| Year |
Citation |
Score |
| 2024 |
Zhang W, Orrú CD, Foutz A, Ding M, Yuan J, Shah SZA, Zhang J, Kotobelli K, Gerasimenko M, Gilliland T, Chen W, Tang M, Cohen M, Safar J, Xu B, ... ... Zou WQ, et al. Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases. Acta Neuropathologica. 147: 17. PMID 38231266 DOI: 10.1007/s00401-023-02661-2 |
0.381 |
|
| 2023 |
Jeong MJ, Wang Z, Zou WQ, Kim YC, Jeong BH. The first report of polymorphisms of the prion protein gene () in Pekin ducks (). Frontiers in Veterinary Science. 10: 1273050. PMID 38026621 DOI: 10.3389/fvets.2023.1273050 |
0.403 |
|
| 2023 |
Myers RR, John A, Zhang W, Zou WQ, Cembran A, Fernandez-Funez P. Y225A induces long-range conformational changes in human prion protein that are protective in Drosophila. The Journal of Biological Chemistry. 104881. PMID 37269948 DOI: 10.1016/j.jbc.2023.104881 |
0.373 |
|
| 2022 |
Wood AR, Foliaki ST, Groveman BR, Walters RO, Williams K, Yuan J, Zou WQ, Haigh CL. Hereditary E200K mutation within the prion protein gene alters human iPSC derived cardiomyocyte function. Scientific Reports. 12: 15788. PMID 36138047 DOI: 10.1038/s41598-022-19631-5 |
0.307 |
|
| 2021 |
Wang Z, Qin K, Camacho MV, Cali I, Yuan J, Shen P, Greenlee J, Kong Q, Mastrianni JA, Zou WQ. Generation of human chronic wasting disease in transgenic mice. Acta Neuropathologica Communications. 9: 158. PMID 34565488 DOI: 10.1186/s40478-021-01262-y |
0.479 |
|
| 2021 |
Trichka J, Zou WQ. Modulation of Neuroinflammation by the Gut Microbiota in Prion and Prion-Like Diseases. Pathogens (Basel, Switzerland). 10. PMID 34358037 DOI: 10.3390/pathogens10070887 |
0.315 |
|
| 2021 |
Ding M, Teruya K, Zhang W, Lee HW, Yuan J, Oguma A, Foutz A, Camacho MV, Mitchell M, Greenlee JJ, Kong Q, Doh-Ura K, Cui L, Zou WQ. Decrease in Skin Prion-Seeding Activity of Prion-Infected Mice Treated with a Compound Against Human and Animal Prions: a First Possible Biomarker for Prion Therapeutics. Molecular Neurobiology. PMID 33983547 DOI: 10.1007/s12035-021-02418-6 |
0.401 |
|
| 2021 |
Zhang W, Xiao X, Ding M, Yuan J, Foutz A, Moudjou M, Kitamoto T, Langeveld JPM, Cui L, Zou WQ. Further Characterization of Glycoform-Selective Prions of Variably Protease-Sensitive Prionopathy. Pathogens (Basel, Switzerland). 10. PMID 33922765 DOI: 10.3390/pathogens10050513 |
0.499 |
|
| 2020 |
Shen P, Dang J, Wang Z, Zhang W, Yuan J, Lang Y, Ding M, Mitchell M, Kong Q, Feng J, Rozemuller AJM, Cui L, Petersen RB, Zou WQ. Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro. Molecular Neurobiology. PMID 32889654 DOI: 10.1007/S12035-020-02098-8 |
0.509 |
|
| 2020 |
Foliaki ST, Groveman BR, Yuan J, Walters R, Zhang S, Tesar P, Zou W, Haigh CL. Pathogenic Prion Protein Isoforms Are Not Present in Cerebral Organoids Generated from Asymptomatic Donors Carrying the E200K Mutation Associated with Familial Prion Disease. Pathogens (Basel, Switzerland). 9. PMID 32570796 DOI: 10.3390/Pathogens9060482 |
0.516 |
|
| 2019 |
Wang Z, Manca M, Foutz A, Camacho MV, Raymond GJ, Race B, Orru CD, Yuan J, Shen P, Li B, Lang Y, Dang J, Adornato A, Williams K, Maurer NR, ... ... Zou WQ, et al. Publisher Correction: Early preclinical detection of prions in the skin of prion-infected animals. Nature Communications. 10: 640. PMID 30718499 DOI: 10.1038/S41467-019-08648-6 |
0.552 |
|
| 2019 |
Wang Z, Manca M, Foutz A, Camacho MV, Raymond GJ, Race B, Orru CD, Yuan J, Shen P, Li B, Lang Y, Dang J, Adornato A, Williams K, Maurer NR, ... ... Zou WQ, et al. Early preclinical detection of prions in the skin of prion-infected animals. Nature Communications. 10: 247. PMID 30651538 DOI: 10.1038/S41467-018-08130-9 |
0.581 |
|
| 2019 |
Wang Z, Yuan J, Shen P, Abskharon R, Lang Y, Dang J, Adornato A, Xu L, Chen J, Feng J, Moudjou M, Kitamoto T, Langeveld J, Appleby B, Ma J, ... ... Zou WQ, et al. In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation. Molecular Neurobiology. PMID 30612334 DOI: 10.1007/S12035-018-1459-0 |
0.441 |
|
| 2019 |
Abskharon R, Wang F, Wohlkonig A, Ruan J, Soror S, Giachin G, Pardon E, Zou W, Legname G, Ma J, Steyaert J. Structural evidence for the critical role of the prion protein hydrophobic region in forming an infectious prion. Plos Pathogens. 15. DOI: 10.2210/Pdb6Hhd/Pdb |
0.504 |
|
| 2017 |
Orrú CD, Yuan J, Appleby BS, Li B, Li Y, Winner D, Wang Z, Zhan YA, Rodgers M, Rarick J, Wyza RE, Joshi T, Wang GX, Cohen ML, Zhang S, ... ... Zou WQ, et al. Prion seeding activity and infectivity in skin samples from patients with sporadic Creutzfeldt-Jakob disease. Science Translational Medicine. 9. PMID 29167394 DOI: 10.1126/Scitranslmed.Aam7785 |
0.409 |
|
| 2017 |
Abskharon R, Dang J, Elfarash A, Wang Z, Shen P, Zou LS, Hassan S, Wang F, Fujioka H, Steyaert J, Mulaj M, Surewicz WK, Castilla J, Wohlkonig A, Zou WQ. Soluble polymorphic bank vole prion proteins induced by co-expression of quiescin sulfhydryl oxidase in E. coli and their aggregation behaviors. Microbial Cell Factories. 16: 170. PMID 28978309 DOI: 10.1186/S12934-017-0782-X |
0.519 |
|
| 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 |
0.651 |
|
| 2016 |
Zhan YA, Abskharon R, Li Y, Yuan J, Zeng L, Dang J, Martinez MC, Wang Z, Mikol J, Lehmann S, Bu S, Steyaert J, Cui L, Petersen RB, Kong Q, ... ... Zou WQ, et al. Quiescin-sulfhydryl oxidase inhibits prion formation in vitro. Aging. PMID 27959866 DOI: 10.18632/aging.101132 |
0.455 |
|
| 2016 |
Das AS, Zou WQ. Prions: Beyond a Single Protein. Clinical Microbiology Reviews. 29: 633-58. PMID 27226089 DOI: 10.1128/CMR.00046-15 |
0.335 |
|
| 2015 |
Zhang B, Cowden D, Zhang F, Yuan J, Siedlak S, Abouelsaad M, Zeng L, Zhou X, O'Toole J, Das AS, Kofskey D, Warren M, Bian Z, Cui Y, Tan T, ... ... Zou WQ, et al. Prion Protein Protects against Renal Ischemia/Reperfusion Injury. Plos One. 10: e0136923. PMID 26327228 DOI: 10.1371/Journal.Pone.0136923 |
0.316 |
|
| 2015 |
Orrú CD, Groveman BR, Raymond LD, Hughson AG, Nonno R, Zou W, Ghetti B, Gambetti P, Caughey B. Correction: Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains. Plos Pathogens. 11: e1005117. PMID 26284358 DOI: 10.1371/Journal.Ppat.1005117 |
0.541 |
|
| 2015 |
Orrú CD, Groveman BR, Raymond LD, Hughson AG, Nonno R, Zou W, Ghetti B, Gambetti P, Caughey B. Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains. Plos Pathogens. 11: e1004983. PMID 26086786 DOI: 10.1371/Journal.Ppat.1004983 |
0.63 |
|
| 2015 |
Ghoshal N, Perry A, McKeel D, Schmidt RE, Carter D, Norton J, Zou WQ, Xiao X, Puoti G, Notari S, Gambetti P, Morris JC, Cairns NJ. Variably Protease-sensitive Prionopathy in an Apparent Cognitively Normal 93-Year-Old. Alzheimer Disease and Associated Disorders. 29: 173-6. PMID 24845762 DOI: 10.1097/Wad.0000000000000049 |
0.473 |
|
| 2014 |
Xiao X, Yuan J, Qing L, Cali I, Mikol J, Delisle MB, Uro-Coste E, Zeng L, Abouelsaad M, Gazgalis D, Martinez MC, Wang GX, Brown P, Ironside JW, Gambetti P, ... ... Zou WQ, et al. Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease. Journal of Clinical & Cellular Immunology. 5. PMID 25419482 DOI: 10.4172/2155-9899.1000240 |
0.672 |
|
| 2014 |
Notari S, Xiao X, Espinosa JC, Cohen Y, Qing L, Aguilar-Calvo P, Kofskey D, Cali I, Cracco L, Kong Q, Torres JM, Zou W, Gambetti P. Transmission characteristics of variably protease-sensitive prionopathy. Emerging Infectious Diseases. 20: 2006-14. PMID 25418590 DOI: 10.3201/Eid2012.140548 |
0.71 |
|
| 2014 |
Cannon A, Bieniek KF, Lin WL, Notari S, Zou WQ, Gambetti P, Pedraza O, Graff-Radford NR, Ferman TJ, Dickson DW. Concurrent variably protease-sensitive prionopathy and amyotrophic lateral sclerosis. Acta Neuropathologica. 128: 313-5. PMID 24928712 DOI: 10.1007/S00401-014-1309-8 |
0.553 |
|
| 2014 |
Ghetti BF, Miller DC, Zou W, Cohen Y, Richardson R, Oblak AL, Gambetti P, Murrell JR. Early Onset And Rapid Course Of Alzheimer Disease Associated With The I143T Psen1 Mutation Alzheimers & Dementia. 10: 629. DOI: 10.1016/J.Jalz.2014.05.1095 |
0.584 |
|
| 2013 |
Zou WQ, Gambetti P, Xiao X, Yuan J, Langeveld J, Pirisinu L. Prions in variably protease-sensitive prionopathy: an update. Pathogens (Basel, Switzerland). 2: 457-71. PMID 25437202 DOI: 10.3390/Pathogens2030457 |
0.727 |
|
| 2013 |
Yuan J, Zhan YA, Abskharon R, Xiao X, Martinez MC, Zhou X, Kneale G, Mikol J, Lehmann S, Surewicz WK, Castilla J, Steyaert J, Zhang S, Kong Q, Petersen RB, ... ... Zou WQ, et al. Recombinant human prion protein inhibits prion propagation in vitro. Scientific Reports. 3: 2911. PMID 24105336 DOI: 10.1038/Srep02911 |
0.531 |
|
| 2013 |
Pirisinu L, Nonno R, Esposito E, Benestad SL, Gambetti P, Agrimi U, Zou WQ. Small ruminant nor98 prions share biochemical features with human gerstmann-sträussler-scheinker disease and variably protease-sensitive prionopathy. Plos One. 8: e66405. PMID 23826096 DOI: 10.1371/Journal.Pone.0066405 |
0.715 |
|
| 2013 |
Xiao X, Yuan J, Haïk S, Cali I, Zhan Y, Moudjou M, Li B, Laplanche JL, Laude H, Langeveld J, Gambetti P, Kitamoto T, Kong Q, Brandel JP, Cobb BA, ... ... Zou WQ, et al. Glycoform-selective prion formation in sporadic and familial forms of prion disease. Plos One. 8: e58786. PMID 23527023 DOI: 10.1371/Journal.Pone.0058786 |
0.681 |
|
| 2013 |
Xiao X, Cali I, Dong Z, Puoti G, Yuan J, Qing L, Wang H, Kong Q, Gambetti P, Zou WQ. Protease-sensitive prions with 144-bp insertion mutations. Aging. 5: 155-73. PMID 23515139 |
0.65 |
|
| 2013 |
Xiao X, Yuan J, Haïk S, Cali I, Zhan Y, Moudjou M, Li B, Laplanche J, Laude H, Langeveld J, Gambetti P, Kitamoto T, Kong Q, Brandel J, Cobb BA, ... ... Zou W, et al. Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease Plos One. 8. DOI: 10.1371/Annotation/5391F30A-0875-4145-A1Ea-74Aedbbcd1E4 |
0.598 |
|
| 2013 |
Zou WQ, Gambetti P. Prions and diseases Prions and Diseases. 2: 1-295. DOI: 10.1007/978-1-4614-5338-3 |
0.441 |
|
| 2012 |
Xiao X, Yuan J, Zou WQ. Isolation of soluble and insoluble PrP oligomers in the normal human brain. Journal of Visualized Experiments : Jove. PMID 23070047 DOI: 10.3791/3788 |
0.436 |
|
| 2011 |
Zhou X, Bi H, Wong J, Shimoji M, Wang Y, Yuan J, Xiao X, Wang GX, Zou WQ. Alkylating antitumor drug mechlorethamine conceals a structured PrP domain and inhibits in vitro prion amplification. Journal of Toxicology and Environmental Health. Part A. 74: 1493-503. PMID 22043910 DOI: 10.1080/15287394.2011.618978 |
0.508 |
|
| 2011 |
Moody KM, Schonberger LB, Maddox RA, Zou WQ, Cracco L, Cali I. Sporadic fatal insomnia in a young woman: a diagnostic challenge: case report. Bmc Neurology. 11: 136. PMID 22040318 DOI: 10.1186/1471-2377-11-136 |
0.335 |
|
| 2011 |
Zou RS, Fujioka H, Guo JP, Xiao X, Shimoji M, Kong C, Chen C, Tasnadi M, Voma C, Yuan J, Moudjou M, Laude H, Petersen RB, Zou WQ. Characterization of spontaneously generated prion-like conformers in cultured cells. Aging. 3: 968-84. PMID 21990137 DOI: 10.18632/AGING.100370 |
0.408 |
|
| 2011 |
Fernandez-Funez P, Zhang Y, Sanchez-Garcia J, Jensen K, Zou WQ, Rincon-Limas DE. Pulling rabbits to reveal the secrets of the prion protein. Communicative & Integrative Biology. 4: 262-6. PMID 21980555 DOI: 10.4161/cib.4.3.15054 |
0.492 |
|
| 2011 |
Zou WQ, Zhou X, Yuan J, Xiao X. Insoluble cellular prion protein and its association with prion and Alzheimer diseases. Prion. 5: 172-8. PMID 21847014 DOI: 10.4161/Pri.5.3.16894 |
0.509 |
|
| 2011 |
Gambetti P, Puoti G, Zou WQ. Variably protease-sensitive prionopathy: a novel disease of the prion protein. Journal of Molecular Neuroscience : Mn. 45: 422-4. PMID 21584652 DOI: 10.1007/S12031-011-9543-1 |
0.681 |
|
| 2011 |
Vital A, Laplanche JL, Bastard JR, Xiao X, Zou WQ, Vital C. A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion. Neuropathology and Applied Neurobiology. 37: 554-9. PMID 21426368 DOI: 10.1111/J.1365-2990.2011.01174.X |
0.383 |
|
| 2011 |
Gambetti P, Cali I, Notari S, Kong Q, Zou WQ, Surewicz WK. Molecular biology and pathology of prion strains in sporadic human prion diseases. Acta Neuropathologica. 121: 79-90. PMID 21058033 DOI: 10.1007/S00401-010-0761-3 |
0.675 |
|
| 2011 |
Gambetti P, Puoti G, Kong Q, Zou W. A New Prion Disease: Protease-Sensitive Prionopathy Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 350-353. DOI: 10.1002/9781444341256.ch35 |
0.37 |
|
| 2010 |
Parchi P, Cescatti M, Notari S, Schulz-Schaeffer WJ, Capellari S, Giese A, Zou WQ, Kretzschmar H, Ghetti B, Brown P. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. Brain : a Journal of Neurology. 133: 3030-42. PMID 20823086 DOI: 10.1093/Brain/Awq234 |
0.496 |
|
| 2010 |
Fernandez-Funez P, Zhang Y, Casas-Tinto S, Xiao X, Zou WQ, Rincon-Limas DE. Sequence-dependent prion protein misfolding and neurotoxicity. The Journal of Biological Chemistry. 285: 36897-908. PMID 20817727 DOI: 10.1074/jbc.M110.174391 |
0.442 |
|
| 2010 |
Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Annals of Neurology. 68: 162-72. PMID 20695009 DOI: 10.1002/Ana.22094 |
0.67 |
|
| 2010 |
Dagdanova A, Ilchenko S, Notari S, Yang Q, Obrenovich ME, Hatcher K, McAnulty P, Huang L, Zou W, Kong Q, Gambetti P, Chen SG. Characterization of the prion protein in human urine. The Journal of Biological Chemistry. 285: 30489-95. PMID 20670940 DOI: 10.1074/Jbc.M110.161794 |
0.659 |
|
| 2010 |
Notari S, Moleres FJ, Hunter SB, Belay ED, Schonberger LB, Cali I, Parchi P, Shieh WJ, Brown P, Zaki S, Zou WQ, Gambetti P. Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. Plos One. 5: e8765. PMID 20098730 DOI: 10.1371/Journal.Pone.0008765 |
0.624 |
|
| 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 |
0.622 |
|
| 2009 |
Xiao X, Miravalle L, Yuan J, McGeehan J, Dong Z, Wyza R, MacLennan GT, Golichowski AM, Kneale G, King N, Kong Q, Spina S, Vidal R, Ghetti B, Roos K, ... ... Zou WQ, et al. Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease. The American Journal of Pathology. 174: 1602-8. PMID 19349373 DOI: 10.2353/Ajpath.2009.081045 |
0.617 |
|
| 2009 |
Zou WQ, Gambetti P. Variant Creutzfeldt-Jakob disease: French versus British. Annals of Neurology. 65: 233-5. PMID 19334065 DOI: 10.1002/ana.21637 |
0.66 |
|
| 2008 |
Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 283: 30557-65. PMID 18753138 DOI: 10.1074/Jbc.M801877200 |
0.66 |
|
| 2008 |
Mehta LR, Huddleston BJ, Skalabrin EJ, Burns JB, Zou WQ, Gambetti P, Chin SS. Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome. Archives of Neurology. 65: 971-3. PMID 18625868 DOI: 10.1001/Archneur.65.7.971 |
0.587 |
|
| 2008 |
Gambetti P, Dong Z, Yuan J, Xiao X, Zheng M, Alshekhlee A, Castellani R, Cohen M, Barria MA, Gonzalez-Romero D, Belay ED, Schonberger LB, Marder K, Harris C, Burke JR, ... ... Zou WQ, et al. A novel human disease with abnormal prion protein sensitive to protease. Annals of Neurology. 63: 697-708. PMID 18571782 DOI: 10.1002/Ana.21420 |
0.691 |
|
| 2008 |
Kong Q, Zheng M, Casalone C, Qing L, Huang S, Chakraborty B, Wang P, Chen F, Cali I, Corona C, Martucci F, Iulini B, Acutis P, Wang L, Liang J, ... ... Zou WQ, et al. Evaluation of the human transmission risk of an atypical bovine spongiform encephalopathy prion strain. Journal of Virology. 82: 3697-701. PMID 18234793 DOI: 10.1128/Jvi.02561-07 |
0.614 |
|
| 2008 |
Yuan J, Dong Z, Guo JP, McGeehan J, Xiao X, Wang J, Cali I, McGeer PL, Cashman NR, Bessen R, Surewicz WK, Kneale G, Petersen RB, Gambetti P, Zou WQ. Accessibility of a critical prion protein region involved in strain recognition and its implications for the early detection of prions. Cellular and Molecular Life Sciences : Cmls. 65: 631-43. PMID 18193391 DOI: 10.1007/S00018-007-7478-Z |
0.647 |
|
| 2007 |
Lefebvre-Roque M, Kremmer E, Gilch S, Zou WQ, Féraudet C, Gilles CM, Salès N, Grassi J, Gambetti P, Baron T, Schätzl H, Lasmézas CI. Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice. Prion. 1: 198-206. PMID 19164902 DOI: 10.4161/Pri.1.3.4870 |
0.504 |
|
| 2007 |
Zou WQ, Gambetti P. Prion: the chameleon protein. Cellular and Molecular Life Sciences : Cmls. 64: 3266-70. PMID 17965827 DOI: 10.1007/S00018-007-7380-8 |
0.696 |
|
| 2006 |
Yuan J, Xiao X, McGeehan J, Dong Z, Cali I, Fujioka H, Kong Q, Kneale G, Gambetti P, Zou WQ. Insoluble aggregates and protease-resistant conformers of prion protein in uninfected human brains. The Journal of Biological Chemistry. 281: 34848-58. PMID 16987816 DOI: 10.1074/Jbc.M602238200 |
0.628 |
|
| 2006 |
Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain : a Journal of Neurology. 129: 2266-77. PMID 16923954 DOI: 10.1093/Brain/Awl224 |
0.579 |
|
| 2006 |
Aralasmak A, Crain BJ, Zou WQ, Yousem DM. A prion disease--possible Gerstmann-Straussler-Scheinker disease: a case report. Journal of Computer Assisted Tomography. 30: 135-9. PMID 16365589 DOI: 10.1097/01.Rct.0000193816.42051.1A |
0.355 |
|
| 2006 |
Xie Z, O'Rourke KI, Dong Z, Jenny AL, Langenberg JA, Belay ED, Schonberger LB, Petersen RB, Zou W, Kong Q, Gambetti P, Chen SG. Chronic wasting disease of elk and deer and Creutzfeldt-Jakob disease: comparative analysis of the scrapie prion protein. The Journal of Biological Chemistry. 281: 4199-206. PMID 16338930 DOI: 10.1074/Jbc.M509052200 |
0.718 |
|
| 2005 |
Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. The American Journal of Pathology. 167: 1729-38. PMID 16314483 DOI: 10.1016/S0002-9440(10)61254-0 |
0.68 |
|
| 2005 |
Belay ED, Sejvar JJ, Shieh WJ, Wiersma ST, Zou WQ, Gambetti P, Hunter S, Maddox RA, Crockett L, Zaki SR, Schonberger LB. Variant Creutzfeldt-Jakob disease death, United States. Emerging Infectious Diseases. 11: 1351-4. PMID 16229761 DOI: 10.3201/eid1109.050371 |
0.508 |
|
| 2005 |
Kong Q, Huang S, Zou W, Vanegas D, Wang M, Wu D, Yuan J, Zheng M, Bai H, Deng H, Chen K, Jenny AL, O'Rourke K, Belay ED, Schonberger LB, et al. Chronic wasting disease of elk: transmissibility to humans examined by transgenic mouse models. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 7944-9. PMID 16135751 DOI: 10.1523/Jneurosci.2467-05.2005 |
0.648 |
|
| 2005 |
Zou WQ, Gambetti P. From microbes to prions the final proof of the prion hypothesis. Cell. 121: 155-7. PMID 15851020 DOI: 10.1016/j.cell.2005.04.002 |
0.616 |
|
| 2005 |
Yuan J, Kinter M, McGeehan J, Perry G, Kneale G, Gambetti P, Zou WQ. Concealment of epitope by reduction and alkylation in prion protein. Biochemical and Biophysical Research Communications. 326: 652-9. PMID 15596149 DOI: 10.1016/j.bbrc.2004.11.088 |
0.584 |
|
| 2004 |
Mishra RS, Basu S, Gu Y, Luo X, Zou WQ, Mishra R, Li R, Chen SG, Gambetti P, Fujioka H, Singh N. Protease-resistant human prion protein and ferritin are cotransported across Caco-2 epithelial cells: implications for species barrier in prion uptake from the intestine. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 11280-90. PMID 15601934 DOI: 10.1523/Jneurosci.2864-04.2004 |
0.609 |
|
| 2004 |
Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology. 63: 436-42. PMID 15304573 DOI: 10.1212/01.Wnl.0000135153.96325.3B |
0.484 |
|
| 2004 |
Zou WQ, Zheng J, Gray DM, Gambetti P, Chen SG. Antibody to DNA detects scrapie but not normal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 101: 1380-5. PMID 14734804 DOI: 10.1073/Pnas.0307825100 |
0.642 |
|
| 2004 |
Gorochov G, Deslys JP, Paramithiotis E, Pinard M, Lawton T, LaBoissiere S, Leathers VL, Zou WQ, Estey LA, Lamontagne J, Lehto MT, Kondejewski LH, Francoeur GP, Papadopoulos M, Haghighat A, et al. Properties of a disease-specific prion probe [1] (multiple letters) Nature Medicine. 10: 11-12. PMID 14702617 |
0.355 |
|
| 2004 |
Kong Q, Surewicz WK, Petersen RB, Zou W, Chen SG, Gambetti P, Parchi P, Capellari S, Goldfarb L, Montagna P, Lugaresi E, Piccardo P, Ghetti B. 14 Inherited Prion Diseases Cold Spring Harbor Monograph Archive. 41: 673-775. DOI: 10.1101/087969693.41.673 |
0.601 |
|
| 2004 |
Zou W, Gambetti P. Is Sporadic Creutzfeldt-Jakob Disease Systemic? Nejm Journal Watch. 2004. DOI: 10.1056/Jn200402260000001 |
0.475 |
|
| 2004 |
Paramithiotis E, Pinard M, Lawton T, LaBoissiere S, Leathers VL, Zou W, Estey LA, Lamontagne J, Lehto MT, Kondejewski LH, Francoeur GP, Papadopoulos M, Haghighat A, Spatz SJ, Head M, et al. Reply to “Properties of a disease-specific prion probe” Nature Medicine. 10: 11-12. DOI: 10.1038/Nm0104-11B |
0.523 |
|
| 2004 |
Zou WQ, Gambetti P. Modeling of human prions and prion diseases in vitro and in vivo Drug Discovery Today: Disease Models. 1: 157-164. DOI: 10.1016/J.Ddmod.2004.09.011 |
0.672 |
|
| 2003 |
Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. British Medical Bulletin. 66: 213-39. PMID 14522861 DOI: 10.1093/Bmb/66.1.213 |
0.649 |
|
| 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 |
0.66 |
|
| 2003 |
Paramithiotis E, Pinard M, Lawton T, LaBoissiere S, Leathers VL, Zou WQ, Estey LA, Lamontagne J, Lehto MT, Kondejewski LH, Francoeur GP, Papadopoulos M, Haghighat A, Spatz SJ, Head M, et al. A prion protein epitope selective for the pathologically misfolded conformation. Nature Medicine. 9: 893-9. PMID 12778138 DOI: 10.1038/Nm883 |
0.469 |
|
| 2003 |
Zou W, Colucci M, Gambetti P, Chen SG. Characterization of prion proteins. Methods in Molecular Biology (Clifton, N.J.). 217: 305-14. PMID 12491943 DOI: 10.1385/1-59259-330-5:305 |
0.581 |
|
| 2003 |
Zou W, Gambetti P. Less Invasive Diagnosis of Sporadic Creutzfeldt-Jakob Disease? Nejm Journal Watch. 2003. DOI: 10.1056/Jn200305090000009 |
0.535 |
|
| 2002 |
Zou WQ, Cashman NR. Acidic pH and detergents enhance in vitro conversion of human brain PrPC to a PrPSc-like form. The Journal of Biological Chemistry. 277: 43942-7. PMID 12161431 DOI: 10.1074/Jbc.M203611200 |
0.339 |
|
| 2000 |
Chen SG, Zou W, Parchi P, Gambetti P. PrP(Sc) typing by N-terminal sequencing and mass spectrometry. Archives of Virology. Supplementum. 209-16. PMID 11214924 DOI: 10.1007/978-3-7091-6308-5_20 |
0.528 |
|
| 2000 |
Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG. Genetic influence on the structural variations of the abnormal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 97: 10168-72. PMID 10963679 DOI: 10.1073/Pnas.97.18.10168 |
0.648 |
|
| 1998 |
Parchi P, Chen SG, Brown P, Zou W, Capellari S, Budka H, Hainfellner J, Reyes PF, Golden GT, Hauw JJ, Gajdusek DC, Gambetti P. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 8322-7. PMID 9653185 DOI: 10.1073/Pnas.95.14.8322 |
0.58 |
|
| 1997 |
Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nature Medicine. 3: 1009-15. PMID 9288728 DOI: 10.1038/Nm0997-1009 |
0.658 |
|
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