(Q34091913)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11565031%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy (English)

1 reference

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11 November 2019

0 references

5

1 reference

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11 November 2019

author name string

Moll J

1

1 reference

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11 November 2019

Barzaghi P

2

1 reference

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11 November 2019

Lin S

3

1 reference

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11 November 2019

Bezakova G

4

1 reference

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11 November 2019

Engvall E

6

1 reference

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11 November 2019

Müller U

7

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11 November 2019

Ruegg MA

8

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11 November 2019

language of work or name

English

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publication date

1 September 2001

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11 November 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11565031%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

volume

413

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11 November 2019

page(s)

302-307

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11 November 2019

issue

6853

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https://scigraph.springernature.com/pub.10.1038/35095054

11 November 2019

exact match

0 references

cites work

Merosin and congenital muscular dystrophy

1 reference

7 January 2021

Form and function: the laminin family of heterotrimers

1 reference

7 January 2021

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

7 January 2021

Absence of integrin alpha 7 causes a novel form of muscular dystrophy

1 reference

7 January 2021

Agrin orchestrates synaptic differentiation at the vertebrate neuromuscular junction

1 reference

7 January 2021

Agrin binds to the nerve-muscle basal lamina via laminin

1 reference

7 January 2021

Agrin is a high-affinity binding protein of dystroglycan in non-muscle tissue

1 reference

7 January 2021

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

1 reference

7 January 2021

Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice.

1 reference

7 January 2021

Structural and functional analysis of the recombinant G domain of the laminin alpha4 chain and its proteolytic processing in tissues

1 reference

7 January 2021

Electron microscopic structure of agrin and mapping of its binding site in laminin-1

1 reference

7 January 2021

Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction

1 reference

7 January 2021

Transcriptional regulation of the muscle creatine kinase gene and regulated expression in transfected mouse myoblasts

1 reference

7 January 2021

Identification of upstream and intragenic regulatory elements that confer cell-type-restricted and differentiation-specific expression on the muscle creatine kinase gene

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The laminin alpha2 expressed by dystrophic dy(2J) mice is defective in its ability to form polymers

1 reference

7 January 2021

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

1 reference

7 January 2021

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

1 reference

7 January 2021

A role for dystroglycan in basement membrane assembly

1 reference

7 January 2021

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

1 reference

7 January 2021

A minigene of neural agrin encoding the laminin-binding and acetylcholine receptor-aggregating domains is sufficient to induce postsynaptic differentiation in muscle fibres

1 reference

7 January 2021

Differential expression of five laminin alpha (1-5) chains in developing and adult mouse kidney

1 reference

7 January 2021

Structural properties of recombinant domain III-3 of perlecan containing a globular domain inserted into an epidermal-growth-factor-like motif

1 reference

7 January 2021

Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy

1 reference

7 January 2021

A quantitative fluorescence-imaging technique for studying acetylcholine receptor turnover at neuromuscular junctions in living animals

1 reference

7 January 2021

Identifiers

DOI

10.1038/35095054

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11565031%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 November 2019

0 references

1 reference