Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research (Q37531866)

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scientific article published on 06 December 2013

Language	Label	Description	Also known as
English	Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research	scientific article published on 06 December 2013

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scholarly article

1 reference

Europe PubMed Central

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2 March 2020

Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research (English)

1 reference

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2 March 2020

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congenital disorder

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congenital muscular dystrophy

1 reference

based on heuristic

inferred from title

congenital merosin-deficient muscular dystrophy 1A

1 reference

based on heuristic

inferred from title

James A Windelborn

5

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2 March 2020

8

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2 March 2020

author name string

Soonsang Yoon

1

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2 March 2020

Guido Stadler

2

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2 March 2020

Mary Lou Beermann

3

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2 March 2020

Eric V Schmidt

4

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2 March 2020

Peter Schneiderat

6

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2 March 2020

Woodring E Wright

7

1 reference

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2 March 2020

publication date

6 December 2013

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2 March 2020

Skeletal Muscle

1 reference

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2 March 2020

3

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2 March 2020

1

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2 March 2020

28

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2 March 2020

https://scigraph.springernature.com/pub.10.1186/2044-5040-3-28

0 references

Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Establishment of clonal myogenic cell lines from severely affected dystrophic muscles - CDK4 maintains the myogenic population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Ku70 regulates Bax-mediated pathogenesis in laminin-alpha2-deficient human muscle cells and mouse models of congenital muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Developmental and pathogenic mechanisms of basement membrane assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Pathology is alleviated by doxycycline in a laminin-alpha2-null model of congenital muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

SIRT3 is a stress-responsive deacetylase in cardiomyocytes that protects cells from stress-mediated cell death by deacetylation of Ku70

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Regulation of the proapoptotic factor Bax by Ku70-dependent deubiquitylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

The double life of the Ku protein: facing the DNA breaks and the extracellular environment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Immunochemical analysis of myosin heavy chain during avian myogenesis in vivo and in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

23 August 2017

Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production

1 reference

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23 August 2017

Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

14 September 2017

Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

14 September 2017

Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

14 September 2017

Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

28 September 2017

Autophagy is increased in laminin α2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

2 September 2018

Inexpensive low-oxygen incubators.

1 reference

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2 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3906772

2 September 2018

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/24314268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/24314268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of caspase-3 apoptotic pathways in skeletal muscle fibers in laminin alpha2-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/24314268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/24314268

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/2044-5040-3-28

1 reference

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2 March 2020

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1 reference

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2 March 2020

1 reference

Europe PubMed Central

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2 March 2020

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