| Year |
Citation |
Score |
| 2023 |
Cracco L, Cali I, Cohen ML, Aslam R, Notari S, Kong Q, Newell KL, Ghetti B, Appleby BS, Gambetti P. Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host. Brain : a Journal of Neurology. PMID 38000783 DOI: 10.1093/brain/awad399 |
0.663 |
|
| 2023 |
Bayazid R, Orru' C, Aslam R, Cohen Y, Silva-Rohwer A, Lee SK, Occhipinti R, Kong Q, Shetty S, Cohen ML, Caughey B, Schonberger LB, Appleby BS, Cali I. Correction: A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques. Acta Neuropathologica. PMID 37253983 DOI: 10.1007/s00401-023-02592-y |
0.362 |
|
| 2022 |
Greenlee JJ, Moore SJ, Cassmann ED, Lambert ZJ, Kokemuller RD, Smith JD, Kunkle RA, Kong Q, Greenlee MHW. White-Tailed Deer are Susceptible to the Agent of Classical Sheep Scrapie after Experimental Oronasal Exposure. The Journal of Infectious Diseases. PMID 36344485 DOI: 10.1093/infdis/jiac443 |
0.353 |
|
| 2022 |
Otero A, Barrio T, Eraña H, Charco JM, Betancor M, Díaz-Domínguez CM, Marín B, Andréoletti O, Torres JM, Kong Q, Badiola JJ, Bolea R, Castilla J. Glycans are not necessary to maintain the pathobiological features of bovine spongiform encephalopathy. Plos Pathogens. 18: e1010900. PMID 36206325 DOI: 10.1371/journal.ppat.1010900 |
0.366 |
|
| 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 |
0.496 |
|
| 2021 |
Dexter E, Kong Q. Neuroprotective effect and potential of cellular prion protein and its cleavage products for treatment of neurodegenerative disorders part I. a literature review. Expert Review of Neurotherapeutics. 1-14. PMID 34470561 DOI: 10.1080/14737175.2021.1965881 |
0.398 |
|
| 2021 |
Dexter E, Kong Q. Neuroprotective effect and potential of cellular prion protein and its cleavage products for treatment of neurodegenerative disorders part II: strategies for therapeutics development. Expert Review of Neurotherapeutics. 1-9. PMID 34470554 DOI: 10.1080/14737175.2021.1965882 |
0.375 |
|
| 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 |
0.423 |
|
| 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 |
0.524 |
|
| 2020 |
Kondru N, Manne S, Kokemuller R, Greenlee J, Greenlee MHW, Nichols T, Kong Q, Anantharam V, Kanthasamy A, Halbur P, Kanthasamy AG. An Ex Vivo Brain Slice Culture Model of Chronic Wasting Disease: Implications for Disease Pathogenesis and Therapeutic Development. Scientific Reports. 10: 7640. PMID 32376941 DOI: 10.1038/S41598-020-64456-9 |
0.455 |
|
| 2020 |
Moore J, Tatum T, Hwang S, Vrentas C, West Greenlee MH, Kong Q, Nicholson E, Greenlee J. Novel Strain of the Chronic Wasting Disease Agent Isolated From Experimentally Inoculated Elk With LL132 Prion Protein. Scientific Reports. 10: 3148. PMID 32081886 DOI: 10.1038/S41598-020-59819-1 |
0.522 |
|
| 2019 |
Camacho MV, Telling G, Kong Q, Gambetti P, Notari S. Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 31249376 DOI: 10.1038/S41374-019-0282-1 |
0.68 |
|
| 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, ... ... Kong Q, 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 |
0.538 |
|
| 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, ... ... Kong Q, 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 |
0.589 |
|
| 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, ... Kong Q, 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 |
0.543 |
|
| 2018 |
Kim C, Xiao X, Chen S, Haldiman T, Smirnovas V, Kofskey D, Warren M, Surewicz K, Maurer NR, Kong Q, Surewicz W, Safar JG. Artificial strain of human prions created in vitro. Nature Communications. 9: 2166. PMID 29867164 DOI: 10.1038/S41467-018-04584-Z |
0.511 |
|
| 2018 |
Ashok A, Karmakar S, Chandel R, Ravikumar R, Dalal S, Kong Q, Singh N. Prion protein modulates iron transport in the anterior segment: Implications for ocular iron homeostasis and prion transmission. Experimental Eye Research. PMID 29859760 DOI: 10.1016/J.Exer.2018.05.031 |
0.354 |
|
| 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, ... ... Kong Q, 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 |
0.418 |
|
| 2017 |
Elezgarai SR, Fernández-Borges N, Eraña H, Sevillano AM, Charco JM, Harrathi C, Saá P, Gil D, Kong Q, Requena JR, Andréoletti O, Castilla J. Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome. Scientific Reports. 7: 9584. PMID 28851967 DOI: 10.1038/S41598-017-09489-3 |
0.535 |
|
| 2017 |
Asthana A, Baksi S, Ashok A, Karmakar S, Mammadova N, Kokemuller R, Greenlee MH, Kong Q, Singh N. Prion protein facilitates retinal iron uptake and is cleaved at the β-site: Implications for retinal iron homeostasis in prion disorders. Scientific Reports. 7: 9600. PMID 28851903 DOI: 10.1038/S41598-017-08821-1 |
0.375 |
|
| 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, et al. Quiescin-sulfhydryl oxidase inhibits prion formation in vitro. Aging. PMID 27959866 DOI: 10.18632/aging.101132 |
0.483 |
|
| 2016 |
Choi JK, Cali I, Surewicz K, Kong Q, Gambetti P, Surewicz WK. Amyloid fibrils from the N-terminal prion protein fragment are infectious. Proceedings of the National Academy of Sciences of the United States of America. PMID 27849581 DOI: 10.1073/Pnas.1610716113 |
0.662 |
|
| 2016 |
Nichols TA, Spraker TR, Gidlewski T, Cummings B, Hill D, Kong Q, Balchandran A, VerCauteren KC, Zabel MD. Dietary Magnesium and Copper Affect Survival Time and Neuroinflammation in Chronic Wasting Disease. Prion. 0. PMID 27216881 DOI: 10.1080/19336896.2016.1181249 |
0.326 |
|
| 2015 |
Nichols TA, Fischer JW, Spraker TR, Kong Q, VerCauteren KC. CWD Prions Remain Infectious after Passage Through the Digestive System of Coyotes (Canis latrans). Prion. 0. PMID 26636258 DOI: 10.1080/19336896.2015.1086061 |
0.465 |
|
| 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, ... ... Kong Q, et al. Prion Protein Protects against Renal Ischemia/Reperfusion Injury. Plos One. 10: e0136923. PMID 26327228 DOI: 10.1371/Journal.Pone.0136923 |
0.343 |
|
| 2015 |
Kurt TD, Jiang L, Fernández-Borges N, Bett C, Liu J, Yang T, Spraker TR, Castilla J, Eisenberg D, Kong Q, Sigurdson CJ. Human prion protein sequence elements impede cross-species chronic wasting disease transmission. The Journal of Clinical Investigation. 125: 2548. PMID 25961458 DOI: 10.1172/Jci82647 |
0.396 |
|
| 2015 |
Kurt TD, Jiang L, Fernández-Borges N, Bett C, Liu J, Yang T, Spraker TR, Castilla J, Eisenberg D, Kong Q, Sigurdson CJ. Human prion protein sequence elements impede cross-species chronic wasting disease transmission. The Journal of Clinical Investigation. 125: 1485-96. PMID 25705888 DOI: 10.1172/Jci79408 |
0.491 |
|
| 2015 |
Xiao X, Cali I, Yuan J, Cracco L, Curtiss P, Zeng L, Abouelsaad M, Gazgalis D, Wang GX, Kong Q, Fujioka H, Puoti G, Zou WQ. Synthetic Aβ peptides acquire prion-like properties in the brain. Oncotarget. 6: 642-50. PMID 25460507 DOI: 10.18632/Oncotarget.2819 |
0.363 |
|
| 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, ... Kong Q, 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 |
0.663 |
|
| 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 |
0.7 |
|
| 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 |
0.543 |
|
| 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, et al. Recombinant human prion protein inhibits prion propagation in vitro. Scientific Reports. 3: 2911. PMID 24105336 DOI: 10.1038/Srep02911 |
0.552 |
|
| 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 |
0.492 |
|
| 2013 |
Kong Q, Mills JL, Kundu B, Li X, Qing L, Surewicz K, Cali I, Huang S, Zheng M, Swietnicki W, Sönnichsen FD, Gambetti P, Surewicz WK. Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo. Cell Reports. 4: 248-54. PMID 23871665 DOI: 10.1016/J.Celrep.2013.06.030 |
0.689 |
|
| 2013 |
Bett C, Kurt TD, Lucero M, Trejo M, Rozemuller AJ, Kong Q, Nilsson KP, Masliah E, Oldstone MB, Sigurdson CJ. Defining the conformational features of anchorless, poorly neuroinvasive prions. Plos Pathogens. 9: e1003280. PMID 23637596 DOI: 10.1371/Journal.Ppat.1003280 |
0.574 |
|
| 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, 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 |
0.67 |
|
| 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 |
0.629 |
|
| 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, 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 |
0.586 |
|
| 2012 |
Liang J, Kong Q. α-Cleavage of cellular prion protein. Prion. 6: 453-60. PMID 23052041 DOI: 10.4161/Pri.22511 |
0.564 |
|
| 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 |
0.568 |
|
| 2012 |
Luo JJ, Truant AL, Kong Q, Zou WQ. Sporadic fatal insomnia with clinical, laboratory, and genetic findings. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 19: 1188-92. PMID 22717776 DOI: 10.1016/J.Jocn.2011.11.023 |
0.339 |
|
| 2012 |
Liang J, Wang W, Sorensen D, Medina S, Ilchenko S, Kiselar J, Surewicz WK, Booth SA, Kong Q. Cellular prion protein regulates its own α-cleavage through ADAM8 in skeletal muscle. The Journal of Biological Chemistry. 287: 16510-20. PMID 22447932 DOI: 10.1074/Jbc.M112.360891 |
0.547 |
|
| 2012 |
Notari S, Qing L, Pocchiari M, Dagdanova A, Hatcher K, Dogterom A, Groisman JF, Lumholtz IB, Puopolo M, Lasmezas C, Chen SG, Kong Q, Gambetti P. Assessing prion infectivity of human urine in sporadic Creutzfeldt-Jakob disease. Emerging Infectious Diseases. 18: 21-8. PMID 22260924 DOI: 10.3201/Eid1801.110589 |
0.661 |
|
| 2012 |
Singh A, Qing L, Kong Q, Singh N. Change in the characteristics of ferritin induces iron imbalance in prion disease affected brains. Neurobiology of Disease. 45: 930-8. PMID 22182691 DOI: 10.1016/J.Nbd.2011.12.012 |
0.458 |
|
| 2011 |
Li B, Qing L, Yan J, Kong Q. Instability of the octarepeat region of the human prion protein gene. Plos One. 6: e26635. PMID 22028931 DOI: 10.1371/Journal.Pone.0026635 |
0.427 |
|
| 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 |
0.651 |
|
| 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 |
0.326 |
|
| 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, ... ... Kong Q, 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 |
0.671 |
|
| 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 |
0.662 |
|
| 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 |
0.461 |
|
| 2010 |
Kim JI, Cali I, Surewicz K, Kong Q, Raymond GJ, Atarashi R, Race B, Qing L, Gambetti P, Caughey B, Surewicz WK. Mammalian prions generated from bacterially expressed prion protein in the absence of any mammalian cofactors. The Journal of Biological Chemistry. 285: 14083-7. PMID 20304915 DOI: 10.1074/Jbc.C110.113464 |
0.65 |
|
| 2010 |
Zou WQ, Langeveld J, Xiao X, Chen S, McGeer PL, Yuan J, Payne MC, Kang HE, McGeehan J, Sy MS, Greenspan NS, Kaplan D, Wang GX, Parchi P, Hoover E, ... ... Kong Q, et al. PrP conformational transitions alter species preference of a PrP-specific antibody. The Journal of Biological Chemistry. 285: 13874-84. PMID 20194495 DOI: 10.1074/Jbc.M109.088831 |
0.404 |
|
| 2010 |
Zou WQ, Langeveld J, Xiao X, Chen S, McGeer PL, Yuan J, Payne MC, Kang HE, McGeehan J, Sy MS, Greenspan NS, Kaplan D, Wang GX, Parchi P, Hoover E, ... ... Kong Q, et al. Reply to Kascsak: Definition of the PrP 3F4 epitope revisited Journal of Biological Chemistry. 285: le6. DOI: 10.1074/Jbc.N109.088831 |
0.303 |
|
| 2009 |
Singh A, Kong Q, Luo X, Petersen RB, Meyerson H, Singh N. Prion protein (PrP) knock-out mice show altered iron metabolism: a functional role for PrP in iron uptake and transport. Plos One. 4: e6115. PMID 19568430 DOI: 10.1371/Journal.Pone.0006115 |
0.414 |
|
| 2009 |
Liang J, Parchaliuk D, Medina S, Sorensen G, Landry L, Huang S, Wang M, Kong Q, Booth SA. Activation of p53-regulated pro-apoptotic signaling pathways in PrP-mediated myopathy. Bmc Genomics. 10: 201. PMID 19400950 DOI: 10.1186/1471-2164-10-201 |
0.525 |
|
| 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, 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 |
0.655 |
|
| 2009 |
Singh A, Isaac AO, Luo X, Mohan ML, Cohen ML, Chen F, Kong Q, Bartz J, Singh N. Abnormal brain iron homeostasis in human and animal prion disorders. Plos Pathogens. 5: e1000336. PMID 19283067 DOI: 10.1371/Journal.Ppat.1000336 |
0.391 |
|
| 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, ... ... Kong Q, 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 |
0.686 |
|
| 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, 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 |
0.671 |
|
| 2007 |
Basu S, Mohan ML, Luo X, Kundu B, Kong Q, Singh N. Modulation of proteinase K-resistant prion protein in cells and infectious brain homogenate by redox iron: implications for prion replication and disease pathogenesis. Molecular Biology of the Cell. 18: 3302-12. PMID 17567949 DOI: 10.1091/Mbc.E07-04-0317 |
0.485 |
|
| 2007 |
Huang S, Liang J, Zheng M, Li X, Wang M, Wang P, Vanegas D, Wu D, Chakraborty B, Hays AP, Chen K, Chen SG, Booth S, Cohen M, Gambetti P, ... Kong Q, et al. Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 104: 6800-5. PMID 17420473 DOI: 10.1073/Pnas.0608885104 |
0.627 |
|
| 2006 |
Kong Q. RNAi: a novel strategy for the treatment of prion diseases. The Journal of Clinical Investigation. 116: 3101-3. PMID 17143323 DOI: 10.1172/JCI30663 |
0.455 |
|
| 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 |
0.631 |
|
| 2006 |
Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits. Journal of Neuropathology and Experimental Neurology. 65: 642-51. PMID 16825951 DOI: 10.1097/01.Jnen.0000228198.81797.4D |
0.644 |
|
| 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 |
0.673 |
|
| 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 |
0.656 |
|
| 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 |
0.573 |
|
| 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 |
0.619 |
|
| 1999 |
Kong Q, Maizels N. PMS2-deficiency diminishes hypermutation of a λ1 transgene in young but not older mice Molecular Immunology. 36: 83-91. PMID 10378680 DOI: 10.1016/S0161-5890(99)00027-9 |
0.302 |
|
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