(Q36128434)

12 August 2017

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title

Pathogenesis of spinocerebellar ataxias viewed from the RNA perspective (English)

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12 August 2017

author

Włodzimierz Krzyżosiak

series ordinal

2

object named as

Wlodzimierz J Krzyzosiak

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12 August 2017

1

Gracjan Michlewski

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12 August 2017

publication date

1 January 2005

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12 August 2017

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12 August 2017

volume

4

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12 August 2017

issue

1

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12 August 2017

page(s)

19-24

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https://scigraph.springernature.com/pub.10.1080/14734220510007905

12 August 2017

exact match

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cites work

The fragile-X premutation: a maturing perspective

1 reference

12 December 2020

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

1 reference

12 December 2020

Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.

1 reference

12 December 2020

Myotonic dystrophy: RNA pathogenesis comes into focus

1 reference

12 December 2020

Facile FMR1 mRNA structure regulation by interruptions in CGG repeats

1 reference

12 December 2020

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

1 reference

12 December 2020

Structures of trinucleotide repeats in human transcripts and their functional implications.

1 reference

12 December 2020

RNA gains a new function: a mediator of neurodegeneration

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12 December 2020

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

1 reference

12 December 2020

SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia

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12 December 2020

The spinocerebellar ataxia 8 noncoding RNA causes neurodegeneration and associates with staufen in Drosophila.

1 reference

12 December 2020

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.

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12 December 2020

Spinocerebellar ataxia type 6 mutation alters P-type calcium channel function

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12 December 2020

Muscleblind proteins regulate alternative splicing

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12 December 2020

Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats

1 reference

12 December 2020

A muscleblind knockout model for myotonic dystrophy

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12 December 2020

CAG repeats containing CAA interruptions form branched hairpin structures in spinocerebellar ataxia type 2 transcripts

1 reference

12 December 2020

Insulin receptor splicing alteration in myotonic dystrophy type 2.

1 reference

12 December 2020

RNA structure of trinucleotide repeats associated with human neurological diseases

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12 December 2020

Pathogenesis of polyglutamine disorders: aggregation revisited

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12 December 2020

Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons

1 reference

12 December 2020

Double-stranded RNA-dependent protein kinase, PKR, binds preferentially to Huntington's disease (HD) transcripts and is activated in HD tissue

1 reference

12 December 2020

RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila

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12 December 2020

Imperfect CAG repeats form diverse structures in SCA1 transcripts

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12 December 2020

A fragile balance: FMR1 expression levels

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12 December 2020

Polyglutamines placed into context

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12 December 2020

Pathogenic RNA repeats: an expanding role in genetic disease

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12 December 2020

Biomedicine. Reconstructing myotonic dystrophy

1 reference

12 December 2020

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

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12 December 2020

Molecular architecture of CAG repeats in human disease related transcripts

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12 December 2020

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis

1 reference

12 December 2020

10.1080/14734220510007905

Identifiers

DOI

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Dimensions Publication ID

12 August 2017

1046593912

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1 reference