Distinct genetic regions modify specific muscle groups in muscular dystrophy (Q34518008)

2 August 2017

Distinct genetic regions modify specific muscle groups in muscular dystrophy (English)

1 reference

2 August 2017

Kayleigh A Swaggart

1

1 reference

2 August 2017

Ahlke Heydemann

series ordinal

2

1 reference

2 August 2017

Abraham A Palmer

series ordinal

3

1 reference

2 August 2017

Elizabeth M McNally

series ordinal

4

1 reference

2 August 2017

19 October 2010

1 reference

2 August 2017

Physiological Genomics

1 reference

2 August 2017

43

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2 August 2017

1

1 reference

2 August 2017

24-31

1 reference

Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Tnni3k modifies disease progression in murine models of cardiomyopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Genetic modifier screens reveal new components that interact with the Drosophila dystroglycan-dystrophin complex

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Muscle diseases: the muscular dystrophies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Dystrophin, its interactions with other proteins, and implications for muscular dystrophy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Mutations in dynamin 2 cause dominant centronuclear myopathy

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Sarcoglycans in vascular smooth and striated muscle

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

ADAM12 alleviates the skeletal muscle pathology in mdx dystrophic mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Disruption of the gene encoding the latent transforming growth factor-beta binding protein 4 (LTBP-4) causes abnormal lung development, cardiomyopathy, and colorectal cancer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Leakage-resistant blood vessels in mice transgenically overexpressing angiopoietin-1

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Two myogenic lineages within the developing somite

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Mind bomb 2, a founder myoblast-specific protein, regulates myoblast fusion and muscle stability

7 July 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00172.2010

Aquaporin-4 deficiency in skeletal muscle and brain of dystrophic mdx mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00172.2010

Genetic background influences muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00172.2010

21 January 2018

NO more muscle fatigue

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00172.2010

Multiple quantitative trait loci modify the heart failure phenotype in murine cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00172.2010

Independent regulation of short and long forms of latent TGF-beta binding protein (LTBP)-4 in cultured fibroblasts and human tissues

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3026347

Intrafamilial variability in dystrophin abundance correlated with difference in the severity of the phenotype

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20959497

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Contractile systolic and diastolic dysfunction in renin-induced hypertensive cardiomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20959497

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1152/PHYSIOLGENOMICS.00172.2010

1 reference

2 August 2017

1 reference

2 August 2017

1 reference