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

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scientific article published on October 19, 2010

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English	Distinct genetic regions modify specific muscle groups in muscular dystrophy	scientific article published on October 19, 2010

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

title

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

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

author

Elizabeth M. McNally

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4

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Elizabeth M. McNally

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stated in

Europe PubMed Central

PubMed publication ID

20959497

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

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5 August 2024

author name string

Ahlke Heydemann

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2

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

Kayleigh A. Swaggart

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1

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Europe PubMed Central

PubMed publication ID

20959497

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

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Abraham A. Palmer

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3

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Europe PubMed Central

PubMed publication ID

20959497

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

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5 August 2024

language of work or name

English

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National Center for Biotechnology Information

PubMed publication ID

20959497

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20959497

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publication date

19 October 2010

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

full work available at URL

https://europepmc.org/articles/pmc3026347

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HTML

online access status

open access

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Europe PubMed Central

PubMed publication ID

20959497

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

retrieved

5 August 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20959497/?tool=EBI

file format

HTML

online access status

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content deliverer

PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20959497

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

retrieved

5 August 2024

https://europepmc.org/articles/PMC3026347

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20959497

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

retrieved

5 August 2024

https://doi.org/10.1152/physiolgenomics.00172.2010

online access status

open access

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stated in

Europe PubMed Central

PubMed publication ID

20959497

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20959497

retrieved

5 August 2024

https://www.physiology.org/doi/pdf/10.1152/physiolgenomics.00172.2010

1 reference

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Crossref

DOI

10.1152/PHYSIOLGENOMICS.00172.2010

reference URL

https://api.crossref.org/works/10.1152/PHYSIOLGENOMICS.00172.2010

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5 August 2024

published in

Physiological Genomics

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Europe PubMed Central

PubMed publication ID

20959497

retrieved

2 August 2017

volume

43

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stated in

Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

issue

1

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

page(s)

24-31

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Europe PubMed Central

PubMed publication ID

20959497

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2 August 2017

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

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Muscle diseases: the muscular dystrophies

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

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

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

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ADAM12 alleviates the skeletal muscle pathology in mdx dystrophic mice

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

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

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

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NO more muscle fatigue

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

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12 December 2020

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Contractile systolic and diastolic dysfunction in renin-induced hypertensive cardiomyopathy

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PubMed

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

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12 December 2020

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Journal of Cellular Physiology

series ordinal

12

volume

223

page(s)

727

author name string

Kantola AK

publication date

2010

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Crossref

DOI

10.1152/PHYSIOLGENOMICS.00172.2010

reference URL

https://api.crossref.org/works/10.1152/PHYSIOLGENOMICS.00172.2010

retrieved

5 August 2024

Identifiers

DOI

10.1152/PHYSIOLGENOMICS.00172.2010

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20959497

retrieved

2 August 2017

PMC publication ID

3026347

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20959497

retrieved

2 August 2017

PubMed publication ID

20959497

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20959497

retrieved

2 August 2017

ResearchGate publication ID

47500066

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