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La ricerca find articoli where soggetti phrase all words 'PRNP GENE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 32 riferimenti
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    1. Sumudhu, W; Perera, S; Hooper, NM
      Ablation of the metal ion-induced endocytosis of the prion protein by disease-associated mutation of the octarepeat region

      CURRENT BIOLOGY
    2. Masullo, C; Macchi, G
      Does PRNP gene control the clinical and pathological phenotype of human spongiform transmissible encephalopathies?

      CLINICAL NEUROPATHOLOGY
    3. McLennan, NF; Rennison, KA; Bell, JE; Ironside, JW
      In situ hybridization analysis of PrP mRNA in human CNS tissues

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    4. Barrette, I; Poisson, G; Gendron, P; Major, F
      Pseudoknots in prion protein mRNAs confirmed by comparative sequence analysis and pattern searching

      NUCLEIC ACIDS RESEARCH
    5. 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
    6. Moore, RC; Xiang, FQ; Monaghan, J; Han, D; Zhang, ZP; Edstrom, L; Anvret, M; Prusiner, SB
      Huntington disease phenocopy is a familial prion disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. Collins, S; Boyd, A; Fletcher, A; Byron, K; Harper, C; McLean, CA; Masters, CL
      Novel prion protein gene mutation in an octogenarian with Creutzfeldt-Jakob disease

      ARCHIVES OF NEUROLOGY
    8. Skworc, KH; Windl, O; Schulz-Schaeffer, WJ; Giese, A; Bergk, J; Nagele, A; Vieregge, P; Zerr, I; Poser, S; Kretzschmar, HA
      Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene

      ANNALS OF NEUROLOGY
    9. Windl, O; Giese, A; Schulz-Schaeffer, W; Zerr, I; Skworc, K; Arendt, S; Oberdieck, C; Bodemer, M; Poser, S; Kretzschmar, HA
      Molecular genetics of human prion diseases in Germany

      HUMAN GENETICS
    10. Cervenakova, L; Buetefisch, C; Lee, HS; Taller, I; Stone, G; Gibbs, CJ; Brown, P; Hallett, M; Goldfarb, LG
      Novel PRNP sequence variant associated with familial encephalopathy

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Mouillet-Richard, S; Teil, C; Lenne, M; Hugon, S; Taleb, O; Laplanche, JL
      Mutation at codon 210 (V210I) of the prion protein gene in a North Africanpatient with Creutzfeldt-Jakob disease

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    12. VITAL C; GRAY F; VITAL A; PARCHI P; CAPELLARI S; PETERSEN RB; FERRER X; JARNIER D; JULIEN J; GAMBETTI P
      PRION ENCEPHALOPATHY WITH INSERTION OF OCTAPEPTIDE REPEATS - THE NUMBER OF REPEATS DETERMINES THE TYPE OF CEREBELLAR DEPOSITS

      Neuropathology and applied neurobiology
    13. CHAPMAN J; CERVENAKOVA L; LEE HS; ESTUPINAN J; RICHARDSON S; VNENCAKJONES CL; GAJDUSEK DC; KORCZYN AD; BROWN P; GOLDFARB LG
      APOE IN NON-ALZHEIMER AMYLOIDOSES - TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES

      Neurology
    14. PICCARDO P; DLOUHY SR; LIEVENS PMJ; YOUNG K; THOMAS DP; NOCHLIN D; DICKSON DW; VINTERS HV; ZIMMERMAN TR; MACKENZIE IRA; KISH SJ; ANG LC; DECARLI C; POCCHIARI M; BROWN P; GIBBS CJ; GAJDUSEK DC; BUGIANI O; IRONSIDE J; TAGLIAVINI F; GHETTI B
      PHENOTYPIC VARIABILITY OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE IS ASSOCIATED WITH PRION PROTEIN HETEROGENEITY

      Journal of neuropathology and experimental neurology
    15. SMID HM
      CHEMICAL MATE GUARDING AND OVIPOSITION STIMULATION IN INSECTS - A MODEL MECHANISM ALTERNATIVE TO THE DROSOPHILA SEX-PEPTIDE PARADIGM

      Proceedings of the Koninklijke Nederlandse Akademie van Wetenschappen
    16. ELHACHIMI KH; CHAUNU MP; CERVENAKOVA L; BROWN P; FONCIN JF
      PUTATIVE NEUROSURGICAL TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE WITHANALYSIS OF DONOR AND RECIPIENT - AGENT STRAINS

      Comptes rendus de l'Academie des sciences. Serie 3, Sciences de la vie
    17. ROSENMANN H; HALIMI M; KAHANA I; BIRAN I; GABIZON R
      DIFFERENTIAL ALLELIC EXPRESSION OF PRP MESSENGER-RNA IN CARRIERS OF THE E200K MUTATION

      Neurology
    18. CAPELLARI S; VITAL C; PARCHI P; PETERSEN RB; FERRER X; JARNIER D; PEGORARO E; GAMBETTI P; JULIEN J
      FAMILIAL PRION DISEASE WITH A NOVEL 144-BP INSERTION IN THE PRION PROTEIN GENE IN A BASQUE FAMILY

      Neurology
    19. ELHACHIMI KH; CERVENAKOVA L; BROWN P; GOLDFARB LG; RUBENSTEIN R; GAJDUSEK DC; FONCIN JF
      MIXED FEATURES OF ALZHEIMER-DISEASE AND CREUTZFELDT-JAKOB-DISEASE IN A FAMILY WITH A PRESENILIN-1 MUTATION IN CHROMOSOME-14

      AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION
    20. GHETTI B; PICCARDO P; FRANGIONE B; BUGIANI O; GIACCONE G; YOUNG K; PRELLI F; FARLOW MR; DLOUHY SR; TAGLIAVINI F
      PRION PROTEIN HEREDITARY AMYLOIDOSIS - PARENCHYMAL AND VASCULAR

      Seminars in virology
    21. MASTRIANNI JA; IANNICOLA C; MYERS RM; DEARMOND S; PRUSINER SB
      MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN FAMILIAL CREUTZFELDT-JAKOB-DISEASE

      Neurology
    22. COCHRAN EJ; BENNETT DA; CERVENAKOVA L; KENNEY K; BERNARD B; FOSTER NL; BENSON DF; GOLDFARB LG; BROWN P
      FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH A 5-REPEAT OCTAPEPTIDE INSERTMUTATION

      Neurology
    23. KRASEMANN S; GROSCHUP M; HUNSMANN G; BODEMER W
      INDUCTION OF ANTIBODIES AGAINST HUMAN PRION PROTEINS (PRP) BY DNA-MEDIATED IMMUNIZATION OF PRP0 0 MICE/

      Journal of immunological methods
    24. HOQUE MZ; KITAMOTO T; FURUKAWA H; MURAMOTO T; TATEISHI J
      MUTATION IN THE PRION PROTEIN GENE AT CODON-232 IN JAPANESE PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE - A CLINICOPATHOLOGICAL, IMMUNOHISTOCHEMICAL AND TRANSMISSION STUDY

      Acta Neuropathologica
    25. LAPLANCHE JL; BEAUDRY P; RIPOLL L; LAUNAY JM
      PRION PROTEIN - STRUCTURE, FUNCTIONS AND HUMAN SPONGIFORM ENCEPHALOPATHIES-ASSOCIATED POLYMORPHISMS

      Pathologie et biologie
    26. KRASEMANN S; ZERR I; WEBER T; POSER S; KRETZSCHMAR H; HUNSMANN G; BODEMER W
      PRION DISEASE-ASSOCIATED WITH A NOVEL 9 OCTAPEPTIDE REPEAT INSERTION IN THE PRNP GENE

      Molecular brain research
    27. GOLDFARB LG; BROWN P
      THE TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES

      Annual review of medicine
    28. LAPLANCHE JL
      MOLECULAR-BASIS OF FAMILIAL AND SPORADIC HUMAN PRION DISEASES

      Transfusion clinique et biologique
    29. GOLDFARB LG; BROWN P; CERVENAKOVA L; GAJDUSEK DC
      MOLECULAR-GENETIC STUDIES OF CREUTZFELDT-JAKOB-DISEASE

      Molecular neurobiology
    30. CERVENAKOVA L; BROWN P; GOLDFARB LG; NAGLE J; PETTRONE K; RUBENSTEIN R; DUBNICK M; GIBBS CJ; GAJDUSEK DC
      INFECTIOUS AMYLOID PRECURSOR GENE-SEQUENCES IN PRIMATES USED FOR EXPERIMENTAL TRANSMISSION OF HUMAN SPONGIFORM ENCEPHALOPATHY

      Proceedings of the National Academy of Sciences of the United Statesof America
    31. HITOSHI S; NAGURA H; YAMANOUCHI H; KITAMOTO T
      DOUBLE MUTATIONS AT CODON 180 AND CODON 232 OF THE PRNP GENE IN AN APPARENTLY SPORADIC CASE OF CREUTZFELDT-JAKOB-DISEASE

      Journal of the neurological sciences
    32. KOVANEN J
      CLINICAL CHARACTERISTICS OF FAMILIAL AND SPORADIC CREUTZFELDT-JAKOB-DISEASE IN FINLAND

      Acta neurologica Scandinavica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 06:06:52