Evolution of Simple Repeats in DNA and Their Relation to Human Disease
- 1 July 1998
- Vol. 94 (2) , 155-160
- https://doi.org/10.1016/s0092-8674(00)81415-4
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- GAA Instability in Friedreich's Ataxia Shares a Common, DNA-Directed and Intraallelic Mechanism with Other Trinucleotide DiseasesMolecular Cell, 1998
- Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyNature Genetics, 1998
- Truncated Forms of the Androgen Receptor are Associated with Polyglutamine Expansion in X-Linked Spinal and Bulbar Muscular AtrophyHuman Molecular Genetics, 1998
- Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in BrainScience, 1997
- Comparison of bicoid-dependent regulation of hunchback between Musca domestica and Drosophila melanogasterMechanisms of Development, 1997
- Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections.Microbiology and Molecular Biology Reviews, 1997
- Molecular Cloning and Characterization of a Novel Mouse Macrophage Gene That Encodes a Nuclear Protein Comprising Polyglutamine Repeats and Interspersing HistidinesPublished by Elsevier ,1996
- Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndromeHuman Molecular Genetics, 1996
- Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic miceNature Genetics, 1995
- Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type INature Genetics, 1993