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La ricerca find articoli where soggetti phrase all words 'VARIANT CJD' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 118 riferimenti
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    1. Knight, R
      Creutzfeldt-Jakob disease: A protein disease

      PROTEOMICS
    2. Aguzzi, A; Montrasio, F; Kaeser, PS
      Prions: Health scare and biological challenge

      NATURE REVIEWS MOLECULAR CELL BIOLOGY
    3. Crozet, C; Bencsik, A; Flamant, F; Lezmi, S; Samarut, J; Baron, T
      Florid plaques in ovine PrP transgenic mice infected with an experimental ovine BSE

      EMBO REPORTS
    4. Deslys, JP; Lasmezas, CI; Comoy, E; Domont, D
      Diagnosis of bovine spongiform encephalopathy

      VETERINARY JOURNAL
    5. Negro, A; Ballarin, C; Bertoli, A; Massimino, ML; Sorgato, MC
      The metabolism and imaging in live cells of the bovine prion protein in its native form or carrying single amino acid substitutions

      MOLECULAR AND CELLULAR NEUROSCIENCE
    6. Gravenor, MB; Cox, DR; Hoinville, LJ; Hoek, A; McLean, AR
      The flock-to-flock force of infection for scrapie in Britain

      PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    7. Vostal, JG; Holada, K; Simak, J
      Expression of cellular prion protein on blood cells: Potential functions in cell physiology and pathophysiology of transmissible spongiform encephalopathy diseases

      TRANSFUSION MEDICINE REVIEWS
    8. Nunery, WR
      Risk of prion transmission with the use of xenografts and allografts in surgery

      OPHTHALMIC PLASTIC AND RECONSTRUCTIVE SURGERY
    9. Head, MW; Tissingh, G; Uitdehaag, BMJ; Barkhof, F; Bunn, TJR; Ironside, JW; Kamphorst, W; Scheltens, P
      Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: Atypical molecular phenotype

      ANNALS OF NEUROLOGY
    10. Myers, MJ; Friedman, SL; Farrell, DE; Dove-Pettit, DA; Bucker, MF; Kelly, S; Madzo, S; Campbell, W; Wang, RF; Paine, D; Cerniglia, CE
      Validation of a polymerase chain reaction method for the detection of rendered bovine-derived materials in feedstuffs

      JOURNAL OF FOOD PROTECTION
    11. Van Everbroeck, B; Pals, P; Quoilin, S; Martin, JJ; Cras, P
      The many faces of human prion diseases in Belgium and the world

      ACTA NEUROLOGICA BELGICA
    12. Aguzzi, A
      From cattle to humans: which connections?

      BIOFUTUR
    13. Sarradin, P; Lantier, F
      Mad sheep?

      BIOFUTUR
    14. Brugere-Picoux, J; Brugere, H
      Bovine spongiform encephalopathy: A turning point in the evolution of the epidemic?

      REVUE DE MEDECINE INTERNE
    15. Bolton, DJ; Doherty, AM; Sheridan, JJ
      Beef HACCP: intervention and non-intervention systems

      INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY
    16. Volkel, D; Zimmermann, K; Zerr, I; Bodemer, M; Lindner, T; Turecek, PL; Poser, S; Schwarz, HP
      Immunochemical determination of cellular prion protein in plasma from healthy subjects and patients with sporadic CJD or other neurologic diseases

      TRANSFUSION
    17. Heppner, FL; Musahl, C; Arrighi, I; Klein, MA; Rulicke, T; Oesch, B; Zinkernagel, RM; Kalinke, U; Aguzzi, A
      Prevention of scrapie pathogenesis by transgenic expression of anti-prion protein antibodies

      SCIENCE
    18. Lasmezas, CI; Fournier, JG; Nouvel, V; Boe, H; Marce, D; Lamoury, F; Kopp, N; Hauw, JJ; Ironside, J; Bruce, M; Dormont, D; Deslys, JP
      Adaptation of the bovine spongiform encephalopathy agent to primates and comparison with Creutzfeldt-Jakob disease: Implications for human health

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    19. Lloyd, SE; Onwuazor, ON; Beck, JA; Mallinson, G; Farrall, M; Targonski, P; Collinge, J; Fisher, EMC
      Identification of multiple quantitative trait loci linked to prion diseaseincubation period in mice

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    20. Walker, P
      Pediatric adenoidectomy under vision using suction-diathermy ablation

      LARYNGOSCOPE
    21. Baron, TGM; Biacabe, AG
      Molecular analysis of the abnormal prion protein during coinfection of mice by bovine spongiform encephalopathy and a scrapie agent

      JOURNAL OF VIROLOGY
    22. Brown, P; Cervenakova, L; Diringer, H
      Blood infectivity and the prospects for a diagnostic screening test in Creutzfeldt-Jakob disease

      JOURNAL OF LABORATORY AND CLINICAL MEDICINE
    23. Winklhofer, KF; Hartl, FU; Tatzelt, J
      A sensitive filter retention assay for the detection of PrPSc and the screening of anti-prion compounds

      FEBS LETTERS
    24. Collie, DA; Sellar, RJ; Zeidler, M; Colchester, ACF; Knight, R; Will, RG
      MRI of Creutzfeldt-Jakob disease: Imaging features and recommended MRI protocol

      CLINICAL RADIOLOGY
    25. Brown, DR
      BSE: a post-industrial disease?

      CHEMISTRY & INDUSTRY
    26. Awan, T; Forloni, G; Ragg, E; Iussich, S; Rossi, G; Colombo, L; Girola, L; Massignan, T; Bugiani, O; Salmona, M; Tagliavini, F
      Therapeutic approaches to prion diseases: In vitro studies with tetracycline compounds

      ALZHEIMER'S DISEASE
    27. Hillier, CEM; Salmon, RL
      Is there evidence for exogenous risk factors in the aetiology and spread of Creutzfeldt-Jakob disease?

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    28. Evatt, B
      Creutzfeldt-Jakob Disease and haemophilia: assessment of risk

      HAEMOPHILIA
    29. Hinton, MH
      Infections and intoxications associated with animal feed and forage which may present a hazard to human health

      VETERINARY JOURNAL
    30. Parchi, P; Capellari, S; Gambetti, P
      Intracerebral distribution of the abnormal isoform of the prion protein insporadic Creutzfeldt-Jakob disease and fatal insomnia

      MICROSCOPY RESEARCH AND TECHNIQUE
    31. Detwiler, LA; Rubenstein, R
      Bovine spongiform encephalopathy: An overview

      ASAIO JOURNAL
    32. Yang, CM
      Evidence for oxidative damage to prion protein in prion diseases

      CHINESE SCIENCE BULLETIN
    33. Hagenaars, TJ; Ferguson, NM; Donnelly, CA; Ghani, AC; Anderson, RM
      Feed-borne transmission and case clustering of BSE

      PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    34. Ghani, AC; Donnelly, CA; Ferguson, NM; Anderson, RM
      Assessment of the prevalence of vCJD through testing tonsils and appendices for abnormal prion protein

      PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    35. McLean, AR; Bostock, CJ
      Scrapie infections initiated at varying doses: an analysis of 117 titration experiments

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    36. Jackson, GS; Clarke, AR
      Mammalian prion proteins

      CURRENT OPINION IN STRUCTURAL BIOLOGY
    37. Harris, DA
      Prion diseases

      NUTRITION
    38. Rogers, M; Doyle, D; Geise, M
      Prions: strategies for control of BSE and scrapie

      IRISH JOURNAL OF AGRICULTURAL AND FOOD RESEARCH
    39. Haltia, M
      Human prion diseases

      ANNALS OF MEDICINE
    40. Politopoulou, G; Seebach, JD; Schmugge, M; Schwarz, HP; Aguzzi, A
      Age-related expression of the cellular prion protein in human peripheral blood leukocytes

      HAEMATOLOGICA
    41. Kenney, K; Brechtel, C; Takahashi, H; Kurohara, K; Anderson, P; Gibbs, CJ
      An enzyme-linked immunosorbent assay to quantify 14-3-3 proteins in the cerebrospinal fluid of suspected Creutzfeldt-Jakob disease patients

      ANNALS OF NEUROLOGY
    42. Ironside, JW; Head, MW; Bell, JE; McCardle, L; Will, RG
      Laboratory diagnosis of variant Creutzfeldt-Jakob disease

      HISTOPATHOLOGY
    43. Hilton, DA
      vCJD - predicting the future?

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    44. Campbell, S; Dennehy, U; Telling, G
      Analyzing the influence of PrP primary structure on prion pathogenesis in transgenic mice

      ARCHIVES OF VIROLOGY
    45. Scott, MR; Supattapone, S; Nguyen, HOB; DeArmond, SJ; Prusiner, SB
      Transgenic models of prion disease

      ARCHIVES OF VIROLOGY
    46. Giese, A; Bieschke, J; Eigen, M; Kretzschmar, HA
      Putting prions into focus: application of single molecule detection to thediagnosis of prion diseases

      ARCHIVES OF VIROLOGY
    47. Baron, TGM; Madec, JY; Calavas, D; Richard, Y; Barillet, F
      Comparison of French natural scrapie isolates with bovine spongiform encephalopathy and experimental scrapie infected sheep

      NEUROSCIENCE LETTERS
    48. Bradley, R
      Veterinary research at the Central Veterinary Laboratory, Weybridge, with special reference to scrapie and bovine spongiform encephalopathy

      REVUE SCIENTIFIQUE ET TECHNIQUE DE L OFFICE INTERNATIONAL DES EPIZOOTIES
    49. Manzoni, M; Bergomi, S; Rollini, M; Cavazzoni, V; Felisaz, C; Marinoni, C
      Extracellular K5 polysaccharidic antigen recovery performed by different cell separation technologies

      BIOTECHNOLOGY LETTERS
    50. Orge, L; Simas, JP; Fernandes, AC; Ramos, M; Galo, A
      Similarity of the lesion profile of BSE in Portuguese cattle to that described in British cattle

      VETERINARY RECORD
    51. Priola, SA; Raines, A; Caughey, WS
      Porphyrin and phthalocyanine antiscrapie compounds

      SCIENCE
    52. Daszak, P; Cunningham, AA; Hyatt, AD
      Wildlife ecology - Emerging infectious diseases of wildlife - Threats to biodiversity and human health

      SCIENCE
    53. Gravenor, MB; Cox, DR; Hoinville, LJ; Hoek, A; McLean, AR
      Encephalopathies - Scrapie in Britain during the BSE years

      NATURE
    54. Parchi, P; Zou, WQ; Wang, W; Brown, P; Capellari, S; Ghetti, B; Kopp, N; Schulz-Schaeffer, WJ; Kretzschmar, HA; Head, MW; Ironside, JW; Gambetti, P; Chen, SG
      Genetic influence on the structural variations of the abnormal prion protein

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    55. Hill, AF; Joiner, S; Linehan, J; Desbruslais, M; Lantos, PL; Collinge, J
      Species-barrier-independent prion replication in apparently resistant species

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    56. Garcia, FL; Zahn, R; Riek, R; Wuthrich, K
      NMR structure of the bovine prion protein

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    57. Perrier, V; Wallace, AC; Kaneko, K; Safar, J; Prusiner, SB; Cohen, FE
      Mimicking dominant negative inhibition of prion replication through structure-based drug design

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    58. Polak, MP; Zmudzinski, JF
      Diagnosis of transmissible spongiform encephalopathies

      MEDYCYNA WETERYNARYJNA
    59. d'Aignaux, JH; Laplanche, JL; Delasnerie-Laupretre, N; Brandel, JP; Peoc'h, K; Salomon, D; Hauw, JJ; Alperovitch, A
      Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    60. Tagliavini, F; Forloni, G; Colombo, L; Rossi, G; Girola, L; Canciani, B; Angeretti, N; Giampaolo, L; Peressini, E; Awan, T; De Gioia, L; Ragg, E; Bugiani, O; Salmona, M
      Tetracycline affects abnormal properties of synthetic PrP peptides and PrPSc in vitro

      JOURNAL OF MOLECULAR BIOLOGY
    61. Sweeney, T; Kuczius, T; McElroy, M; Parada, MG; Groschup, MH
      Molecular analysis of Irish sheep scrapie cases

      JOURNAL OF GENERAL VIROLOGY
    62. Porter, S; Scully, C; Ridgway, GL; Bell, J
      The human transmissible spongiform encephalopathies (TSEs): implications for dental practitioners

      BRITISH DENTAL JOURNAL
    63. Van Everbroeck, B; Pals, P; Dziedzic, T; Dom, R; Godfraind, C; Sciot, R; Brucher, JM; Martin, JJ; Cras, P
      Retrospective study of Creutzfeldt-Jakob disease in Belgium: neuropathological findings

      ACTA NEUROPATHOLOGICA
    64. Aguzzi, A
      Prion diseases: an update

      BIOLOGICAL RESOURCE MANAGEMENT: CONNECTING SCIENCE AND POLICY
    65. Wadsworth, JDF; Hill, AF; Joiner, S; Jackson, GS; Clarke, AR; Collinge, J
      Strain-specific prion-protein conformation determined by metal ions

      NATURE CELL BIOLOGY
    66. Priola, SA; Caughey, B; Caughey, WS
      Novel therapeutic uses for porphyrins and phthalocyanines in the transmissible spongiform encephalopathies - Commentary

      CURRENT OPINION IN MICROBIOLOGY
    67. Van Everbroeck, B; O'Rourke, KI; Cras, P
      Immunoreactivity of the monoclonal antibody F89/160.1.5 for human prion protein

      EUROPEAN JOURNAL OF HISTOCHEMISTRY
    68. Brewer, MS
      Current status of bovine spongiform encephalopathy - A review

      JOURNAL OF MUSCLE FOODS
    69. Ferguson, NM; Donnelly, CA; Woolhouse, MEJ; Anderson, RM
      Estimation of the basic reproduction number of BSE: the intensity of transmission in British cattle

      PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    70. Jenkins, ES; Combes, RD
      The welfare problems associated with using transgenic mice to bioassay forbovine spongiform encephalopathy

      ANIMAL WELFARE
    71. Foster, PR
      Assessment of the potential of plasma fractionation processes to remove causative agents of transmissible spongiform encephalopathy

      TRANSFUSION MEDICINE
    72. Sol-Caubel, I; Castela, F; Brousse, V; Faivre, L; Guigonis, V; Thiriez, G; de Villemeur, TB
      Prion diseases in pediatrics

      ARCHIVES DE PEDIATRIE
    73. Will, RG
      The transmission of prions to humans

      ACTA PAEDIATRICA
    74. Brandel, JP
      Clinical aspects of human spongiform encephalopathies, with the exception of iatrogenic forms

      BIOMEDICINE & PHARMACOTHERAPY
    75. Parchi, P; Giese, A; Capellari, S; Brown, P; Schulz-Schaeffer, W; Windl, O; Zerr, I; Budka, H; Kopp, N; Piccardo, P; Poser, S; Rojiani, A; Streichemberger, N; Julien, J; Vital, C; Ghetti, B; Gambetti, P; Kretzschmar, H
      Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

      ANNALS OF NEUROLOGY
    76. Drohan, WN; Cervenakova, L
      Safety of blood products: Are transmissible spongiform encephalopathies (prion diseases) a risk?

      THROMBOSIS AND HAEMOSTASIS
    77. Nandi, PK; Leclerc, E
      Polymerization of murine recombinant prion protein in nucleic acid solution

      ARCHIVES OF VIROLOGY
    78. Hogan, RN; Brown, P; Heck, E; Cavanagh, HD
      Risk of prion disease transmission from ocular donor tissue transplantation

      CORNEA
    79. Wenisch, S; Lucker, E; Eigenbrodt, E; Leiser, R; Bulte, M
      Detection of central nervous tissue in meat products - An immunohistochemical approach

      NUTRITION RESEARCH
    80. Jackson, GS; Hill, SF; Joseph, C; Hosszu, L; Power, A; Waltho, JP; Clarke, AR; Collinge, J
      Multiple folding pathways for heterologously expressed human prion protein

      BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
    81. Tan, LJ; Williams, MA; Khan, MK; Champion, HC; Nielsen, NH
      Risk of transmission of bovine spongiform encephalopathy to humans in the United States - Report of the Council on Scientific Affairs

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    82. Baron, TGM; Madec, JY; Calavas, D
      Similar signature of the prion protein in natural sheep scrapie and bovinespongiform encephalopathy-linked diseases

      JOURNAL OF CLINICAL MICROBIOLOGY
    83. Belay, ED
      Transmissible spongiform encephalopathies in humans

      ANNUAL REVIEW OF MICROBIOLOGY
    84. MacGregor, I; Hope, J; Barnard, G; Kirby, L; Drummond, O; Pepper, D; Hornsey, V; Barclay, R; Bessos, H; Turner, M; Prowse, C
      Application of a time-resolved fluoroimmunoassay for the analysis of normal prion protein in human blood and its components

      VOX SANGUINIS
    85. Shinobu, LA; Frosch, MP; Budzik, RF
      A 68-year-old woman with rapidly progressive dementia and a gait disorder - Creutzfeldt-Jakob disease.

      NEW ENGLAND JOURNAL OF MEDICINE
    86. d'Aignaux, JH; Costagliola, D; Maccario, J; de Villemeur, TB; Brandel, JP; Deslys, JP; Hauw, JJ; Chaussain, JL; Agid, Y; Dormont, D; Alperovitch, A
      Incubation period of Creutzfeldt-Jakob disease in human growth hormone recipients in France

      NEUROLOGY
    87. Scott, MR; Will, R; Ironside, J; Nguyen, HOB; Tremblay, P; DeArmond, SJ; Prusiner, SB
      Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    88. Frosh, A
      Prions and the ENT surgeon

      JOURNAL OF LARYNGOLOGY AND OTOLOGY
    89. Somerville, RA
      Host and transmissible spongiform encephalopathy agent strain control glycosylation of PrP

      JOURNAL OF GENERAL VIROLOGY
    90. O'Rourke, KI; Besser, TE; Miller, MW; Cline, TF; Spraker, TR; Jenny, AL; Wild, MA; Zebarth, GL; Williams, ES
      PrP genotypes of captive and free-ranging Rocky Mountain elk (Cervus elaphus nelsoni) with chronic wasting disease

      JOURNAL OF GENERAL VIROLOGY
    91. Hope, J; Wood, SCER; Birkett, CR; Chong, A; Bruce, ME; Cairns, D; Goldmann, W; Hunter, N; Bostock, CJ
      Molecular analysis of ovine prion protein identifies similarities between BSE and an experimental isolate of natural scrapie, CH1641

      JOURNAL OF GENERAL VIROLOGY
    92. McHattie, S; Wells, GAH; Bee, J; Edington, N
      Clusterin in bovine spongiform encephalopathy (BSE)

      JOURNAL OF COMPARATIVE PATHOLOGY
    93. Nixon, RR
      Prions and prion diseases

      LABORATORY MEDICINE
    94. Barclay, GR; Hope, J; Birkett, CR; Turner, ML
      Distribution of cell-associated prion protein in normal adult blood determined by flow cytometry

      BRITISH JOURNAL OF HAEMATOLOGY
    95. Demart, S; Fournier, JG; Creminon, C; Frobert, Y; Lamoury, F; Marce, D; Lasmezas, C; Dormont, D; Grassi, J; Deslys, JP
      New insight into abnormal prion protein using monoclonal antibodies

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    96. McHattie, S; Edington, N
      Clusterin prevents aggregation of neuropeptide 106-126 in vitro

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    97. White, AR; Collins, SJ; Maher, F; Jobling, MF; Stewart, LR; Thyer, JM; Beyreuther, K; Masters, CL; Cappai, R
      Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity

      AMERICAN JOURNAL OF PATHOLOGY
    98. Groschup, MH; Beekes, M; McBride, PA; Hardt, M; Hainfellner, JA; Budka, H
      Deposition of disease-associated prion protein involves the peripheral nervous system in experimental scrapie

      ACTA NEUROPATHOLOGICA
    99. Bruce, ME; Will, RG; Ironside, JW; Fraser, H
      Comparison of the biological characteristics of BSE and CJD in mice

      ALZHEIMER'S DISEASE AND RELATED DISORDERS
    100. FOSTER J; HUNTER N
      TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - TRANSMISSION, MECHANISM OF DISEASE, AND PERSISTENCE

      CURRENT OPINION IN MICROBIOLOGY


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Documento generato il 03/06/20 alle ore 22:23:26