The expanded CAG repeat associated with juvenile Huntington disease shows a common origin of most or all neurons and glia in human cerebrum

This publication has 18 references indexed in Scilit:

• Identification of a Neural Stem Cell in the Adult Mammalian Central Nervous System
  Cell, 1999
• Transglutaminase Action Imitates Huntington's Disease: Selective Polymerization of Huntingtin Containing Expanded Polyglutamine
  Molecular Cell, 1998
• Avoiding errors in the diagnosis of (CAG)n expansion in the huntingtin gene.
  Journal of Medical Genetics, 1997
• Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy
  Human Genetics, 1996
• CAG expansion affects the expression of mutant huntingtin in the Huntington's disease brain
  Neuron, 1995
• Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum
  Human Molecular Genetics, 1995
• Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1
  Nature Genetics, 1995
• A self-renewing multipotential stem cell in embryonic rat cerebral cortex
  Nature, 1994
• A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
  Cell, 1993
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970