Instability of the CAG repeat in immortalized fibroblast cell cultures from Huntington's Disease transgenic mice

This publication has 24 references indexed in Scilit:

• Spinocerebellar ataxia type 6: CAG repeat expansion in α_1a voltage‐dependent calcium channel gene and clinical variations in japanese population
  Annals of Neurology, 1997
• Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
  Nature Genetics, 1996
• Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
  Nature Genetics, 1996
• Integrated Map of the Chromosome 8p12–p21 Region, a Region Involved in Human Cancers and Werner Syndrome
  Genomics, 1996
• CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
  Nature Genetics, 1994
• Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)
  Nature Genetics, 1994
• Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
  Nature Genetics, 1994
• Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
  Nature Genetics, 1993
• A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
  Cell, 1993
• Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
  Nature, 1991