Dystroglycan is a binding protein of laminin and merosin in peripheral nerve (Q28238540)

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T Shimizu

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T Tanaka

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K P Campbell

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K Matsumura

Association of dystrophin and an integral membrane glycoprotein.

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language of work or name

English

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publication date

19 September 1994

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published in

FEBS Letters

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volume

352

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page(s)

49-53

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issue

1

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cites work

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Glycoprotein complex anchoring dystrophin to sarcolemma

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Membrane organization of the dystrophin-glycoprotein complex

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Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

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Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization

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A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

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A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering

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Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

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Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development

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Merosin, a tissue-specific basement membrane protein, is a laminin-like protein

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Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

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Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

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A dual laminin/collagen receptor acts in peripheral nerve regeneration

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Association of dystrophin-related protein with dystrophin-associated proteins in mdx mouse muscle

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Abnormal localization of laminin subunits in muscular dystrophies

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Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

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Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

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Neural abnormalities in the dystrophic mouse

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Extracellular matrix molecules and their receptors: functions in neural development

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Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle

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Dystrophin-glycoprotein complex and laminin colocalize to the sarcolemma and transverse tubules of cardiac muscle

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Identification and purification of an agrin receptor from Torpedo postsynaptic membranes: a heteromeric complex related to the dystroglycans

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Differential expression of dystrophin, utrophin and dystrophin-associated proteins in peripheral nerve

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Basement membranes during development of human nerve: Schwann cells and perineurial cells display marked changes in their expression profiles for laminin subunits and beta 1 and beta 4 integrins

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Purification of dystrophin-related protein (utrophin) from lung and its identification in pulmonary artery endothelial cells

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Genetically determined defect of Schwann cell basement membrane in dystrophic mouse

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