메뉴 건너뛰기




Volumn 2, Issue 1, 2014, Pages

Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases

Author keywords

Creutzfeldt Jakob disease; Curvilinear PrPSc; E200K; Familial CJD; Synaptic PrPSc

Indexed keywords


EID: 85005896404     PISSN: None     EISSN: 20515960     Source Type: Journal    
DOI: 10.1186/2051-5960-1-80     Document Type: Article
Times cited : (25)

References (50)
  • 1
    • 1842644947 scopus 로고    scopus 로고
    • Inherited prion diseases
    • 2nd edition. Edited by: Prusiner SB. City: Cold Spring Harbor Laboratory Press
    • Kong Q, Surewicz WK, Petersen RB, et al.: Inherited prion diseases. In Prion Biology and Diseases. 2nd edition. Edited by: Prusiner SB. City: Cold Spring Harbor Laboratory Press; 2004:673-775.
    • (2004) Prion Biology and Diseases , pp. 673-775
    • Kong, Q.1    Surewicz, W.K.2    Petersen, R.B.3
  • 2
    • 0141514771 scopus 로고    scopus 로고
    • Sporadic and familial CJD: classification and characterisation
    • Gambetti P, Kong Q, Zou W, Parchi P, Chen SG: Sporadic and familial CJD: classification and characterisation. Br Med Bull 2003, 66: 213-239. 10.1093/bmb/66.1.213
    • (2003) Br Med Bull , vol.66 , pp. 213-239
    • Gambetti, P.1    Kong, Q.2    Zou, W.3    Parchi, P.4    Chen, S.G.5
  • 3
    • 0024467653 scopus 로고
    • Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker's syndrome
    • Goldgaber D, Goldfarb LG, Brown P, et al.: Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker's syndrome. Exp Neurol 1989, 106: 204-206. 10.1016/0014-4886(89)90095-2
    • (1989) Exp Neurol , vol.106 , pp. 204-206
    • Goldgaber, D.1    Goldfarb, L.G.2    Brown, P.3
  • 4
    • 0342505312 scopus 로고    scopus 로고
    • Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
    • Lee HS, Sambuughin N, Cervenakova L, et al.: Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. Am J Hum Genet 1999, 64: 1063-1070. 10.1086/302340
    • (1999) Am J Hum Genet , vol.64 , pp. 1063-1070
    • Lee, H.S.1    Sambuughin, N.2    Cervenakova, L.3
  • 5
    • 0026406817 scopus 로고
    • A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin
    • Korczyn AD, Chapman J, Goldfarb LG, Brown P, Gajdusek DC: A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian origin. Ann N Y Acad Sci 1991, 640: 171-176.
    • (1991) Ann N Y Acad Sci , vol.640 , pp. 171-176
    • Korczyn, A.D.1    Chapman, J.2    Goldfarb, L.G.3    Brown, P.4    Gajdusek, D.C.5
  • 6
    • 27944483780 scopus 로고    scopus 로고
    • Genetic prion disease: the EUROCJD experience
    • Kovacs GG, Puopolo M, Ladogana A, et al.: Genetic prion disease: the EUROCJD experience. Hum Genet 2005, 118: 166-174. 10.1007/s00439-005-0020-1
    • (2005) Hum Genet , vol.118 , pp. 166-174
    • Kovacs, G.G.1    Puopolo, M.2    Ladogana, A.3
  • 8
    • 0035996287 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development
    • Mitrova E, Belay G: Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Acta Virol 2002, 46: 31-39.
    • (2002) Acta Virol , vol.46 , pp. 31-39
    • Mitrova, E.1    Belay, G.2
  • 9
    • 0025869213 scopus 로고
    • Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease
    • Hsiao K, Meiner Z, Kahana E, et al.: Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease. N Engl J Med 1991, 324: 1091-1097. 10.1056/NEJM199104183241604
    • (1991) N Engl J Med , vol.324 , pp. 1091-1097
    • Hsiao, K.1    Meiner, Z.2    Kahana, E.3
  • 10
    • 0031183207 scopus 로고    scopus 로고
    • Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews
    • Meiner Z, Gabizon R, Prusiner SB: Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews. Medicine (Baltimore) 1997, 76: 227-237. 10.1097/00005792-199707000-00001
    • (1997) Medicine (Baltimore) , vol.76 , pp. 227-237
    • Meiner, Z.1    Gabizon, R.2    Prusiner, S.B.3
  • 11
    • 13344295093 scopus 로고    scopus 로고
    • Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP
    • Ghetti B, Piccardo P, Spillantini MG, et al.: Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. Proc Natl Acad Sci USA 1996, 93: 744-748. 10.1073/pnas.93.2.744
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 744-748
    • Ghetti, B.1    Piccardo, P.2    Spillantini, M.G.3
  • 12
    • 49849091894 scopus 로고    scopus 로고
    • Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease
    • Debatin L, Streffer J, Geissen M, Matschke J, Aguzzi A, Glatzel M: Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease. Neurodegener Dis 2008, 5: 347-354. doi: 10.1159/000121389 10.1159/000121389
    • (2008) Neurodegener Dis , vol.5 , pp. 347-354
    • Debatin, L.1    Streffer, J.2    Geissen, M.3    Matschke, J.4    Aguzzi, A.5    Glatzel, M.6
  • 13
    • 70350450945 scopus 로고    scopus 로고
    • Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype
    • Ghoshal N, Cali I, Perrin RJ, et al.: Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype. Arch Neurol 2009, 66: 1240-1246.
    • (2009) Arch Neurol , vol.66 , pp. 1240-1246
    • Ghoshal, N.1    Cali, I.2    Perrin, R.J.3
  • 14
    • 78651257339 scopus 로고    scopus 로고
    • Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy
    • Kovacs GG, Seguin J, I Q, et al.: Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy. Acta Neuropathol 2011, 121: 39-57. doi: 10.1007/s00401-010-0713-y 10.1007/s00401-010-0713-y
    • (2011) Acta Neuropathol , vol.121 , pp. 39-57
    • Kovacs, G.G.1    Seguin, J.I.Q.2
  • 15
    • 68249146549 scopus 로고    scopus 로고
    • The nigrostriatal pathway in Creutzfeldt-Jakob disease
    • Vital A, Fernagut PO, Canron MH, et al.: The nigrostriatal pathway in Creutzfeldt-Jakob disease. J Neuropathol Exp Neurol 2009, 68: 809-815. doi: 10.1097/NEN.0b013e3181abdae8 10.1097/NEN.0b013e3181abdae8
    • (2009) J Neuropathol Exp Neurol , vol.68 , pp. 809-815
    • Vital, A.1    Fernagut, P.O.2    Canron, M.H.3
  • 16
    • 84870337113 scopus 로고    scopus 로고
    • MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease
    • Carswell C, Thompson A, A L, et al.: MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease. BMC Neurol 2012, 12: 153. doi: 10.1186/1471-2377-12-153 10.1186/1471-2377-12-153
    • (2012) BMC Neurol , vol.12 , pp. 153
    • Carswell, C.1    Thompson, A.A.L.2
  • 17
    • 0033853890 scopus 로고    scopus 로고
    • Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation
    • Puoti G, Rossi G, G G, et al.: Polymorphism at codon 129 of PRNP affects the phenotypic expression of Creutzfeldt-Jakob disease linked to E200K mutation. Ann Neurol 2000, 48: 269-270.
    • (2000) Ann Neurol , vol.48 , pp. 269-270
    • Puoti, G.1    Rossi, G.G.G.2
  • 18
    • 62949172413 scopus 로고    scopus 로고
    • Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease
    • Geschwind MD, Potter CA, Sattavat M, et al.: Correlating DWI MRI with pathologic and other features of Jakob-Creutzfeldt disease. Alzheimer Dis Assoc Disord 2009, 23: 82-87. 10.1097/WAD.0b013e31818323ef
    • (2009) Alzheimer Dis Assoc Disord , vol.23 , pp. 82-87
    • Geschwind, M.D.1    Potter, C.A.2    Sattavat, M.3
  • 20
    • 0029741936 scopus 로고    scopus 로고
    • Diagnostic criteria for sporadic Creutzfeldt-Jakob disease
    • Kretzschmar HA, Ironside JW, DeArmond SJ, Tateishi J: Diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Arch Neurol 1996, 53: 913-920. 10.1001/archneur.1996.00550090125018
    • (1996) Arch Neurol , vol.53 , pp. 913-920
    • Kretzschmar, H.A.1    Ironside, J.W.2    DeArmond, S.J.3    Tateishi, J.4
  • 21
    • 0033045425 scopus 로고    scopus 로고
    • The efficiency of systematic sampling in stereology-reconsidered
    • Gundersen HJ, Jensen EB, Kieu K, Nielsen J: The efficiency of systematic sampling in stereology-reconsidered. J Microsc 1999, 193: 199-211. 10.1046/j.1365-2818.1999.00457.x
    • (1999) J Microsc , vol.193 , pp. 199-211
    • Gundersen, H.J.1    Jensen, E.B.2    Kieu, K.3    Nielsen, J.4
  • 22
    • 0032816292 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    • Parchi P, Giese A, Capellari S, et al.: Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999, 46: 224-233. 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W
    • (1999) Ann Neurol , vol.46 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3
  • 23
    • 33749254251 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease revisited
    • Cali I, Castellani R, J Y, et al.: Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain 2006, 129: 2266-2277. 10.1093/brain/awl224
    • (2006) Brain , vol.129 , pp. 2266-2277
    • Cali, I.1    Castellani, R.J.Y.2
  • 24
    • 0023499868 scopus 로고
    • Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins
    • Kascsak RJ, Rubenstein R, Merz PA, et al.: Mouse polyclonal and monoclonal antibody to scrapie-associated fibril proteins. J Virol 1987, 61: 3688-3693.
    • (1987) J Virol , vol.61 , pp. 3688-3693
    • Kascsak, R.J.1    Rubenstein, R.2    Merz, P.A.3
  • 25
    • 77953027708 scopus 로고    scopus 로고
    • Sporadic corticobasal syndrome due to FTLD-TDP
    • Tartaglia MC, Sidhu M, V L, et al.: Sporadic corticobasal syndrome due to FTLD-TDP. Acta Neuropathol 2010, 119: 365-374. doi: 10.1007/s00401-009-0605-1 10.1007/s00401-009-0605-1
    • (2010) Acta Neuropathol , vol.119 , pp. 365-374
    • Tartaglia, M.C.1    Sidhu, M.V.L.2
  • 26
    • 84857612755 scopus 로고    scopus 로고
    • Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease
    • Kovacs GG, Molnar K, Keller E, Botond G, Budka H, Laszlo L: Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease. J Neuropathol Exp Neurol 2012, 71: 223-232. doi: 10.1097/NEN.0b013e318248aa70 10.1097/NEN.0b013e318248aa70
    • (2012) J Neuropathol Exp Neurol , vol.71 , pp. 223-232
    • Kovacs, G.G.1    Molnar, K.2    Keller, E.3    Botond, G.4    Budka, H.5    Laszlo, L.6
  • 27
    • 0028351904 scopus 로고
    • Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism
    • Monari L, Chen SG, P B, et al.: Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proc Natl Acad Sci USA 1994, 91: 2839-2842. 10.1073/pnas.91.7.2839
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 2839-2842
    • Monari, L.1    Chen, S.G.P.B.2
  • 28
    • 0030953939 scopus 로고    scopus 로고
    • Typing prion isoforms
    • Parchi P, Capellari S, Chen SG: Typing prion isoforms. Nature 1997, 386: 232-234. 10.1038/386232a0
    • (1997) Nature , vol.386 , pp. 232-234
    • Parchi, P.1    Capellari, S.2    Chen, S.G.3
  • 29
    • 0032975733 scopus 로고    scopus 로고
    • A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
    • Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H: A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Ann Neurol 1999, 45: 812-816. 10.1002/1531-8249(199906)45:6<812::AID-ANA20>3.0.CO;2-2
    • (1999) Ann Neurol , vol.45 , pp. 812-816
    • Hainfellner, J.A.1    Parchi, P.2    Kitamoto, T.3    Jarius, C.4    Gambetti, P.5    Budka, H.6
  • 31
    • 84862534521 scopus 로고    scopus 로고
    • The EEG in E200K familial CJD: relation to MRI patterns
    • Appel SA, Chapman J, Prohovnik I, Hoffman C, Cohen OS, Blatt I: The EEG in E200K familial CJD: relation to MRI patterns. J Neurol 2012, 259: 491-496. doi: 10.1007/s00415-011-6208-5 10.1007/s00415-011-6208-5
    • (2012) J Neurol , vol.259 , pp. 491-496
    • Appel, S.A.1    Chapman, J.2    Prohovnik, I.3    Hoffman, C.4    Cohen, O.S.5    Blatt, I.6
  • 33
    • 0026095028 scopus 로고
    • The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
    • Brown P, Goldfarb LG, Gibbs CJ Jr, Gajdusek DC: The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease. Eur J Epidemiol 1991, 7: 469-476. 10.1007/BF00143124
    • (1991) Eur J Epidemiol , vol.7 , pp. 469-476
    • Brown, P.1    Goldfarb, L.G.2    Gibbs, C.J.3    Gajdusek, D.C.4
  • 34
    • 0022973492 scopus 로고
    • Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases
    • Brown P, Cathala F, Castaigne P, Gajdusek DC: Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases. Ann Neurol 1986, 20: 597-602. 10.1002/ana.410200507
    • (1986) Ann Neurol , vol.20 , pp. 597-602
    • Brown, P.1    Cathala, F.2    Castaigne, P.3    Gajdusek, D.C.4
  • 35
    • 0038452462 scopus 로고    scopus 로고
    • Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease
    • Jarius C, Kovacs GG, Belay G, Hainfellner JA, Mitrova E, Budka H: Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease. Acta Neuropathol 2003, 105: 449-454. doi: 10.1007/s00401-002-0664-z
    • (2003) Acta Neuropathol , vol.105 , pp. 449-454
    • Jarius, C.1    Kovacs, G.G.2    Belay, G.3    Hainfellner, J.A.4    Mitrova, E.5    Budka, H.6
  • 36
    • 78651246462 scopus 로고    scopus 로고
    • Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis
    • Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P: Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis. Acta Neuropathol 2011, 121: 21-37. 10.1007/s00401-010-0760-4
    • (2011) Acta Neuropathol , vol.121 , pp. 21-37
    • Capellari, S.1    Strammiello, R.2    Saverioni, D.3    Kretzschmar, H.4    Parchi, P.5
  • 37
    • 0037065769 scopus 로고    scopus 로고
    • Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease
    • Taratuto AL, Piccardo P, Reich EG: Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology 2002, 58: 362-367. 10.1212/WNL.58.3.362
    • (2002) Neurology , vol.58 , pp. 362-367
    • Taratuto, A.L.1    Piccardo, P.2    Reich, E.G.3
  • 38
    • 0026552043 scopus 로고
    • Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
    • Medori R, Tritschler HJ, A LB, et al.: Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene. N Engl J Med 1992, 326: 444-449. doi: 10.1056/NEJM199202133260704 10.1056/NEJM199202133260704
    • (1992) N Engl J Med , vol.326 , pp. 444-449
    • Medori, R.1    Tritschler, H.J.2
  • 39
    • 0032976574 scopus 로고    scopus 로고
    • A subtype of sporadic prion disease mimicking fatal familial insomnia
    • Parchi P, Capellari S, S C, et al.: A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology 1999, 52: 1757-1763. 10.1212/WNL.52.9.1757
    • (1999) Neurology , vol.52 , pp. 1757-1763
    • Parchi, P.1    Capellari, S.S.C.2
  • 40
    • 84857029808 scopus 로고    scopus 로고
    • Hyperphosphorylated tau in young and middle-aged subjects
    • Elobeid A, Soininen H, Alafuzoff I: Hyperphosphorylated tau in young and middle-aged subjects. Acta Neuropathol 2012, 123: 97-104. doi: 10.1007/s00401-011-0906-z 10.1007/s00401-011-0906-z
    • (2012) Acta Neuropathol , vol.123 , pp. 97-104
    • Elobeid, A.1    Soininen, H.2    Alafuzoff, I.3
  • 41
    • 0026751775 scopus 로고
    • Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
    • Kitamoto T, Shin RW, K D-u: Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 1992, 140: 1285-1294.
    • (1992) Am J Pathol , vol.140 , pp. 1285-1294
    • Kitamoto, T.1    Shin, R.W.2
  • 42
    • 0020051603 scopus 로고
    • Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway
    • Fraser H: Neuronal spread of scrapie agent and targeting of lesions within the retino-tectal pathway. Nature 1982, 295: 149-150. 10.1038/295149a0
    • (1982) Nature , vol.295 , pp. 149-150
    • Fraser, H.1
  • 43
    • 0026686855 scopus 로고
    • Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis
    • Scott JR, Davies D, Fraser H: Scrapie in the central nervous system: neuroanatomical spread of infection and Sinc control of pathogenesis. J Gen Virol 1992,73(Pt 7):1637-1644.
    • (1992) J Gen Virol , vol.73 , Issue.PART. 7 , pp. 1637-1644
    • Scott, J.R.1    Davies, D.2    Fraser, H.3
  • 44
    • 0031881510 scopus 로고    scopus 로고
    • Cerebral targeting indicates vagal spread of infection in hamsters fed with scrapie
    • Beekes M, McBride PA, Baldauf E: Cerebral targeting indicates vagal spread of infection in hamsters fed with scrapie. J Gen Virol 1998,79(Pt 3):601-607.
    • (1998) J Gen Virol , vol.79 , Issue.PART. 3 , pp. 601-607
    • Beekes, M.1    McBride, P.A.2    Baldauf, E.3
  • 45
    • 3843142665 scopus 로고    scopus 로고
    • The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system
    • Bouzamondo-Bernstein E, Hopkins SD, P S, et al.: The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system. J Neuropathol Exp Neurol 2004, 63: 882-899.
    • (2004) J Neuropathol Exp Neurol , vol.63 , pp. 882-899
    • Bouzamondo, -B.E.1    Hopkins, S.D.P.S.2
  • 46
    • 84878325700 scopus 로고    scopus 로고
    • Intrinsic connectivity network disruption in progressive supranuclear palsy
    • Gardner RC, Boxer AL, A T, et al.: Intrinsic connectivity network disruption in progressive supranuclear palsy. Ann Neurol 2013. doi: 10.1002/ana.23844
    • (2013) Ann Neurol
    • Gardner, R.C.1    Boxer, A.L.A.T.2
  • 47
    • 63649160214 scopus 로고    scopus 로고
    • Conformational diversity of wild-type Tau fibrils specified by templated conformation change
    • Frost B, Ollesch J, Wille H, Diamond MI: Conformational diversity of wild-type Tau fibrils specified by templated conformation change. J Biol Chem 2009, 284: 3546-3551.
    • (2009) J Biol Chem , vol.284 , pp. 3546-3551
    • Frost, B.1    Ollesch, J.2    Wille, H.3    Diamond, M.I.4
  • 48
    • 67649273927 scopus 로고    scopus 로고
    • Propagation of tau misfolding from the outside to the inside of a cell
    • Frost B, Jacks RL, Diamond MI: Propagation of tau misfolding from the outside to the inside of a cell. J Biol Chem 2009, 284: 12845-12852. 10.1074/jbc.M808759200
    • (2009) J Biol Chem , vol.284 , pp. 12845-12852
    • Frost, B.1    Jacks, R.L.2    Diamond, M.I.3
  • 49
    • 84861758226 scopus 로고    scopus 로고
    • Trans-cellular propagation of Tau aggregation by fibrillar species
    • Kfoury N, Holmes BB, Jiang H, Holtzman DM, Diamond MI: Trans-cellular propagation of Tau aggregation by fibrillar species. J Biol Chem 2012, 287: 19440-19451. doi: 10.1074/jbc.M112.346072 10.1074/jbc.M112.346072
    • (2012) J Biol Chem , vol.287 , pp. 19440-19451
    • Kfoury, N.1    Holmes, B.B.2    Jiang, H.3    Holtzman, D.M.4    Diamond, M.I.5
  • 50
    • 81755183039 scopus 로고    scopus 로고
    • Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease
    • Friedman-Levi Y, Meiner Z, Canello T, et al.: Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease. PLoS Pathog 2011, 7: e1002350. doi: 10.1371/journal.ppat.1002350 PPATHOGENS-D-11-01077 10.1371/journal.ppat.1002350
    • (2011) PLoS Pathog , vol.7
    • Friedman-Levi, Y.1    Meiner, Z.2    Canello, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.