(Q48466850)

11 February 2018

title

Electrophysiology of the neuromuscular junction of the laminin-2 (merosin) deficient C57 BL/6J dy2J/dy2J dystrophic mouse. (English)

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11 February 2018

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neuromuscular junction

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Edwards JP

1

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11 February 2018

Hatton PA

series ordinal

2

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11 February 2018

Wareham AC

series ordinal

3

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11 February 2018

language of work or name

English

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publication date

1 March 1998

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11 February 2018

published in

Brain Research

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11 February 2018

volume

788

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11 February 2018

issue

1-2

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11 February 2018

page(s)

262-268

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11 February 2018

Neuromuscular junctions shrink and expand as muscle fiber size is manipulated: in vivo observations in the androgen-sensitive bulbocavernosus muscle of mice

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Histochemical and structural analyses of the phenotypic expression of the dystrophic gene in the 129/ReJ dy/dy and the C57BL/6J dy2J/dy2J mice

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The basement membrane at the neuromuscular junction: a synaptic mediatrix

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Histochemical and morphological study of dystrophic () and normal muscle

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The evolution of an experimental distal motor axonopathy. Physiological studies of changes in neuromuscular transmission caused by cycloleucine, an inhibitor of methionine adenosyltransferase

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Ultrastructural Alterations of the Motor End Plate in Myotonic Dystrophy of the Mouse (dy2J/dy2J)

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The Conus toxin geographutoxin IL distinguishes two functional sodium channel subtypes in rat muscle cells developing in vitro

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The resting membrane potential of fibres of fast and slow twitch muscles in normal and dystrophic mice

7 January 2021

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Some mechanical and electrical properties of distal hind limb muscles of genetically dystrophic mice (C57BL/6Jdy2J/dy2J)

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Muscular dystrophy in the mouse: neuromuscular transmission and the concept of functional denervation

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Abnormal localization of laminin subunits in muscular dystrophies

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Use of geographutoxin II (mu-conotoxin) for the study of neuromuscular transmission in mouse

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Correlation between nerve terminal size and transmitter release at the neuromuscular junction of the frog

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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

7 January 2021

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7 January 2021

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A further study of the statistical composition on the end-plate potential

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Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

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Changes in MEPP and EPP amplitude distributions in the mouse diaphragm during synapse formation and degeneration.

7 January 2021

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Neuromuscular transmission in the mdx mouse

7 January 2021

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Aberrant differentiation of neuromuscular junctions in mice lacking s-laminin/laminin beta 2

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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

7 January 2021

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Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

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7 January 2021

Identifiers

DOI

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11 February 2018

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11 February 2018