Current knowledge of dystrophin and dystrophin-associated proteins in the retina

Histology and Histopathology

Volumn 15, Issue 3, 2000, Pages 753-760

  Ueda, H ^a   Baba, T ^a   Ohno, S ^a  

^a UNIVERSITY OF YAMANASHI   (Japan)

Author keywords

Dystrophin; Dystrophin associated proteins; Muller cells; Photoreceptor cells; Retina

Indexed keywords

DYSTROBREVIN; DYSTROGLYCAN; DYSTROPHIN; SARCOGLYCAN; SYNTROPHIN; UNCLASSIFIED DRUG; UTROPHIN;

BLOOD VESSEL; HUMAN; MEMBRANE; NEUROMUSCULAR SYNAPSE; NEUROTRANSMISSION; PHOTORECEPTOR CELL; PROTEIN LOCALIZATION; RETINA; RETINA CONE; RETINA ROD; REVIEW;

ANIMALS; CONES (RETINA); CYTOSKELETAL PROTEINS; DYSTROGLYCANS; DYSTROPHIN; DYSTROPHIN-ASSOCIATED PROTEINS; HUMANS; MEMBRANE GLYCOPROTEINS; MEMBRANE PROTEINS; MICE; MUSCLE PROTEINS; MUSCULAR DYSTROPHY, DUCHENNE; MUTAGENESIS; RETINA; RODS (RETINA); UTROPHIN;

EID: 0033925182     PISSN: 02133911     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (84)

1. The structural and functional diversity of dystrophin
2. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide
3. Calcium action in synaptic transmitter release
4. A novel product of the Duchenne muscular dystrophy gene which greatly differs from the known isoforms in its structure and tissue distribution
5. Different distributions of dystrophin and related proteins at nerve-muscle junctions
6. Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein
7. Subcellular concentration of β-dystroglycan in photoreceptors and glial cells of the chick retina
8. Dystrophin and β-dystroglycan in photoreceptor terminals from normal and mdx(3Cv) mouse retinae
9. Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: A heteromeric complex related to the dystroglycans
10. The ultrastructure of rat rod synaptic terminals: Effects of dark-adaptation
11. Dystrophin-associated proteins and the muscular dystrophies: A glossary
12. An alternative dystrophin transcript specific to peripheral nerve
13. A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering
14. Identification of α-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus
15. Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice
16. The effects of dystrophin gene mutations on the ERG in mice and humans
17. New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophin
18. Distribution of microtubule-associated protein 2 in the nervous system of the rat studied by immunofluorescence
19. Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice
20. Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
21. A novel dystrophin isoform is required for normal retinal electrophysiology
22. Dystroglycan in development and disease
23. A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin
24. Retinal signal transmission in Duchenne muscular dystrophy: Evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway
25. 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
26. Dystroglycan-α, a dystrophin-associated glycoprotein, is a functional agrin receptor
27. Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
28. Subtle neuromuscular defects in utrophin-deficient mice
29. Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: A model for Duchenne muscular dystrophy
30. Dystroglycan: An extracellular matrix receptor linked to the cytoskeleton
31. The cytoskeletal architecture of the presynaptic terminal and molecular structure of synapsin 1
32. Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina
33. Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix
34. Differential expression of dystrophin isoforms in strains of mdx mice with different mutations
35. Dystrophin in central nervous system: A developmental, regional distribution and subcellular localization study
36. Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of β-dystroglycan in the outer plexiform layer of the retina
37. A study of synaptic transmission in the absence of nerve impulses
38. The subcellular distribution of chromosome 6-encoded dystrophin-related protein in the brain
39. Differential distribution of β-dystroglycan in rabbit and rat retina
40. The organization of cytoplasm at the presynaptic active zone of a central nervous system synapse
41. Talin, vinculin and DRP (utrophin) concentrations are increased at mdx myotendinous junctions following onset of necrosis
42. A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-wave
43. Dp140: Alternatively spliced isoforms in brain and kidney
44. Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons
45. The distribution of dystrophin in the murine central nervous system: An immunocytochemical study
46. Dp140: A novel 140 kDa CNS transcript from the dystrophin locus
47. Ultrastructural evidence that horizontal cell axon terminals are presynaptic in the human retina
48. An autosomal transcript in skeletal muscle with homology to dystrophin
49. Synapsins in the vertebrate retina: Absence from ribbon synapses and heterogeneous distribution among conventional synapses
50. Cell types using glutamate as a neurotransmitter in the vertebrate retina
51. Immunohistochemical dystrophin reaction in synaptic regions
52. Dystroglycan expression in the wild type and mdx mouse neural retina: Synaptic colocalization with dystrophin, dystrophin-related protein but not laminin
53. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention
54. + hypothesis
55. The Muller cell: A functional element of the retina
56. Towards an understanding of the dystrophin-glycoprotein complex: Linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers
57. Dystrophin-associated proteins in muscular dystrophy
58. From dystrophinopathy to sarcoglycanopathy: Evolution of a concept of muscular dystrophy
59. Dystrophin expression in the human retina is required for normal function as defined by electroretinography
60. mdx(Cv3) mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy
61. Effects of dystrophin isoforms on signal transduction through neural retina: Genotype-phenotype analysis of Duchenne muscular dystrophy mouse mutants
62. Role of α-dystroglycan as a Schwann cell receptor for Mycobacterium leprae
63. Mammalian rod terminal: Architecture of a binary synapse
64. Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane
65. Characterization of the transmembrane molecular architecture of the dystroglycan complex in Schwann cells
66. Colocalization of retinal dystrophin and actin in postsynaptic dendrites of rod and cone photoreceptor synapses
67. Localization of dystrophin and β-dystroglycan in bovine retinal photoreceptor processes extending into the postsynaptic dendritic complex
68. Dystrophin in the retina
69. Specific interactions between the syntrophin PDZ domain and voltage-gated sodium channels
70. The intermediate filament complement of the retina: A comparison between different mammalian species
71. The molecular basis of muscular dystrophy in the mdx mouse: A point mutation
72. Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy
73. B-wave of the electroretinogram. A reflection of ON bipolar cell activity
74. Dystroglycan in the cerebellum is a laminin alpha 2-chain binding protein at the glial-vascular interface and is expressed in Purkinje cells
75. Dystrophin localization at presynapse in rat retina revealed by immunoelectron microscopy
76. Dystrophin in rod spherules; Submembranous dense regions facing bipolar cell processes
77. Immunocytochemical study of dystrophin localization in cone cells of mouse retinas
78. β-dystroglycan localization in the photoreceptor and Muller cells in the rat retina revealed by immunoelectron microscopy
79. Immunoelectron microscopic localization of dystrophin in myofibers
80. Ion-selective microelectrodes suitable for recording rapid changes in extracellular ion concentration
81. Distribution of orthogonal arrays of particles in the Muller cell membrane of the mouse retina
82. Dystroglycan is a binding protein of laminin and merosin in peripheral nerve
83. Dystrophin in control and mdx retina
84. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle