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  • Author: Cox BS
  • References

Author: Cox BS


References 45 references


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  • Ness F, et al. (2017) Over-expression of the molecular chaperone Hsp104 in Saccharomyces cerevisiae results in the malpartition of [PSI+ ] propagons. Mol Microbiol 104(1):125-143 PMID:28073182
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  • Tuite MF, et al. (2015) [PSI(+)] turns 50. Prion 9(5):318-32 PMID:26645632
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  • Byrne LJ, et al. (2009) The number and transmission of [PSI] prion seeds (Propagons) in the yeast Saccharomyces cerevisiae. PLoS One 4(3):e4670 PMID:19262693
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  • Tuite MF and Cox BS (2009) Prions remodel gene expression in yeast. Nat Cell Biol 11(3):241-3 PMID:19255570
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  • Byrne LJ, et al. (2007) Cell division is essential for elimination of the yeast [PSI+] prion by guanidine hydrochloride. Proc Natl Acad Sci U S A 104(28):11688-93 PMID:17606924
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  • Cox BS, et al. (2007) Prion stability. Prion 1(3):170-8 PMID:19164897
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  • Tuite MF and Cox BS (2007) The genetic control of the formation and propagation of the [PSI+] prion of yeast. Prion 1(2):101-9 PMID:19164924
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  • Tuite MF and Cox BS (2006) The [PSI+] prion of yeast: a problem of inheritance. Methods 39(1):9-22 PMID:16757178
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  • Osherovich LZ, et al. (2004) Dissection and design of yeast prions. PLoS Biol 2(4):E86 PMID:15045026
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  • Tuite MF and Cox BS (2003) Propagation of yeast prions. Nat Rev Mol Cell Biol 4(11):878-90 PMID:14625537
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  • Ness F, et al. (2002) Guanidine hydrochloride inhibits the generation of prion "seeds" but not prion protein aggregation in yeast. Mol Cell Biol 22(15):5593-605 PMID:12101251
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  • Ferreira PC, et al. (2001) The elimination of the yeast [PSI+] prion by guanidine hydrochloride is the result of Hsp104 inactivation. Mol Microbiol 40(6):1357-69 PMID:11442834
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  • Eaglestone SS, et al. (2000) Guanidine hydrochloride blocks a critical step in the propagation of the prion-like determinant [PSI(+)] of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A 97(1):240-4 PMID:10618402
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  • Resnick MA and Cox BS (2000) Yeast as an honorary mammal. Mutat Res 451(1-2):1-11 PMID:10915861
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  • Eaglestone SS, et al. (1999) Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion-mediated mechanism. EMBO J 18(7):1974-81 PMID:10202160
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  • Kochneva-Pervukhova NV, et al. (1998) Mechanism of inhibition of Psi+ prion determinant propagation by a mutation of the N-terminus of the yeast Sup35 protein. EMBO J 17(19):5805-10 PMID:9755180
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  • Stansfield I, et al. (1995) The products of the SUP45 (eRF1) and SUP35 genes interact to mediate translation termination in Saccharomyces cerevisiae. EMBO J 14(17):4365-73 PMID:7556078
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  • Doel SM, et al. (1994) The dominant PNM2- mutation which eliminates the psi factor of Saccharomyces cerevisiae is the result of a missense mutation in the SUP35 gene. Genetics 137(3):659-70 PMID:8088511
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  • Nierras CR and Cox BS (1994) Expression and inheritance of the yeast extrachromosomal element psi do not depend on RNA polymerase I. Curr Genet 25(1):49-51 PMID:8082166
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  • McCready SJ, et al. (1989) The Saccharomyces cerevisiae RAD2 gene complements a Schizosaccharomyces pombe repair mutation. Curr Genet 15(1):27-30 PMID:2663184
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  • Cox BS, et al. (1988) The psi factor of yeast: a problem in inheritance. Yeast 4(3):159-78 PMID:3059716
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  • McCready SJ, et al. (1987) Excision repair in the yeast, Saccharomyces cerevisiae. J Cell Sci Suppl 6:25-38 PMID:3308920
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  • Plesset J, et al. (1987) Effect of cell cycle position on thermotolerance in Saccharomyces cerevisiae. J Bacteriol 169(2):779-84 PMID:3542970
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  • Tuite MF, et al. (1987) A ribosome-associated inhibitor of in vitro nonsense suppression in [psi-] strains of yeast. FEBS Lett 225(1-2):205-8 PMID:3319694
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  • Dai H, et al. (1986) Transformation of psi- Saccharomyces cerevisiae to psi+ with DNA co-purified with 3 micron circles. Curr Genet 11(1):79-82 PMID:3329046
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  • Whittaker J, et al. (1986) Part of the human ribosomal RNA locus stabilizes a plasmid in yeast. Nucleic Acids Res 14(14):5683-92 PMID:3016661
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  • Futcher AB and Cox BS (1983) Maintenance of the 2 microns circle plasmid in populations of Saccharomyces cerevisiae. J Bacteriol 154(2):612-22 PMID:6341357
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  • Tuite MF, et al. (1983) In vitro nonsense suppression in [psi+] and [psi-] cell-free lysates of Saccharomyces cerevisiae. Proc Natl Acad Sci U S A 80(10):2824-8 PMID:6344070
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  • McCready SJ and Cox BS (1982) The role of the cdc9 ligase in replication and excision repair in Saccharomyces cerevisiae. Curr Genet 6(1):29-30 PMID:24186368
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  • Tuite MF, et al. (1982) Relationship of the [psi] factor with other plasmids of Saccharomyces cerevisiae. Plasmid 8(2):103-11 PMID:6757991
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  • Lund PM and Cox BS (1981) Reversion analysis of [psi-] mutations in Saccharomyces cerevisiae. Genet Res 37(2):173-82 PMID:7021322
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  • Tuite MF and Cox BS (1981) RAD6+ gene of Saccharomyces cerevisiae codes for two mutationally separable deoxyribonucleic acid repair functions. Mol Cell Biol 1(2):153-7 PMID:6765597
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  • Tuite MF, et al. (1981) Agents that cause a high frequency of genetic change from [psi+] to [psi-] in Saccharomyces cerevisiae. Genetics 98(4):691-711 PMID:7037537
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  • Waldron C, et al. (1981) Yeast ochre suppressor SUQ5-ol is an altered tRNA Ser UCA. Nucleic Acids Res 9(13):3077-88 PMID:7024909
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  • di Caprio L and Cox BS (1981) DNA synthesis in UV-irradiated yeast. Mutat Res 82(1):69-85 PMID:7022172
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  • Cox BS, et al. (1980) Reversion from suppression to nonsuppression in SUQ5 [psi+] strains of yeast: the classificaion of mutations. Genetics 95(3):589-609 PMID:7002720
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  • Dobson MJ, et al. (1980) Control of recombination within and between DNA plasmids of Saccharomyces cerevisiae. Curr Genet 2(3):193-200 PMID:24189909
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  • Dobson MJ, et al. (1980) Loss of 2 um DNA from Saccharomyces cerevisiae transformed with the chimaeric plasmid pJDB219. Curr Genet 2(3):201-5 PMID:24189910
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  • McCready SJ and Cox BS (1980) Repair of 2 um Plasmid DNA in Saccharomyces cerevisiae. Curr Genet 2(3):207-10 PMID:24189911
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  • Tuite MF and Cox BS (1980) Ultraviolet mutagenesis studies of [psi], a cytoplasmic determinant of Saccharomyces cerevisiae. Genetics 95(3):611-30 PMID:7002721
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  • Waldron C and Cox BS (1978) Ribosomal proteins of yeast strains carrying mutations which affect the efficiency of nonsense suppression. Mol Gen Genet 159(2):223-5 PMID:345095
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  • McCready SJ, et al. (1977) The extrachromosomal control of nonsense suppression in yeast: an analysis of the elimination of [psi+] in the presence of a nuclear gene PNM. Mol Gen Genet 150(3):265-70 PMID:321935
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  • Young CS and Cox BS (1975) Extrachromosomal elements in a super-suppression system of yeast. III. Enhanced detection of weak suppressors in certain non-suppressed psi-strains. Heredity (Edinb) 34(1):83-93 PMID:1091604
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  • Cox BS (1971) A recessive lethal super-suppressor mutation in yeast and other psi phenomena. Heredity (Edinb) 26(2):211-32 PMID:5286385
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  • Cox BS and Parry JM (1968) The isolation, genetics and survival characteristics of ultraviolet light-sensitive mutants in yeast. Mutat Res 6(1):37-55 PMID:5708072
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