Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where soggetti phrase all words 'AMYLOID PRECURSOR GENE' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 55 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Leuck, CJ; McIlwaine, GG; Zeidler, M
      Creutzfeldt-Jakob disease and the eye. I. Background and patient management

      EYE
    2. Mastrianni, JA; Roos, RP
      The prion diseases

      SEMINARS IN NEUROLOGY
    3. 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
    4. Tohgi, H; Utsugisawa, K; Nagane, Y; Yoshimura, M; Genda, Y; Ukitsu, M
      Reduction with age in methylcytosine in the promoter region-224 similar to-101 of the amyloid precursor protein gene in autopsy human cortex

      MOLECULAR BRAIN RESEARCH
    5. Laplanche, JL; El Hachimi, KH; Durieux, I; Thuillet, P; Defebvre, L; Delasnerie-Laupretre, N; Peoc'h, K; Foncin, JF; Destee, A
      Prominent psychiatric features and early onset in an inherited prion disease with a new insertional mutation in the prion protein gene

      BRAIN
    6. Lee, HS; Sambuughin, N; Cervenakova, L; Chapman, J; Pocchiari, M; Litvak, S; Qi, HY; Budka, H; del Ser, T; Furukawa, H; Brown, P; Gajdusek, DC; Long, JC; Korczyn, AD; Goldfarb, LG
      Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    7. CHATELAIN J; DELASNERIELAUPRETRE N; LEMAIRE MH; CATHALA F; LAUNAY JM; LAPLANCHE JL
      CLUSTER OF CREUTZFELDT-JAKOB-DISEASE IN FRANCE ASSOCIATED WITH THE CODON-200 MUTATION (E200K) IN THE PRION PROTEIN GENE

      European journal of neurology
    8. Mastrianni, JA
      The prion diseases: Creutzfeldt-Jakob, Gerstmann-Straussler-Scheinker, andrelated disorders

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    9. Riekkinen, P; Schmidt, BH; van der Staay, FJ
      Animal models in the development of symptomatic and preventive drug therapies for Alzheimer's disease

      ANNALS OF MEDICINE
    10. 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
    11. Miyakawa, T; Inoue, K; Iseki, E; Kawanishi, C; Sugiyama, N; Onishi, H; Yamada, Y; Suzuki, K; Iwabuchi, K; Kosaka, K
      Japanese Creutzfeldt-Jakob disease patients exhibiting high incidence of the E200K PRNP mutation and located in the basin of a river

      NEUROLOGICAL RESEARCH
    12. DORMONT D
      BIOLOGY OF THE TRANSMISSIBLE SPONGIFORM E NCEPHALOPATHY AGENTS (PRIONS)

      Revue neurologique
    13. KRAKAUER DC; ZANOTTO PMD; PAGEL M
      PRIONS PROGRESS - PATTERNS AND RATES OF MOLECULAR EVOLUTION IN RELATION TO SPONGIFORM DISEASE

      Journal of molecular evolution
    14. MOORE RC; MELTON DW
      TRANSGENIC ANALYSIS OF PRION DISEASES

      Molecular human reproduction
    15. PRUSINER SB; SCOTT MR
      GENETICS OF PRIONS

      Annual review of genetics
    16. ROSENMANN H; HALIMI M; KAHANA I; BIRAN I; GABIZON R
      DIFFERENTIAL ALLELIC EXPRESSION OF PRP MESSENGER-RNA IN CARRIERS OF THE E200K MUTATION

      Neurology
    17. MEINER Z; GABIZON R; PRUSINER SB
      FAMILIAL CREUTZFELDT-JAKOB-DISEASE - CODON-200 PRION DISEASE IN LIBYAN JEWS

      Medicine
    18. GABIZON R; TELLING G; MEINER Z; HALIMI H; KAHANA I; PRUSINER SB
      INSOLUBLE WILD-TYPE AND PROTEASE-RESISTANT MUTANT PRION PROTEIN IN BRAINS OF PATIENTS WITH INHERITED PRION DISEASE

      Nature medicine
    19. PRUSINER SB; TELLING G; COHEN FE; DEARMOND SJ
      PRION DISEASES OF HUMANS AND ANIMALS

      Seminars in virology
    20. COLLINS SJ; CAPPAI R; MASTERS CL
      RECENT DEVELOPMENTS IN THE TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - IMPLICATIONS FOR CLINICAL-PRACTICE

      Journal of clinical neuroscience
    21. LAPLANCHE JL
      MOLECULAR-GENETICS OF FAMILIAL AND SPORAD IC FORMS OF HUMAN PRION DISEASES

      Medecine et maladies infectieuses
    22. PRUSINER SB
      MOLECULAR-BIOLOGY AND GENETICS OF PRION DISEASES

      Cold Spring Harbor Symposia on Quantitative Biology
    23. 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
    24. ANTOINE JC; LAPLANCHE JL; MOSNIER JF; BEAUDRY P; CHATELAIN J; MICHEL D
      DEMYELINATING PERIPHERAL NEUROPATHY WITH CREUTZFELDT-JAKOB-DISEASE AND MUTATION AT CODON-200 OF THE PRION PROTEIN GENE

      Neurology
    25. CHAPMAN J; ARLAZOROFF A; GOLDFARB LG; CERVENAKOVA L; NEUFELD MY; WERBER E; HERBERT M; BROWN P; GAJDUSEK DC; KORCZYN AD
      FATAL INSOMNIA IN A CASE OF FAMILIAL CREUTZFELDT-JAKOB-DISEASE WITH THE CODON 200(LYS) MUTATION

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

      Pathologie et biologie
    27. FORSELL C; LANNFELT L
      AMYLOID PRECURSOR PROTEIN MUTATION AT CODON-713 (ALA-]VAL) DOES NOT CAUSE SCHIZOPHRENIA - NONPATHOGENIC VARIANT FOUND AT CODON-705 (SILENT)

      Neuroscience letters
    28. EGENSPERGER R; KOSEL S; SCHNABEL R; MEHRAEIN P; GRAEBER MB
      APOLIPOPROTEIN-E GENOTYPE AND NEUROPATHOLOGICAL PHONOTYPE IN 2 MEMBERS OF A GERMAN FAMILY WITH CHROMOSOME 14-LINKED EARLY-ONSET ALZHEIMERS-DISEASE

      Acta Neuropathologica
    29. LIBERSKI PP
      PRIONS, BETA-SHEETS AND TRANSMISSIBLE DEMENTIAS - IS THERE STILL SOMETHING MISSING

      Acta Neuropathologica
    30. LAPLANCHE JL
      MOLECULAR-BASIS OF FAMILIAL AND SPORADIC HUMAN PRION DISEASES

      Transfusion clinique et biologique
    31. COLLINGE J; PALMER MS
      MOLECULAR-GENETICS OF HUMAN PRION DISEASES

      Philosophical transactions-Royal Society of London. Biological sciences
    32. GOLDFARB LG; BROWN P; CERVENAKOVA L; GAJDUSEK DC
      GENETIC-ANALYSIS OF CREUTZFELDT-JAKOB-DISEASE AND RELATED DISORDERS

      Philosophical transactions-Royal Society of London. Biological sciences
    33. KITAMOTO T; TATEISHI J
      HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN

      Philosophical transactions-Royal Society of London. Biological sciences
    34. COLLINGE J; PALMER MS
      HUMAN PRION DISEASES

      Bailliere's clinical neurology
    35. GOLDFARB LG; BROWN P; CERVENAKOVA L; GAJDUSEK DC
      MOLECULAR-GENETIC STUDIES OF CREUTZFELDT-JAKOB-DISEASE

      Molecular neurobiology
    36. PRUSINER SB; HSIAO KK
      HUMAN PRION DISEASES

      Annals of neurology
    37. SALVATORE M; GENUARDI M; PETRAROLI R; MASULLO C; DALESSANDRO M; POCCHIARI M
      POLYMORPHISMS OF THE PRION PROTEIN GENE IN ITALIAN PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE

      Human genetics
    38. ACKERMAN SL; KNOWLES BB; ANDREWS PW
      GENE-REGULATION DURING NEURONAL AND NONNEURONAL DIFFERENTIATION OF NTERA2 HUMAN TERATOCARCINOMA-DERIVED STEM-CELLS

      Molecular brain research
    39. PRUSINER SB; DEARMOND SJ
      PRION DISEASES AND NEURODEGENERATION

      Annual review of neuroscience
    40. PRUSINER SB
      NEURODEGENERATION IN HUMANS CAUSED BY PRIONS

      Western journal of medicine
    41. INOUE I; KITAMOTO T; DOHURA K; SHII H; GOTO I; TATEISHI J
      JAPANESE FAMILY WITH CREUTZFELDT-JAKOB-DISEASE WITH CODON-200 POINT MUTATION OF THE PRION PROTEIN GENE

      Neurology
    42. BOGUMIL T; BEUCHE W; SCHINDLER C; SCHACHENMAYR W; KRETZSCHMAR HA
      CREUTZFELDT-JAKOB-DISEASE - PRESENTATION OF A CASE WITH AN UNUSUALLY LONG CLINICAL COURSE AND A SHORT REVIEW OF THE LITERATURE

      Nervenarzt
    43. 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
    44. DOIYI R; KITAMOTO T; OGOMORI K; MEHRAEIN P; TATEISHI J
      DISTRIBUTION OF PRION PROTEIN IN GERMAN PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE IS DIFFERENT FROM THAT IN JAPANESE PATIENTS

      Acta Neuropathologica
    45. FUKUDA R; HATTORI M; SASAKI T; KAZAMATSURI H; KUWATA S; SHIBATA Y; NANKO S
      NO EVIDENCE FOR A POINT MUTATION AT CODON-713 AND CODON-717 OF AMYLOID PRECURSOR PROTEIN GENE IN JAPANESE SCHIZOPHRENICS

      Japanese journal of human genetics
    46. TANAKA H; NARUSE S; SEKI K; ONODERA O; KOBAYASHI H; MIYATAKE T; SHIBATA A; SAKAKI Y; KAMINO K; MIKI T; NUKINA N; IMAGAWA M; NAKANO I; SHIMIZU T; KOJIMA T; HARDY J; TSUJI S
      ABSENCE OF LINKAGE DISEQUILIBRIUM AT AMYLOID PRECURSOR PROTEIN GENE LOCUS IN JAPANESE FAMILIAL ALZHEIMERS-DISEASE WITH 717VAL-]ILE MUTATION

      Neuroscience letters
    47. ASHERSON P; MANT R; TAYLOR C; SARGEANT M; COLLIER D; CLEMENTS A; NANKO S; WHATLEY S; GILL M; MCGUFFIN P; OWEN M
      FAILURE TO FIND LINKAGE BETWEEN SCHIZOPHRENIA AND GENETIC-MARKERS ON CHROMOSOME-21

      American journal of medical genetics
    48. COON H; HOFF M; HOLIK J; DELISI LE; CROWE T; FREEDMAN R; SHIELDS G; BOCCIO AM; LERMAN M; GERSHON ES; GEJMAN PV; LEPPERT M; BYERLEY W
      C-NUCLEOTIDE TO T-NUCLEOTIDE SUBSTITUTION IN CODON 713 OF AMYLOID PRECURSOR PROTEIN GENE NOT FOUND IN 86 UNRELATED SCHIZOPHRENICS FROM MULTIPLEX FAMILIES

      American journal of medical genetics
    49. GOLDFARB LG; BROWN P; LITTLE BW; CERVENAKOVA L; KENNEY K; GIBBS CJ; GAJDUSEK DC
      A NEW (2-REPEAT) OCTAPEPTIDE CODING INSERT MUTATION IN CREUTZFELDT-JAKOB-DISEASE

      Neurology
    50. RIPOLL L; LAPLANCHE JL; SALZMANN M; JOUVET A; PLANQUES B; DUSSAUCY M; CHATELAIN J; BEAUDRY P; LAUNAY JM
      A NEW POINT MUTATION IN THE PRION PROTEIN GENE AT CODON 210 IN CREUTZFELDT-JAKOB-DISEASE

      Neurology
    51. 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
    52. YOSHIZAWA T; KOMATSUZAKI Y; IWAMOTO H; MIZUSAWA H; KANAZAWA I
      SCREENING OF THE MIS-SENSE MUTATION PRODUCING THE (717)VAL-]ILE SUBSTITUTION IN THE AMYLOID PRECURSOR PROTEIN IN JAPANESE FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE

      Journal of the neurological sciences
    53. DEARMOND SJ; PRUSINER SB
      THE NEUROCHEMISTRY OF PRION DISEASES

      Journal of neurochemistry
    54. ARNHOLT JC; SOBELL JL; HESTON LL; SOMMER SS
      APP MUTATIONS AND SCHIZOPHRENIA

      Biological psychiatry
    55. PRUSINER SB
      GENETIC AND INFECTIOUS PRION DISEASES

      Archives of neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 12/08/20 alle ore 17:58:27