| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2017 |
Mente KP, O'Donnell JK, Jones SE, Cohen ML, Thompson NR, Bizzi A, Gambetti P, Safar JG, Appleby BS. Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) Correlation of Histopathology and MRI in Prion Disease. Alzheimer Disease and Associated Disorders. PMID 28121634 DOI: 10.1097/Wad.0000000000000188 |
0.01 |
|
| 2017 |
Cracco L, Notari S, Cali I, Sy MS, Chen SG, Cohen ML, Ghetti B, Appleby BS, Zou WQ, Caughey B, Safar JG, Gambetti P. Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type. Scientific Reports. 7: 38280. PMID 28091514 DOI: 10.1038/Srep38280 |
0.01 |
|
| 2016 |
Foutz A, Appleby BS, Hamlin C, Liu X, Yang S, Cohen Y, Chen W, Blevins J, Fausett C, Wang H, Gambetti P, Zhang S, Hughson A, Tatsuoka C, Schonberger LB, ... ... Safar JG, et al. Diagnostic and Prognostic Value of Human Prion Detection in Cerebrospinal Fluid. Annals of Neurology. PMID 27893164 DOI: 10.1002/Ana.24833 |
0.01 |
|
| 2016 |
Cohen M, Appleby B, Safar JG. Distinct prion-like strains of amyloid beta implicated in phenotypic diversity of Alzheimer's disease. Prion. 10: 9-17. PMID 26809345 DOI: 10.1080/19336896.2015.1123371 |
0.01 |
|
| 2015 |
Mays CE, van der Merwe J, Kim C, Haldiman T, McKenzie D, Safar JG, Westaway D. Prion infectivity plateaus and conversion to symptomatic disease originate from falling precursor levels and increased oligomeric PrPSc species. Journal of Virology. PMID 26423957 DOI: 10.1128/JVI.02142-15 |
0.01 |
|
| 2015 |
Safar JG, Xiao X, Kabir ME, Chen S, Kim C, Haldiman T, Cohen Y, Chen W, Cohen ML, Surewicz WK. Structural determinants of phenotypic diversity and replication rate of human prions. Plos Pathogens. 11: e1004832. PMID 25875953 DOI: 10.1371/Journal.Ppat.1004832 |
0.01 |
|
| 2015 |
Petersen RB, Lissemore FM, Appleby B, Aggarwal N, Boyatzis R, Casadesus G, Cummings J, Jack A, Perry G, Safar J, Sajatovic M, Surewicz W, Wang Y, Whitehouse P, Lerner A. From Neurodegeneration to Brain Health: An Integrated Approach. Journal of Alzheimer's Disease : Jad. PMID 25720413 DOI: 10.3233/Jad-150043 |
0.01 |
|
| 2015 |
Cohen ML, Kim C, Haldiman T, ElHag M, Mehndiratta P, Pichet T, Lissemore F, Shea M, Cohen Y, Chen W, Blevins J, Appleby BS, Surewicz K, Surewicz WK, Sajatovic M, ... ... Safar JG, et al. Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β. Brain : a Journal of Neurology. 138: 1009-22. PMID 25688081 DOI: 10.1093/Brain/Awv006 |
0.01 |
|
| 2015 |
Lau A, McDonald A, Daude N, Mays CE, Walter ED, Aglietti R, Mercer RC, Wohlgemuth S, van der Merwe J, Yang J, Gapeshina H, Kim C, Grams J, Shi B, Wille H, ... ... Safar JG, et al. Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation. Embo Molecular Medicine. 7: 339-56. PMID 25661904 DOI: 10.15252/Emmm.201404588 |
0.01 |
|
| 2014 |
Choulet F, Alberti A, Theil S, Glover N, Barbe V, Daron J, Pingault L, Sourdille P, Couloux A, Paux E, Leroy P, Mangenot S, Guilhot N, Le Gouis J, Balfourier F, ... ... Safar J, et al. Structural and functional partitioning of bread wheat chromosome 3B. Science (New York, N.Y.). 345: 1249721. PMID 25035497 DOI: 10.1126/Science.1249721 |
0.01 |
|
| 2014 |
Nevrtalova E, Baloun J, Hudzieczek V, Cegan R, Vyskot B, Dolezel J, Safar J, Milde D, Hobza R. Expression response of duplicated metallothionein 3 gene to copper stress in Silene vulgaris ecotypes. Protoplasma. 251: 1427-39. PMID 24748066 DOI: 10.1007/s00709-014-0644-x |
0.01 |
|
| 2014 |
Mays CE, Kim C, Haldiman T, van der Merwe J, Lau A, Yang J, Grams J, Di Bari MA, Nonno R, Telling GC, Kong Q, Langeveld J, McKenzie D, Westaway D, Safar JG. Prion disease tempo determined by host-dependent substrate reduction. The Journal of Clinical Investigation. 124: 847-58. PMID 24430187 DOI: 10.1172/Jci72241 |
0.01 |
|
| 2014 |
Kabir ME, Safar JG. Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases. Prion. 8: 111-6. PMID 24401672 DOI: 10.4161/pri.27661 |
0.01 |
|
| 2013 |
Haldiman T, Kim C, Cohen Y, Chen W, Blevins J, Qing L, Cohen ML, Langeveld J, Telling GC, Kong Q, Safar JG. Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection. The Journal of Biological Chemistry. 288: 29846-61. PMID 23974118 DOI: 10.1074/Jbc.M113.500108 |
0.01 |
|
| 2012 |
Kim C, Haldiman T, Surewicz K, Cohen Y, Chen W, Blevins J, Sy MS, Cohen M, Kong Q, Telling GC, Surewicz WK, Safar JG. Small protease sensitive oligomers of PrPSc in distinct human prions determine conversion rate of PrP(C). Plos Pathogens. 8: e1002835. PMID 22876179 DOI: 10.1371/Journal.Ppat.1002835 |
0.01 |
|
| 2012 |
Puoti G, Bizzi A, Forloni G, Safar JG, Tagliavini F, Gambetti P. Sporadic human prion diseases: molecular insights and diagnosis. The Lancet. Neurology. 11: 618-28. PMID 22710755 DOI: 10.1016/S1474-4422(12)70063-7 |
0.01 |
|
| 2012 |
Safar JG. Molecular pathogenesis of sporadic prion diseases in man. Prion. 6: 108-15. PMID 22421210 DOI: 10.4161/pri.18666 |
0.01 |
|
| 2011 |
Kim C, Haldiman T, Cohen Y, Chen W, Blevins J, Sy MS, Cohen M, Safar JG. Protease-sensitive conformers in broad spectrum of distinct PrPSc structures in sporadic Creutzfeldt-Jakob disease are indicator of progression rate. Plos Pathogens. 7: e1002242. PMID 21931554 DOI: 10.1371/Journal.Ppat.1002242 |
0.01 |
|
| 2011 |
Safar JG, Giles K, Lessard P, Letessier F, Patel S, Serban A, Dearmond SJ, Prusiner SB. Conserved properties of human and bovine prion strains on transmission to guinea pigs. Laboratory Investigation; a Journal of Technical Methods and Pathology. 91: 1326-36. PMID 21727894 DOI: 10.1038/Labinvest.2011.89 |
0.01 |
|
| 2010 |
Stanker LH, Serban AV, Cleveland E, Hnasko R, Lemus A, Safar J, DeArmond SJ, Prusiner SB. Conformation-dependent high-affinity monoclonal antibodies to prion proteins. Journal of Immunology (Baltimore, Md. : 1950). 185: 729-37. PMID 20530267 DOI: 10.4049/jimmunol.0902930 |
0.01 |
|
| 2009 |
Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain : a Journal of Neurology. 132: 2643-58. PMID 19734292 DOI: 10.1093/Brain/Awp196 |
0.01 |
|
| 2009 |
Choi EM, Geschwind MD, Deering C, Pomeroy K, Kuo A, Miller BL, Safar JG, Prusiner SB. Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt-Jakob disease. Laboratory Investigation; a Journal of Technical Methods and Pathology. 89: 624-35. PMID 19434060 DOI: 10.1038/Labinvest.2009.30 |
0.01 |
|
| 2009 |
Nové-Josserand L, Costa P, Liotard JP, Safar JF, Walch G, Zilber S. Results of latissimus dorsi tendon transfer for irreparable cuff tears. Orthopaedics & Traumatology, Surgery & Research : Otsr. 95: 108-13. PMID 19349223 DOI: 10.1016/j.otsr.2008.10.002 |
0.01 |
|
| 2009 |
Wille H, Shanmugam M, Murugesu M, Ollesch J, Stubbs G, Long JR, Safar JG, Prusiner SB. Surface charge of polyoxometalates modulates polymerization of the scrapie prion protein. Proceedings of the National Academy of Sciences of the United States of America. 106: 3740-5. PMID 19223590 DOI: 10.1073/Pnas.0812770106 |
0.01 |
|
| 2008 |
Paux E, Sourdille P, Salse J, Saintenac C, Choulet F, Leroy P, Korol A, Michalak M, Kianian S, Spielmeyer W, Lagudah E, Somers D, Kilian A, Alaux M, Vautrin S, ... ... Safar J, et al. A physical map of the 1-gigabase bread wheat chromosome 3B. Science (New York, N.Y.). 322: 101-4. PMID 18832645 DOI: 10.1126/Science.1161847 |
0.01 |
|
| 2008 |
Safar JG, Lessard P, Tamgüney G, Freyman Y, Deering C, Letessier F, Dearmond SJ, Prusiner SB. Transmission and detection of prions in feces. The Journal of Infectious Diseases. 198: 81-9. PMID 18505383 DOI: 10.1086/588193 |
0.01 |
|
| 2007 |
King DJ, Safar JG, Legname G, Prusiner SB. Thioaptamer interactions with prion proteins: sequence-specific and non-specific binding sites. Journal of Molecular Biology. 369: 1001-14. PMID 17481659 DOI: 10.1016/j.jmb.2007.02.004 |
0.01 |
|
| 2007 |
Phuan PW, Zorn JA, Safar J, Giles K, Prusiner SB, Cohen FE, May BC. Discriminating between cellular and misfolded prion protein by using affinity to 9-aminoacridine compounds. The Journal of General Virology. 88: 1392-401. PMID 17374787 DOI: 10.1099/Vir.0.82601-0 |
0.01 |
|
| 2006 |
Tamgüney G, Giles K, Bouzamondo-Bernstein E, Bosque PJ, Miller MW, Safar J, DeArmond SJ, Prusiner SB. Transmission of elk and deer prions to transgenic mice. Journal of Virology. 80: 9104-14. PMID 16940522 DOI: 10.1128/JVI.00098-06 |
0.01 |
|
| 2006 |
Safar JG, Wille H, Geschwind MD, Deering C, Latawiec D, Serban A, King DJ, Legname G, Weisgraber KH, Mahley RW, Miller BL, Dearmond SJ, Prusiner SB. Human prions and plasma lipoproteins. Proceedings of the National Academy of Sciences of the United States of America. 103: 11312-7. PMID 16849426 DOI: 10.1073/Pnas.0604021103 |
0.01 |
|
| 2006 |
Hobza R, Hrusakova P, Safar J, Bartos J, Janousek B, Zluvova J, Michu E, Dolezel J, Vyskot B. MK17, a specific marker closely linked to the gynoecium suppression region on the Y chromosome in Silene latifolia. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. 113: 280-7. PMID 16791694 DOI: 10.1007/s00122-006-0293-3 |
0.01 |
|
| 2006 |
Peretz D, Supattapone S, Giles K, Vergara J, Freyman Y, Lessard P, Safar JG, Glidden DV, McCulloch C, Nguyen HO, Scott M, Dearmond SJ, Prusiner SB. Inactivation of prions by acidic sodium dodecyl sulfate. Journal of Virology. 80: 322-31. PMID 16352557 DOI: 10.1128/Jvi.80.1.322-331.2006 |
0.01 |
|
| 2005 |
Lee IS, Long JR, Prusiner SB, Safar JG. Selective precipitation of prions by polyoxometalate complexes. Journal of the American Chemical Society. 127: 13802-3. PMID 16201796 DOI: 10.1021/Ja055219Y |
0.01 |
|
| 2005 |
Safar JG, DeArmond SJ, Kociuba K, Deering C, Didorenko S, Bouzamondo-Bernstein E, Prusiner SB, Tremblay P. Prion clearance in bigenic mice. The Journal of General Virology. 86: 2913-23. PMID 16186247 DOI: 10.1099/vir.0.80947-0 |
0.01 |
|
| 2005 |
Safar JG, Kellings K, Serban A, Groth D, Cleaver JE, Prusiner SB, Riesner D. Search for a prion-specific nucleic acid. Journal of Virology. 79: 10796-806. PMID 16051871 DOI: 10.1128/Jvi.79.16.10796-10806.2005 |
0.01 |
|
| 2005 |
Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB. Diagnosis of human prion disease. Proceedings of the National Academy of Sciences of the United States of America. 102: 3501-6. PMID 15741275 DOI: 10.1073/Pnas.0409651102 |
0.01 |
|
| 2004 |
Bouzamondo-Bernstein E, Hopkins SD, Spilman P, Uyehara-Lock J, Deering C, Safar J, Prusiner SB, Ralston HJ, DeArmond SJ. The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system. Journal of Neuropathology and Experimental Neurology. 63: 882-99. PMID 15330342 DOI: 10.1093/Jnen/63.8.882 |
0.01 |
|
| 2004 |
Goldman JS, Miller BL, Safar J, de Tourreil S, Martindale JL, Prusiner SB, Geschwind MD. When sporadic disease is not sporadic: the potential for genetic etiology. Archives of Neurology. 61: 213-6. PMID 14967768 DOI: 10.1001/Archneur.61.2.213 |
0.01 |
|
| 2004 |
Tremblay P, Ball HL, Kaneko K, Groth D, Hegde RS, Cohen FE, DeArmond SJ, Prusiner SB, Safar JG. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains. Journal of Virology. 78: 2088-99. PMID 14747574 DOI: 10.1128/Jvi.78.4.2088-2099.2004 |
0.01 |
|
| 2003 |
Leclerc E, Peretz D, Ball H, Solforosi L, Legname G, Safar J, Serban A, Prusiner SB, Burton DR, Williamson RA. Conformation of PrP(C) on the cell surface as probed by antibodies. Journal of Molecular Biology. 326: 475-83. PMID 12559915 DOI: 10.1016/S0022-2836(02)01365-7 |
0.01 |
|
| 2002 |
Safar JG, Scott M, Monaghan J, Deering C, Didorenko S, Vergara J, Ball H, Legname G, Leclerc E, Solforosi L, Serban H, Groth D, Burton DR, Prusiner SB, Williamson RA. Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice. Nature Biotechnology. 20: 1147-50. PMID 12389035 DOI: 10.1038/nbt748 |
0.01 |
|
| 2002 |
Perrier V, Kaneko K, Safar J, Vergara J, Tremblay P, DeArmond SJ, Cohen FE, Prusiner SB, Wallace AC. Dominant-negative inhibition of prion replication in transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 99: 13079-84. PMID 12271119 DOI: 10.1073/pnas.182425299 |
0.01 |
|
| 2001 |
Supattapone S, Wille H, Uyechi L, Safar J, Tremblay P, Szoka FC, Cohen FE, Prusiner SB, Scott MR. Branched polyamines cure prion-infected neuroblastoma cells. Journal of Virology. 75: 3453-61. PMID 11238871 DOI: 10.1128/Jvi.75.7.3453-3461.2001 |
0.01 |
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| 2000 |
Safar J, Cohen FE, Prusiner SB. Quantitative traits of prion strains are enciphered in the conformation of the prion protein. Archives of Virology. Supplementum. 227-35. PMID 11214926 DOI: 10.1007/978-3-7091-6308-5_22 |
0.01 |
|
| 2000 |
Perrier V, Wallace AC, Kaneko K, Safar J, Prusiner SB, Cohen FE. Mimicking dominant negative inhibition of prion replication through structure-based drug design. Proceedings of the National Academy of Sciences of the United States of America. 97: 6073-8. PMID 10823951 DOI: 10.1073/pnas.97.11.6073 |
0.01 |
|
| 2000 |
Kaneko K, Ball HL, Wille H, Zhang H, Groth D, Torchia M, Tremblay P, Safar J, Prusiner SB, DeArmond SJ, Baldwin MA, Cohen FE. A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice. Journal of Molecular Biology. 295: 997-1007. PMID 10656806 DOI: 10.1006/jmbi.1999.3386 |
0.01 |
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| 1999 |
Safar JA, Davis RD, Overton JD. Effect of saliva contamination on the bond of dentin to resin-modified glass-ionomer cement. Operative Dentistry. 24: 351-7. PMID 10823084 |
0.01 |
|
| 1999 |
Supattapone S, Bosque P, Muramoto T, Wille H, Aagaard C, Peretz D, Nguyen HO, Heinrich C, Torchia M, Safar J, Cohen FE, DeArmond SJ, Prusiner SB, Scott M. Prion protein of 106 residues creates an artifical transmission barrier for prion replication in transgenic mice. Cell. 96: 869-78. PMID 10102274 DOI: 10.1016/S0092-8674(00)80596-6 |
0.01 |
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| 1998 |
Safar J, Prusiner SB. Molecular studies of prion diseases. Progress in Brain Research. 117: 421-34. PMID 9932423 DOI: 10.1016/S0079-6123(08)64030-3 |
0.01 |
|
| 1998 |
Safar J, Wille H, Itri V, Groth D, Serban H, Torchia M, Cohen FE, Prusiner SB. Eight prion strains have PrP(Sc) molecules with different conformations. Nature Medicine. 4: 1157-65. PMID 9771749 DOI: 10.1038/2654 |
0.01 |
|
| 1998 |
Stöckel J, Safar J, Wallace AC, Cohen FE, Prusiner SB. Prion protein selectively binds copper(II) ions. Biochemistry. 37: 7185-93. PMID 9585530 DOI: 10.1021/bi972827k |
0.01 |
|
| 1997 |
Scott MR, Safar J, Telling G, Nguyen O, Groth D, Torchia M, Koehler R, Tremblay P, Walther D, Cohen FE, DeArmond SJ, Prusiner SB. Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 94: 14279-84. PMID 9405603 DOI: 10.1073/pnas.94.26.14279 |
0.01 |
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| 1996 |
Pergami P, Jaffe H, Safar J. Semipreparative chromatographic method to purify the normal cellular isoform of the prion protein in nondenatured form. Analytical Biochemistry. 236: 63-73. PMID 8619497 DOI: 10.1006/abio.1996.0132 |
0.01 |
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| 1996 |
Safar J. The folding intermediate concept of prion protein formation and conformational links to infectivity. Current Topics in Microbiology and Immunology. 207: 69-76. PMID 8575207 |
0.01 |
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| 1995 |
Safar JA. Subcutaneous emphysema during removal of an overhang. General Dentistry. 43: 424-6. PMID 8941733 |
0.01 |
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| 1995 |
Brown P, Kenney K, Little B, Ironside J, Will R, Cervenáková L, Bjork RJ, San Martin RA, Safar J, Roos R, Haltia M, Gibbs CJ, Gajdusek DC. Intracerebral distribution of infectious amyloid protein in spongiform encephalopathy Annals of Neurology. 38: 245-253. PMID 7654073 DOI: 10.1002/Ana.410380218 |
0.01 |
|
| 1994 |
Safar J, Roller PP, Gajdusek DC, Gibbs CJ. Scrapie amyloid (prion) protein has the conformational characteristics of an aggregated molten globule folding intermediate. Biochemistry. 33: 8375-83. PMID 8031772 |
0.01 |
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| 1994 |
Safar J. Infectious amyloid, prions, unconventional viruses, and disease. Neurobiology of Aging. 15: 279-81. PMID 7838313 |
0.01 |
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| 1994 |
Di Martino A, Safar J, Gibbs CJ. The consistent use of organic solvents for purification of phospholipids from brain tissue effectively removes scrapie infectivity. Biologicals : Journal of the International Association of Biological Standardization. 22: 221-5. PMID 7811455 DOI: 10.1006/biol.1994.1032 |
0.01 |
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| 1993 |
Safar J, Roller PP, Ruben GC, Gajdusek DC, Gibbs CJ. Secondary structure of proteins associated in thin films. Biopolymers. 33: 1461-76. PMID 8400035 DOI: 10.1002/bip.360330915 |
0.01 |
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| 1993 |
Di Martino A, Safar J, Callegaro L, Salem N, Gibbs CJ. Ganglioside composition changes in spongiform encephalopathies: analyses of 263K scrapie-infected hamster brains. Neurochemical Research. 18: 907-13. PMID 8371832 |
0.01 |
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| 1993 |
Di Martino A, Safar J, Ceroni M, Gibbs CJ. Inactivation of the scrapie agent in a scaled-down procedure for the purification of gangliosides from brain tissue. Developments in Biological Standardization. 80: 187-94. PMID 8270108 |
0.01 |
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| 1993 |
Guiroy DC, Mellini M, Miyazaki M, Hilbich C, Safar J, Garruto RM, Yanagihara R, Beyreuther K, Gajdusek DC. Neurofibrillary tangles of Guamanian amyotrophic lateral sclerosis, parkinsonism-dementia and neurologically normal Guamanians contain a 4- to 4.5-kilodalton protein which is immunoreactive to anti-amyloid beta/A4-protein antibodies. Acta Neuropathologica. 86: 265-74. PMID 8213085 DOI: 10.1007/Bf00304141 |
0.01 |
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| 1993 |
Safar J, Roller PP, Gajdusek DC, Gibbs CJ. Conformational transitions, dissociation, and unfolding of scrapie amyloid (prion) protein. The Journal of Biological Chemistry. 268: 20276-84. PMID 8104185 |
0.01 |
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| 1993 |
Safar J, Roller PP, Gajdusek DC, Gibbs CJ. Thermal stability and conformational transitions of scrapie amyloid (prion) protein correlate with infectivity. Protein Science : a Publication of the Protein Society. 2: 2206-16. PMID 7905316 DOI: 10.1002/pro.5560021220 |
0.01 |
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| 1992 |
Di Martino A, Safar J, Ceroni M, Gibbs CJ. Purification of non-infectious ganglioside preparations from scrapie-infected brain tissue. Archives of Virology. 124: 111-21. PMID 1571012 |
0.01 |
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| 1992 |
Berry CW, Moore TJ, Safar JA, Henry CA, Wagner MJ. Antibacterial activity of dental implant metals. Implant Dentistry. 1: 59-65. PMID 1288798 |
0.01 |
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| Hide low-probability matches. |