(Q36128445)

12 August 2017

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title

Recent progress in spinocerebellar ataxia type-10 (SCA10). (English)

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12 August 2017

spinocerebellar ataxia

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Xi Lin

1

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PubMed ID

15895557

12 August 2017

Tetsuo Ashizawa

series ordinal

2

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12 August 2017

1 January 2005

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12 August 2017

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12 August 2017

4

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12 August 2017

1

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12 August 2017

37-42

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https://scigraph.springernature.com/pub.10.1080/14734220510007897

12 August 2017

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cites work

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

1 reference

12 December 2020

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

1 reference

12 December 2020

Aberrant regulation of insulin receptor alternative splicing is associated with insulin resistance in myotonic dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Asynchronous replication of imprinted genes is established in the gametes and maintained during development

1 reference

12 December 2020

The need for enhancers is acquired upon formation of a diploid nucleus during early mouse development.

1 reference

12 December 2020

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.

1 reference

12 December 2020

Changes in histone synthesis and modification at the beginning of mouse development correlate with the establishment of chromatin mediated repression of transcription.

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12 December 2020

Spinocerebellar ataxia type 10 in the French population.

1 reference

12 December 2020

Localized torsional tension in the DNA of human cells

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12 December 2020

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy

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12 December 2020

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

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12 December 2020

SCA10 and ATTCT repeat expansion: clinical features and molecular aspects

1 reference

12 December 2020

Ataxin-10, the spinocerebellar ataxia type 10 neurodegenerative disorder protein, is essential for survival of cerebellar neurons

1 reference

12 December 2020

Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

1 reference

12 December 2020

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

1 reference

12 December 2020

Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10

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12 December 2020

Transcriptional state of the mouse mammary tumor virus promoter can affect topological domain size in vivo

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12 December 2020

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

1 reference

12 December 2020

The inefficient replication origin from yeast ribosomal DNA is naturally impaired in the ARS consensus sequence and in DNA unwinding.

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia

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12 December 2020

In vitro replication of plasmids containing human c-myc DNA.

1 reference

12 December 2020

Pathogenic RNA repeats: an expanding role in genetic disease

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12 December 2020

Unpaired structures in SCA10 (ATTCT)n.(AGAAT)n repeats

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12 December 2020

Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy

1 reference

12 December 2020

Measurement of unrestrained negative supercoiling and topological domain size in living human cells

1 reference

12 December 2020

Expanded CUG repeats trigger aberrant splicing of ClC-1 chloride channel pre-mRNA and hyperexcitability of skeletal muscle in myotonic dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1080/14734220510007897

Identifiers

DOI

1 reference

PubMed ID

15895557

Dimensions Publication ID

12 August 2017

0 references

1 reference

PubMed ID

15895557