Search Results - "Pryde, Fiona E."

Limitations of silencing at native yeast telomeres by Pryde, F.E, Louis, E.J

“…Silencing at native yeast telomeres, in which the subtelomeric elements are intact, is different from silencing at terminal truncations. The repression of URA3…”
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Repressive and non-repressive chromatin at native telomeres in Saccharomyces cerevisiae by Loney, Esther R, Inglis, Peter W, Sharp, Sarah, Pryde, Fiona E, Kent, Nicholas A, Mellor, Jane, Louis, Edward J

“…In Saccharomyces cerevisiae genes that are located close to a telomere can become transcriptionally repressed by an epigenetic process known as telomere…”
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SGS1 is required for telomere elongation in the absence of telomerase by Huang, Pei-Hsiu, Pryde, Fiona E, Lester, Darren, Maddison, Rachelle L, Borts, Rhona H, Hickson, Ian D, Louis, Edward J

“…In S. cerevisiae, mutations in genes that encode telomerase components, such as the genes EST1, EST2, EST3, and TLC1, result in the loss of telomerase activity…”
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Chromosome ends: all the same under their caps by Pryde, Fiona E, Gorham, Hazel C, Louis, Edward J

“…The recent characterisation of subtelomeric regions from a variety of organisms from yeast to man has led to the realisation that all chromosome ends are…”
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Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres by Laroche, Thierry, Martin, Sophie G., Gotta, Monica, Gorham, Hazel C., Pryde, Fiona E., Louis, Edward J., Gasser, Susan M.

“…The mammalian Ku70 and Ku86 proteins form a heterodimer that binds to the ends of double-stranded DNA in vitro and is required for repair of radiation-induced…”
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Sequence analysis of the right end of chromosome XV in Saccharomyces cerevisiae: an insight into the structural and functional significance of sub-telomeric repeat sequences by Pryde, F E, Huckle, T C, Louis, E J

“…Approximately 3.9 kb of DNA, centromere proximal to the previously sequenced Y' element at the right end of chromosome XV in Saccharomyces cerevisiae strain…”
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Analysis of Three Deletion Breakpoints in Xp21.1 and the Further Localization of RP3 by Brown, John, Dry, Katherine L., Edgar, Alexander J., Pryde, Fiona E., Hardwick, Lee J., Aldred, Micheala A., Lester, Douglas H., Boyle, Shelagh, Kaplan, Josseline, Dufier, Jean-Louis, Ho, Meng-Fatt, Monaco, Anthony M., Musarella, Maria A., Wright, Alan F.

“…The gene responsible for X-linked retinitis pigmentosa (xlRP) in Xp21.1 (RP3) was initially localized by deletion analysis to within a 150- to 170-kb region…”
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