Диссертация (1144700), страница 31
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622 - 626.201.Paushkin S.V., Kushnirov V.V., Smirnov V.N., Ter-Avanesyan M.D.Interaction between yeast Sup45p (eRF1) and Sup35p (eRF3) polypeptide chainrelease factors: implications for prion-dependent regulation. // Mol Cell Biol. –1997. – Vol. 17, № 5. – P. 2798 - 2805.202.Peterson C.L., Herskowitz I. Characterization of the yeast SWI1, SWI2,and SWI3 genes, which encode a global activator of transcription. // Cell. - 1992.– Vol. 68, № 3. – P.
573 - 583.203.Polymeropoulos M.H., Lavedan C., Leroy E., Ide S.E., Dehejia A. et al.Mutation in the alpha-synuclein gene identified in families with Parkinson'sdisease. // Science. – 1997. – Vol. 276. – P. 2045 – 2047.204.Porzoor A., Macreadie I.G. Application of yeast to study the tau andamyloid-β abnormalities of Alzheimer's disease. // J Alzheimers Dis. – 2013. –Vol.
35, № 2. – P. 217 - 225.205.Poulopoulos M., Levy O.A., Alcalay R.N. The neuropathology of geneticParkinson's disease.// Mov Disord. – 2012. – Vol. 27. – P. 831 – 842.196206.Pratt-Hyatt M., Pai D.A., Haeusler R.A., Wozniak G.G., Good P.D. et al.Mod5 protein binds to tRNA gene complexes and affects local transcriptionalsilencing. // Proc Natl Acad Sci U S A. – 2013.
– Vol. 110. № 33. – P. 3081 3089.207.Prusiner S.B. Scrapie prions // Am. Rev. Microbiol. – 1989. – Vol. 43. – Р.345 – 374.208.Prusiner S.B. Shattuck lecture-neurodegenerative diseases and prions // NEngl J Med. – 2001. – V. 344, №20. – P.1516 – 1526.209.Prusiner S.B. Biology and genetics of prions causing neurodegeneration.
//Annu Rev Genet. – 2013. – Vol. 47. - P. 601 - 23.210.Prusiner S.B., Scott M.R. Genetics of prions // Annu Rev Genet. – 1997. –Vol. 31. – Р. 139 – 175.211.Radovanovic I., Braun N., Giger O.T., Mertz K., Miele G. et al. Truncatedprion protein and Doppel are myelinotoxic in the absence of oligodendrocyticPrPC. // J Neurosci. - 2005. - Vol.
25. - P. 4879-4888.212.Rank K.B., Pauley A.M., Bhattacharya K., Wang Z., Evans D.B. Directinteraction of soluble human recombinant tau protein with Abeta 1-42 results intau aggregation and hyperphosphorylation by tau protein kinase II // FEBS Lett. 2002. - Vol. 514, № 2-3. - P. 263-268.213.Raveendra B.L., Siemer A.B., Puthanveetti S.V., Hendrickson W.A.,Kandel E.R., McDermott A.E. Characterization of prion-like conformationalchanges of the neuronal isoform of Aplysia CPEB. // Nat Struct Mol Biol. – 2013.– Vol. 20, № 4. – P. 495 - 501.214.Ren P.H., Lauckner J.E., Kachirskaia I., Heuser J.E., Melki R., Kopito R.R.Cytoplasmic penetration and persistent infection of mammalian cells bypolyglutamine aggregates. // Nat Cell Biol. – 2009.
– Vol. 11. – P. 219 – 25.215.Resenberger U.K., Harmeier A., Woerner A.C., Goodman J.L., Müller V.et al. The cellular prion protein mediates neurotoxic signalling of β-sheet-richconformers independent of prion replication. // EMBO J. - 2011 - Vol. 30. - P.2057 - 2070.197216.Roberson E.D., Scearce-Levie K., Palop J.J., Yan F., Cheng I.H. et al.Reducing endogenous tau ameliorates amyloid β-induced deficits in anAlzheimer’s disease mouse model. // Science. - 2007.
– Vol. 316. P. 750 – 754.217.Roberts B.T., Wickner R.B. Heritable activity: a prion that propagates bycovalent autoactivation // Genes Dev. – 2003. – Vol. 17, №17. – P. 2083 – 2087.218.Rogoza T., Goginashvili A., Rodionova S., Ivanov M., Viktorovskaya O.,et al. Non-Mendelian determinant [ISP+] in yeast is a nuclear-residing prion formof the global transcriptional regulator Sfp1. // Proc Natl Acad Sci USA. - 2010. –Vol. 107. – P.
10573 - 10577.219.Rolli E., Ragni E., Rodriguez-Pena J.M., Arroyo J., Popolo L. GAS3, adevelopmentally regulated gene, encodes a highly mannosylated and inactiveprotein of the Gas family of Saccharomyces cerevisiae. // Yeast.
– 2010. – Vol.27, № 8. – P. 597 - 610.220.Romanova N.V., Chernoff Y.O. Hsp104 and prion propagation. // ProteinPept Lett. – 2009. - V. 16, №6. – P. 598-605.221.Rose M.D., Winstone F., Hieter P. Methods in yeast genetics // CSHLPress. – 1990. – 198 p.222.Rosen R.F., Fritz J.J., Dooyema J., Cintron A.F., Hamaguchi T., et al.Exogenous seeding of cerebral β-amyloid deposition in βAPP-transgenic rats. // JNeurochem. – 2012.
– Vol. 120. – P. 660 – 666.223.Roszik J., Toth G., Szollosi J., Vereb G. Validating pharmacologicaldisruption of protein-protein interactions by acceptor photobleaching FRETimaging. // Methods Mol Biol. – 2013, № 986. – P. 165 - 178.224.Ruan Q.X., Zhou P., Hu B.W., Ji D. An investigation into the effect ofpotassium ions on the folding of silk fibroin studied by generalized twodimensional NMR-NMR correlation and Raman spectroscopy.
// FEBS J. – 2008.– V. 275. №2. - P. 219-232.225.Rubel A.A., Ryzhova T.A., Antonets K.S., Chernoff Y.O, Galkin, A.P.Identification of PrP sequences essential for the interaction between the PrP198polymers and Aβ peptide in a yeast-based assay. // Prion. – 2013. – Vol. 7, № 6. –P. 469 - 476.226.Saifitdinova A.F., Nizhnikov A.A., Lada A.G., Rubel A.A, MagomedovaZ.M., Ignatova V.V., Inge-Vechtomov S.G., Galkin A.P. [NSI+]: a novel nonMendelian nonsense suppressor determinant in Saccharomyces cerevisiae.
// CurrGenet. – 2010. – Vol. 56, № 5. – P. 467 - 478.227.Sipe J.D., Cohen A.S. Review: history of the amyloid fibril. // J Struct Biol.- 2000. - Vol. 130. № 2-3. – P. 88-98.228.Sipe J.D., Benson M.D., Buxbaum J.N., Ikeda S., Merlini G. et al.Nomenclature 2014: Amyloid fibril proteins and clinical classification of theamyloidosis. // Amyloid. – 2014. – Vol.
21. №. – P. 221 – 224.229.Sambrook J., Fritsch E.F., Maniatis T. Molecular cloning. A laboratorymanual // New York: Cold Spring Harbor Lab. Press. – 1989. – 1626 p.230.Sarantseva S., Timoshenko S., Bolshakova O., Karaseva E., Rodin D. et al.Apolipoprotein E-mimetics inhibit neurodegeneration and restore cognitivefunctions in a transgenic Drosophila model of Alzheimer's disease. // PLoS One.– 2009. – Vol. 4, № 12. - e8191.231.Saupe S.J.
The [Het-s] prion of Podospora anserina and its role inheterokaryon incompatibility. // Semin Cell Dev Biol. – 2011. – V. 22, №5. - P.460 - 468.232.Schilling G., Becher M.W., Sharp A.H., Jinnah H.A., Duan K. et al.Intranuclear inclusions and neuritic aggregates in transgenic mice expressing amutant N-terminal fragment of huntingtin. // Hum Mol Genet. – 1999. – Vol. 8. –P. 397 – 407.233.Schwarze-Eicker K., Keyvani K., Gortz N., Westaway D., Sachser N.,Paulus W. Prion protein (PrPc) promotes beta-amyloid plaque formation //Neurobiol. Aging. - 2005.
- V. 26, № 8. - P. 1177 - 1182.234.Schwimmer C., Masison D.C. Antagonistic interactions between yeast[PSI(+)] and [URE3] prions and curing of [URE3] by Hsp70 protein chaperone199Ssa1p but not by Ssa2p. // Mol Cell Biol. – 2002. – Vol. 22, № 11. – P. 3590 3598.235.Selkoe D.J. Alzheimer's disease. // Cold Spring Harb Perspect Biol. – 2011.- Vol.
3, № 7. - pii: a004457.236.Serio T.R., Cashikar A.G., Kowal A.S., Sawicki G.J., Moslehi J.J. et al. //Nucleated conformational conversion and the replication of conformationalinformation by a prion determinant. // Science. – 2000. – Vol. 289. – P. 1317 1321.237.Sherman F., Fink G.R., Hinks J.B. Methods in Yeast Genetics. // ColdSpring Harbor Lab Press, New-York.
- 1986.238.Shewmaker F., McGlinchey R.P., Wickner R.B. Structural insights intofunctional and pathological amyloid. // J Biol Chem. – 2011. – Vol. 286, №19. –P. 16533 - 16540.239.Si K., Choi Y., White-Grindley E., MajumdarA., Kandel E. Aplysia CPEBcan form prion-like multimers in sensory neurons that contribute to long-termfacilitation. // Cell.
- 2010. – V. 140, №3. - P. 421 - 435.240.Sikorski R.S., Hieter P. A system of shuttle vectors and yeast host strainsdesigned for efficient manipulation of DNA in Saccharomyces cerevisiae. //Genetics. – 1989. – Vol. 122. – P. 19-27.241.Snow A.D., Sekiguchi R., Nochlin D., Fraser P., Kimata K. et al. Animportant role of heparan sulfate proteoglycan (Perlecan) in a model system forthe deposition and persistence of fibrillar A beta-amyloid in rat brain. // Neuron.
–1994. – Vol. 12, № 1. – P. 219 - 234.242.Sondheimer N. and Lindquist S. Rnq1: an epigenetic modifier of proteinfunction in yeast // Mol. Cell. - 2000. - Vol. 5. - P. 163 - 172.243.Sondheimer N, Lopez N, Craig EA, Lindquist S. The role of Sis1 in themaintenance of the [RNQ+] prion. // EMBO J. – 2001. – Vol. 20, № 10. – P.2435 - 2442.200244.Speransky V.V., Taylor K.L., Edskes H.K., Wickner R.B., Steven A.C.Prion filament networks in [URE3] cells of Saccharomyces cerevisiae // J.
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