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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

Author

Huda Zoghbi

Published in: Nature Genetics

Date of publication: 1993-07-01

Language: angličtina

Main subject: spinocerebellar ataxia

Bibliographic databases:

Cites articles 33

Date

Title

Authors

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Spinocerebellar ataxia: study of a large kindred. I. General information and genetics
1977-05-01

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing
1978-07-01

Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions
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A family with hereditary ataxia: HLA typing
1981-12-01

Genetic aspects of autosomal dominant late onset cerebellar ataxia
1984-12-01

Spinocerebellar ataxia in a large kindred: age at onset, reproduction, and genetic linkage studies
1985-12-01

Nucleotide sequence from the neurogenic locus notch implies a gene product that shares homology with proteins containing EGF-like repeats
1988-06-01

Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.

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1989-10-01

Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings
1989-12-01

Synergistic activation by the glutamine-rich domains of human transcription factor Sp1
1989-06-01

Isolation of single-copy human genes from a library of yeast artificial chromosome clones
1990-06-01

Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents
1991-12-20

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox,Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991-07-01

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
1991-01-01

The 56/58 kDa androgen-binding protein in male genital skin fibroblasts with a deleted androgen receptor gene.
1991-11-01

prospero is expressed in neuronal precursors and encodes a nuclear protein that is involved in the control of axonal outgrowth in Drosophila
1991-06-01

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
1991-05-01

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

, ,
1992-02-01

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member
1992-02-06

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1992-10-01

A second-generation linkage map of the human genome
1992-02-01

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
1992-03-01

An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1992-05-01

Unstable DNA sequence in myotonic dystrophy
1992-03-01

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
1992-12-01

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
1992-07-01

Evidence of founder chromosomes in fragile X syndrome
1992-04-01

Complete deletion of the androgen receptor gene: definition of the null phenotype of the androgen insensitivity syndrome and determination of carrier status
1992-11-01

The Drosophila couch potato protein is expressed in nuclei of peripheral neuronal precursors and shows homology to RNA-binding proteins
1993-07

The gene for Machado-Joseph disease maps to human chromosome 14q
1993-07

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
1993-02-01

Brief report: reverse mutation in myotonic dystrophy

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