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La ricerca find articoli where soggetti phrase all words 'PRION PROTEIN' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 966 riferimenti
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    1. Hooper, NM
      Determination of glycosyl-phosphatidylinositol membrane protein anchorage

      PROTEOMICS
    2. Knight, R
      Creutzfeldt-Jakob disease: A protein disease

      PROTEOMICS
    3. Narang, HK
      Lingering doubts about spongiform encephalopathy and Creutzfeldt-Jakob disease

      EXPERIMENTAL BIOLOGY AND MEDICINE
    4. Langenhan, JM; Fisk, JD; Gellman, SH
      Evaluation of hydrogen bonding complementarity between a secondary sulfonamide and an alpha-amino acid residue

      ORGANIC LETTERS
    5. 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
    6. Jansen, GH; Vogelaar, CF; Elshof, SM
      Distribution of cellular prion protein in normal human cerebral cortex - Does it have relevance to Creutzfeldt-Jakob disease?

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    7. Ball, HL; King, DS; Cohen, FE; Prusiner, SB; Baldwin, MA
      Engineering the prion protein using chemical synthesis

      JOURNAL OF PEPTIDE RESEARCH
    8. Ferrillo, F; Plazzi, G; Nobili, L; Beelke, M; De Carli, F; Cortelli, P; Tinuper, P; Avoni, P; Vandi, S; Gambetti, P; Lugaresi, E; Montagna, P
      Absence of sleep EEG markers in fatal familial insomnia healthy carriers: a spectral analysis study

      CLINICAL NEUROPHYSIOLOGY
    9. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; Leguern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    10. Dezutter, NA; Landman, WJM; Jager, PL; de Groot, TJ; Dupont, PJ; Tooten, PCJ; Zekarias, B; Gruys, E; Verbruggen, AM
      Evaluation of Tc-99m-MAMA-chrysamine G as an in vivo probe for amyloidosis

      AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS
    11. Kawashima, T; Doh-ura, K; Ogomori, K; Iwaki, T
      Apoptotic bodies in the cerebellum of Japanese patients with Creutzfeldt-Jakob disease

      PATHOLOGY INTERNATIONAL
    12. Mabbott, NA; Bruce, ME; Botto, M; Walport, MJ; Pepys, MB
      Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie

      NATURE MEDICINE
    13. Miele, G; Manson, J; Clinton, M
      A novel erythroid-specific marker of transmissible spongiform encephalopathies

      NATURE MEDICINE
    14. Turner, ML
      Variant Creutzfeldt-Jakob disease and blood transfusion

      CURRENT OPINION IN HEMATOLOGY
    15. Griffiths, PD
      Variant CJD epidemiology: joining up the dots

      REVIEWS IN MEDICAL VIROLOGY
    16. Wong, BS; Liu, T; Paisley, D; Li, RL; Pan, T; Chen, SG; Perry, G; Petersen, RB; Smith, MA; Melton, DW; Gambetti, P; Brown, DR; Sy, MS
      Induction of HO-1 and NOS in doppel-expressing mice devoid of PrP: Implications for doppel function

      MOLECULAR AND CELLULAR NEUROSCIENCE
    17. Hamir, AN; Miller, JM; Schmerr, MJ; Stack, MJ; Chaplin, MJ; Cutlip, RC
      Diagnosis of preclinical and subclinical scrapie in a naturally infected sheep flock utilizing currently available postmortem diagnostic techniques

      JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION
    18. Hamir, AN; Cutlip, RC; Miller, JM; Williams, ES; Stack, MJ; Miller, MW; O'Rourke, KI; Chaplin, MJ
      Preliminary findings on the experimental transmission of chronic wasting disease agent of mule deer to cattle

      JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION
    19. Kovacs, GG; Kurucz, I; Budka, H; Adori, C; Muller, F; Acs, P; Kloppel, S; Schatzl, HM; Mayer, RJ; Laszlo, L
      Prominent stress response of Purkinje cells in Creutzfeldt-Jakob disease

      NEUROBIOLOGY OF DISEASE
    20. Reiersen, H; Rees, AR
      The hunchback and its neighbours: proline as an environmental modulator

      TRENDS IN BIOCHEMICAL SCIENCES
    21. Clarke, AR; Jackson, GS; Collinge, J
      The molecular biology of prion propagation

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    22. Smith, DP; Radford, SE
      Role of the single disulphide bond of beta(2)-microglobulin in amyloidosisin vitro

      PROTEIN SCIENCE
    23. Peretz, D; Scott, MR; Groth, D; Williamson, RA; Burton, DR; Cohen, FE; Prusiner, SB
      Strain-specified relative conformational stability of the scrapie prion protein

      PROTEIN SCIENCE
    24. Jamieson, E; Jeffrey, M; Ironside, JW; Fraser, JR
      Activation of Fas and caspase 3 precedes PrP accumulation in 87V scrapie

      NEUROREPORT
    25. Laine, J; Marc, ME; Sy, MS; Axelrad, H
      Cellular and subcellular morphological localization of normal prion protein in rodent cerebellum

      EUROPEAN JOURNAL OF NEUROSCIENCE
    26. Niklas, N; Hampel, F; Liehr, G; Zahl, A; Alsfasser, R
      The reactivity of N-coordinated amides in metallopeptide frameworks: Molecular events in metal-induced pathogenic pathways?

      CHEMISTRY-A EUROPEAN JOURNAL
    27. Funke-Kaiser, H; Theis, S; Behrouzi, T; Thomas, A; Scheuch, K; Zollmann, FS; Paterka, M; Paul, M; Orzechowski, HD
      Functional characterization of the human prion protein promoter in neuronal and endothelial cells

      JOURNAL OF MOLECULAR MEDICINE-JMM
    28. Schlapfer, J; Stahlberger-Saitbekova, N; Womack, JE; Gaillard, C; Dolf, G
      Assignment of six genes to bovine chromosome 13

      JOURNAL OF ANIMAL BREEDING AND GENETICS-ZEITSCHRIFT FUR TIERZUCHTUNG UND ZUCHTUNGSBIOLOGIE
    29. Armstrong, RA; Lantos, PL; Cairns, NJ
      Correlations between the clustering patterns of the pathological changes in sporadic Creutzfeldt-Jakob disease

      NEUROSCIENCE RESEARCH COMMUNICATIONS
    30. Rossi, L; Marchese, E; Lombardo, MF; Rotilio, G; Ciriolo, MR
      Increased susceptibility of copper-deficient neuroblastoma cells to oxidative stress-mediated apoptosis

      FREE RADICAL BIOLOGY AND MEDICINE
    31. Hoots, WK; Abrams, C; Tankersley, D
      The impact of Creutzfeldt-Jakob disease and variant Creutzfeldt-Jakob disease on plasma safety

      TRANSFUSION MEDICINE REVIEWS
    32. Levy, Y; Hanan, E; Solomon, B; Becker, OM
      Helix-coil transition of PrP106-126: Molecular dynamic study

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    33. Matsunaga, Y; Peretz, D; Williamson, A; Burton, D; Mehlhorn, I; Groth, D; Cohen, FE; Prusiner, SB; Baldwin, MA
      Cryptic epitopes in N-terminally truncated prion protein are exposed in the full-length molecule: Dependence of conformation on pH

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    34. Romero, P; Obradovic, Z; Li, XH; Garner, EC; Brown, CJ; Dunker, AK
      Sequence complexity of disordered protein

      PROTEINS-STRUCTURE FUNCTION AND GENETICS
    35. Coulthart, MB; Cashman, NR
      Variant Creutzfeldt-Jakob disease: a summary of current scientific knowledge in relation to public health

      CANADIAN MEDICAL ASSOCIATION JOURNAL
    36. Masullo, C; Macchi, G
      Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies?

      CLINICAL NEUROPATHOLOGY
    37. Lindner, H; Helliger, W
      Age-dependent deamidation of asparagine residues in proteins

      EXPERIMENTAL GERONTOLOGY
    38. Plaitakis, A; Viskadouraki, AK; Tzagournissakis, M; Zaganas, I; Verghese-Nikolakaki, S; Karagiorgis, V; Panagiotides, I; Kilindireas, C; Patsouris, E; Haberler, C; Budka, H; Sklaviadis, T
      Increased incidence of sporadic Creutzfeldt-Jakob disease on the island ofCrete associated with a high rate of PRNP 129-methionine homozygosity in the local population

      ANNALS OF NEUROLOGY
    39. 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
    40. Campbell, A; Smith, MA; Sayre, LM; Bondy, SC; Perry, G
      Mechanisms by which metals promote events connected to neurodegenerative diseases

      BRAIN RESEARCH BULLETIN
    41. Kourie, JI; Henry, CL
      Protein aggregation and deposition: Implications for ion channel formationand membrane damage

      CROATIAN MEDICAL JOURNAL
    42. Ratzka, P; Schroter, A; Cepek, L; Henkel, K; Wiltfang, J; Kretzschmar, HA; Prange, H; Poser, S; Otto, M
      Unaltered apoptotic behaviour of mononuclear cells from patients with sporadic Creutzfeldt-Jakob disease

      JOURNAL OF NEUROLOGY
    43. Saiz, A; Nos, C; Yague, J; Dominguez, A; Graus, F; Munoz, P
      The impact of the introduction of the 14-3-3 protein assay in the surveillance of sporadic Creutzfeldt-Jakob disease in Catalonia

      JOURNAL OF NEUROLOGY
    44. Brown, DR
      BSE did not cause variant CJD: an alternative cause related to post-industrial environmental contamination

      MEDICAL HYPOTHESES
    45. Ledoux, JM
      Bovine spastic paresis: etiological hypotheses

      MEDICAL HYPOTHESES
    46. McLennan, NF; Rennison, KA; Bell, JE; Ironside, JW
      In situ hybridization analysis of PrP mRNA in human CNS tissues

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    47. Satoh, JI; Kuroda, Y
      Ubiquitin C-terminal hydrolase-L1 (PGP9.5) expression in human neural celllines following induction of neuronal differentiation and exposure to cytokines, neurotrophic factors or heat stress

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    48. Vaccari, G; Petraroli, R; Agrimi, U; Eleni, C; Perfetti, MG; Di Bari, MA; Morelli, L; Ligios, C; Busani, L; Nonno, R; Di Guardo, G
      PrP genotype in Sarda breed sheep and its relevance to scrapie

      ARCHIVES OF VIROLOGY
    49. Van Everbroeck, B; Croes, EA; Pals, P; Dermaut, B; Jansen, G; van Duijn, CM; Cruts, M; Van Broeckhoven, C; Martin, JJ; Cras, P
      Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype

      NEUROSCIENCE LETTERS
    50. Peoc'h, K; Schroder, HC; Laplanche, JL; Ramljak, S; Muller, WEG
      Determination of 14-3-3 protein levels in cerebrospinal fluid from Creutzfeldt-Jakob patients by a highly sensitive capture assay

      NEUROSCIENCE LETTERS
    51. Pereira, GS; Walz, R; Bonan, CD; Battastini, AMO; Izquierdo, I; Martins, VR; Brentani, RR; Sarkis, JJF
      Changes in cortical and hippocampal ectonucleotidase activities in mice lacking cellular prion protein

      NEUROSCIENCE LETTERS
    52. Laffling, AJ; Baird, A; Birkett, CR; John, HA
      A monoclonal antibody that enables specific immunohistological detection of prion protein in bovine spongiform encephalopathy cases

      NEUROSCIENCE LETTERS
    53. Armstrong, RA; Lantos, PL; Cairns, NJ
      The spatial patterns of prion protein deposits in Creutzfeldt-Jakob disease: comparison with beta-amyloid deposits in Alzheimer's disease

      NEUROSCIENCE LETTERS
    54. Thielen, C; Melot, F; Jolois, O; Leclereq, F; Tsunoda, R; Frobert, Y; Heinen, E; Antoine, N
      Isolation of bovine follicular dendritic cells allows the demonstration ofa particular cellular prion protein

      CELL AND TISSUE RESEARCH
    55. 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
    56. Johansson, J
      Membrane properties and amyloid fibril formation of lung surfactant protein

      BIOCHEMICAL SOCIETY TRANSACTIONS
    57. Ironside, JW
      From BSE to Creutzfeldt-Jakob

      BIOFUTUR
    58. Dormont, D
      The mechanisms of the neuronal death

      BIOFUTUR
    59. Aguzzi, A
      From cattle to humans: which connections?

      BIOFUTUR
    60. Cesbron, JY; Lemaire, C; Gagnon, J
      The way infection spreads

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

      BIOFUTUR
    62. La Bonnardiere, C
      Screening tests move forward

      BIOFUTUR
    63. Melov, S; Doctrow, SR; Schneider, JA; Haberson, J; Patel, M; Coskun, PE; Huffman, K; Wallace, DC; Malfroy, B
      Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics

      JOURNAL OF NEUROSCIENCE
    64. Leclerc, E; Peretz, D; Ball, H; Sakurai, H; Legname, G; Serban, A; Prusiner, SB; Burton, DR; Williamson, RA
      Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form

      EMBO JOURNAL
    65. Rossi, D; Cozzio, A; Flechsig, E; Klein, MA; Rulicke, T; Aguzzi, A; Weissmann, C
      Onset of ataxia and Purkinje cell loss in PrP null mice inversely correlated with Dpl level in brain

      EMBO JOURNAL
    66. Priola, SA; Lawson, VA
      Glycosylation influences cross-species formation of protease-resistant prion protein

      EMBO JOURNAL
    67. Barron, RM; Thomson, V; Jamieson, E; Melton, DW; Ironside, J; Will, R; Manson, JC
      Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers

      EMBO JOURNAL
    68. Gilch, S; Winklhofer, KF; Groschup, MH; Nunziante, M; Lucassen, R; Spielhaupter, C; Muranyi, W; Riesner, D; Tatzelt, J; Schatzl, HM
      Intracellular re-routing of prion protein prevents propagation of PrPSc and delays onset of prion disease

      EMBO JOURNAL
    69. Birkett, CR; Hennion, RM; Bembridge, DA; Clarke, MC; Chree, A; Bruce, ME; Bostock, CJ
      Scrapie strains maintain biological phenotypes on propagation in a cell line in culture

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

      REVUE DE MEDECINE INTERNE
    71. Wegiel, J; Wang, KC; Imaki, H; Rubenstein, R; Wronska, A; Osuchowski, M; Lipinski, WJ; Walker, LC; LeVine, H
      The role of microglial cells and astrocytes in fibrillar plaque evolution in transgenic APP(SW) mice

      NEUROBIOLOGY OF AGING
    72. Machen, MR
      Scrapie: Deciphering its pathophysiology and cause

      COMPENDIUM ON CONTINUING EDUCATION FOR THE PRACTICING VETERINARIAN
    73. Righetti, PG; Verzola, B
      Folding/unfolding/refolding of proteins: Present methodologies in comparison with capillary zone electrophoresis

      ELECTROPHORESIS
    74. Hopp, P; Ulvund, MJ; Jarp, J
      A case-control study on scrapie in Norwegian sheep flocks

      PREVENTIVE VETERINARY MEDICINE
    75. Thompson, AJ; Barnham, KJ; Norton, RS; Barrow, CJ
      The Val-210-Ile pathogenic Creutzfeldt-Jakob disease mutation increases both the helical and aggregation propensities of a sequence corresponding to helix-3 of PrPC

      BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
    76. Lezmi, S; Bencsik, A; Baron, T
      CNA42 monoclonal antibody identifies FDC as PrPsc accumulating cells in the spleen of scrapie affected sheep

      VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY
    77. Glatzel, M; Aguzzi, A
      The shifting biology of prions

      BRAIN RESEARCH REVIEWS
    78. Rezaie, P; Lantos, PL
      Microglia and the pathogenesis of spongiform encephalopathies

      BRAIN RESEARCH REVIEWS
    79. Ladogana, A; Almonti, S; Petraroli, R; Giaccaglini, E; Ciarmatori, C; Liu, QG; Bevivino, S; Squitieri, F; Pocchiari, M
      Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    80. Collinge, J
      Prion diseases of humans and animals: Their causes and molecular basis

      ANNUAL REVIEW OF NEUROSCIENCE
    81. Jacchieri, SG
      Stepwise assembling of polypeptide chain energy distributions

      COMPUTERS & CHEMISTRY
    82. Miller, JLC; Petteway, SR; Lee, DC
      Ensuring the pathogen safety of intravenous immunoglobulin and other humanplasma-derived therapeutic proteins

      JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
    83. Perna, AF; Castaldo, P; De Santo, NG; Di Carlo, E; Cimmino, A; Galletti, P; Zappia, V; Ingrosso, D
      Plasma proteins containing damaged L-isoaspartyl residues are increased inuremia: Implications for mechanism

      KIDNEY INTERNATIONAL
    84. Aguzzi, A; Brandner, S; Fischer, MB; Furukawa, H; Glatzel, M; Hawkins, C; Heppner, FL; Montrasio, F; Navarro, B; Parizek, P; Pekarik, V; Prinz, M; Raeber, AJ; Rockl, C; Klein, MA
      Spongiform encephalopathies: Insights from transgenic models

      ADVANCES IN VIRUS RESEARCH, VOL 56
    85. Asante, EA; Collinge, J
      Transgenic studies of the influence of the PrP structure on TSE diseases

      ADVANCES IN PROTEIN CHEMISTRY, VOL 57
    86. Bratosiewicz, J; Liberski, PP; Kulczycki, J; Kordek, R
      Codon 129 polymorphism of the PRNP gene in normal Polish population and inCreutzfeldt-Jakob disease, and the search for new mutations in PRNP gene

      ACTA NEUROBIOLOGIAE EXPERIMENTALIS
    87. Jesionek-Kupnicka, D; Kordek, R; Buczynski, J; Liberski, PP
      Apoptosis in relation to neuronal loss in experimental Creutzfeldt-Jakob disease in mice

      ACTA NEUROBIOLOGIAE EXPERIMENTALIS
    88. Kolb, E
      Recent studies on the properties of the infectious molecules of BSE and sheep scrapie and means of infection

      TIERARZTLICHE UMSCHAU
    89. Kolb, E
      Are there inter-relationships between the BSE and transmissible mink encephalopathy? Did BSE exist before 1985?

      TIERARZTLICHE UMSCHAU
    90. Beiglbock, C
      Chronic Wasting Disease (CWD) in cervids in North America - a review

      WIENER TIERARZTLICHE MONATSSCHRIFT
    91. Velinova, M; Thielen, C; Melot, F; Donga, J; Eicher, S; Heinen, E; Antoine, N
      New histochemical and ultrastructural observations on normal bovine tonsils

      VETERINARY RECORD
    92. Ryder, SJ; Wells, GAH; Bradshaw, JM; Pearson, GR
      Inconsistent detection of PrP in extraneural tissues of cats with feline spongiform encephalopathy

      VETERINARY RECORD
    93. Ryder, SJ; Spencer, YI; Bellerby, PJ; March, SA
      Immunohistochemical detection of PrP in the medulla oblongata of sheep: the spectrum of staining in normal and scrapie-affected sheep

      VETERINARY RECORD
    94. Brown, P
      Transfusion medicine and spongiform encephalopathy

      TRANSFUSION
    95. Krailadsiri, P; Seghatchian, J; Williamson, LM
      Platelet storage lesion of WBG-reduced, pooled, buffy coat-derived platelet concentrates prepared in three in-process filter/storage bag combinations

      TRANSFUSION
    96. Dell, A; Morris, HR
      Glycoprotein structure determination mass spectrometry

      SCIENCE
    97. Gray, F; Chretien, F; Keohane, C
      Hereditary cerebral amyloid angiopathy

      REVUE NEUROLOGIQUE
    98. Bridges, BA
      Radiation and germline mutation at repeat sequences: Are we in the middle of a paradigm shift?

      RADIATION RESEARCH
    99. Kolb, E
      Newer biochemical and pathobiochemical knowledge in the genesis, development and prevention of scrapie

      PRAKTISCHE TIERARZT
    100. Thompson, C
      In search of a cure for CJD

      NATURE


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Documento generato il 23/10/20 alle ore 05:57:54