(Q37227124)

19 August 2017

Haploinsufficiency of utrophin gene worsens skeletal muscle inflammation and fibrosis in mdx mice (English)

1 reference

19 August 2017

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9

Richard M Ransohoff

1 reference

19 August 2017

Lan Zhou

1

1 reference

19 August 2017

Jill A Rafael-Fortney

2

1 reference

19 August 2017

Ping Huang

3

1 reference

19 August 2017

Xinyu S Zhao

4

1 reference

19 August 2017

Georgiana Cheng

5

1 reference

19 August 2017

Xiaohua Zhou

6

1 reference

19 August 2017

Henry J Kaminski

7

1 reference

19 August 2017

Liping Liu

8

1 reference

19 August 2017

language of work or name

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24 September 2007

1 reference

Journal of the Neurological Sciences

19 August 2017

1 reference

19 August 2017

264

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19 August 2017

1-2

1 reference

19 August 2017

106-111

1 reference

Dystrophin and utrophin: genetic analyses of their role in skeletal muscle

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Expression of full-length utrophin prevents muscular dystrophy in mdx mice

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Population frequencies of inherited neuromuscular diseases—A world survey

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Muscular dystrophy in the mdx mouse: histopathology of the soleus and extensor digitorum longus muscles.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Severe disease, unaltered leukocyte migration, and reduced IFN-gamma production in CXCR3-/- mice with experimental autoimmune encephalomyelitis.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Temporal and spatial mRNA expression patterns of TGF-beta1, 2, 3 and TbetaRI, II, III in skeletal muscles of mdx mice.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2696235

The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation

3 September 2018

1 reference

12 December 2020

Ultrastructure of the skeletal muscle in the X chromosome-linked dystrophic (mdx) mouse. Comparison with Duchenne muscular dystrophy

1 reference

12 December 2020

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy

1 reference

12 December 2020

Differential expression of muscular dystrophy in diaphragm versus hindlimb muscles of mdx mice

1 reference

12 December 2020

A simplified method for the analysis of hydroxyproline in biological tissues

1 reference

12 December 2020

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy

1 reference

12 December 2020

Utrophin deficiency worsens cardiac contractile dysfunction present in dystrophin-deficient mdx mice

1 reference

12 December 2020

10.1016/J.JNS.2007.08.029

Identifiers

DOI

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

17889902

1 reference