Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene (Q34319775)

1 August 2017

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

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1 August 2017

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Xu H

1

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1 August 2017

Wu XR

series ordinal

2

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1 August 2017

Wewer UM

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3

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1 August 2017

Engvall E

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4

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1 August 2017

language of work or name

English

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publication date

1 November 1994

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1 August 2017

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1 August 2017

8

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1 August 2017

3

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1 August 2017

297-302

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https://scigraph.springernature.com/pub.10.1038/ng1194-297

1 August 2017

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cites work

A new nomenclature for the laminins

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

A laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

The dermal-epidermal junction of human skin contains a novel laminin variant

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Laminin variants: why, where and when?

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https://api.crossref.org/works/10.1038%2FNG1194-297

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Abnormal localization of laminin subunits in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

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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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Muscular dystrophy in the mouse caused by an allele at the dy-locus.

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Comparison of dy and dy2J, Two Alleles Expressing Forms of Muscular Dystrophy in the Mouse

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Histopathology of hereditary, progressive muscular dystrophy in inbred strain 129 mice

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Primary structure of the human laminin A chain. Limited expression in human tissues

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Molecular Cloning of the cDNA Encoding Human Laminin A Chain

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Biochemical Mechanisms of Constitutive and Regulated Pre-mRNA Splicing

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Laminins and other strange proteins

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https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Aberrant PNS development in dystrophic mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Reciprocal expression of laminin A-chain isoforms along the crypt-villus axis in the human small intestine

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Differential expression of laminin isoforms and alpha 6-beta 4 integrin subunits in the developing human and mouse intestine.

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Laminin-like antigen in rat CNS neurons: distribution and changes upon brain injury and nerve growth factor treatment.

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Molecular genetics of epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Molecular genetics of the cutaneous basement membrane zone. Perspectives on epidermolysis bullosa and other blistering skin diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Laminin from rat yolk sac tumor: isolation, partial characterization, and comparison with mouse laminin

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-297

7 January 2021

Identifiers

DOI

10.1038/NG1194-297

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1 August 2017

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