Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

@en

Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

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P1476

Silencing Nfix rescues muscular dystrophy by delaying muscle regeneration.

@en

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Anna Innocenzi

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Chiara Bonfanti

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Marielle Saclier

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Mattia Bastoni

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Stefania Antonini

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Stefania Monteverde

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P2860

Glucocorticoid corticosteroids for Duchenne muscular dystrophy

Stem cells for skeletal muscle regeneration: therapeutic potential and roadblocks

A phase I/IItrial of MYO-029 in adult subjects with muscular dystrophy

Nfix regulates fetal-specific transcription in developing skeletal muscle

The transcription factor Nfix is essential for normal brain development.

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.

Roles of the NFI/CTF gene family in transcription and development.

Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres.

NF1 transcriptional factor(s) is required for basal promoter activation of the human intestinal NaPi-IIb cotransporter gene.

Progress and prospects of gene therapy clinical trials for the muscular dystrophies.

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s41467-017-01098-y

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scholarly article

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10.1038/S41467-017-01098-Y

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P407

English

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P478

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Giuliana Rossi

Graziella Messina

Valentina Taglietti

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2017-10-20T00:00:00Z

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P6179

1092252208

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29057908

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5651883

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