| Year |
Citation |
Score |
| 2023 |
Thackray AM, McNulty EE, Nalls AV, Cardova A, Tran L, Telling G, Benestad SL, Gilch S, Mathiason CK, Bujdoso R. Genetic modulation of CWD prion propagation in cervid PrP Drosophila. The Biochemical Journal. 480: 1485-1501. PMID 37747806 DOI: 10.1042/BCJ20230247 |
0.492 |
|
| 2023 |
Eraña H, Díaz-Domínguez CM, Charco JM, Vidal E, González-Miranda E, Pérez-Castro MA, Piñeiro P, López-Moreno R, Sampedro-Torres-Quevedo C, Fernández-Veiga L, Tasis-Galarza J, Lorenzo NL, Santini-Santiago A, Lázaro M, García-Martínez S, ... ... Telling GC, et al. Understanding the key features of the spontaneous formation of bona fide prions through a novel methodology that enables their swift and consistent generation. Acta Neuropathologica Communications. 11: 145. PMID 37679832 DOI: 10.1186/s40478-023-01640-8 |
0.441 |
|
| 2023 |
Sun JL, Telling GC. New developments in prion disease research using genetically modified mouse models. Cell and Tissue Research. 392: 33-46. PMID 36929219 DOI: 10.1007/s00441-023-03761-x |
0.422 |
|
| 2023 |
Sun JL, Kim S, Crowell J, Webster BK, Raisley EK, Lowe DC, Bian J, Korpenfelt SL, Benestad SL, Telling GC. Novel Prion Strain as Cause of Chronic Wasting Disease in a Moose, Finland. Emerging Infectious Diseases. 29: 323-332. PMID 36692340 DOI: 10.3201/eid2902.220882 |
0.477 |
|
| 2022 |
Vidal E, Sánchez-Martín MA, Eraña H, Lázaro SP, Pérez-Castro MA, Otero A, Charco JM, Marín B, López-Moreno R, Díaz-Domínguez CM, Geijo M, Ordóñez M, Cantero G, di Bari M, Lorenzo NL, ... ... Telling G, et al. Bona fide atypical scrapie faithfully reproduced for the first time in a rodent model. Acta Neuropathologica Communications. 10: 179. PMID 36514160 DOI: 10.1186/s40478-022-01477-7 |
0.535 |
|
| 2022 |
Mays CE, Trinh THT, Telling G, Kang HE, Ryou C. Endoproteolysis of cellular prion protein by plasmin hinders propagation of prions. Frontiers in Molecular Neuroscience. 15: 990136. PMID 36117913 DOI: 10.3389/fnmol.2022.990136 |
0.42 |
|
| 2022 |
Wagner K, Pierce R, Gordon E, Hay A, Lessard A, Telling GC, Ballard JR, Moreno JA, Zabel MD. Tissue-Specific Biochemical Differences Between Chronic Wasting Disease Prions Isolated From Free-Ranging White-Tailed Deer (Odocoileus virginianus). The Journal of Biological Chemistry. 101834. PMID 35304100 DOI: 10.1016/j.jbc.2022.101834 |
0.484 |
|
| 2021 |
Bian J, Kim S, Kane SJ, Crowell J, Sun JL, Christiansen J, Saijo E, Moreno JA, DiLisio J, Burnett E, Pritzkow S, Gorski D, Soto C, Kreeger TJ, Balachandran A, ... ... Telling GC, et al. Adaptive selection of a prion strain conformer corresponding to established North American CWD during propagation of novel emergent Norwegian strains in mice expressing elk or deer prion protein. Plos Pathogens. 17: e1009748. PMID 34310663 DOI: 10.1371/journal.ppat.1009748 |
0.5 |
|
| 2021 |
Pritzkow S, Gorski D, Ramirez F, Telling GC, Benestad SL, Soto C. North American and Norwegian Chronic Wasting Disease prions exhibit different potential for interspecies transmission and zoonotic risk. The Journal of Infectious Diseases. PMID 34302479 DOI: 10.1093/infdis/jiab385 |
0.425 |
|
| 2020 |
Nonno R, Di Bari MA, Pirisinu L, D'Agostino C, Vanni I, Chiappini B, Marcon S, Riccardi G, Tran L, Vikøren T, Våge J, Madslien K, Mitchell G, Telling GC, Benestad SL, et al. Studies in bank voles reveal strain differences between chronic wasting disease prions from Norway and North America. Proceedings of the National Academy of Sciences of the United States of America. PMID 33229531 DOI: 10.1073/pnas.2013237117 |
0.341 |
|
| 2020 |
Yu CG, Bondada V, Joshi A, Reneer DV, Telling G, Saatman KE, Geddes JW. Calpastatin overexpression protects against excitotoxic hippocampal injury and traumatic spinal cord injury. Journal of Neurotrauma. PMID 32718209 DOI: 10.1089/Neu.2020.7122 |
0.325 |
|
| 2020 |
Kang HE, Bian J, Kane SJ, Kim S, Selwyn V, Crowell J, Bartz JC, Telling GC. Incomplete glycosylation during prion infection unmasks a prion protein epitope that facilitates prion detection and strain discrimination. The Journal of Biological Chemistry. PMID 32513872 DOI: 10.1074/Jbc.Ra120.012796 |
0.512 |
|
| 2020 |
Parrie LE, Crowell JAE, Moreno JA, Suinn SS, Telling GC, Bessen RA. The cellular prion protein promotes neuronal regeneration after acute nasotoxic injury. Prion. 14: 31-41. PMID 31950869 DOI: 10.1080/19336896.2020.1714373 |
0.337 |
|
| 2019 |
Kramm C, Gomez-Gutierrez R, Soto C, Telling G, Nichols T, Morales R. In Vitro detection of Chronic Wasting Disease (CWD) prions in semen and reproductive tissues of white tailed deer bucks (Odocoileus virginianus). Plos One. 14: e0226560. PMID 31887141 DOI: 10.1371/Journal.Pone.0226560 |
0.413 |
|
| 2019 |
Slapšak U, Salzano G, Ilc G, Giachin G, Bian J, Telling G, Legname G, Plavec J. Unique Structural Features of Mule Deer Prion Protein Provide Insights into Chronic Wasting Disease. Acs Omega. 4: 19913-19924. PMID 31788624 DOI: 10.1021/acsomega.9b02824 |
0.412 |
|
| 2019 |
Telling GC. Breakthroughs in antemortem diagnosis of neurodegenerative diseases. Proceedings of the National Academy of Sciences of the United States of America. PMID 31666323 DOI: 10.1073/Pnas.1917054116 |
0.404 |
|
| 2019 |
Eraña H, Charco JM, Di Bari MA, Díaz-Domínguez CM, López-Moreno R, Vidal E, González-Miranda E, Pérez-Castro MA, García-Martínez S, Bravo S, Fernández-Borges N, Geijo M, D'Agostino C, Garrido J, Bian J, ... ... Telling GC, et al. Development of a new largely scalable in vitro prion propagation method for the production of infectious recombinant prions for high resolution structural studies. Plos Pathogens. 15: e1008117. PMID 31644574 DOI: 10.1371/Journal.Ppat.1008117 |
0.804 |
|
| 2019 |
Mays CE, Armijo E, Morales R, Kramm C, Flores A, Tiwari A, Bian J, Telling GC, Pandita TK, Hunt CR, Soto C. Prion disease is accelerated in mice lacking stress-induced heat shock protein 70 (HSP70). The Journal of Biological Chemistry. PMID 31320473 DOI: 10.1074/Jbc.Ra118.006186 |
0.515 |
|
| 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 |
0.542 |
|
| 2019 |
Bian J, Christiansen JR, Moreno JA, Kane SJ, Khaychuk V, Gallegos J, Kim S, Telling GC. Primary structural differences at residue 226 of deer and elk PrP dictate selection of distinct CWD prion strains in gene-targeted mice. Proceedings of the National Academy of Sciences of the United States of America. PMID 31147460 DOI: 10.1073/Pnas.1903947116 |
0.801 |
|
| 2019 |
Lyon A, Mays CE, Borriello F, Telling GC, Soto C, Pritzkow S. Application of PMCA to screen for prion infection in a human cell line used to produce biological therapeutics. Scientific Reports. 9: 4847. PMID 30890734 DOI: 10.1038/S41598-019-41055-X |
0.401 |
|
| 2018 |
Ricci A, Allende A, Bolton D, Chemaly M, Davies R, Fernández Escámez PS, Gironés R, Herman L, Koutsoumanis K, Lindqvist R, Nørrung B, Robertson L, Ru G, Sanaa M, ... ... Telling GC, et al. Scientific opinion on chronic wasting disease (II). Efsa Journal. European Food Safety Authority. 16: e05132. PMID 32625679 DOI: 10.2903/J.Efsa.2018.5132 |
0.404 |
|
| 2018 |
Benestad SL, Telling GC. Chronic wasting disease: an evolving prion disease of cervids. Handbook of Clinical Neurology. 153: 135-151. PMID 29887133 DOI: 10.1016/B978-0-444-63945-5.00008-8 |
0.487 |
|
| 2018 |
Davenport KA, Christiansen JR, Bian J, Young M, Gallegos J, Kim S, Balachandran A, Mathiason CK, Hoover EA, Telling GC. Comparative analysis of prions in nervous and lymphoid tissues of chronic wasting disease-infected cervids. The Journal of General Virology. PMID 29580373 DOI: 10.1099/Jgv.0.001053 |
0.798 |
|
| 2018 |
Parrie LE, Crowell JAE, Telling GC, Bessen RA. The cellular prion protein promotes olfactory sensory neuron survival and axon targeting during adult neurogenesis. Developmental Biology. PMID 29577883 DOI: 10.1016/J.Ydbio.2018.03.012 |
0.367 |
|
| 2018 |
Yuan Q, Telling G, Bartelt-Hunt SL, Bartz JC. Dehydration of prions on environmentally relevant surfaces protects them from inactivation by freezing and thawing. Journal of Virology. PMID 29386284 DOI: 10.1128/Jvi.02191-17 |
0.503 |
|
| 2017 |
Ricci A, Allende A, Bolton D, Chemaly M, Davies R, Fernández Escámez PS, Gironés R, Herman L, Koutsoumanis K, Lindqvist R, Nørrung B, Robertson L, Sanaa M, Skandamis P, ... ... Telling GC, et al. Chronic wasting disease (CWD) in cervids. Efsa Journal. European Food Safety Authority. 15: e04667. PMID 32625260 DOI: 10.2903/J.Efsa.2017.4667 |
0.444 |
|
| 2017 |
Kane SJ, Farley TK, Gordon EO, Estep J, Bender HR, Moreno JA, Bartz J, Telling GC, Pickering MC, Zabel MD. Complement Regulatory Protein Factor H Is a Soluble Prion Receptor That Potentiates Peripheral Prion Pathogenesis. Journal of Immunology (Baltimore, Md. : 1950). PMID 29070671 DOI: 10.4049/Jimmunol.1701100 |
0.577 |
|
| 2017 |
Davenport KA, Hoover CE, Bian J, Telling GC, Mathiason CK, Hoover EA. PrPC expression and prion seeding activity in the alimentary tract and lymphoid tissue of deer. Plos One. 12: e0183927. PMID 28880938 DOI: 10.1371/Journal.Pone.0183927 |
0.435 |
|
| 2017 |
Moreno JA, Telling GC. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases. Methods in Molecular Biology (Clifton, N.J.). 1658: 219-252. PMID 28861793 DOI: 10.1007/978-1-4939-7244-9_16 |
0.591 |
|
| 2017 |
Hannaoui S, Amidian S, Cheng YC, Duque Velásquez C, Dorosh L, Law S, Telling G, Stepanova M, McKenzie D, Wille H, Gilch S. Destabilizing polymorphism in cervid prion protein hydrophobic core determines prion conformation and conversion efficiency. Plos Pathogens. 13: e1006553. PMID 28800624 DOI: 10.1371/Journal.Ppat.1006553 |
0.601 |
|
| 2017 |
Iwamaru Y, Mathiason CK, Telling GC, Hoover EA. Chronic wasting disease prion infection of differentiated neurospheres. Prion. 1-7. PMID 28762865 DOI: 10.1080/19336896.2017.1336273 |
0.552 |
|
| 2017 |
Moreno JA, Telling GC. Molecular Mechanisms of Chronic Wasting Disease Prion Propagation. Cold Spring Harbor Perspectives in Medicine. PMID 28193766 DOI: 10.1101/Cshperspect.A024448 |
0.494 |
|
| 2017 |
Bian J, Khaychuk V, Angers RC, Fernández-Borges N, Vidal E, Meyerett-Reid C, Kim S, Calvi CL, Bartz JC, Hoover EA, Agrimi U, Richt JA, Castilla J, Telling GC. Prion replication without host adaptation during interspecies transmissions. Proceedings of the National Academy of Sciences of the United States of America. PMID 28096357 DOI: 10.1073/Pnas.1611891114 |
0.841 |
|
| 2017 |
Waqas M, Lee HM, Kim J, Telling G, Kim JK, Kim DH, Ryou C. Effect of poly-L-arginine in inhibiting scrapie prion protein of cultured cells. Molecular and Cellular Biochemistry. PMID 28063003 DOI: 10.1007/S11010-016-2916-6 |
0.47 |
|
| 2016 |
Wyckoff AC, Kane S, Lockwood K, Seligman J, Michel B, Hill D, Ortega A, Mangalea MR, Telling GC, Miller MW, Vercauteren K, Zabel MD. Clay Components in Soil Dictate Environmental Stability and Bioavailability of Cervid Prions in Mice. Frontiers in Microbiology. 7: 1885. PMID 27933048 DOI: 10.3389/Fmicb.2016.01885 |
0.422 |
|
| 2015 |
Davenport KA, Henderson DM, Bian J, Telling GC, Mathiason CK, Hoover EA. Insights into Chronic Wasting Disease and Bovine Spongiform Encephalopathy Species Barriers by Use of Real-Time Conversion. Journal of Virology. 89: 9524-31. PMID 26157118 DOI: 10.1128/Jvi.01439-15 |
0.479 |
|
| 2015 |
Telling G. Neurodegeneration: Evolved protection against human prions. Nature. 522: 423-4. PMID 26061767 DOI: 10.1038/Nature14534 |
0.574 |
|
| 2015 |
Pritzkow S, Morales R, Moda F, Khan U, Telling GC, Hoover E, Soto C. Grass plants bind, retain, uptake, and transport infectious prions. Cell Reports. 11: 1168-75. PMID 25981035 DOI: 10.1016/J.Celrep.2015.04.036 |
0.433 |
|
| 2015 |
Yuan Q, Eckland T, Telling G, Bartz J, Bartelt-Hunt S. Mitigation of prion infectivity and conversion capacity by a simulated natural process--repeated cycles of drying and wetting. Plos Pathogens. 11: e1004638. PMID 25665187 DOI: 10.1371/Journal.Ppat.1004638 |
0.386 |
|
| 2015 |
Yuan Q, Eckland T, Telling G, Bartz J, Bartelt-Hunt S. Repeated cycles of drying and wetting extend the incubation period of prion infection. Plos Pathogens. DOI: 10.1371/Journal.Ppat.1004638.G008 |
0.316 |
|
| 2015 |
Yuan Q, Eckland T, Telling G, Bartz J, Bartelt-Hunt S. Reduced total protein abundance in HY TME brain homogenate. Plos Pathogens. DOI: 10.1371/Journal.Ppat.1004638.G001 |
0.32 |
|
| 2014 |
Angers R, Christiansen J, Nalls AV, Kang HE, Hunter N, Hoover E, Mathiason CK, Sheetz M, Telling GC. Structural effects of PrP polymorphisms on intra- and interspecies prion transmission Proceedings of the National Academy of Sciences of the United States of America. 111: 11169-11174. PMID 25034251 DOI: 10.1073/Pnas.1404739111 |
0.845 |
|
| 2014 |
Bian J, Kang HE, Telling GC. Quinacrine promotes replication and conformational mutation of chronic wasting disease prions. Proceedings of the National Academy of Sciences of the United States of America. 111: 6028-33. PMID 24711410 DOI: 10.1073/Pnas.1322377111 |
0.609 |
|
| 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 |
0.579 |
|
| 2014 |
Vickery CM, Lockey R, Holder TM, Thorne L, Beck KE, Wilson C, Denyer M, Sheehan J, Marsh S, Webb PR, Dexter I, Norman A, Popescu E, Schneider A, Holden P, ... ... Telling GC, et al. Assessing the susceptibility of transgenic mice overexpressing deer prion protein to bovine spongiform encephalopathy. Journal of Virology. 88: 1830-3. PMID 24257620 DOI: 10.1128/Jvi.02762-13 |
0.58 |
|
| 2013 |
Saijo E, Kang HE, Bian J, Bowling KG, Browning S, Kim S, Hunter N, Telling GC. Epigenetic dominance of prion conformers. Plos Pathogens. 9: e1003692. PMID 24204258 DOI: 10.1371/Journal.Ppat.1003692 |
0.75 |
|
| 2013 |
Michel B, Ferguson A, Johnson T, Bender H, Meyerett-Reid C, Wyckoff AC, Pulford B, Telling GC, Zabel MD. Complement protein C3 exacerbates prion disease in a mouse model of chronic wasting disease. International Immunology. 25: 697-702. PMID 24038599 DOI: 10.1093/Intimm/Dxt034 |
0.573 |
|
| 2013 |
Piccardo P, King D, Telling G, Manson JC, Barron RM. Dissociation of prion protein amyloid seeding from transmission of a spongiform encephalopathy. Journal of Virology. 87: 12349-56. PMID 24027305 DOI: 10.1128/Jvi.00673-13 |
0.653 |
|
| 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 |
0.499 |
|
| 2013 |
Nichols TA, Spraker TR, Rigg TD, Meyerett-Reid C, Hoover C, Michel B, Bian J, Hoover E, Gidlewski T, Balachandran A, O'Rourke K, Telling GC, Bowen R, Zabel MD, VerCauteren KC. Intranasal inoculation of white-tailed deer (Odocoileus virginianus) with lyophilized chronic wasting disease prion particulate complexed to montmorillonite clay. Plos One. 8: e62455. PMID 23671598 DOI: 10.1371/Journal.Pone.0062455 |
0.484 |
|
| 2013 |
Telling GC. The importance of prions. Plos Pathogens. 9: e1003090. PMID 23382670 DOI: 10.1371/Journal.Ppat.1003090 |
0.492 |
|
| 2013 |
Schoch KM, von Reyn CR, Bian J, Telling GC, Meaney DF, Saatman KE. Brain injury-induced proteolysis is reduced in a novel calpastatin-overexpressing transgenic mouse. Journal of Neurochemistry. 125: 909-20. PMID 23305291 DOI: 10.1111/Jnc.12144 |
0.371 |
|
| 2012 |
Michel B, Ferguson A, Johnson T, Bender H, Meyerett-Reid C, Pulford B, von Teichman A, Seelig D, Weis JH, Telling GC, Aguzzi A, Zabel MD. Genetic depletion of complement receptors CD21/35 prevents terminal prion disease in a mouse model of chronic wasting disease. Journal of Immunology (Baltimore, Md. : 1950). 189: 4520-7. PMID 23002439 DOI: 10.4049/Jimmunol.1201579 |
0.534 |
|
| 2012 |
Kang HE, Weng CC, Saijo E, Saylor V, Bian J, Kim S, Ramos L, Angers R, Langenfeld K, Khaychuk V, Calvi C, Bartz J, Hunter N, Telling GC. Characterization of conformation-dependent prion protein epitopes. The Journal of Biological Chemistry. 287: 37219-32. PMID 22948149 DOI: 10.1074/Jbc.M112.395921 |
0.788 |
|
| 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 |
0.586 |
|
| 2012 |
Michel B, Meyerett-Reid C, Johnson T, Ferguson A, Wyckoff C, Pulford B, Bender H, Avery A, Telling G, Dow S, Zabel MD. Incunabular immunological events in prion trafficking. Scientific Reports. 2: 440. PMID 22679554 DOI: 10.1038/Srep00440 |
0.344 |
|
| 2012 |
Nichols TA, Spraker TR, Gidlewski T, Powers JG, Telling GC, VerCauteren KC, Zabel MD. Detection of prion protein in the cerebrospinal fluid of elk (Cervus canadensis nelsoni) with chronic wasting disease using protein misfolding cyclic amplification. Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 24: 746-9. PMID 22621952 DOI: 10.1177/1040638712448060 |
0.455 |
|
| 2012 |
Pulford B, Spraker TR, Wyckoff AC, Meyerett C, Bender H, Ferguson A, Wyatt B, Lockwood K, Powers J, Telling GC, Wild MA, Zabel MD. Detection of PrPCWD in feces from naturally exposed Rocky Mountain elk (Cervus elaphus nelsoni) using protein misfolding cyclic amplification. Journal of Wildlife Diseases. 48: 425-34. PMID 22493117 DOI: 10.7589/0090-3558-48.2.425 |
0.47 |
|
| 2012 |
Haley NJ, Mathiason CK, Carver S, Telling GC, Zabel MD, Hoover EA. Sensitivity of protein misfolding cyclic amplification versus immunohistochemistry in ante-mortem detection of chronic wasting disease. The Journal of General Virology. 93: 1141-50. PMID 22278825 DOI: 10.1099/Vir.0.039073-0 |
0.41 |
|
| 2012 |
Telling GC. Transgenic studies of prion diseases. Methods in Molecular Medicine. 59: 111-27. PMID 21374501 DOI: 10.1385/1-59259-134-5:111 |
0.568 |
|
| 2011 |
Seelig DM, Mason GL, Telling GC, Hoover EA. Chronic wasting disease prion trafficking via the autonomic nervous system. The American Journal of Pathology. 179: 1319-28. PMID 21777560 DOI: 10.1016/J.Ajpath.2011.05.057 |
0.621 |
|
| 2011 |
Telling GC. Transgenic mouse models and prion strains. Topics in Current Chemistry. 305: 79-99. PMID 21769720 DOI: 10.1007/128_2011_166 |
0.416 |
|
| 2011 |
Kurt TD, Seelig DM, Schneider JR, Johnson CJ, Telling GC, Heisey DM, Hoover EA. Alteration of the chronic wasting disease species barrier by in vitro prion amplification. Journal of Virology. 85: 8528-37. PMID 21697475 DOI: 10.1128/Jvi.00809-11 |
0.553 |
|
| 2011 |
Saijo E, Scheff SW, Telling GC. Unaltered prion protein expression in Alzheimer disease patients. Prion. 5: 109-16. PMID 21654203 DOI: 10.4161/Pri.5.2.16355 |
0.395 |
|
| 2011 |
Haley NJ, Mathiason CK, Carver S, Zabel M, Telling GC, Hoover EA. Detection of chronic wasting disease prions in salivary, urinary, and intestinal tissues of deer: potential mechanisms of prion shedding and transmission. Journal of Virology. 85: 6309-18. PMID 21525361 DOI: 10.1128/Jvi.00425-11 |
0.494 |
|
| 2011 |
Mays CE, Yeom J, Kang HE, Bian J, Khaychuk V, Kim Y, Bartz JC, Telling GC, Ryou C. In vitro amplification of misfolded prion protein using lysate of cultured cells. Plos One. 6: e18047. PMID 21464935 DOI: 10.1371/Journal.Pone.0018047 |
0.804 |
|
| 2011 |
Barria MA, Telling GC, Gambetti P, Mastrianni JA, Soto C. Generation of a new form of human PrP(Sc) in vitro by interspecies transmission from cervid prions. The Journal of Biological Chemistry. 286: 7490-5. PMID 21209079 DOI: 10.1074/Jbc.M110.198465 |
0.572 |
|
| 2011 |
Denkers ND, Telling GC, Hoover EA. Minor oral lesions facilitate transmission of chronic wasting disease. Journal of Virology. 85: 1396-9. PMID 21084472 DOI: 10.1128/Jvi.01655-10 |
0.447 |
|
| 2010 |
Telling GC. Nucleic acid-free mutation of prion strains. Prion. 4: 252-5. PMID 20948302 DOI: 10.4161/Pri.4.4.13675 |
0.429 |
|
| 2010 |
Bian J, Napier D, Khaychuck V, Angers R, Graham C, Telling G. Cell-based quantification of chronic wasting disease prions Journal of Virology. 84: 8322-8326. PMID 20519392 DOI: 10.1128/Jvi.00633-10 |
0.831 |
|
| 2010 |
Angers RC, Kang HE, Napier D, Browning S, Seward T, Mathiason C, Balachandran A, McKenzie D, Castilla J, Soto C, Jewell J, Graham C, Hoover EA, Telling GC. Prion strain mutation determined by prion protein conformational compatibility and primary structure. Science (New York, N.Y.). 328: 1154-8. PMID 20466881 DOI: 10.1126/Science.1187107 |
0.819 |
|
| 2010 |
Seelig DM, Mason GL, Telling GC, Hoover EA. Pathogenesis of chronic wasting disease in cervidized transgenic mice. The American Journal of Pathology. 176: 2785-97. PMID 20395435 DOI: 10.2353/Ajpath.2010.090710 |
0.627 |
|
| 2010 |
Mathiason CK, Hayes-Klug J, Hays SA, Powers J, Osborn DA, Dahmes SJ, Miller KV, Warren RJ, Mason GL, Telling GC, Young AJ, Hoover EA. B cells and platelets harbor prion infectivity in the blood of deer infected with chronic wasting disease. Journal of Virology. 84: 5097-107. PMID 20219916 DOI: 10.1128/Jvi.02169-09 |
0.421 |
|
| 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, ... ... Telling G, 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 |
0.429 |
|
| 2010 |
Denkers ND, Seelig DM, Telling GC, Hoover EA. Aerosol and nasal transmission of chronic wasting disease in cervidized mice. The Journal of General Virology. 91: 1651-8. PMID 20164261 DOI: 10.1099/Vir.0.017335-0 |
0.585 |
|
| 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, ... ... Telling G, et al. Reply to Kascsak: Definition of the PrP 3F4 epitope revisited Journal of Biological Chemistry. 285: le6. DOI: 10.1074/Jbc.N109.088831 |
0.3 |
|
| 2009 |
Haley NJ, Mathiason CK, Zabel MD, Telling GC, Hoover EA. Detection of sub-clinical CWD infection in conventional test-negative deer long after oral exposure to urine and feces from CWD+ deer. Plos One. 4: e7990. PMID 19956732 DOI: 10.1371/Journal.Pone.0007990 |
0.508 |
|
| 2009 |
Nichols TA, Pulford B, Wyckoff AC, Meyerett C, Michel B, Gertig K, Hoover EA, Jewell JE, Telling GC, Zabel MD. Detection of protease-resistant cervid prion protein in water from a CWD-endemic area. Prion. 3: 171-83. PMID 19823039 DOI: 10.4161/Pri.3.3.9819 |
0.404 |
|
| 2009 |
Mays CE, Titlow W, Seward T, Telling GC, Ryou C. Enhancement of protein misfolding cyclic amplification by using concentrated cellular prion protein source. Biochemical and Biophysical Research Communications. 388: 306-10. PMID 19664595 DOI: 10.1016/J.Bbrc.2009.07.163 |
0.525 |
|
| 2009 |
Angers RC, Seward TS, Napier D, Green M, Hoover E, Spraker T, O'Rourke K, Balachandran A, Telling GC. Chronic wasting disease prions in elk antler velvet. Emerging Infectious Diseases. 15: 696-703. PMID 19402954 DOI: 10.3201/Eid1505.081458 |
0.859 |
|
| 2009 |
Haley NJ, Seelig DM, Zabel MD, Telling GC, Hoover EA. Detection of CWD prions in urine and saliva of deer by transgenic mouse bioassay. Plos One. 4: e4848. PMID 19293928 DOI: 10.1371/Journal.Pone.0004848 |
0.593 |
|
| 2009 |
Kurt TD, Telling GC, Zabel MD, Hoover EA. Trans-species amplification of PrP(CWD) and correlation with rigid loop 170N. Virology. 387: 235-43. PMID 19269662 DOI: 10.1016/J.Virol.2009.02.025 |
0.458 |
|
| 2008 |
Meyerett C, Michel B, Pulford B, Spraker TR, Nichols TA, Johnson T, Kurt T, Hoover EA, Telling GC, Zabel MD. In vitro strain adaptation of CWD prions by serial protein misfolding cyclic amplification. Virology. 382: 267-76. PMID 18952250 DOI: 10.1016/J.Virol.2008.09.023 |
0.443 |
|
| 2008 |
Saunders SE, Bartz JC, Telling GC, Bartelt-Hunt SL. Environmentally-relevant forms of the prion protein. Environmental Science & Technology. 42: 6573-9. PMID 18800532 DOI: 10.1021/Es800590K |
0.539 |
|
| 2008 |
Green KM, Castilla J, Seward TS, Napier DL, Jewell JE, Soto C, Telling GC. Accelerated high fidelity prion amplification within and across prion species barriers. Plos Pathogens. 4: e1000139. PMID 18769716 DOI: 10.1371/Journal.Ppat.1000139 |
0.757 |
|
| 2008 |
Telling GC. Transgenic mouse models of prion diseases. Methods in Molecular Biology (Clifton, N.J.). 459: 249-63. PMID 18576160 DOI: 10.1007/978-1-59745-234-2_17 |
0.572 |
|
| 2008 |
Green KM, Browning SR, Seward TS, Jewell JE, Ross DL, Green MA, Williams ES, Hoover EA, Telling GC. The elk PRNP codon 132 polymorphism controls cervid and scrapie prion propagation. The Journal of General Virology. 89: 598-608. PMID 18198392 DOI: 10.1099/Vir.0.83168-0 |
0.768 |
|
| 2007 |
Kurt TD, Perrott MR, Wilusz CJ, Wilusz J, Supattapone S, Telling GC, Zabel MD, Hoover EA. Efficient in vitro amplification of chronic wasting disease PrPRES. Journal of Virology. 81: 9605-8. PMID 17553879 DOI: 10.1128/Jvi.00635-07 |
0.773 |
|
| 2007 |
Nazor KE, Seward T, Telling GC. Motor behavioral and neuropathological deficits in mice deficient for normal prion protein expression. Biochimica Et Biophysica Acta. 1772: 645-53. PMID 17531449 DOI: 10.1016/J.Bbadis.2007.04.004 |
0.816 |
|
| 2006 |
Mathiason CK, Powers JG, Dahmes SJ, Osborn DA, Miller KV, Warren RJ, Mason GL, Hays SA, Hayes-Klug J, Seelig DM, Wild MA, Wolfe LL, Spraker TR, Miller MW, Sigurdson CJ, ... Telling GC, et al. Infectious prions in the saliva and blood of deer with chronic wasting disease. Science (New York, N.Y.). 314: 133-6. PMID 17023660 DOI: 10.1126/Science.1132661 |
0.457 |
|
| 2006 |
Angers RC, Browning SR, Seward TS, Sigurdson CJ, Miller MW, Hoover EA, Telling GC. Prions in skeletal muscles of deer with chronic wasting disease. Science (New York, N.Y.). 311: 1117. PMID 16439622 DOI: 10.1126/Science.1122864 |
0.819 |
|
| 2006 |
Bian J, Nazor KE, Angers R, Jernigan M, Seward T, Centers A, Green M, Telling GC. GFP-tagged PrP supports compromised prion replication in transgenic mice. Biochemical and Biophysical Research Communications. 340: 894-900. PMID 16386707 DOI: 10.1016/J.Bbrc.2005.12.085 |
0.8 |
|
| 2005 |
Telling G. Anchors away--of plaques and pathology in prion disease. The New England Journal of Medicine. 353: 1177-9. PMID 16162891 DOI: 10.1056/Nejmcibr052527 |
0.473 |
|
| 2005 |
Nazor KE, Kuhn F, Seward T, Green M, Zwald D, Pürro M, Schmid J, Biffiger K, Power AM, Oesch B, Raeber AJ, Telling GC. Immunodetection of disease-associated mutant PrP, which accelerates disease in GSS transgenic mice. The Embo Journal. 24: 2472-80. PMID 15962001 DOI: 10.1038/Sj.Emboj.7600717 |
0.835 |
|
| 2004 |
Browning SR, Mason GL, Seward T, Green M, Eliason GA, Mathiason C, Miller MW, Williams ES, Hoover E, Telling GC. Transmission of prions from mule deer and elk with chronic wasting disease to transgenic mice expressing cervid PrP. Journal of Virology. 78: 13345-50. PMID 15542685 DOI: 10.1128/Jvi.78.23.13345-13350.2004 |
0.775 |
|
| 2004 |
Moroncini G, Kanu N, Solforosi L, Abalos G, Telling GC, Head M, Ironside J, Brockes JP, Burton DR, Williamson RA. Motif-grafted antibodies containing the replicative interface of cellular PrP are specific for PrPSc. Proceedings of the National Academy of Sciences of the United States of America. 101: 10404-9. PMID 15240877 DOI: 10.1073/Pnas.0403522101 |
0.436 |
|
| 2004 |
Telling GC. The mechanism of prion strain propagation. Genome Biology. 5: 222. PMID 15128438 DOI: 10.1186/Gb-2004-5-5-222 |
0.461 |
|
| 2004 |
Yadavalli R, Guttmann RP, Seward T, Centers AP, Williamson RA, Telling GC. Calpain-dependent endoproteolytic cleavage of PrPSc modulates scrapie prion propagation. The Journal of Biological Chemistry. 279: 21948-56. PMID 15026410 DOI: 10.1074/Jbc.M400793200 |
0.469 |
|
| 2003 |
Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Proceedings of the National Academy of Sciences of the United States of America. 100: 4784-9. PMID 12684540 DOI: 10.1073/Pnas.2627989100 |
0.653 |
|
| 2002 |
Bosque PJ, Ryou C, Telling G, Peretz D, Legname G, DeArmond SJ, Prusiner SB. Prions in skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America. 99: 3812-7. PMID 11904434 DOI: 10.1073/Pnas.052707499 |
0.619 |
|
| 2002 |
Connolly JG, Tate RJ, Telling GC, Fraser J, Brown D, Head MW. Expression of cellular prion protein in Xenopus oocytes Biochemical Society Transactions. 30: A82-A82. DOI: 10.1042/Bst030A082A |
0.358 |
|
| 2001 |
Mastrianni JA, Capellari S, Telling GC, Han D, Bosque P, Prusiner SB, DeArmond SJ. Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. Neurology. 57: 2198-205. PMID 11756597 DOI: 10.1212/Wnl.57.12.2198 |
0.669 |
|
| 2001 |
Telling G. Protein-based PCR for prion diseases? Nature Medicine. 7: 778-9. PMID 11433339 DOI: 10.1038/89895 |
0.489 |
|
| 2001 |
Campbell S, Dennehy U, Telling G. Analyzing the influence of PrP primary structure on prion pathogenesis in transgenic mice. Archives of Virology. Supplementum. 87-94. PMID 11214937 DOI: 10.1007/978-3-7091-6308-5_7 |
0.556 |
|
| 2000 |
Telling GC. Prion protein genes and prion diseases: Studies in transgenic mice Neuropathology and Applied Neurobiology. 26: 209-220. PMID 10886679 DOI: 10.1046/j.1365-2990.2000.00253.x |
0.531 |
|
| 1999 |
Mastrianni JA, Nixon R, Layzer R, Telling GC, Han D, DeArmond SJ, Prusiner SB. Prion protein conformation in a patient with sporadic fatal insomnia. The New England Journal of Medicine. 340: 1630-8. PMID 10341275 DOI: 10.1056/Nejm199905273402104 |
0.632 |
|
| 1998 |
Fisher E, Telling G, Collinge J. Prions and the prion disorders. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 9: 497-502. PMID 9657843 DOI: 10.1007/S003359900807 |
0.346 |
|
| 1997 |
Muramoto T, DeArmond SJ, Scott M, Telling GC, Cohen FE, Prusiner SB. Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix. Nature Medicine. 3: 750-5. PMID 9212101 DOI: 10.1038/nm0797-750 |
0.581 |
|
| 1997 |
Telling GC, Tremblay P, Torchia M, Dearmond SJ, Cohen FE, Prusiner SB. N-terminally tagged prion protein supports prion propagation in transgenic mice. Protein Science : a Publication of the Protein Society. 6: 825-33. PMID 9098892 DOI: 10.1002/pro.5560060409 |
0.594 |
|
| 1996 |
Bamborough P, Wille H, Telling GC, Yehiely F, Prusiner SB, Cohen FE. Prion protein structure and scrapie replication: theoretical, spectroscopic, and genetic investigations. Cold Spring Harbor Symposia On Quantitative Biology. 61: 495-509. PMID 9246476 DOI: 10.1101/Sqb.1996.061.01.050 |
0.425 |
|
| 1996 |
Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, Mastrianni J, Lugaresi E, Gambetti P, Prusiner SB. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Science (New York, N.Y.). 274: 2079-82. PMID 8953038 DOI: 10.1126/Science.274.5295.2079 |
0.66 |
|
| 1996 |
Telling GC, Haga T, Torchia M, Tremblay P, DeArmond SJ, Prusiner SB. Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes & Development. 10: 1736-50. PMID 8698234 DOI: 10.1101/Gad.10.14.1736 |
0.616 |
|
| 1996 |
Scott MR, Telling GC, Prusiner SB. Transgenetics and gene targeting in studies of prion diseases. Current Topics in Microbiology and Immunology. 207: 95-123. PMID 8575209 DOI: 10.1007/978-3-642-60983-1_8 |
0.545 |
|
| 1996 |
Gabizon R, Telling G, Meiner Z, Halimi M, Kahana I, Prusiner SB. Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease. Nature Medicine. 2: 59-64. PMID 8564843 DOI: 10.1038/nm0196-59 |
0.569 |
|
| 1996 |
Prusiner SB, Telling G, Cohen FE, DeArmond SJ. Prion diseases of humans and animals Seminars in Virology. 7: 159-173. DOI: 10.1006/smvy.1996.0021 |
0.548 |
|
| 1995 |
Telling GC, Scott M, Mastrianni J, Gabizon R, Torchia M, Cohen FE, DeArmond SJ, Prusiner SB. Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell. 83: 79-90. PMID 7553876 DOI: 10.1016/0092-8674(95)90236-8 |
0.62 |
|
| 1994 |
Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ, Prusiner SB. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Proceedings of the National Academy of Sciences of the United States of America. 91: 9936-40. PMID 7937921 DOI: 10.1073/Pnas.91.21.9936 |
0.666 |
|
| 1994 |
Carlson GA, Ebeling C, Yang SL, Telling G, Torchia M, Groth D, Westaway D, DeArmond SJ, Prusiner SB. Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 91: 5690-4. PMID 7911243 DOI: 10.1073/Pnas.91.12.5690 |
0.63 |
|
| 1993 |
Borchelt DR, Rogers M, Stahl N, Telling G, Prusiner SB. Release of the cellular prion protein from cultured cells after loss of its glycoinositol phospholipid anchor. Glycobiology. 3: 319-29. PMID 7691278 DOI: 10.1093/Glycob/3.4.319 |
0.727 |
|
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