Muscle fatigue, nNOS and muscle fiber atrophy in limb girdle muscular dystrophy (Q28083989)

limb-girdle muscular dystrophy

main subject

1 reference

11 October 2019

nitric oxide synthase 1

1 reference

28 September 2019

1 reference

11 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Elisabetta Tasca

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Anna Chiara Nascimbeni

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Marina Fanin

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

language of work or name

1 reference

December 2014

1 reference

1 December 2014

6 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

6 October 2019

11 October 2019

8 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

6 October 2019

11 October 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

page(s)

119-126

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

1 June 2020

6 references

13 March 2019

22 April 2019

25 April 2019

28 September 2019

6 October 2019

on focus list of Wikimedia project

11 October 2019

ScienceSource

0 references

cites work

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Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

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Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutations

20 March 2017

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Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2E

20 March 2017

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Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy

20 March 2017

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20 March 2017

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Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy

20 March 2017

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Sildenafil does not improve cardiomyopathy in Duchenne/Becker muscular dystrophy.

7 April 2017

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Genetic basis of limb-girdle muscular dystrophies: the 2014 update

29 September 2017

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Fatigue in muscular dystrophies

29 September 2017

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Sildenafil reduces respiratory muscle weakness and fibrosis in the mdx mouse model of Duchenne muscular dystrophy

29 September 2017

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Exercise training attenuates MuRF-1 expression in the skeletal muscle of patients with chronic heart failure independent of age: the randomized Leipzig Exercise Intervention in Chronic Heart Failure and Aging catabolism study

29 September 2017

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A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy

29 September 2017

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Arginine metabolism by macrophages promotes cardiac and muscle fibrosis in mdx muscular dystrophy

29 September 2017

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Golgi and sarcolemmal neuronal NOS differentially regulate contraction-induced fatigue and vasoconstriction in exercising mouse skeletal muscle

29 September 2017

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Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?

29 September 2017

1 reference

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Sarcolemma-localized nNOS is required to maintain activity after mild exercise

29 September 2017

1 reference

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Branched-chain amino acids and arginine suppress MaFbx/atrogin-1 mRNA expression via mTOR pathway in C2C12 cell line.

29 September 2017

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Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes

29 September 2017

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Molecular diagnosis in LGMD2A: mutation analysis or protein testing?

29 September 2017

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Smooth muscle cell-extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy

29 September 2017

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The 10 autosomal recessive limb-girdle muscular dystrophies

29 September 2017

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Influence of estrogen on skeletal muscle damage, inflammation, and repair

29 September 2017

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Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy

29 September 2017

1 reference

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Physiology of a microgravity environment invited review: microgravity and skeletal muscle

29 September 2017

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Impaired metabolic modulation of alpha-adrenergic vasoconstriction in dystrophin-deficient skeletal muscle

29 September 2017

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Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy

29 September 2017

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Gender difference in limb-girdle muscular dystrophy: a muscle fiber morphometric study in 101 patients

29 September 2017

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Muscle atrophy, ubiquitin-proteasome, and autophagic pathways in dysferlinopathy.

27 November 2018

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Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study

27 November 2018

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Exercise training has beneficial anti-atrophy effects by inhibiting oxidative stress-induced MuRF1 upregulation in rats with diabetes

27 November 2018

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Dietary L-carnitine alters gene expression in skeletal muscle of piglets

27 November 2018

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27 November 2018

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27 November 2018

NO more muscle fatigue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Reduction of skeletal muscle atrophy by a proteasome inhibitor in a rat model of denervation

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Absence of neuronal nitric oxide synthase (nNOS) as a pathological marker for the diagnosis of Becker muscular dystrophy with rod domain deletions

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Functional nitric oxide synthase mislocalization in cardiomyopathy

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Clinical variability in calpainopathy: what makes the difference?

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

NO vascular control in Duchenne muscular dystrophy

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4369848

Limb-girdle muscular dystrophy with apparently different clinical courses within sexes in a large inbred kindred.

27 November 2018

1 reference

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Evaluation of cardiac and respiratory involvement in sarcoglycanopathies

27 November 2018

1 reference

12 December 2020

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach

1 reference

12 December 2020

LGMD2E patients risk developing dilated cardiomyopathy

1 reference

12 December 2020

Heart involvement in muscular dystrophies due to sarcoglycan gene mutations

1 reference

12 December 2020

Prior resistance training and sex influence muscle responses to arm suspension

1 reference

12 December 2020

EPA inhibits the inhibitor of κBα (IκBα)/NF-κB/muscle RING finger 1 pathway in C2C12 myotubes in a PPARγ-dependent manner

1 reference

12 December 2020

Fenofibrate, a PPARα agonist, decreases atrogenes and myostatin expression and improves arthritis-induced skeletal muscle atrophy

1 reference

12 December 2020

Identifiers

2138980

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2138980

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

PubMed publication ID

25873780

2 references

Consolidated OpenCitations Corpus – April 2017

2138980

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25873780%20AND%20SRC:MED&resulttype=core&format=json