Absence of acetylcholinesterase at the neuromuscular junctions of perlecan-null mice (Q28588415)

Molecular and cellular biology of cholinesterases

GOA release 2020-03-11

neuromuscular junction

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Eri Arikawa-Hirasawa

1

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31 January 2017

Susana G. Rossi

series ordinal

2

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31 January 2017

Richard L. Rotundo

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3

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31 January 2017

Yoshihiko Yamada

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4

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31 January 2017

language of work or name

English

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publication date

1 February 2002

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31 January 2017

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31 January 2017

5

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31 January 2017

2

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31 January 2017

119–123

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31 January 2017

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7 January 2021

[Acetylcholinesterase of fish electric organs (torpedo and electric eel); membrane complexes]

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7 January 2021

Multiple forms of acetylcholinesterase and their distribution in endplate and non-endplate regions of rat diaphragm muscle

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7 January 2021

Molecular forms of acetylcholinesterase from Torpedo californica: their relation to synaptic membranes

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7 January 2021

The Dependence of Acetylcholinesterase Aggregation at Low Ionic Strength upon a Polyanionic Component

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7 January 2021

Interaction of heparin with multimolecular aggregates of acetylcholinesterase

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7 January 2021

Genetic analysis of collagen Q: roles in acetylcholinesterase and butyrylcholinesterase assembly and in synaptic structure and function

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7 January 2021

Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme

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7 January 2021

Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)

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7 January 2021

Cholinesterase is associated with the basal lamina at the neuromuscular junction

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7 January 2021

Transient interactions between collagen-tailed acetylcholinesterase and sulfated proteoglycans prior to immobilization on the extracellular matrix

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7 January 2021

Compartmentalization of acetylcholinesterase mRNA and enzyme at the vertebrate neuromuscular junction

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7 January 2021

Developmental regulation of acetylcholinesterase transcripts in the mouse diaphragm: alternative splicing and focalization

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7 January 2021

Neural regulation of acetylcholinesterase mRNAs at mammalian neuromuscular synapses

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7 January 2021

Cell surface acetylcholinesterase molecules on multinucleated myotubes are clustered over the nucleus of origin

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7 January 2021

Aggregates of acetylcholine receptors are associated with plaques of a basal lamina heparan sulfate proteoglycan on the surface of skeletal muscle fibers

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7 January 2021

Extracellular matrix organization in developing muscle: correlation with acetylcholine receptor aggregates

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7 January 2021

Expression of several adhesive macromolecules (N-CAM, L1, J1, NILE, uvomorulin, laminin, fibronectin, and a heparan sulfate proteoglycan) in embryonic, adult, and denervated adult skeletal muscle

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7 January 2021

The biology of perlecan: the multifaceted heparan sulphate proteoglycan of basement membranes and pericellular matrices

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7 January 2021

Perlecan is essential for cartilage and cephalic development

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7 January 2021

Perlecan maintains the integrity of cartilage and some basement membranes

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7 January 2021

Acetylcholinesterase clustering at the neuromuscular junction involves perlecan and dystroglycan

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7 January 2021

Transplantation of quail collagen-tailed acetylcholinesterase molecules onto the frog neuromuscular synapse

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7 January 2021

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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7 January 2021

Defective neuromuscular synaptogenesis in agrin-deficient mutant mice

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7 January 2021

Chondroitinases release acetylcholinesterase from chick skeletal muscle

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7 January 2021

The small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscle

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7 January 2021

Co-solubilization of asymmetric acetylcholinesterase and dermatan sulfate proteoglycan from the extracellular matrix of rat skeletal muscles

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7 January 2021

The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction.

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7 January 2021

Binding of the G domains of laminin alpha1 and alpha2 chains and perlecan to heparin, sulfatides, alpha-dystroglycan and several extracellular matrix proteins

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7 January 2021

The dystroglycan complex is necessary for stabilization of acetylcholine receptor clusters at neuromuscular junctions and formation of the synaptic basement membrane

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7 January 2021

Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.

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7 January 2021

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).

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7 January 2021

A rapid, simple radiometric assay for cholinesterase, suitable for multiple determinations

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7 January 2021