Search Results - "Burman, R W"

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  1. 1

    Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation by BURMAN, R. W, POPOVICH, B. W, JACKY, P. B, TURKER, M. S

    Published in Human molecular genetics (01-11-1999)
    “…The fragile X syndrome is characterized at the molecular level by expansion and methylation of a CGG trinucleotide repeat located within the FMR1 locus. The…”
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    Journal Article
  2. 2

    Hypomethylation of an Expanded FMR1 Allele Is Not Associated with a Global DNA Methylation Defect by Burman, Robert W., Yates, Phillip A., Green, Lindsay D., Jacky, Peter B., Turker, Mitchell S., Popovich, Bradley W.

    Published in American journal of human genetics (01-11-1999)
    “…The vast majority of fragile-X full mutations are heavily methylated throughout the expanded CGG repeat and the surrounding CpG island. Hypermethylation…”
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    Journal Article
  3. 3

    Tandem B1 Elements Located in a Mouse Methylation Center Provide a Target for de Novo DNA Methylation by Yates, P A, Burman, R W, Mummaneni, P, Krussel, S, Turker, M S

    Published in The Journal of biological chemistry (17-12-1999)
    “…A cis-acting methylation center that signals de novo DNA methylation is located upstream of the mouse Aprt gene. In the current study, two approaches were…”
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  4. 4
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    Fragile X full mutations are more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics by Burman, R W, Anoe, K S, Popovich, B W

    Published in Genetics in medicine (01-07-2000)
    “…We sought to compare patterns of full mutation repeat-length variability in the peripheral blood DNA of patients with fragile X syndrome to determine whether…”
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  6. 6

    Fully Expanded FMR1CGG Repeats Exhibit a Length-and Differentiation-Dependent Instability in Cell Hybrids That is Independent of DNA Methylation by Burman, Robert W., Popovich, Bradley W., Jacky, Peter B., Turker, Mitchell S.

    Published in Human molecular genetics (01-11-1999)
    “…The fragile X syndrome is characterized at the molecular level by expansion and methylation of a CGG trinucleotide repeat located within the FMR1 locus. The…”
    Get full text
    Journal Article
  7. 7