Human skeletal muscle xenograft as a new preclinical model for muscle disorders (Q33649287)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24452336%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

title

Human skeletal muscle xenograft as a new preclinical model for muscle disorders (English)

1 reference

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6 March 2020

1 reference

Yuanfan Zhang

1

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6 March 2020

Fedik Rahimov

3

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6 March 2020

Takako I Jones

4

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6 March 2020

Christopher W Ward

5

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6 March 2020

Naili Liu

7

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6 March 2020

Charles P Emerson

8

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6 March 2020

Louis M Kunkel

9

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6 March 2020

Terence A Partridge

10

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6 March 2020

Kathryn R Wagner

11

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6 March 2020

publication date

22 January 2014

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6 March 2020

published in

Human Molecular Genetics

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6 March 2020

volume

23

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6 March 2020

issue

12

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6 March 2020

page(s)

3180-3188

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Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD

6 March 2020

cites work

1 reference

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The mdx mouse model as a surrogate for Duchenne muscular dystrophy

21 June 2018

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Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy

21 June 2018

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Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.

21 June 2018

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Microtubules underlie dysfunction in duchenne muscular dystrophy.

21 June 2018

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Bodywide skipping of exons 45-55 in dystrophic mdx52 mice by systemic antisense delivery

21 June 2018

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

21 June 2018

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Structural and functional evaluation of branched myofibers lacking intermediate filaments

21 June 2018

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Glucocorticoid-treated mice are an inappropriate positive control for long-term preclinical studies in the mdx mouse

21 June 2018

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DUX4 activates germline genes, retroelements, and immune mediators: implications for facioscapulohumeral dystrophy.

21 June 2018

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Mice null for calsequestrin 1 exhibit deficits in functional performance and sarcoplasmic reticulum calcium handling

21 June 2018

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A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

21 June 2018

1 reference

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Slowing down differentiation of engrafted human myoblasts into immunodeficient mice correlates with increased proliferation and migration

21 June 2018

1 reference

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Genetic deletion of trkB.T1 increases neuromuscular function

21 June 2018

1 reference

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Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions

21 June 2018

1 reference

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Duchenne muscular dystrophy gene therapy: Lost in translation?

21 June 2018

1 reference

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DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

21 June 2018

1 reference

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Contribution of human muscle-derived cells to skeletal muscle regeneration in dystrophic host mice

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030773

Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030773

A unifying genetic model for facioscapulohumeral muscular dystrophy

21 June 2018

1 reference

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Biphasic myopathic phenotype of mouse DUX, an ORF within conserved FSHD-related repeats.

21 June 2018

1 reference

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Malformed mdx myofibers have normal cytoskeletal architecture yet altered EC coupling and stress-induced Ca2+ signaling

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030773

Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030773

Application and potential limitations of animal models utilized in the development of trastuzumab (Herceptin): a case study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4030773

Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1

21 June 2018

1 reference

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Development of the proteasome inhibitor PS-341.

21 June 2018

1 reference

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

21 June 2018

1 reference

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Sustained cell proliferation in denervated skeletal muscle of mice

21 June 2018

1 reference

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Randomized, double-blind six-month trial of prednisone in Duchenne's muscular dystrophy

21 June 2018

1 reference

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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

21 June 2018

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Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice

21 June 2018

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A New Immunodeficient Mouse Model for Human Myoblast Transplantation

21 January 2018

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Non-obese diabetic-recombination activating gene-1 (NOD-Rag1 null) interleukin (IL)-2 receptor common gamma chain (IL2r gamma null) null mice: a radioresistant model for human lymphohaematopoietic engraftment.

21 January 2018

1 reference

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Efficacy of systemic morpholino exon-skipping in Duchenne dystrophy dogs

21 January 2018

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A soluble activin type IIB receptor improves function in a mouse model of amyotrophic lateral sclerosis

21 January 2018

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Inhibition of myostatin reverses muscle fibrosis through apoptosis.

21 January 2018

1 reference

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Skeletal muscle stem cells adopt a dormant cell state post mortem and retain regenerative capacity.

21 January 2018

1 reference

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Mdx muscle grafts retain the mdx phenotype in normal hosts

30 October 2018

1 reference

12 December 2020

Fast skeletal muscle troponin activator in the dy2J muscular dystrophy model

1 reference

12 December 2020

Prednisone in Duchenne dystrophy. A randomized, controlled trial defining the time course and dose response. Clinical Investigation of Duchenne Dystrophy Group

1 reference

12 December 2020

Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDU028

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24452336%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

1 reference

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6 March 2020

PubMed publication ID

24452336

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24452336%20AND%20SRC:MED&resulttype=core&format=json