Neurodegenerative disease: 'Fifty shades of grey' in the Huntington disease gene
暂无分享,去创建一个
[1] J. Jankovic,et al. Characterization of the Huntington intermediate CAG repeat expansion phenotype in PHAROS , 2013, Neurology.
[2] Jessica K. Lee,et al. Measures of growth in children at risk for Huntington disease , 2012, Neurology.
[3] P. Nopoulos,et al. Substance abuse may be a risk factor for earlier onset of Huntington disease , 2012, Journal of Neurology.
[4] P. Detloff,et al. DNA instability in postmitotic neurons , 2008, Proceedings of the National Academy of Sciences.
[5] Jane S. Paulsen,et al. Psychiatric Symptoms in Huntington’s Disease before Diagnosis: The Predict-HD Study , 2007, Biological Psychiatry.
[6] H. Zoghbi,et al. RORα-Mediated Purkinje Cell Development Determines Disease Severity in Adult SCA1 Mice , 2006, Cell.
[7] M. MacDonald,et al. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. , 2005, Human molecular genetics.
[8] Larry J Young,et al. Microsatellite Instability Generates Diversity in Brain and Sociobehavioral Traits , 2005, Science.
[9] Karen Marder,et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[10] G. Nguyen,et al. DNA stability and schizophrenia in twins , 2003, Schizophrenia Research.