Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy (Q40300149)

19 September 2017

title

Laminin alpha1 chain improves laminin alpha2 chain deficient peripheral neuropathy (English)

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19 September 2017

Kinga I Gawlik

1

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19 September 2017

Jia-Yi Li

series ordinal

2

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19 September 2017

Asa Petersén

series ordinal

3

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19 September 2017

Madeleine Durbeej

series ordinal

4

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19 September 2017

publication date

7 August 2006

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19 September 2017

published in

Human Molecular Genetics

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19 September 2017

volume

15

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19 September 2017

issue

18

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19 September 2017

page(s)

2690-2700

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A simplified laminin nomenclature

19 September 2017

cites work

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

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Merosin and congenital muscular dystrophy

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Hypermyelinating neuropathy, mental retardation and epilepsy in a case of merosin deficiency

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Dysmyelinating sensory-motor neuropathy in merosin-deficient congenital muscular dystrophy.

21 January 2018

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The nodes of Ranvier in the nerves of mice with muscular dystrophy

21 January 2018

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Atypical axon-Schwann cell relationships in the common peroneal nerve of the dystrophic mouse: an ultrastructural study

21 January 2018

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

21 January 2018

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

21 January 2018

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Identification of a novel mutant transcript of laminin α2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J mice

21 January 2018

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Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

21 January 2018

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Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

21 January 2018

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Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

21 January 2018

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Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice

21 January 2018

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Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier.

21 January 2018

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An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

21 January 2018

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Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin

21 January 2018

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Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy

21 January 2018

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Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice

21 January 2018

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Laminin {alpha}1 chain corrects male infertility caused by absence of laminin {alpha}2 chain

21 January 2018

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Distribution and function of laminins in the neuromuscular system of developing, adult, and mutant mice

21 January 2018

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Laminin gamma1 is critical for Schwann cell differentiation, axon myelination, and regeneration in the peripheral nerve

21 January 2018

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Coordinate control of axon defasciculation and myelination by laminin-2 and -8.

21 January 2018

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Impeded interaction between Schwann cells and axons in the absence of laminin alpha4.

21 January 2018

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Conditional disruption of beta 1 integrin in Schwann cells impedes interactions with axons

21 January 2018

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Unique role of dystroglycan in peripheral nerve myelination, nodal structure, and sodium channel stabilization

21 January 2018

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Laminin alpha1 chain mediated reduction of laminin alpha2 chain deficient muscular dystrophy involves integrin alpha7beta1 and dystroglycan

21 January 2018

1 reference

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Differentiation of axon-related Schwann cells in vitro. I. Ascorbic acid regulates basal lamina assembly and myelin formation

21 January 2018

1 reference

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Role of the extracellular matrix in myelination of peripheral nerve

21 January 2018

1 reference

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Expression of laminin alpha 1, alpha 5 and beta 2 chains during embryogenesis of the kidney and vasculature.

21 January 2018

1 reference

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Laminin α2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL201

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL201

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19 September 2017

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