| Year |
Citation |
Score |
| 2019 |
Ke J, Wu G, Zhang J, Li H, Gao S, Shao M, Gao Z, Sy MS, Cao Y, Yang X, Xu J, Li C. Melanoma migration is promoted by prion protein via Akt-hsp27 signaling axis. Biochemical and Biophysical Research Communications. PMID 31870551 DOI: 10.1016/J.Bbrc.2019.12.042 |
0.355 |
|
| 2018 |
Gao Z, Shi J, Cai L, Luo M, Wong BS, Dong X, Sy MS, Li C. Prion dimer is heterogenous and is modulated by multiple negative and positive motifs. Biochemical and Biophysical Research Communications. PMID 30600179 DOI: 10.1016/J.Bbrc.2018.12.113 |
0.413 |
|
| 2017 |
Wu GR, Mu TC, Gao ZX, Wang J, Sy MS, Li CY. Prion protein is required for tumor necrosis factor alpha (TNFα)-triggered nuclear factor kappa B (NF-κB) signaling and cytokine production. The Journal of Biological Chemistry. PMID 28900035 DOI: 10.1074/Jbc.M117.787283 |
0.339 |
|
| 2016 |
Ni CL, Seth D, Fonseca FV, Wang L, Xiao TS, Gruber P, Sy MS, Stamler JS, Tartakoff AM. Polyglutamine Tract Expansion Increases S-Nitrosylation of Huntingtin and Ataxin-1. Plos One. 11: e0163359. PMID 27658206 DOI: 10.1371/Journal.Pone.0163359 |
0.315 |
|
| 2016 |
Wang Y, Yu S, Huang D, Cui M, Hu H, Zhang L, Wang W, Parameswaran N, Jackson M, Osborne B, Bedogni B, Li C, Sy MS, Xin W, Zhou L. Cellular Prion Protein Mediates Pancreatic Cancer Cell Survival and Invasion through Association with and Enhanced Signaling of Notch1. The American Journal of Pathology. PMID 27639164 DOI: 10.1016/J.Ajpath.2016.07.010 |
0.369 |
|
| 2016 |
Yang L, Gao Z, Hu L, Wu G, Yang X, Zhang L, Zhu Y, Wong BS, Xin W, Sy MS, Li C. Glycosylphosphatidylinositol anchor modification machinery deficiency is responsible for the formation of pro-prion protein (PrP) in BxPC-3 cells and increases cancer cell motility. The Journal of Biological Chemistry. 291: 6785. PMID 27016554 DOI: 10.1074/Jbc.A115.705830 |
0.365 |
|
| 2015 |
Yang L, Gao Z, Hu L, Wu G, Yang X, Zhang L, Zhu Y, Wong BS, Xin W, Sy MS, Li C. GPI Anchor Modification Machinery Deficiency is Responsible for the Formation of Pro-PrP in BxPC-3 and Increases Cancer Cell Motility. The Journal of Biological Chemistry. PMID 26683373 DOI: 10.1074/Jbc.M115.705830 |
0.42 |
|
| 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 |
0.452 |
|
| 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 |
0.414 |
|
| 2010 |
Wang F, Yin S, Wang X, Zha L, Sy MS, Ma J. Role of the highly conserved middle region of prion protein (PrP) in PrP-lipid interaction. Biochemistry. 49: 8169-76. PMID 20718504 DOI: 10.1021/Bi101146V |
0.323 |
|
| 2010 |
Li C, Xin W, Sy MS. Binding of pro-prion to filamin A: by design or an unfortunate blunder. Oncogene. 29: 5329-45. PMID 20697352 DOI: 10.1038/onc.2010.307 |
0.327 |
|
| 2010 |
Das D, Luo X, Singh A, Gu Y, Ghosh S, Mukhopadhyay CK, Chen SG, Sy MS, Kong Q, Singh N. Paradoxical role of prion protein aggregates in redox-iron induced toxicity. Plos One. 5: e11420. PMID 20625431 DOI: 10.1371/Journal.Pone.0011420 |
0.41 |
|
| 2010 |
Sy MS, Li C, Yu S, Xin W. The fatal attraction between pro-prion and filamin A: prion as a marker in human cancers. Biomarkers in Medicine. 4: 453-64. PMID 20550479 DOI: 10.2217/Bmm.10.14 |
0.334 |
|
| 2009 |
Li C, Yu S, Nakamura F, Yin S, Xu J, Petrolla AA, Singh N, Tartakoff A, Abbott DW, Xin W, Sy MS. Binding of pro-prion to filamin A disrupts cytoskeleton and correlates with poor prognosis in pancreatic cancer. The Journal of Clinical Investigation. 119: 2725-36. PMID 19690385 DOI: 10.1172/Jci39542 |
0.319 |
|
| 2008 |
Pham N, Yin S, Yu S, Wong P, Kang SC, Li C, Sy MS. Normal cellular prion protein with a methionine at position 129 has a more exposed helix 1 and is more prone to aggregate. Biochemical and Biophysical Research Communications. 368: 875-81. PMID 18275852 DOI: 10.1016/j.bbrc.2008.01.172 |
0.315 |
|
| 2007 |
Watts JC, Drisaldi B, Ng V, Yang J, Strome B, Horne P, Sy MS, Yoong L, Young R, Mastrangelo P, Bergeron C, Fraser PE, Carlson GA, Mount HT, Schmitt-Ulms G, et al. The CNS glycoprotein Shadoo has PrP(C)-like protective properties and displays reduced levels in prion infections. The Embo Journal. 26: 4038-50. PMID 17703189 DOI: 10.1038/Sj.Emboj.7601830 |
0.466 |
|
| 2007 |
Li C, Wong P, Pan T, Xiao F, Yin S, Chang B, Kang SC, Ironside J, Sy MS. Normal cellular prion protein is a ligand of selectins: binding requires Le(X) but is inhibited by sLe(X). The Biochemical Journal. 406: 333-41. PMID 17497959 DOI: 10.1042/Bj20061857 |
0.432 |
|
| 2007 |
Yin S, Pham N, Yu S, Li C, Wong P, Chang B, Kang SC, Biasini E, Tien P, Harris DA, Sy MS. Human prion proteins with pathogenic mutations share common conformational changes resulting in enhanced binding to glycosaminoglycans. Proceedings of the National Academy of Sciences of the United States of America. 104: 7546-51. PMID 17456603 DOI: 10.1073/pnas.0610827104 |
0.316 |
|
| 2007 |
Yu S, Yin S, Li C, Wong P, Chang B, Xiao F, Kang SC, Yan H, Xiao G, Tien P, Sy MS. Aggregation of prion protein with insertion mutations is proportional to the number of inserts. The Biochemical Journal. 403: 343-51. PMID 17187581 DOI: 10.1042/BJ20061592 |
0.323 |
|
| 2007 |
Goh AX, Li C, Sy MS, Wong BS. Altered prion protein glycosylation in the aging mouse brain. Journal of Neurochemistry. 100: 841-54. PMID 17144900 DOI: 10.1111/j.1471-4159.2006.04268.x |
0.376 |
|
| 2007 |
Chang B, Cheng X, Yin S, Pan T, Zhang H, Wong P, Kang SC, Xiao F, Yan H, Li C, Wolfe LL, Miller MW, Wisniewski T, Greene MI, Sy MS. Test for detection of disease-associated prion aggregate in the blood of infected but asymptomatic animals. Clinical and Vaccine Immunology : Cvi. 14: 36-43. PMID 17079434 DOI: 10.1128/Cvi.00341-06 |
0.421 |
|
| 2007 |
Adamson CS, Yao Y, Vasiljevic S, Sy MS, Ren J, Jones IM. Novel single chain antibodies to the prion protein identified by phage display. Virology. 358: 166-77. PMID 16996555 DOI: 10.1016/j.virol.2006.08.023 |
0.328 |
|
| 2006 |
Pankiewicz J, Prelli F, Sy MS, Kascsak RJ, Kascsak RB, Spinner DS, Carp RI, Meeker HC, Sadowski M, Wisniewski T. Clearance and prevention of prion infection in cell culture by anti-PrP antibodies. The European Journal of Neuroscience. 23: 2635-47. PMID 16817866 DOI: 10.1111/J.1460-9568.2006.04805.X |
0.342 |
|
| 2006 |
Yin S, Yu S, Li C, Wong P, Chang B, Xiao F, Kang SC, Yan H, Xiao G, Grassi J, Tien P, Sy MS. Prion proteins with insertion mutations have altered N-terminal conformation and increased ligand binding activity and are more susceptible to oxidative attack. The Journal of Biological Chemistry. 281: 10698-705. PMID 16478730 DOI: 10.1074/jbc.M511819200 |
0.347 |
|
| 2005 |
Pan T, Chang B, Wong P, Li C, Li R, Kang SC, Robinson JD, Thompsett AR, Tein P, Yin S, Barnard G, McConnell I, Brown DR, Wisniewski T, Sy MS. An aggregation-specific enzyme-linked immunosorbent assay: detection of conformational differences between recombinant PrP protein dimers and PrP(Sc) aggregates. Journal of Virology. 79: 12355-64. PMID 16160162 DOI: 10.1128/Jvi.79.19.12355-12364.2005 |
0.504 |
|
| 2005 |
Pan T, Li R, Wong BS, Kang SC, Ironside J, Sy MS. Novel antibody-lectin enzyme-linked immunosorbent assay that distinguishes prion proteins in sporadic and variant cases of Creutzfeldt-Jakob disease. Journal of Clinical Microbiology. 43: 1118-26. PMID 15750071 DOI: 10.1128/Jcm.43.3.1118-1126.2005 |
0.456 |
|
| 2005 |
Pan T, Wong P, Chang B, Li C, Li R, Kang SC, Wisniewski T, Sy MS. Biochemical fingerprints of prion infection: accumulations of aberrant full-length and N-terminally truncated PrP species are common features in mouse prion disease. Journal of Virology. 79: 934-43. PMID 15613322 DOI: 10.1128/Jvi.79.2.934-943.2005 |
0.422 |
|
| 2005 |
Pan T, Li R, Kang SC, Pastore M, Wong BS, Ironside J, Gambetti P, Sy MS. Biochemical fingerprints of prion diseases: scrapie prion protein in human prion diseases that share prion genotype and type. Journal of Neurochemistry. 92: 132-42. PMID 15606903 DOI: 10.1111/J.1471-4159.2004.02859.X |
0.46 |
|
| 2005 |
Wang X, Wang F, Sy MS, Ma J. Calpain and other cytosolic proteases can contribute to the degradation of retro-translocated prion protein in the cytosol. The Journal of Biological Chemistry. 280: 317-25. PMID 15525638 DOI: 10.1074/jbc.M410649200 |
0.358 |
|
| 2005 |
Cardinale A, Filesi I, Vetrugno V, Pocchiari M, Sy MS, Biocca S. Trapping prion protein in the endoplasmic reticulum impairs PrPC maturation and prevents PrPSc accumulation. The Journal of Biological Chemistry. 280: 685-94. PMID 15513919 DOI: 10.1074/jbc.M407360200 |
0.38 |
|
| 2004 |
Drisaldi B, Coomaraswamy J, Mastrangelo P, Strome B, Yang J, Watts JC, Chishti MA, Marvi M, Windl O, Ahrens R, Major F, Sy MS, Kretzschmar H, Fraser PE, Mount HT, et al. Genetic mapping of activity determinants within cellular prion proteins: N-terminal modules in PrPC offset pro-apoptotic activity of the Doppel helix B/B' region. The Journal of Biological Chemistry. 279: 55443-54. PMID 15459186 DOI: 10.1074/Jbc.M404794200 |
0.371 |
|
| 2004 |
Pan T, Li R, Kang SC, Wong BS, Wisniewski T, Sy MS. Epitope scanning reveals gain and loss of strain specific antibody binding epitopes associated with the conversion of normal cellular prion to scrapie prion. Journal of Neurochemistry. 90: 1205-17. PMID 15312175 DOI: 10.1111/J.1471-4159.2004.02582.X |
0.416 |
|
| 2004 |
Kang SC, Brown DR, Whiteman M, Li R, Pan T, Perry G, Wisniewski T, Sy MS, Wong BS. Prion protein is ubiquitinated after developing protease resistance in the brains of scrapie-infected mice. The Journal of Pathology. 203: 603-8. PMID 15095484 DOI: 10.1002/Path.1555 |
0.477 |
|
| 2003 |
Zou WQ, Capellari S, Parchi P, Sy MS, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 278: 40429-36. PMID 12917418 DOI: 10.1074/Jbc.M308550200 |
0.36 |
|
| 2003 |
Cui T, Daniels M, Wong BS, Li R, Sy MS, Sassoon J, Brown DR. Mapping the functional domain of the prion protein. European Journal of Biochemistry / Febs. 270: 3368-76. PMID 12899694 DOI: 10.1046/J.1432-1033.2003.03717.X |
0.37 |
|
| 2003 |
Wong BS, Li R, Sassoon J, Kang SC, Liu T, Pan T, Greenspan NS, Wisniewski T, Brown DR, Sy MS. Mapping the antigenicity of copper-treated cellular prion protein with the scrapie isoform. Cellular and Molecular Life Sciences : Cmls. 60: 1224-34. PMID 12861388 DOI: 10.1007/S00018-003-3057-0 |
0.513 |
|
| 2003 |
Li R, Liu T, Yoshihiro F, Tary-Lehmann M, Obrenovich M, Kuekrek H, Kang SC, Pan T, Wong BS, Medof ME, Sy MS. On the same cell type GPI-anchored normal cellular prion and DAF protein exhibit different biological properties. Biochemical and Biophysical Research Communications. 303: 446-51. PMID 12659837 DOI: 10.1016/S0006-291X(03)00354-1 |
0.533 |
|
| 2003 |
Kang SC, Li R, Wang C, Pan T, Liu T, Rubenstein R, Barnard G, Wong BS, Sy MS. Guanidine hydrochloride extraction and detection of prion proteins in mouse and hamster prion diseases by ELISA. The Journal of Pathology. 199: 534-41. PMID 12635145 DOI: 10.1002/Path.1294 |
0.494 |
|
| 2003 |
Sigurdsson EM, Sy MS, Li R, Scholtzova H, Kascsak RJ, Kascsak R, Carp R, Meeker HC, Frangione B, Wisniewski T. Anti-prion antibodies for prophylaxis following prion exposure in mice. Neuroscience Letters. 336: 185-7. PMID 12505623 DOI: 10.1016/S0304-3940(02)01192-8 |
0.33 |
|
| 2002 |
Liu T, Li R, Pan T, Liu D, Petersen RB, Wong BS, Gambetti P, Sy MS. Intercellular transfer of the cellular prion protein. The Journal of Biological Chemistry. 277: 47671-8. PMID 12359724 DOI: 10.1074/Jbc.M207458200 |
0.48 |
|
| 2002 |
Pan T, Wong BS, Liu T, Li R, Petersen RB, Sy MS. Cell-surface prion protein interacts with glycosaminoglycans. The Biochemical Journal. 368: 81-90. PMID 12186633 DOI: 10.1042/Bj20020773 |
0.433 |
|
| 2002 |
Pan T, Li R, Wong BS, Liu T, Gambetti P, Sy MS. Heterogeneity of normal prion protein in two- dimensional immunoblot: presence of various glycosylated and truncated forms. Journal of Neurochemistry. 81: 1092-101. PMID 12065622 DOI: 10.1046/J.1471-4159.2002.00909.X |
0.513 |
|
| 2001 |
Wong BS, Brown DR, Pan T, Whiteman M, Liu T, Bu X, Li R, Gambetti P, Olesik J, Rubenstein R, Sy MS. Oxidative impairment in scrapie-infected mice is associated with brain metals perturbations and altered antioxidant activities. Journal of Neurochemistry. 79: 689-98. PMID 11701772 DOI: 10.1046/J.1471-4159.2001.00625.X |
0.449 |
|
| 2001 |
Wong BS, Chen SG, Colucci M, Xie Z, Pan T, Liu T, Li R, Gambetti P, Sy MS, Brown DR. Aberrant metal binding by prion protein in human prion disease. Journal of Neurochemistry. 78: 1400-8. PMID 11579148 DOI: 10.1046/J.1471-4159.2001.00522.X |
0.504 |
|
| 2001 |
Pan T, Colucci M, Wong BS, Li R, Liu T, Petersen RB, Chen S, Gambetti P, Sy MS. Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis. The Journal of Biological Chemistry. 276: 37284-8. PMID 11489910 DOI: 10.1074/Jbc.M107358200 |
0.471 |
|
| 2001 |
Wong BS, Green AJ, Li R, Xie Z, Pan T, Liu T, Chen SG, Gambetti P, Sy MS. Absence of protease-resistant prion protein in the cerebrospinal fluid of Creutzfeldt-Jakob disease. The Journal of Pathology. 194: 9-14. PMID 11329135 DOI: 10.1002/Path.872 |
0.446 |
|
| 2001 |
Wong BS, Liu T, Paisley D, Li R, Pan T, Chen SG, Perry G, Petersen RB, Smith MA, Melton DW, Gambetti P, Brown DR, Sy MS. Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: implications for doppel function. Molecular and Cellular Neurosciences. 17: 768-75. PMID 11312611 DOI: 10.1006/Mcne.2001.0963 |
0.425 |
|
| 2001 |
Liu T, Zwingman T, Li R, Pan T, Wong BS, Petersen RB, Gambetti P, Herrup K, Sy MS. Differential expression of cellular prion protein in mouse brain as detected with multiple anti-PrP monoclonal antibodies. Brain Research. 896: 118-29. PMID 11277980 DOI: 10.1016/S0006-8993(01)02050-9 |
0.56 |
|
| 2001 |
Liu T, Li R, Wong BS, Liu D, Pan T, Petersen RB, Gambetti P, Sy MS. Normal cellular prion protein is preferentially expressed on subpopulations of murine hemopoietic cells. Journal of Immunology (Baltimore, Md. : 1950). 166: 3733-42. PMID 11238614 DOI: 10.4049/Jimmunol.166.6.3733 |
0.513 |
|
| 2001 |
Wong BS, Liu T, Li R, Pan T, Petersen RB, Smith MA, Gambetti P, Perry G, Manson JC, Brown DR, Sy MS. Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein. Journal of Neurochemistry. 76: 565-72. PMID 11208919 DOI: 10.1046/J.1471-4159.2001.00028.X |
0.413 |
|
| 2000 |
Lu K, Wang W, Xie Z, Wong BS, Li R, Petersen RB, Sy MS, Chen SG. Expression and structural characterization of the recombinant human doppel protein. Biochemistry. 39: 13575-83. PMID 11063595 DOI: 10.1021/Bi001523M |
0.358 |
|
| 2000 |
Jin T, Gu Y, Zanusso G, Sy M, Kumar A, Cohen M, Gambetti P, Singh N. The chaperone protein BiP binds to a mutant prion protein and mediates its degradation by the proteasome. The Journal of Biological Chemistry. 275: 38699-704. PMID 10970892 DOI: 10.1074/Jbc.M005543200 |
0.454 |
|
| 2000 |
Li R, Liu T, Wong BS, Pan T, Morillas M, Swietnicki W, O'Rourke K, Gambetti P, Surewicz WK, Sy MS. Identification of an epitope in the C terminus of normal prion protein whose expression is modulated by binding events in the N terminus. Journal of Molecular Biology. 301: 567-73. PMID 10966770 DOI: 10.1006/Jmbi.2000.3986 |
0.465 |
|
| 2000 |
Wong BS, Pan T, Liu T, Li R, Petersen RB, Jones IM, Gambetti P, Brown DR, Sy MS. Prion disease: A loss of antioxidant function? Biochemical and Biophysical Research Communications. 275: 249-52. PMID 10964653 DOI: 10.1006/Bbrc.2000.3158 |
0.486 |
|
| 2000 |
Capellari S, Parchi P, Russo CM, Sanford J, Sy MS, Gambetti P, Petersen RB. Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain. The American Journal of Pathology. 157: 613-22. PMID 10934164 DOI: 10.1016/S0002-9440(10)64572-5 |
0.44 |
|
| 2000 |
Wong BS, Pan T, Liu T, Li R, Gambetti P, Sy MS. Differential contribution of superoxide dismutase activity by prion protein in vivo. Biochemical and Biophysical Research Communications. 273: 136-9. PMID 10873575 DOI: 10.1006/Bbrc.2000.2911 |
0.515 |
|
| 2000 |
Wong B, Brown DR, Clive C, Haswell S, Sy M, Gambetti P, Williamson RA, Burton DR, Jones IM. Effect of copper on recombinant mouse prion protein Biochemical Society Transactions. 28: A36-A36. DOI: 10.1042/Bst028A036B |
0.366 |
|
| 1988 |
Sy MS, Benacerraf B. Suppressor T cells, immunoglobulin and Igh restriction. Immunological Reviews. 101: 133-48. PMID 2965093 DOI: 10.1111/J.1600-065X.1988.Tb00735.X |
0.317 |
|
| 1982 |
Greene MI, Nelles MJ, Sy M, Nisonoff A. Regulation of immunity to the azobenzenearsonate hapten. Advances in Immunology. 32: 253-300. PMID 6214163 DOI: 10.1016/S0065-2776(08)60723-3 |
0.324 |
|
| 1981 |
Sy MS, Brown A, Bach BA, Benacerraf B, Gottlieb PD, Nisonoff A, Greene MI. Genetic and serological analysis of the expression of crossreactive idiotypic determinants on anti-p-azobenzenarsonate antibodies and p-azobenzenarsonate-specific suppressor T cell factors. Proceedings of the National Academy of Sciences of the United States of America. 78: 1143-7. PMID 6165006 DOI: 10.1073/Pnas.78.2.1143 |
0.305 |
|
| 1979 |
Sy MS, Bach BA, Dohi Y, Nisonoff A, Benacerraf B, Greene MI. Antigen- and receptor-driven regulatory mechanisms. I. Induction of suppressor T cells with anti-idiotypic antibodies. The Journal of Experimental Medicine. 150: 1216-28. PMID 91656 DOI: 10.1084/Jem.150.5.1216 |
0.317 |
|
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