Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

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Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

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http://www.wikidata.org/entity/Q39440318

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

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Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@en

Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@nl

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Item

label

Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@en

Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@nl

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Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@en

Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum.

@nl

P1476

Congenital myotonic dystrophy-an RNA-mediated disease across a developmental continuum

@en

P2093

Robert K Bradley

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P2860

Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy

Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy

A muscleblind knockout model for myotonic dystrophy

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy.

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

Dose-Dependent Regulation of Alternative Splicing by MBNL Proteins Reveals Biomarkers for Myotonic Dystrophy

Transcriptome-wide regulation of pre-mRNA splicing and mRNA localization by muscleblind proteins.

RNA splicing factors as oncoproteins and tumour suppressors.

RNA mis-splicing in disease.

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.

P304

1067-1068

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P31

scholarly article

P356

10.1101/GAD.302893.117

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P433

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P478

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P50

Sujatha Jagannathan

P577

2017-06-01T00:00:00Z

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P698

28717044

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P921

birth defect

P932

5538429

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