An unstable triplet repeat in a gene related to myotonic muscular dystrophy.
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T. Ashizawa | A. Pizzuti | Ying-Hui Fu | Y. Fu | R. Fenwick | J. King | S. Rajnarayan | P. Dunne | J. Dubel | G. A. Nasser | P. de Jong | R. Fenwick | Y. Fu | Y. Fu | Y. Fu | Jonathan King | PW Dunne | G. Nasser | P. D. Jong | P. Dunne
[1] K. Titani,et al. Amino acid sequence of the catalytic subunit of bovine type II adenosine cyclic 3',5'-phosphate dependent protein kinase. , 1983, Biochemistry.
[2] Susan S. Taylor,et al. Direct evidence that oncogenic tyrosine kinases and cyclic AMP-dependent protein kinase have homologous ATP-binding sites , 1984, Nature.
[3] Michael Wigler,et al. Three different genes in S. cerevisiae encode the catalytic subunits of the cAMP-dependent protein kinase , 1987, Cell.
[4] A. Beaudet,et al. Spinocerebellar ataxia: Variable age of onset and linkage to human leukocyte antigen in a large kindred , 1988, Annals of neurology.
[5] T. Hunter,et al. The protein kinase family: conserved features and deduced phylogeny of the catalytic domains. , 1988, Science.
[6] R. Gibbs,et al. Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families. , 1990, Genomics.
[7] E. Nimmo,et al. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus. , 1990, American journal of human genetics.
[8] C. Caskey,et al. DNA typing and genetic mapping with trimeric and tetrameric tandem repeats. , 1991, American journal of human genetics.
[9] H. Brunner,et al. Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locus. , 1991, Genomics.
[10] K. Fischbeck,et al. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.
[11] C. Frith,et al. Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting. , 1991, Journal of medical genetics.
[12] Ben A. Oostra,et al. Absence of expression of the FMR-1 gene in fragile X syndrome , 1991, Cell.
[13] J. Sutcliffe,et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome , 1991, Cell.
[14] J. Sutcliffe,et al. Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox , 1991, Cell.
[15] C. Amemiya,et al. Cloning of the essential myotonic dystrophy region and mapping of the putative defect , 1992, Nature.