RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2. (Q47802363)

5 February 2018

title

RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2. (English)

1 reference

5 February 2018

1 reference

Tao Zu

1 reference

5 February 2018

John D Cleary

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5 February 2018

Yuanjing Liu

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5 February 2018

Monica Bañez-Coronel

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5 February 2018

Jodi L Bubenik

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5 February 2018

Fatma Ayhan

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5 February 2018

Tetsuo Ashizawa

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5 February 2018

Guangbin Xia

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5 February 2018

H Brent Clark

1 reference

5 February 2018

Anthony T Yachnis

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5 February 2018

Maurice S Swanson

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5 February 2018

Laura P W Ranum

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5 February 2018

language of work or name

English

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publication date

1 September 2017

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5 February 2018

published in

Neuron

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5 February 2018

volume

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5 February 2018

issue

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5 February 2018

page(s)

1292-1305.e5

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5 February 2018

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5951173/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1.

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Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS

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Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement

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Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy

26 August 2018

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26 August 2018

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26 August 2018

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Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2.

26 August 2018

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Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

26 August 2018

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

26 August 2018

1 reference

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Anterior temporal white matter lesions in myotonic dystrophy with intellectual impairment: an MRI and neuropathological study

26 August 2018

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An unstable triplet repeat in a gene related to myotonic muscular dystrophy

26 August 2018

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Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

26 August 2018

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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

26 August 2018

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Myotonic dystrophies as a brain disorder

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10.1016/J.NEURON.2017.08.039

1 December 2018

Identifiers

DOI

1 reference

5 February 2018

PMC publication ID

5951173

0 references

1 reference

5 February 2018