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La ricerca find articoli where soggetti phrase all words 'NUCLEAR INCLUSIONS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 77 riferimenti
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    1. Margolis, RL; Ross, CA
      Expansion explosion: new clues to the pathogenesis of repeat expansion neurodegenerative diseases

      TRENDS IN MOLECULAR MEDICINE
    2. 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
    3. 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
    4. 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
    5. Insabato, L; Di Vizio, D; Terracciano, LM; Pettinato, G; Staibano, S; Bifano, D; D'Agostino, L
      Primary Kaposi sarcoma of the bowel in a HIV-negative patient

      JOURNAL OF SURGICAL ONCOLOGY
    6. 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
    7. 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
    8. Reddy, SV; Kurihara, N; Menaa, C; Landucci, G; Forthal, D; Koop, BA; Windle, JJ; Roodman, GD
      Osteoclasts formed by measles virus-infected osteoclast precursors from hCD46 transgenic mice express characteristics of pagetic osteoclasts

      ENDOCRINOLOGY
    9. Hill, ME; Creed, GA; McMullan, TFW; Tyers, AG; Hilton-Jones, D; Robinson, DO; Hammans, SR
      Oculopharyngeal muscular dystrophy - Phenotypic and genotypic studies in aUK population

      BRAIN
    10. Yan, CZ; Ikezoe, K; Nonaka, I
      Apoptotic muscle fiber degeneration in distal myopathy with rimmed vacuoles

      ACTA NEUROPATHOLOGICA
    11. Ooi, CG; Walsh, CA; Gallagher, JA; Fraser, WD
      Absence of measles virus and canine distemper virus transcripts in long-term bone marrow cultures from patients with Paget's disease of bone

      BONE
    12. 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
    13. 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
    14. Nagao, Y; Ishiguro, H; Nukina, N
      DMSO and glycerol reduce bacterial death induced by expression of truncated N-terminal huntingtin with expanded polyglutamine tracts

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    15. Helfrich, MH; Hobson, RP; Grabowski, PS; Zurbriggen, A; Cosby, SL; Dickson, GR; Fraser, WD; Ooi, CG; Selby, PL; Crisp, AJ; Wallace, RGH; Kahn, S; Ralston, SH
      A negative search for a paramyxoviral etiology of Paget's disease of bone:Molecular, immunological, and ultrastructural studies in UK patients

      JOURNAL OF BONE AND MINERAL RESEARCH
    16. Birman, S
      Drosophila as a genetic model to study neurodegenerative diseases

      M S-MEDECINE SCIENCES
    17. Becher, MW; Kotzuk, JA; Davis, LE; Bear, DG
      Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A) binding protein 2

      ANNALS OF NEUROLOGY
    18. Morton, AJ; Leavens, W
      Mice transgenic for the human Huntington's disease mutation have reduced sensitivity to kainic acid toxicity

      BRAIN RESEARCH BULLETIN
    19. 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
    20. Resnik, KS; DiLeonardo, M; Maillet, M
      Histopathologic findings in cutaneous cytomegalovirus infection

      AMERICAN JOURNAL OF DERMATOPATHOLOGY
    21. Zoghbi, HY; Orr, HT
      Glutamine repeats and neurodegeneration

      ANNUAL REVIEW OF NEUROSCIENCE
    22. Crook, TW; Rogers, BB; McFarland, RD; Kroft, SH; Muretto, P; Hernandez, JA; Latimer, MJ; McKenna, RW
      Unusual bone marrow manifestations of parvovirus B19 infection in immunocompromised patients

      HUMAN PATHOLOGY
    23. Satyal, SH; Schmidt, E; Kitagawa, K; Sondheimer, N; Lindquist, S; Kramer, JM; Morimoto, RI
      Polyglutamine aggregates alter protein folding homeostasis in Caenorhabditis elegans

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    24. Vig, PJS; Subramony, SH; Qin, Z; McDaniel, DO; Fratkin, JD
      Relationship between ataxin-1 nuclear inclusions and Purkinje cell specific proteins in SCA-1 transgenic mice

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    25. Takahashi, J; Fukuda, T; Tanaka, J; Minamitani, M; Fujigasaki, H; Uchihara, T
      Neuronal intranuclear hyaline inclusion disease with polyglutamine-immunoreactive inclusions

      ACTA NEUROPATHOLOGICA
    26. Evert, BO; Wullner, U; Schulz, JB; Weller, M; Groscurth, P; Trottier, Y; Brice, A; Klockgether, T
      High level expression of expanded full-length ataxin-3 in vitro causes cell death and formation of intranuclear inclusions in neuronal cells

      HUMAN MOLECULAR GENETICS
    27. Davies, SW; Turmaine, M; Cozens, BA; Raza, AS; Mahal, A; Mangiarini, L; Bates, GP
      From neuronal inclusions to neurodegeneration: neuropathological investigation of a transgenic mouse model of Huntington's disease

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    28. Bonini, NM
      A genetic model for human polyglutamine-repeat disease in Drosophila melanogaster

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    29. Fischbeck, KH; Lieberman, A; Bailey, CK; Abel, A; Merry, DE
      Androgen receptor mutation in Kennedy's disease

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    30. Ordway, JM; Cearley, JA; Detloff, PJ
      CAG-polyglutamine-repeat mutations: independence from gene context

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    31. Singer, FR
      Update on the viral etiology of Paget's disease of bone

      JOURNAL OF BONE AND MINERAL RESEARCH
    32. Blumen, SC; Brais, B; Korczyn, AD; Medinsky, S; Chapman, J; Asherov, A; Nisipeanu, P; Codere, F; Bouchard, JP; Fardeau, M; Tome, FMS; Rouleau, GA
      Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease

      ANNALS OF NEUROLOGY
    33. Levine, MS; Klapstein, GJ; Koppel, A; Gruen, E; Cepeda, C; Vargas, ME; Jokel, ES; Carpenter, EM; Zanjani, H; Hurst, RS; Efstratiadis, A; Zeitlin, S; Chesselet, MF
      Enhanced sensitivity to N-methyl-D-aspartate receptor activation in transgenic and knockin mouse models of Huntington's disease

      JOURNAL OF NEUROSCIENCE RESEARCH
    34. Gutekunst, CA; Li, SH; Yi, H; Mulroy, JS; Kuemmerle, S; Jones, R; Rye, D; Ferrante, RJ; Hersch, SM; Li, XJ
      Nuclear and neuropil aggregates in Huntington's disease: Relationship to neuropathology

      JOURNAL OF NEUROSCIENCE
    35. Kim, M; Lee, HS; LaForet, G; McIntyre, C; Martin, EJ; Chang, P; Kim, TW; Williams, M; Reddy, PH; Tagle, D; Boyce, FM; Won, L; Heller, A; Aronin, N; DiFiglia, M
      Mutant huntingtin expression in clonal striatal cells: Dissociation of inclusion formation and neuronal survival by caspase inhibition

      JOURNAL OF NEUROSCIENCE
    36. Chai, YH; Koppenhafer, SL; Bonini, NM; Paulson, HL
      Analysis of the role of heat shock protein (Hsp) molecular chaperones in polyglutamine disease

      JOURNAL OF NEUROSCIENCE
    37. Lesemann, DE
      Virus specific cytological effects in infected plant cells

      PHYTON-ANNALES REI BOTANICAE
    38. Drachenberg, CB; Beskow, CO; Cangro, CB; Bourquin, PM; Simsir, A; Fink, J; Weir, MR; Klassen, DK; Bartlett, ST; Papadimitriou, JC
      Human polyoma virus in renal allograft biopsies: Morphological findings and correlation with urine cytology

      HUMAN PATHOLOGY
    39. Cooper, AJL; Sheu, KFR; Burke, JR; Strittmatter, WJ; Gentile, V; Peluso, G; Blass, JP
      Pathogenesis of inclusion bodies in (CAG)(n)/Q(n)-expansion diseases with special reference to the role of tissue transglutaminase and to selective vulnerability

      JOURNAL OF NEUROCHEMISTRY
    40. BORG K; AHLBERG G; ANVRET M; EDSTROM L
      WELANDER-DISTAL-MYOPATHY - AN OVERVIEW

      Neuromuscular disorders
    41. SIRIS ES
      PAGETS-DISEASE OF BONE

      Journal of bone and mineral research
    42. SEMINOMORA C; DALAKAS MC
      RIMMED VACUOLES WITH BETA-AMYLOID AND UBIQUITINATED FILAMENTOUS DEPOSITS IN THE MUSCLES OF PATIENTS WITH LONG-STANDING DENERVATION (POSTPOLIOMYELITIS MUSCULAR-ATROPHY) - SIMILARITIES WITH INCLUSION-BODY MYOSITIS

      Human pathology
    43. VOGEL H; KORNMAN M; LEDET SC; RAJAGOPALAN L; TABER L; MCCLAIN K
      CONGENITAL PARVOVIRUS INFECTION

      PEDIATRIC PATHOLOGY & LABORATORY MEDICINE
    44. ROWLAND LP; HIRANO M; DIMAURO S; SCHON EA
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY, OTHER OCULAR MYOPATHIES, AND PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA

      Neuromuscular disorders
    45. BOUCHARD JP; BRAIS B; BRUNET D; GOULD PV; ROULEAU GA
      RECENT STUDIES ON OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN QUEBEC

      Neuromuscular disorders
    46. BRUNET G; TOME FMS; EYMARD B; ROBERT JM
      GENEALOGICAL STUDY OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN FRANCE

      Neuromuscular disorders
    47. BLUMEN SC; NISIPEANU P; SADEH M; ASHEROV A; BLUMEN N; WIRGUIN Y; KHILKEVICH O; CARASSO RL; KORCZYN AD
      EPIDEMIOLOGY AND INHERITANCE OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY INISRAEL

      Neuromuscular disorders
    48. UYAMA E; NOHIRA O; TOME FMS; CHATEAU D; TOKUNAGA M; ANDO M; MAKI M; OKABE T; UCHINO M
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN JAPAN

      Neuromuscular disorders
    49. MEOLA G; SANSONE V; ROTONDO G; TOME FMS; BOUCHARD JP
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN ITALY

      Neuromuscular disorders
    50. PORSCHKE H; KRESS W; REICHMANN H; GOEBEL HH; GRIMM T
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN A NORTHERN GERMAN FAMILY LINKEDTO CHROMOSOME 14Q, AND PRESENTING CARNITINE DEFICIENCY

      Neuromuscular disorders
    51. TOME FMS; CHATEAU D; HELBLINGLECLERC A; FARDEAU M
      MORPHOLOGICAL-CHANGES IN MUSCLE-FIBERS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Neuromuscular disorders
    52. BRAIS B; BOUCHARD JP; GOSSELIN F; XIE YG; FARDEAU M; TOME FMS; ROULEAU GA
      USING THE FULL POWER OF LINKAGE ANALYSIS IN 11 FRENCH-CANADIAN FAMILIES TO FINE MAP THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY GENE

      Neuromuscular disorders
    53. ROSE MR; LANDON DN; PAPADIMITRIOU A; MORGANHUGHES JA
      A RAPIDLY PROGRESSIVE ADOLESCENT-ONSET OCULOPHARYNGEAL SOMATIC SYNDROME WITH RIMMED VACUOLES IN 2 SIBLINGS

      Annals of neurology
    54. NEETENS A; MARTIN JJ; BRAIS B; WEIN B; DREUW B; TIJSSEN CC; CEUTERICK C
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY (OPMD)

      Neuro-ophthalmology
    55. TIEGS RD
      PAGETS-DISEASE OF BONE - INDICATIONS FOR TREATMENT AND GOALS OF THERAPY

      Clinical therapeutics
    56. DESEZE J; PASQUIER F; RUCHOUX MM; HURTEVENT JF; PETIT H
      MITOCHONDRIAL ANOMALIES IN OCULO-PHARYNGE AL MUSCULAR-DYSTROPHY

      Revue neurologique
    57. FABBRI F
      ON THE OCCURRENCE OF INTRANUCLEAR PROTEINACEOUS INCLUSIONS IN PTERIDOPHYTA

      Caryologia
    58. CODY JD; SINGER FR; ROODMAN GD; OTTERUND B; LEWIS TB; LEPPERT M; LEACH RJ
      GENETIC-LINKAGE OF PAGET-DISEASE OF THE BONE TO CHROMOSOME 18Q

      American journal of human genetics
    59. ROODMAN GD
      PAGETS-DISEASE AND OSTEOCLAST BIOLOGY

      Bone
    60. SINGER FR
      PAGETS-DISEASE OF BONE - POSSIBLE VIRAL BASIS

      Trends in endocrinology and metabolism
    61. NUNES JFM; FONSECA I; SOARES J
      HELIOID INCLUSIONS IN DEDIFFERENTIATED ACINIC CELL-CARCINOMA OF THE PAROTID-GLAND

      Ultrastructural pathology
    62. BLUMEN SC; SADEH M; KORCZYN AD; ROUCHE A; NISIPEANU P; ASHEROV A; TOME FMS
      INTRANUCLEAR INCLUSIONS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY AMONG BUKHARA JEWS

      Neurology
    63. UYAMA E; NOHIRA O; CHATEAU D; TOKUNAGA M; UCHINO M; OKABE T; ANDO M; TOME FMS
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY 2 UNRELATED JAPANESE FAMILIES

      Neurology
    64. SALVESEN R; BRAUTASET NJ
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN NORWAY - SURVEY OF A LARGE NORWEGIAN FAMILY

      Acta neurologica Scandinavica
    65. ROODMAN GD
      OSTEOCLAST FUNCTION IN PAGETS-DISEASE AND MULTIPLE-MYELOMA

      Bone
    66. BRAIS B; XIE YG; SANSON M; MORGAN K; WEISSENBACH J; KORCZYN AD; BLUMEN SC; FARDEAU M; TOME FMS; BOUCHARD JP; ROULEAU GA
      THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY LOCUS MAPS TO THE REGION OF THE CARDIAC ALPHA-MYOSIN AND BETA-MYOSIN HEAVY-CHAIN GENES ON CHROMOSOME14Q11.2-Q13

      Human molecular genetics
    67. WEIDENHEIM KM; DICKSON DW
      INTRANUCLEAR INCLUSION-BODIES IN AN ELDERLY DEMENTED WOMAN - A FORM OF INTRANUCLEAR INCLUSION-BODY DISEASE

      Clinical neuropathology
    68. SCHRODER JM; KRABBE B; WEIS J
      OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - CLINICAL AND MORPHOLOGICAL FOLLOW-UP-STUDY REVEALS MITOCHONDRIAL ALTERATIONS AND UNIQUE NUCLEAR INCLUSIONS IN A SEVERE AUTOSOMAL RECESSIVE TYPE

      Neuropathology and applied neurobiology
    69. ABE S; OHNO T; PARK P; HIGAKI S; UNNO K; TATEISHI A
      VIRAL BEHAVIOR OF PARACRYSTALLINE INCLUSIONS IN OSTEOCLASTS OF PAGETS-DISEASE OF BONE

      Ultrastructural pathology
    70. CALABRESE LH; CHOU SM
      INCLUSION-BODY MYOSITIS

      Rheumatic diseases clinics of North America
    71. SINGER FR
      PAGETS-DISEASE OF BONE - CLASSICAL PATHOLOGY AND ELECTRON-MICROSCOPY

      Seminars in arthritis and rheumatism
    72. CHOU SM
      INCLUSION-BODY MYOSITIS

      Bailliere's clinical neurology
    73. LAFARGA M; BERCIANO MT; ANDRES MA
      PROTEIN-SYNTHESIS INHIBITION INDUCES PERICHROMATIN GRANULE ACCUMULATION AND INTRANUCLEAR RODLET FORMATION IN OSMOTICALLY STIMULATED SUPRAOPTIC NEURONS

      Anatomy and embryology
    74. MEE AP; SHARPE PT
      DOGS, DISTEMPER AND PAGETS-DISEASE

      BioEssays
    75. BIGAZZI M
      ULTRASTRUCTURAL AND CYTOCHEMICAL INVESTIGATIONS ON THE FUNCTIONAL-ROLE OF PROTEINACEOUS NUCLEAR INCLUSIONS (PNIS) IN CHLORENCHYMA PLANT-CELLS

      Biology of the cell
    76. ALBRECHT S; BILBAO JM
      UBIQUITIN EXPRESSION IN INCLUSION-BODY MYOSITIS - AN IMMUNOHISTOCHEMICAL STUDY

      Archives of pathology and laboratory medicine
    77. HARDIMAN O; HALPERIN JJ; FARRELL MA; SHAPIRO BE; WRAY SH; BROWN RH
      NEUROPATHIC FINDINGS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY - A REPORTOF 7 CASES AND A REVIEW OF THE LITERATURE

      Archives of neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 19:30:30