]  V. Timmerman,et al.  Hereditary Peripheral Neuropathies , 2000 .

[9]  R. Huganir,et al.  PDZ domains in synapse assembly and signalling. , 2000, Trends in cell biology.

[10]  Austin G Smith,et al.  Peripheral Demyelination and Neuropathic Pain Behavior in Periaxin-Deficient Mice , 2000, Neuron.

[11]  G. Cesareni,et al.  Contribution of the different modules in the utrophin carboxy‐terminal region to the formation and regulation of the DAP complex , 2000, FEBS letters.

[12]  D. Sherman,et al.  A Tripartite Nuclear Localization Signal in the PDZ-domain Protein L-periaxin* , 2000, The Journal of Biological Chemistry.

[13]  W. Lim,et al.  Unexpected modes of PDZ domain scaffolding revealed by structure of nNOS-syntrophin complex. , 1999, Science.

[14]  S. Froehner,et al.  A PDZ-containing Scaffold Related to the Dystrophin Complex at the Basolateral Membrane of Epithelial Cells , 1999, The Journal of cell biology.

[15]  Y. Sunada,et al.  Characterization of the Transmembrane Molecular Architecture of the Dystroglycan Complex in Schwann Cells* , 1999, The Journal of Biological Chemistry.

[16]  J. Lupski,et al.  Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms. , 1999, Annual review of medicine.

[17]  J. Ellis,et al.  An epitope structure for the C-terminal domain of dystrophin and utrophin. , 1998, Biochemistry.

[18]  C. Montell,et al.  Coordination of an Array of Signaling Proteins through Homo- and Heteromeric Interactions Between PDZ Domains and Target Proteins , 1998, The Journal of cell biology.

[19]  D. Sherman,et al.  Two PDZ Domain Proteins Encoded by the Murine Periaxin Gene Are the Result of Alternative Intron Retention and Are Differentially Targeted in Schwann Cells* , 1998, The Journal of Biological Chemistry.

[20]  E. Cuppen,et al.  PDZ motifs in PTP-BL and RIL bind to internal protein segments in the LIM domain protein RIL. , 1998, Molecular biology of the cell.

[21]  C. Broeckhoven,et al.  Advances in Charcot–Marie–Tooth Disease Research: Cellular Function of CMT-Related Proteins, Transgenic Animal Models, and Pathomechanisms , 1997, Neurobiology of Disease.

[22]  E. Isacoff,et al.  Synaptic Clustering of Fasciclin II and Shaker: Essential Targeting Sequences and Role of Dlg , 1997, Neuron.

[23]  T. Freeman,et al.  Expression of the dystrophin-related protein 2 (Drp2) transcript in the mouse. , 1997, Journal of molecular biology.

[24]  Emiko Suzuki,et al.  A multivalent PDZ-domain protein assembles signalling complexes in a G-protein-coupled cascade , 1997, Nature.

[25]  P. Seeburg,et al.  Interaction of ion channels and receptors with PDZ domain proteins , 1997, Current Opinion in Neurobiology.

[26]  K. Campbell,et al.  A Role of Dystroglycan in Schwannoma Cell Adhesion to Laminin* , 1997, The Journal of Biological Chemistry.

[27]  K. Campbell,et al.  Muscular dystrophies and the dystrophin-glycoprotein complex. , 1997, Current opinion in neurology.

[28]  N. Severs,et al.  Dystrophin is not a specific component of the cardiac costamere. , 1997, Circulation research.

[29]  Y. Sunada,et al.  Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse , 1997, Neuromuscular Disorders.

[30]  Y. Sunada,et al.  The role of dystroglycan, a novel receptor of laminin and agrin, in cell differentiation. , 1997, Histology and histopathology.

[31]  S. Froehner,et al.  Syntrophins: modular adapter proteins at the neuromuscular junction and the sarcolemma. , 1997, Society of General Physiologists series.

[32]  C. Montell,et al.  Requirement for the PDZ Domain Protein, INAD, for Localization of the TRP Store-Operated Channel to a Signaling Complex , 1997, Neuron.

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

[34]  Z. Levy,et al.  Reduced levels of dystrophin associated proteins in the brains of mice deficient for Dp71. , 1996, Human molecular genetics.

[35]  John H. Lewis,et al.  Crystal Structures of a Complexed and Peptide-Free Membrane Protein–Binding Domain: Molecular Basis of Peptide Recognition by PDZ , 1996, Cell.

[36]  Q. Bone,et al.  Characterization of DRP2, a novel human dystrophin homologue , 1996, Nature Genetics.

[37]  I. Kanazawa,et al.  Characterization of Dystroglycan‐Laminin Interaction in Peripheral Nerve , 1996, Journal of neurochemistry.

[38]  D. Drubin,et al.  Origins of Cell Polarity , 1996, Cell.

[39]  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.

[40]  D. Sherman,et al.  Periaxin expression in myelinating Schwann cells: modulation by axon-glial interactions and polarized localization during development. , 1995, Development.

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

[42]  N. Bresolin,et al.  A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient. , 1995, Human molecular genetics.

[43]  O. Ibraghimov-Beskrovnaya,et al.  Non-muscle alpha-dystroglycan is involved in epithelial development , 1995, The Journal of cell biology.

[44]  E. Elson,et al.  Mechanical function of dystrophin in muscle cells , 1995, The Journal of cell biology.

[45]  K. Campbell,et al.  Dystroglycan is a binding protein of laminin and merosin in peripheral nerve , 1994, FEBS letters.

[46]  K. Campbell,et al.  Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. , 1994, The Journal of biological chemistry.

[47]  Peter J. Brophy,et al.  Periaxin, a novel protein of myelinating schwann cells with a possible role in axonal ensheathment , 1994, Neuron.

[48]  Kensuke Hayashi,et al.  Molecular organization at the glycoprotein-complex-binding site of dystrophin. Three dystrophin-associated proteins bind directly to the carboxy-terminal portion of dystrophin. , 1994, European journal of biochemistry.

[49]  E. Engvall,et al.  Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene. , 1994, Nature genetics.

[50]  F. Giancotti,et al.  Axonal regulation of Schwann cell integrin expression suggests a role for alpha 6 beta 4 in myelination , 1993, The Journal of cell biology.

[51]  K. Campbell,et al.  Differential expression of dystrophin, utrophin and dystrophin‐associated proteins in peripheral nerve , 1993, FEBS letters.

[52]  S. Carbonetto,et al.  Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin. , 1993, The Journal of biological chemistry.

[53]  H. Sweeney,et al.  Dystrophin protects the sarcolemma from stresses developed during muscle contraction. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

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

[55]  G. Sobue,et al.  Laminin A, B1, and B2 Chain Gene Expression in Transected and Regenerating Nerves: Regulation by Axonal Signals , 1993, Journal of neurochemistry.

[56]  T. Tsukahara,et al.  Laminin in Animal Models for Muscular Dystrophy Defect of Laminin M in Skeletal and Cardiac Muscles and Peripheral Nerve of the Homozygous Dystrophic dy/dy Mice. , 1993 .

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

[58]  J. Vance,et al.  Hereditary motor and sensory neuropathies. , 1991, Journal of medical genetics.

[59]  J. Ervasti,et al.  Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle , 1990, Nature.

[60]  R. Bunge,et al.  Schwann Cell Function Depends upon Axonal Signals and Basal Lamina Components a , 1990, Annals of the New York Academy of Sciences.

[61]  D. Hill,et al.  An autosomal transcript in skeletal muscle with homology to dystrophin , 1989, Nature.

[62]  R. Bunge,et al.  Differentiation of axon-related Schwann cells in vitro: II. Control of myelin formation by basal lamina , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[63]  M. Chao,et al.  Axons regulate Schwann cell expression of the major myelin and NGF receptor genes. , 1988, Development.

[64]  C. M. Rafferty,et al.  Schwann cell myelination: induction by exogenous basement membrane-like extracellular matrix , 1986, The Journal of cell biology.

[65]  M. Bunge,et al.  Linkage between axonal ensheathment and basal lamina production by Schwann cells. , 1986, Annual review of neuroscience.

[66]  R. Bunge,et al.  Evidence that contact with connective tissue matrix is required for normal interaction between Schwann cells and nerve fibers , 1978, The Journal of cell biology.