A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.
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M. Pericak-Vance | G. Schellenberg | K. Tashiro | K. Welsh-Bohmer | S. Tsuji | A. Brice | T. Bird | L. Clark | K. Wilhelmsen | H. Sasaki | T. Ikeuchi | H. Takano | K. Sanpei | G. Cancel
[1] Mika Nakamoto,et al. A CAG/CTG expansion in the normal population , 1997, Nature Genetics.
[2] F. McMahon,et al. A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. , 1997, Human molecular genetics.
[3] Y. Agid,et al. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion , 1997, Nature Genetics.
[4] N L Foster,et al. Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference , 1997, Annals of neurology.
[5] J. Mandel. Breaking the rule of three , 1997, Nature.
[6] S. M. Sumi,et al. Chromosome 17 and hereditary dementia , 1997, Neurology.
[7] K. Kidd,et al. Survey of maximum CTG/CAG repeat lengths in humans and non-human primates: total genome scan in populations using the Repeat Expansion Detection method. , 1997, Human molecular genetics.
[8] M. Pericak-Vance,et al. Linkage of frontotemporal dementia to chromosome 17: clinical and neuropathological characterization of phenotype. , 1996, American journal of human genetics.
[9] S. Tsuji,et al. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT , 1996, Nature Genetics.
[10] S. Tsuji. Unstable expansion of triplet repeats as a new disease mechanism for neurodegenerative diseases , 1996, Japanese Journal of Human Genetics.
[11] G. Gyapay,et al. A radiation hybrid map of the human genome. , 1996, Human molecular genetics.
[12] K. Fischbeck,et al. Trinucleotide repeats in neurogenetic disorders. , 1996, Annual review of neuroscience.
[13] G. Pals,et al. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21. , 1996, Human molecular genetics.
[14] J. Weissenbach,et al. Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease. , 1995, Human molecular genetics.
[15] K. Wilhelmsen,et al. Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. , 1994, American journal of human genetics.
[16] O. Onodera,et al. Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) , 1994, Nature Genetics.
[17] T. Hudson,et al. Direct detection of novel expanded trinucleotide repeats in the human genome , 1993, Nature Genetics.
[18] Manish S. Shah,et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes , 1993, Cell.
[19] H. Zoghbi,et al. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I , 1993, Nature Genetics.
[20] R. Myers,et al. Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. , 1990, Science.
[21] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[22] W. Rutter,et al. Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. , 1979, Biochemistry.