Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1 (Q28286194)

Rossella Tupler

12

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Davide Gabellini

Davide Gabellini

1

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Giuseppe D'Antona

Giuseppe D'Antona

2

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Alessandro Prelle

Alessandro Prelle

4

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Maurizio Moggio

3

Maurizio Moggio

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Patrizia Ciscato

8

Patrizia Ciscato

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author name string

Raffaella Adami

6

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Barbara Angeletti

7

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Maria Antonietta Pellegrino

9

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Roberto Bottinelli

10

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Michael R Green

Multiple 5'-flanking regions of the human alpha-skeletal actin gene synergistically modulate muscle-specific expression

11

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language of work or name

English

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publication date

23 February 2006

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published in

Nature

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volume

439

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issue

7079

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page(s)

973-7

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cites work

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D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection

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Facioscapulohumeral muscular dystrophy

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

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Large-scale proteomic analysis of the human spliceosome

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Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.

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

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

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Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old

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Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models.

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Glycosylation eases muscular dystrophy

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Muscular dystrophies: genes to pathogenesis

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Myotonic dystrophy: RNA pathogenesis comes into focus

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Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

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A muscleblind knockout model for myotonic dystrophy

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Definitive molecular diagnosis of facioscapulohumeral dystrophy

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Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

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Role of the fetal and alpha/beta exons in the function of fast skeletal troponin T isoforms: correlation with altered Ca2+ regulation associated with development.

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Genome-wide survey of human alternative pre-mRNA splicing with exon junction microarrays

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Identifiers

DOI

10.1038/NATURE04422

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

3211605

1011731478

0 references

3211605

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference