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 'NEURONAL INTRANUCLEAR INCLUSIONS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 238 riferimenti
Si mostrano 100 riferimenti a partire da 1
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Tao, T; Tartakoff, AM
      Nuclear relocation of normal huntingtin

      TRAFFIC
    2. Bonini, NM
      Drosophila as a genetic approach to human neurodegenerative disease

      PARKINSONISM & RELATED DISORDERS
    3. Sartorelli, V; Puri, PL
      The link between chromatin structure, protein acetylation and cellular differentiation

      FRONTIERS IN BIOSCIENCE
    4. Nance, MA; Myers, RH
      Juvenile onset Huntington's disease - Clinical and research perspectives

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    5. Dyer, RB; McMurray, CT
      Mutant protein in Huntington disease is resistant to proteolysis in affected brain

      NATURE GENETICS
    6. Waelter, S; Boeddrich, A; Lurz, R; Scherzinger, E; Lueder, G; Lehrach, H; Wanker, EE
      Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation

      MOLECULAR BIOLOGY OF THE CELL
    7. Zeron, MM; Chen, NS; Moshaver, A; Lee, ATC; Wellington, CL; Hayden, MR; Raymond, LA
      Mutant huntingtin enhances excitotoxic cell death

      MOLECULAR AND CELLULAR NEUROSCIENCE
    8. Loy, CJ; Yong, EL
      Sex, infertility and the molecular biology of the androgen receptor

      CURRENT OPINION IN OBSTETRICS & GYNECOLOGY
    9. Lievens, JC; Woodman, B; Mahal, A; Spasic-Boscovic, O; Samuel, D; Goff, LKL; Bates, GP
      Impaired glutamate uptake in the R6 Huntington's disease transgenic mice

      NEUROBIOLOGY OF DISEASE
    10. Chun, WJ; Lesort, M; Tucholski, J; Faber, PW; MacDonald, ME; Ross, CA; Johnson, GVW
      Tissue transglutaminase selectively modifies proteins associated with truncated mutant huntingtin in intact cells

      NEUROBIOLOGY OF DISEASE
    11. 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
    12. Sathasivam, K; Woodman, B; Mahal, A; Bertaux, F; Wanker, EE; Shima, DT; Bates, GP
      Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients

      HUMAN MOLECULAR GENETICS
    13. Abel, A; Walcott, J; Woods, J; Duda, J; Merry, DE
      Expression of expanded repeat androgen receptor produces neurologic disease in transgenic mice

      HUMAN MOLECULAR GENETICS
    14. Fain, JN; Del Mar, NA; Meade, CA; Reiner, A; Goldowitz, D
      Abnormalities in the functioning of adipocytes from R6/2 mice that are transgenic for the Huntington's disease mutation

      HUMAN MOLECULAR GENETICS
    15. Wyttenbach, A; Swartz, J; Kita, H; Thykjaer, T; Carmichael, J; Bradley, J; Brown, R; Maxwell, M; Schapira, A; Orntoft, TF; Kato, K; Rubinsztein, DC
      Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease

      HUMAN MOLECULAR GENETICS
    16. Nakamura, K; Jeong, SY; Uchihara, T; Anno, M; Nagashima, K; Nagashima, T; Ikeda, S; Tsuji, S; Kanazawa, I
      SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein

      HUMAN MOLECULAR GENETICS
    17. Sittler, A; Lurz, R; Lueder, G; Priller, J; Hayer-Hartl, MK; Hartl, FU; Lehrach, H; Wanker, EE
      Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease

      HUMAN MOLECULAR GENETICS
    18. Jana, NR; Zemskov, EA; Wang, GH; Nukina, N
      Altered proteasomal function due to the expression of polyglutamine-expanded truncated N-terminal huntingtin induces apoptosis by caspase activation through mitochondrial cytochrome c release

      HUMAN MOLECULAR GENETICS
    19. Yue, S; Serra, HG; Zoghbi, HY; Orr, HT
      The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract

      HUMAN MOLECULAR GENETICS
    20. Nozaki, K; Onodera, O; Takano, H; Tsuji, S
      Amino acid sequences flanking polyglutamine stretches influence their potential for aggregate formation

      NEUROREPORT
    21. Hansson, O; Guatteo, E; Mercuri, NB; Bernardi, G; Li, XJ; Castilho, RF; Brundin, P
      Resistance to NMDA toxicity correlates with appearance of nuclear inclusions, behavioural deficits and changes in calcium homeostasis in mice transgenic for exon 1 of the huntington gene

      EUROPEAN JOURNAL OF NEUROSCIENCE
    22. NicNiocaill, B; Haraldsson, B; Hansson, O; O'Connor, WT; Brundin, P
      Altered striatal amino acid neurotransmitter release monitored using microdialysis in R6/1 Huntington transgenic mice

      EUROPEAN JOURNAL OF NEUROSCIENCE
    23. Cao, F; Levine, JJ; Li, SH; Li, XJ
      Nuclear aggregation of huntingtin is not prevented by deletion of chaperone Hsp104

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    24. Sherman, MY; Goldberg, AL
      Cellular defenses against unfolded proteins: A cell biologist thinks aboutneurodegenerative diseases

      NEURON
    25. Orr, HT
      Beyond the Qs in the polyglutamine diseases

      GENES & DEVELOPMENT
    26. Piccioni, F; Simeoni, S; Andriola, I; Armatura, E; Bassanini, S; Pozzi, P; Poletti, A
      Polyglutamine tract expansion of the androgen receptor in a motoneuronal model of spinal and bulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    27. Okazawa, H; Sudol, M; Rich, T
      PQBP-1 (Np/PQ): A polyglutamine tract-binding and nuclear inclusion-forming protein

      BRAIN RESEARCH BULLETIN
    28. Kagan, BL; Hirakura, Y; Azimov, R; Azimova, R
      The channel hypothesis of Huntington's disease

      BRAIN RESEARCH BULLETIN
    29. Fusco, FR; Viscomi, MT; Bernardi, G; Molinari, M
      Localization of ataxin-2 within the cerebellar cortex of the rat

      BRAIN RESEARCH BULLETIN
    30. Rimoldi, M; Servadio, A; Zimarino, V
      Analysis of heat shock transcription factor for suppression of polyglutamine toxicity

      BRAIN RESEARCH BULLETIN
    31. Deckel, AW
      Nitric oxide and nitric oxide synthase in Huntington's disease

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

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    33. Schilling, G; Coonfield, ML; Ross, CA; Borchelt, DR
      Coenzyme Q10 and remacemide hydrochloride ameliorate motor deficits in a Huntington's disease transgenic mouse model

      NEUROSCIENCE LETTERS
    34. Mende-Mueller, LM; Toneff, T; Hwang, SR; Chesselet, MF; Hook, VYH
      Tissue-specific proteolysis of huntingtin (htt) in human brain: Evidence of enhanced levels of N- and C-terminal htt fragments in Huntington's disease striatum

      JOURNAL OF NEUROSCIENCE
    35. Martin-Aparicio, E; Yamamoto, A; Hernandez, F; Hen, R; Avila, JS; Lucas, JJ
      Proteasomal-dependent aggregate reversal and absence of cell death in a conditional mouse model of Huntington's disease

      JOURNAL OF NEUROSCIENCE
    36. Li, H; Li, SH; Yu, ZX; Shebourne, P; Li, XJ
      Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice

      JOURNAL OF NEUROSCIENCE
    37. 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
    38. Cattaneo, E; Rigamonti, D; Goffredo, D; Zuccato, C; Squitieri, F; Sipione, S
      Loss of normal huntingtin function: new developments in Huntington's disease research

      TRENDS IN NEUROSCIENCES
    39. Becher, MW; Morrison, L; Davis, LE; Maki, WC; King, MK; Bicknell, JM; Reinert, BL; Bartolo, C; Bear, DG
      Oculopharyngeal muscular dystrophy in Hispanic new Mexicans

      JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
    40. Nucifora, FC; Sasaki, M; Peters, MF; Huang, H; Cooper, JK; Yamada, M; Takahashi, H; Tsuji, S; Troncoso, J; Dawson, VL; Dawson, TM; Ross, CA
      Interference by Huntingtin and atrophin-1 with CBP-mediated transcription leading to cellular toxicity

      SCIENCE
    41. Ho, LW; Carmichael, J; Swartz, J; Wyttenbach, A; Rankin, J; Rubinsztein, DC
      The molecular biology of Huntington's disease

      PSYCHOLOGICAL MEDICINE
    42. Lecerf, JM; Shirley, TL; Zhu, Q; Kazantsev, A; Amersdorfer, P; Housman, DE; Messer, A; Huston, JS
      Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    43. Holbert, S; Denghien, I; Kiechle, T; Rosenblatt, A; Wellington, C; Hayden, MR; Margolis, RL; Ross, CA; Dausset, J; Ferrante, RJ; Neri, C
      The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: Neuropathologic and genetic evidence for a role in Huntington's diseasepathogenesis

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    44. Sapp, E; Kegel, KB; Aronin, N; Hashikawa, T; Uchiyama, Y; Tohyama, K; Bhide, PG; Vonsattel, JP; DiFiglia, M
      Early and progressive accumulation of reactive microglia in the Huntingtondisease brain

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    45. Hansson, O; Castilho, RF; Korhonen, L; Lindholm, D; Bates, GP; Brundin, P
      Partial resistance to malonate-induced striatal cell death in transgenic mouse models of Huntington's disease is dependent on age and CAG repeat length

      JOURNAL OF NEUROCHEMISTRY
    46. Morton, AJ; Edwardson, JM
      Progressive depletion of complexin II in a transgenic mouse model of Huntington's disease

      JOURNAL OF NEUROCHEMISTRY
    47. Chen, S; Berthelier, V; Yang, W; Wetzel, R
      Polyglutamine aggregation behavior in vitro supports a recruitment mechanism of cytotoxicity

      JOURNAL OF MOLECULAR BIOLOGY
    48. Chun, WJ; Lesort, M; Tucholski, J; Ross, CA; Johnson, GVW
      Tissue transglutaminase does not contribute to the formation of mutant Huntingtin aggregates

      JOURNAL OF CELL BIOLOGY
    49. Chen, TLL; Wang, PYY; Luo, W; Gwon, SS; Flay, NW; Zheng, J; Guo, CX; Tanzer, ML; Vertel, BM
      Aggrecan domains expected to traffic through the exocytic pathway are misdirected to the nucleus

      EXPERIMENTAL CELL RESEARCH
    50. Berthelier, V; Hamilton, JB; Chen, SM; Wetzel, R
      A microtiter plate assay for polyglutamine aggregate extension

      ANALYTICAL BIOCHEMISTRY
    51. Leavitt, BR; Guttman, JA; Hodgson, JG; Kimel, GH; Singaraja, R; Vogl, AW; Hayden, MR
      Wild-type huntingtin reduces the cellular toxicity of mutant huntingtin invivo

      AMERICAN JOURNAL OF HUMAN GENETICS
    52. Cummings, CJ; Zoghbi, HY
      Trinucleotide repeats: Mechanisms and pathophysiology

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    53. Gusella, JF; MacDonald, ME
      Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease

      NATURE REVIEWS NEUROSCIENCE
    54. Wanker, EE
      Protein aggregation and pathogenesis of Huntington's disease: Mechanisms and correlations

      BIOLOGICAL CHEMISTRY
    55. Wanker, EE
      Protein aggregation in Huntington's and Parkinson's disease: implications for therapy

      MOLECULAR MEDICINE TODAY
    56. Chen, M; Ona, VO; Li, MW; Ferrante, RJ; Fink, KB; Zhu, S; Bian, J; Guo, L; Farrell, LA; Hersch, SM; Hobbs, W; Vonsattel, JP; Cha, JHJ; Friedlander, RM
      Minocycline inhibits caspase-1 and caspase-3 expression and delays mortality in a transgenic mouse model of Huntington disease

      NATURE MEDICINE
    57. Di Prospero, NA; Tagle, DA
      Normal and mutant huntingtin: Partners in crime?

      NATURE MEDICINE
    58. Shimohata, T; Nakajima, T; Yamada, M; Uchida, C; Onodera, O; Naruse, S; Kimura, T; Koide, R; Nozaki, K; Sano, Y; Ishiguro, H; Sakoe, K; Ooshima, T; Sato, A; Ikeuchi, T; Oyake, M; Sato, T; Aoyagi, Y; Hozumi, I; Nagatsu, T; Takiyama, Y; Nishizawa, M; Goto, J; Kanazawa, I; Davidson, I; Tanese, N; Takahashi, H; Tsuji, S
      Expanded polyglutamine stretches interact with TAF(II)130, interfering with CREB-dependent transcription

      NATURE GENETICS
    59. Huynh, DP; Figueroa, K; Hoang, N; Pulst, SM
      Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

      NATURE GENETICS
    60. Stevanin, G; Durr, A; Brice, A
      Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology

      EUROPEAN JOURNAL OF HUMAN GENETICS
    61. Paulson, HL
      Toward an understanding of polyglutamine neurodegeneration

      BRAIN PATHOLOGY
    62. Orr, HT
      The ins and outs of a polyglutamine neurodegenerative disease: Spinocerebellar ataxia type 1 (SCA1)

      NEUROBIOLOGY OF DISEASE
    63. Shibata, H; Huynh, DP; Pulst, SM
      A novel protein with RNA-binding motifs interacts with ataxin-2

      HUMAN MOLECULAR GENETICS
    64. Yanagisawa, H; Bundo, M; Miyashita, T; Okamura-Oho, Y; Tadokoro, K; Tokunaga, K; Yamada, M
      Protein binding of a DRPLA family through arginine-glutamic acid dipeptiderepeats is enhanced by extended polyglutamine

      HUMAN MOLECULAR GENETICS
    65. Cummings, CJ; Zoghbi, HY
      Fourteen and counting: unraveling trinucleotide repeat diseases

      HUMAN MOLECULAR GENETICS
    66. Calado, A; Tome, FMS; Brais, B; Rouleau, G; Kuhn, U; Wahle, E; Carmo-Fonseca, M
      Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

      HUMAN MOLECULAR GENETICS
    67. Gaspar, C; Jannatipour, M; Dion, P; Laganiere, J; Sequeiros, J; Brais, B; Rouleau, GA
      CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation

      HUMAN MOLECULAR GENETICS
    68. Jana, NR; Tanaka, M; Wang, GH; Nukina, N
      Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity

      HUMAN MOLECULAR GENETICS
    69. Marsh, JL; Walker, H; Theisen, H; Zhu, YZ; Fielder, T; Purcell, J; Thompson, LM
      Expanded polyglutamine peptides alone are intrinsically cytotoxic and cause neurodegeneration in Drosophila

      HUMAN MOLECULAR GENETICS
    70. Yoshizawa, T; Yamagishi, Y; Koseki, N; Goto, J; Yoshida, H; Shibasaki, F; Shoji, S; Kanazawa, I
      Cell cycle arrest enhances the in vitro cellular toxicity of the truncatedMachado-Joseph disease gene product with an expanded polyglutamine stretch

      HUMAN MOLECULAR GENETICS
    71. Simeoni, S; Mancini, MA; Stenoien, DL; Marcelli, M; Weigel, NL; Zanisi, M; Martini, L; Poletti, A
      Motoneuronal cell death is not correlated with aggregate formation of androgen receptors containing an elongated polyglutamine tract

      HUMAN MOLECULAR GENETICS
    72. Tobin, AJ; Signer, ER
      Huntington's disease: the challenge for cell biologists

      TRENDS IN CELL BIOLOGY
    73. Morris, GE
      Nuclear proteins and cell death in inherited neuromuscular disease

      NEUROMUSCULAR DISORDERS
    74. Matsuyama, N; Hadano, S; Onoe, K; Osuga, H; Showguchi-Miyata, J; Gondo, Y; Ikeda, JE
      Identification and characterization of the miniature pig Huntington's disease gene homolog: Evidence for conservation and polymorphism in the CAG triplet repeat

      GENOMICS
    75. Klockgether, T; Wullner, U; Spauschus, A; Evert, B
      The molecular biology of the autosomal-dominant cerebellar ataxias

      MOVEMENT DISORDERS
    76. Birman, S
      Drosophila as a genetic model to study neurodegenerative diseases

      M S-MEDECINE SCIENCES
    77. Morton, AJ; Leavens, W
      Mice transgenic for the human Huntington's disease mutation have reduced sensitivity to kainic acid toxicity

      BRAIN RESEARCH BULLETIN
    78. Kouroku, Y; Fujita, E; Urase, K; Tsuru, T; Setsuie, R; Kikuchi, T; Yagi, Y; Momoi, MY; Momoi, T
      Caspases that are activated during generation of nuclear polyglutamine aggregates are necessary for DNA fragmentation but not sufficient for cell death

      JOURNAL OF NEUROSCIENCE RESEARCH
    79. McGowan, DP; van Roon-Mom, W; Holloway, H; Bates, GP; Mangiarini, L; Cooper, GJS; Faull, RLM; Snell, RG
      Amyloid-like inclusions in Huntington's disease

      NEUROSCIENCE
    80. Wellington, CL; Leavitt, BR; Hayden, MR
      Huntington disease: new insights on the role of huntingtin cleavage

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    81. Tsuji, S
      Dentatorubral-pallidoluysian atrophy (DRPLA)

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    82. Evert, BO; Wullner, U; Klockgether, T
      Cell death in polyglutamine diseases

      CELL AND TISSUE RESEARCH
    83. Lesort, M; Tucholski, J; Miller, ML; Johnson, GVW
      Tissue transglutaminase: a possible role in neurodegenerative diseases

      PROGRESS IN NEUROBIOLOGY
    84. Morton, AJ; Lagan, MA; Skepper, JN; Dunnett, SB
      Progressive formation of inclusions in the striatum and hippocampus of mice transgenic for the human Huntington's disease mutation

      JOURNAL OF NEUROCYTOLOGY
    85. Kegel, KB; Kim, M; Sapp, E; McIntyre, C; Castano, JG; Aronin, N; DiFiglia, M
      Huntingtin expression stimulates endosomal-lysosomal activity, endosome tubulation, and autophagy

      JOURNAL OF NEUROSCIENCE
    86. 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
    87. 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
    88. Rigamonti, D; Bauer, JH; De-Fraja, C; Conti, L; Sipione, S; Sciorati, C; Clementi, E; Hackam, A; Hayden, MR; Li, Y; Cooper, JK; Ross, CA; Govoni, S; Vincenz, C; Cattaneo, E
      Wild-type Huntingtin protects from apoptosis upstream of caspase-3

      JOURNAL OF NEUROSCIENCE
    89. Senut, MC; Suhr, ST; Kaspar, B; Gage, FH
      Intraneuronal aggregate formation and cell death after viral expression ofexpanded polyglutamine tracts in the adult rat brain

      JOURNAL OF NEUROSCIENCE
    90. Yazawa, I
      Aberrant phosphorylation of dentatorubral-pallidoluysian atrophy (DRPLA) protein complex in brain tissue

      BIOCHEMICAL JOURNAL
    91. Chen, HY; Ishii, A; Wong, WK; Chen, LB; Lo, SH
      Molecular characterization of human tensin

      BIOCHEMICAL JOURNAL
    92. Rankin, J; Wyttenbach, A; Rubinsztein, DC
      Intracellular green fluorescent protein-polyalanine aggregates are associated with cell death

      BIOCHEMICAL JOURNAL
    93. Furlong, RA; Narain, Y; Rankin, J; Wyttenbach, A; Rubinsztein, DC
      alpha-synuclein overexpression promotes aggregation of mutant huntingtin

      BIOCHEMICAL JOURNAL
    94. Cha, JHJ
      Transcriptional dysregulation in Huntington's disease

      TRENDS IN NEUROSCIENCES
    95. Nijhawan, D; Honarpour, N; Wang, XD
      Apoptosis in neural development and disease

      ANNUAL REVIEW OF NEUROSCIENCE
    96. Zoghbi, HY; Orr, HT
      Glutamine repeats and neurodegeneration

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

      CELL
    98. Duyckaerts, C; Hauw, JJ
      Diagnostic controversies: Another view

      CORTICOBASAL DEGENERATION AND RELATED DISORDERS
    99. Mirabella, M; Silvestri, G; de Rosa, G; Di Giovanni, S; Di Muzio, A; Uncini, A; Tonali, P; Servidei, S
      GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophy

      NEUROLOGY
    100. Yuan, JY; Yankner, BA
      Apoptosis in the nervous system

      NATURE


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 02/06/20 alle ore 17:06:29