SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia (Q34446619)

2 August 2017

1 reference

title

SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia (English)

1 reference

2 August 2017

Holmes SE

1

1 reference

2 August 2017

Hearn EO

series ordinal

2

1 reference

2 August 2017

Ross CA

series ordinal

3

1 reference

2 August 2017

Margolis RL

series ordinal

4

1 reference

2 August 2017

publication date

1 October 2001

1 reference

2 August 2017

published in

Brain Research Bulletin

1 reference

2 August 2017

volume

56

1 reference

2 August 2017

issue

3-4

1 reference

2 August 2017

page(s)

397-403

1 reference

Prediction of complete gene structures in human genomic DNA

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Phosphorylation of microtubule-associated protein tau is regulated by protein phosphatase 2A in mammalian brain. Implications for neurofibrillary degeneration in Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

A conserved downstream element defines a new class of RNA polymerase II promoters

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Altered spacing of promoter elements due to the dodecamer repeat expansion contributes to reduced expression of the cystatin B gene in EPM1.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Structure of the 55-kDa regulatory subunit of protein phosphatase 2A: evidence for a neuronal-specific isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Regulation of protein kinase cascades by protein phosphatase 2A.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Brain protein serine/threonine phosphatases

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Direct detection of novel expanded trinucleotide repeats in the human genome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Protein serine/threonine phosphatases--new avenues for cell regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Regulation of the phosphorylation state and microtubule-binding activity of Tau by protein phosphatase 2A.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Dominantly inherited ataxias

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Protein phosphatase 2A: a panoply of enzymes.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

Glutamine repeats and neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900596-2

7 January 2021

10.1016/S0361-9230(01)00596-2

Identifiers

DOI

1 reference

2 August 2017

1 reference