Qingzhong Kong - Publications

Affiliations: 
Case Western Reserve University, Cleveland Heights, OH, United States 

51 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.88
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  0.88
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. Correction to: In Vitro Seeding Activity of Glycoform-Deficient Prions from Variably Protease-Sensitive Prionopathy and Familial CJD Associated with PrP Mutation. Molecular Neurobiology. PMID 30707392 DOI: 10.1007/s12035-019-1508-3  0.84
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  0.88
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  0.84
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  0.48
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  0.44
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  0.84
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  0.44
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  0.84
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  0.88
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. Correction: Prion Protein Protects against Renal Ischemia/Reperfusion Injury. Plos One. 10: e0141025. PMID 26469069 DOI: 10.1371/journal.pone.0141025  0.84
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  1
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  1
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  1
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  0.88
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2012 Liang J, Kong Q. α-Cleavage of cellular prion protein. Prion. 6: 453-60. PMID 23052041 DOI: 10.4161/pri.22511  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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