(Q40834560)

24 September 2017

IGF-II ameliorates the dystrophic phenotype and coordinately down-regulates programmed cell death (English)

1 reference

24 September 2017

Smith J

1

1 reference

24 September 2017

Goldsmith C

series ordinal

2

1 reference

24 September 2017

Ward A

series ordinal

3

1 reference

24 September 2017

LeDieu R

series ordinal

4

1 reference

24 September 2017

1 November 2000

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Cell Death & Differentiation

24 September 2017

1 reference

24 September 2017

7

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24 September 2017

11

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24 September 2017

1109-1118

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.cdd.4400738

24 September 2017

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cites work

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Association of dystrophin and an integral membrane glycoprotein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Syntrophin binds to an alternatively spliced exon of dystrophin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Dystrophin as a mechanochemical transducer in skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Molecular and genetic mapping of the mouse mdx locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

X chromosome-linked muscular dystrophy (mdx) in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

"mdx" mouse myopathy: histopathological, morphometric and histochemical observations on young mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Acute infantile spinal muscular atrophy. Muscle apoptosis as a proposed pathogenetic mechanism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Visualization of dystrophic muscle fibers in mdx mouse by vital staining with Evans blue: evidence of apoptosis in dystrophin-deficient muscle.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Dystrophic muscle in mice chimeric for expression of alpha5 integrin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Insulin-like growth factor-II is an autocrine survival factor for differentiating myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Disproportionate growth in mice with Igf-2 transgenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Utrophin: a potential replacement for dystrophin?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Reversal of terminal differentiation mediated by p107 in Rb-/- muscle cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

pRb controls proliferation, differentiation, and death of skeletal muscle cells and other lineages during embryogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Myonuclear apoptosis in dystrophic mdx muscle occurs by perforin-mediated cytotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

The molecular and biochemical basis of Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Conversion of mdx myofibres from dystrophin-negative to -positive by injection of normal myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Selection and use of ligands for receptor-mediated gene delivery to myogenic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/enhancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Molecular and functional analysis of the utrophin promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Induction of utrophin gene expression by heregulin in skeletal muscle cells: role of the N-box motif and GA binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Sequence of a placental cDNA encoding the mouse insulin-like growth factor II precursor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

The effects of fibroblast growth factors in long-term primary culture of dystrophic (mdx) mouse muscle myoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Immunoelectron microscopic localization of dystrophin in myofibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

A noninvasive procedure to detect muscle weakness in the mdx mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Enhanced expression of transforming growth factor-beta 1 during thyroid hyperplasia in rats

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

c-Myc-induced apoptosis in fibroblasts is inhibited by specific cytokines.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Ontogeny of somatomedin during development in the mouse. Serum concentrations, molecular forms, binding proteins, and tissue receptors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

High plasma insulin-like growth factor-II and low lipid content in transgenic mice: measurements of lipid metabolism

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Programmed Cell Death and Senescence in Skeletal Muscle Stem Cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Results of a triple blind clinical study of myoblast transplantations without immunosuppressive treatment in young boys with Duchenne muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.CDD.4400738

7 January 2021

Identifiers

DOI

10.1038/SJ.CDD.4400738

1 reference

Dimensions Publication ID

24 September 2017

0 references

1 reference