(Q24681141)

22 June 2017

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy (English)

1 reference

congenital muscular dystrophy

22 June 2017

0 references

0 references

1 reference

Thomas E Hall

1

0 references

Joachim Berger

Joachim Berger

7

0 references

Nicholas J. Cole

Nicholas J Cole

Robert J. Bryson-Richardson

5

0 references

Robert J Bryson-Richardson

2

0 references

Peter D. Currie

Peter D Currie

8

0 references

Silke Berger

3

Silke Berger

1 reference

22 June 2017

4

Arie S Jacoby

1 reference

22 June 2017

6

Georgina E Hollway

1 reference

PubMed ID

17438294

22 June 2017

language of work or name

English

0 references

publication date

16 April 2007

1 reference

22 June 2017

6

1 reference

Proceedings of the National Academy of Sciences of the United States of America

inferred from page(s)

published in

1 reference

22 June 2017

104

1 reference

22 June 2017

17

1 reference

22 June 2017

7092-7097

1 reference

22 June 2017

GeneWise and Genomewise

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Characterization and expression of the laminin gamma3 chain: a novel, non-basement membrane-associated, laminin chain

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Integrins as receptors for laminins

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Expression of dystroglycan and the laminin-alpha 2 chain in the rat peripheral nerve during development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Strength at the extracellular matrix-muscle interface.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Expression and biological role of laminin-1

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Merosin-integrin promotion of skeletal myofiber cell survival: Differentiation state-distinct involvement of p60Fyn tyrosine kinase and p38alpha stress-activated MAP kinase

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Laminins: structure and genetic regulation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Molecular basis of muscular dystrophies.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Radiation hybrid mapping of the zebrafish genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Dystrophin-associated proteins in muscular dystrophy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Functional morphology of serially linked skeletal muscle fibers

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Satellite cells from dystrophic (mdx) mouse muscle are stimulated by fibroblast growth factor in vitro

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

A novel laminin 2 isoform in severe laminin 2 deficient congenital muscular dystrophy

30 May 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0700942104

Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0700942104

Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0700942104

Myosin heavy chain expression in zebrafish and slow muscle composition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0700942104

Zebrafish periostin is required for the adhesion of muscle fiber bundles to the myoseptum and for the differentiation of muscle fibers

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0700942104

Transgenesis and gene trap methods in zebrafish by using the Tol2 transposable element.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Zebrafish mutants identify an essential role for laminins in notochord formation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Neural degeneration mutants in the zebrafish, Danio rerio.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1855385

Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for alpha2 chain of laminin)

28 November 2018

1 reference

12 December 2020

Myosatellite cells, growth, and regeneration in murine dystrophic muscle: a quantitative study

1 reference

12 December 2020

Transient and chronic neonatal denervation of murine muscle: a procedure to modify the phenotypic expression of muscular dystrophy

1 reference

12 December 2020

Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy

1 reference

12 December 2020

Differential heparin sensitivity of alpha-dystroglycan binding to laminins expressed in normal and dy/dy mouse skeletal muscle

1 reference

12 December 2020

Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy

1 reference

12 December 2020

Muscle-specific BCL2 expression ameliorates muscle disease in laminin {alpha}2-deficient, but not in dystrophin-deficient, mice

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0700942104

1 reference

OpenCitations bibliographic resource ID

22 June 2017

0 references

426401

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

PubMed ID

17438294