Contributions of the LG modules and furin processing to laminin-2 functions (Q38291309)

1 September 2017

title

Contributions of the LG modules and furin processing to laminin-2 functions (English)

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1 September 2017

Sergei P Smirnov

1

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1 September 2017

Erin L McDearmon

2

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1 September 2017

Shaohua Li

3

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1 September 2017

James M Ervasti

4

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1 September 2017

Karl Tryggvason

5

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1 September 2017

Peter D Yurchenco

6

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1 September 2017

language of work or name

English

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publication date

8 March 2002

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Journal of Biological Chemistry

1 September 2017

number of pages

10

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based on heuristic

inferred from page(s)

published in

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1 September 2017

volume

277

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1 September 2017

issue

21

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1 September 2017

page(s)

18928-18937

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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

1 September 2017

cites work

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https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Form and function: the laminin family of heterotrimers

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Reduction of postjunctional fold density and depth in dystrophic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Laminin polymerization induces a receptor-cytoskeleton network

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Laminin-induced acetylcholine receptor clustering: an alternative pathway

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M201880200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Recombinant laminin B1 chains exhibit intact short-arm domains but do not form oligomeric molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

The alpha chain of laminin-1 is independently secreted and drives secretion of its beta- and gamma-chain partners.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Role of alpha-dystroglycan as a Schwann cell receptor for Mycobacterium leprae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

A functional role for specific spliced variants of the alpha7beta1 integrin in acetylcholine receptor clustering

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Differential heparin inhibition of skeletal muscle alpha-dystroglycan binding to laminins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Cell and heparin binding in the distal long arm of laminin: identification of active and cryptic sites with recombinant and hybrid glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Mutation of a basic sequence in the laminin alpha2LG3 module leads to a lack of proteolytic processing and has different effects on beta1 integrin-mediated cell adhesion and alpha-dystroglycan binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Regulation of programmed cell death by basement membranes in embryonic development

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Structure of the C-terminal laminin G-like domain pair of the laminin alpha2 chain harbouring binding sites for alpha-dystroglycan and heparin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Laminin-induced clustering of dystroglycan on embryonic muscle cells: comparison with agrin-induced clustering.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Dystroglycan is not required for localization of dystrophin, syntrophin, and neuronal nitric-oxide synthase at the sarcolemma but regulates integrin alpha 7B expression and caveolin-3 distribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Chimeric forms of furin and TGN38 are transported with the plasma membrane in the trans-Golgi network via distinct endosomal pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M201880200

21 January 2018

Identifiers

DOI

10.1074/JBC.M201880200

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1 September 2017

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