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La ricerca find articoli where soggetti phrase all words 'EXPANDED CAG REPEAT' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 27 riferimenti
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    1. Nance, MA; Myers, RH
      Juvenile onset Huntington's disease - Clinical and research perspectives

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    2. Schilling, G; Jinnah, HA; Gonzales, V; Coonfield, ML; Kim, Y; Wood, JD; Price, DL; Li, XJ; Jenkins, N; Copeland, N; Moran, T; Ross, CA; Borchelt, DR
      Distinct behavioral and neuropathological abnormalities in transgenic mouse models of HD and DRPLA

      NEUROBIOLOGY OF DISEASE
    3. Lin, CH; Tallaksen-Greene, S; Chien, WM; Cearley, JA; Jackson, WS; Crouse, AB; Ren, SR; Li, XJ; Albin, RL; Detloff, PJ
      Neurological abnormalities in a knock-in mouse model of Huntington's disease

      HUMAN MOLECULAR GENETICS
    4. Deckel, AW
      Nitric oxide and nitric oxide synthase in Huntington's disease

      JOURNAL OF NEUROSCIENCE RESEARCH
    5. Sieradzan, KA; Mann, DMA
      The selective vulnerability of nerve cells in Huntington's disease

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    6. Reiner, A; Del Mar, N; Meade, CA; Yang, HT; Dragatsis, I; Zeitlin, S; Goldowitz, D
      Neurons lacking huntingtin differentially colonize brain and survive in chimeric mice

      JOURNAL OF NEUROSCIENCE
    7. Luesse, HG; Schiefer, J; Spruenken, A; Puls, C; Block, F; Kosinski, CM
      Evaluation of R6/2 HD transgenic mice for therapeutic studies in Huntington's disease: behavioral testing and impact of diabetes mellitus

      BEHAVIOURAL BRAIN RESEARCH
    8. Ho, LW; Carmichael, J; Swartz, J; Wyttenbach, A; Rankin, J; Rubinsztein, DC
      The molecular biology of Huntington's disease

      PSYCHOLOGICAL MEDICINE
    9. Kusakabe, M; Mangiarini, L; Laywell, ED; Bates, GP; Yoshiki, A; Hiraiwa, N; Inoue, J; Steindler, DA
      Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene

      JOURNAL OF COMPARATIVE NEUROLOGY
    10. Luthi-Carter, R; Strand, A; Peters, NL; Solano, SM; Hollingsworth, ZR; Menon, AS; Frey, AS; Spektor, BS; Penney, EB; Schilling, G; Ross, CA; Borchelt, DR; Tapscott, SJ; Young, AB; Cha, JHJ; Olson, JM
      Decreased expression of striatal signaling genes in a mouse model of Huntington's disease

      HUMAN MOLECULAR GENETICS
    11. Wheeler, VC; White, JK; Gutekunst, CA; Vrbanac, V; Weaver, M; Li, XJ; Li, SH; Yi, H; Vonsattel, JP; Gusella, JF; Hersch, S; Auerbach, W; Joyner, AL; MacDonald, ME
      Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in Hdh(Q92) and Hdh(Q111) knock-in mice

      HUMAN MOLECULAR GENETICS
    12. Haque, NSK; Isacson, O
      Neurotrophic factors NGF and FGF-2 alter levels of huntingtin (IT15) in striatal neuronal cell cultures

      CELL TRANSPLANTATION
    13. Coles, R; Birdsall, M; Wyttenbach, A; Rubinsztein, DC
      12-O-tetradecanoyl-phorbol-13-acetate down-regulates the Huntingtin promoter at Sp I sites

      NEUROREPORT
    14. Carter, RJ; Hunt, MJ; Morton, AJ
      Environmental stimulation increases survival in mice transgenic for exon Iof the Huntington's disease gene

      MOVEMENT DISORDERS
    15. Murphy, KPSJ; Carter, RJ; Lione, LA; Mangiarini, L; Mahal, A; Bates, GP; Dunnett, SB; Morton, AJ
      Abnormal synaptic plasticity and impaired spatial cognition in mice transgenic for exon 1 of the human Huntington's disease mutation

      JOURNAL OF NEUROSCIENCE
    16. Ferrante, RJ; Andreassen, OA; Jenkins, BG; Dedeoglu, A; Kuemmerle, S; Kubilus, JK; Kaddurah-Daouk, R; Hersch, SM; Beal, MF
      Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease

      JOURNAL OF NEUROSCIENCE
    17. Yamamoto, A; Lucas, JJ; Hen, R
      Reversal of neuropathology and motor dysfunction in a conditional model ofHuntington's disease

      CELL
    18. Hickey, MA; Morton, AJ
      Mice transgenic for the Huntington's disease mutation are resistant to chronic 3-nitropropionic acid-induced striatal toxicity

      JOURNAL OF NEUROCHEMISTRY
    19. Shelbourne, PF
      Of mice and men: solving the molecular mysteries of Huntington's disease

      JOURNAL OF ANATOMY
    20. Yen, LS; Strittmatter, SM; Kalb, RG
      Sequence-specific cleavage of Huntingtin mRNA by catalytic DNA

      ANNALS OF NEUROLOGY
    21. SAHBA S; NECHIPORUK A; FIGUEROA KP; NECHIPORUK T; PULST SM
      GENOMIC STRUCTURE OF THE HUMAN GENE FOR SPINOCEREBELLAR ATAXIA TYPE-2(SCA2) ON CHROMOSOME 12Q24.1

      Genomics
    22. STEVANIN G; DAVID G; ABBAS N; AGID Y; BRICE A; YVERT G
      AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA WITH MACULAR DYSTROPHY (SCA7)

      MS. Medecine sciences
    23. WALLING HW; BALDASSARE JJ; WESTFALL TC
      MOLECULAR ASPECTS OF HUNTINGTONS-DISEASE

      Journal of neuroscience research
    24. QUINN N; SCHRAG A
      HUNTINGTONS-DISEASE AND OTHER CHOREAS

      Journal of neurology
    25. COOPER AJL; SHEU KFR; BURKE JR; ONODERA O; STRITTMATTER WJ; ROSES AD; BLASS JP
      INHIBITION OF ALPHA-KETOGLUTARATE-DEHYDROGENASE AND PYRUVATE-DEHYDROGENASE COMPLEXES IN ESCHERICHIA-COLI BY A GLUTATHIONE-S-TRANSFERASE CONTAINING A PATHOLOGICAL LENGTH POLY-Q DOMAIN - A POSSIBLE ROLE OF ENERGY DEFICIT IN NEUROLOGICAL DISEASES ASSOCIATED WITH POLY-Q EXPANSIONS

      Age
    26. LI SH; HOSSEINI SH; GUTEKUNST CA; HERSCH SM; FERRANTE RJ; LI XJ
      A HUMAN HAP1 HOMOLOG - CLONING, EXPRESSION, AND INTERACTION WITH HUNTINGTIN

      The Journal of biological chemistry
    27. ROSS CA; MARGOLIS RL; ROSENBLATT A; RANEN NG; BECHER MW; AYLWARD E
      HUNTINGTON-DISEASE AND THE RELATED DISORDER, DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA)

      Medicine


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/06/20 alle ore 21:04:10