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La ricerca find articoli where soggetti phrase all words 'mutant mouse' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 551 riferimenti
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    1. Kamimura, E; Ueno, Y; Tanaka, S; Sawa, H; Yoshioka, M; Ueno, K; Inoue, T; Li, XB; Koyama, T; Ishikawa, R; Nagashima, K
      New rat model for attention deficit hyperactive disorder (ADHD)

      COMPARATIVE MEDICINE
    2. Black, JL; Krahn, LE; Jalal, SM
      Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome

      MOLECULAR PSYCHIATRY
    3. Oda, S; Hanai, A; Masaki, S; Yonezawa, S
      A new mouse model with cochleo-saccular type inner ear defects

      EXPERIMENTAL ANIMALS
    4. Stanek, J; de Courten-Myers, G; Spaulding, AG; Strub, W; Hopkin, RJ
      Case of complex craniofacial anomalies, bilateral nasal proboscides, palatal pituitary, upper limbs reduction, and amnion rupture sequence: Disorganization phenotype?

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    5. Cosentino, F; Barker, JE; Brand, MP; Heales, SJ; Werner, ER; Tippins, JR; West, N; Channon, KM; Volpe, M; Luscher, TF
      Reactive oxygen species mediate endothelium-dependent relaxations in tetrahydrobiopterin-deficient mice

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    6. Yan, CN; Matzuk, MM
      Transgenic models of ovarian failure

      JOURNAL OF THE SOCIETY FOR GYNECOLOGIC INVESTIGATION
    7. Peterfy, M; Phan, J; Xu, P; Reue, K
      Lipodystrophy in the fld mouse results from mutation of a new gene encoding a nuclear protein, lipin

      NATURE GENETICS
    8. Polleux, F; Dehay, C; Goffinet, A; Kennedy, H
      Pre- and post-mitotic events contribute to the progressive acquisition of area-specific connectional fate in the neocortex

      CEREBRAL CORTEX
    9. Pernas-Alonso, R; Perrone-Capano, C; Volpicelli, F; di Porzio, U
      Regionalized neurofilament accumulation and motoneuron degeneration are linked phenotypes in wobbler neuromuscular disease

      NEUROBIOLOGY OF DISEASE
    10. Yamashita, S; Mita, S; Arima, T; Maeda, Y; Kimura, E; Nishida, Y; Murakami, T; Okado, H; Uchino, M
      Bcl-2 expression by retrograde transport of adenoviral vectors with Cre-IoxP recombination system in motor neurons of mutant SOD1 transgenic mice

      GENE THERAPY
    11. Murdoch, JN; Doudney, K; Paternotte, C; Copp, AJ; Stanier, P
      Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification

      HUMAN MOLECULAR GENETICS
    12. Abe, H; Honma, S; Namihira, M; Masubuchi, S; Honma, K
      Behavioral rhythm splitting in the CS mouse is related to clock gene expression outside the suprachiasmatic nucleus

      EUROPEAN JOURNAL OF NEUROSCIENCE
    13. Sarna, J; Miranda, SRP; Schuchman, EH; Hawkes, R
      Patterned cerebellar Purkinje cell death in a transgenic mouse model of Niemann Pick type A/B disease

      EUROPEAN JOURNAL OF NEUROSCIENCE
    14. Ludwig, T; Fisher, P; Murty, V; Efstratiadis, A
      Development of mammary adenocarcinomas by tissue-specific knockout of Brca2 in mice

      ONCOGENE
    15. Niederreither, K; Vermot, J; Messaddeq, N; Schuhbaur, B; Chambon, P; Dolle, P
      Embryonic retinoic acid synthesis is essential for heart morphogenesis in the mouse

      DEVELOPMENT
    16. Mansouri, A; Pla, P; Larue, L; Gruss, P
      Pax3 acts cell autonomously in the neural tube and somites by controlling cell surface properties

      DEVELOPMENT
    17. Hornyak, TJ; Hayes, DJ; Chiu, LY; Ziff, EB
      Transcription factors in melanocyte development: distinct roles for Pax-3 and Mitf

      MECHANISMS OF DEVELOPMENT
    18. Kusumi, K; Dunwoodie, SL; Krumlauf, R
      Dynamic expression patterns of the pudgy/spondylocostal dysostosis gene Dll3 in the developing nervous system

      MECHANISMS OF DEVELOPMENT
    19. Boyle, MET; Berglund, EO; Murai, KK; Weber, L; Peles, E; Ranscht, B
      Contactin orchestrates assembly of the septate-like junctions at the paranode in myelinated peripheral nerve

      NEURON
    20. Boiko, T; Rasband, MN; Levinson, SR; Caldwell, JH; Mandel, G; Trimmer, JS; Matthews, G
      Compact myelin dictates the differential targeting of two sodium channel isoforms in the same axon

      NEURON
    21. Uschkureit, T; Sporkel, O; Bussow, H; Stoffel, W
      Rumpshaker-like proteolipid protein (PLP) ratio in a mouse model with unperturbed structural and functional integrity of the myelin sheath and axons in the central nervous system

      GLIA
    22. Feutz, AC; Pham-Dinh, D; Allinquant, B; Miehe, M; Ghandour, MS
      An immortalized jimpy oligodendrocyte cell line: Defects in cell cycle andcAMP pathway

      GLIA
    23. Ludwig, T; Fisher, P; Ganesan, S; Efstratiadis, A
      Tumorigenesis in mice carrying a truncating Brca1 mutation

      GENES & DEVELOPMENT
    24. Hartmann, N; Martrette, JM; Westphal, A
      Influence of the lurcher mutation on myosin heavy chain expression in skeletal and cardiac muscles

      JOURNAL OF CELLULAR BIOCHEMISTRY
    25. Konrad-Martin, D; Norton, SJ; Mascher, KE; Tempel, BL
      Effects of PMCA2 mutation on DPOAE amplitudes and latencies in deafwaddlermice

      HEARING RESEARCH
    26. Yamazoe, I; Takeuchi, Y; Matsushita, H; Kawano, H; Sawada, T
      Serotonergic heterotypic sprouting in the unilaterally dopamine-depleted mouse neostriatum

      DEVELOPMENTAL NEUROSCIENCE
    27. Sharp, AH; Black, JL; Dubel, SJ; Sundarraj, S; Shen, JP; Yunker, AMR; Copeland, TD; McEnery, MW
      Biochemical and anatomical evidence for specialized voltage-dependent calcium channel gamma isoform expression in the epileptic and ataxic mouse, stargazer

      NEUROSCIENCE
    28. Lopez-Bendito, G; Shigemoto, R; Lujan, R; Juiz, JM
      Developmental changes in the localisation of the mGluR1 alpha subtype of metabotropic glutamate receptors in purkinje cells

      NEUROSCIENCE
    29. Van Lieshout, EMM; Van der Heijden, I; Hendriks, WJAJ; Van der Zee, CEEM
      A decrease in size and number of basal forebrain cholinergic neurons is paralleled by diminished hippocampal cholinergic innervation in mice lacking leukocyte common antigen related protein tyrosine phosphatase activity

      NEUROSCIENCE
    30. Kearney, JA; Plummer, NW; Smith, MR; Kapur, J; Cummins, TR; Waxman, SG; Goldin, AL; Meisler, MH
      A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities

      NEUROSCIENCE
    31. Blondet, B; Ait-Ikhlef, A; Murawsky, M; Rieger, F
      Transient massive DNA fragmentation in nervous system during the early course of a murine neurodegenerative disease.

      NEUROSCIENCE LETTERS
    32. Zwingman, TA; Neumann, PE; Noebels, JL; Herrup, K
      Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a

      JOURNAL OF NEUROSCIENCE
    33. Doerre, G; Malicki, J
      A mutation of early photoreceptor development, mikre oko, reveals cell-cell interactions involved in the survival and differentiation of zebrafish photoreceptors

      JOURNAL OF NEUROSCIENCE
    34. Barclay, J; Balaguero, N; Mione, M; Ackerman, SL; Letts, VA; Brodbeck, J; Canti, C; Meir, A; Page, KM; Kusumi, K; Perez-Reyes, E; Lander, ES; Frankel, WN; Gardiner, RM; Dolphin, AC; Rees, M
      Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells

      JOURNAL OF NEUROSCIENCE
    35. Zine, A; Aubert, A; Qiu, JP; Therianos, S; Guillemot, F; Kageyama, R; de Ribaupierre, F
      Hes1 and Hes5 activities are required for the normal development of the hair cells in the mammalian inner ear

      JOURNAL OF NEUROSCIENCE
    36. Wang, YS; Huso, D; Cahill, H; Ryugo, D; Nathans, J
      Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene

      JOURNAL OF NEUROSCIENCE
    37. Maeda, K; Hara, R; Gillardon, F; Hossmann, KA
      Aggravation of brain injury after transient focal ischemia in p53-deficient mice

      MOLECULAR BRAIN RESEARCH
    38. Ichikawa, H; Matsuo, S; Silos-Santiago, I; Jacquin, MF; Sugimoto, T
      Developmental dependency of Merkel endings on trks in the palate

      MOLECULAR BRAIN RESEARCH
    39. van der Staay, FJ; Steckler, T
      Behavioural phenotyping of mouse mutants

      BEHAVIOURAL BRAIN RESEARCH
    40. Miller, RJ
      Rocking and rolling with Ca2+ channels

      TRENDS IN NEUROSCIENCES
    41. Luscher, C; Frerking, M
      Restless AMPA receptors: implications for synaptic transmission and plasticity

      TRENDS IN NEUROSCIENCES
    42. Hadj-Sahraoui, N; Frederic, F; Zanjani, H; Delhaye-Bouchaud, N; Herrup, K; Mariani, J
      Progressive atrophy of cerebellar Purkinje cell dendrites during aging of the heterozygous staggerer mouse (Rora (+/sg))

      DEVELOPMENTAL BRAIN RESEARCH
    43. Cohen, MM
      Asymmetry: Molecular, biologic, embryopathic, and clinical perspectives

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Rice, DS; Curran, T
      Role of the Reelin signaling pathway in central nervous system development

      ANNUAL REVIEW OF NEUROSCIENCE
    45. Bennett, CL; Brunkow, ME; Ramsdell, F; O'Briant, KC; Zhu, Q; Fuleihan, RL; Shigeoka, AO; Ochs, HD; Chance, PF
      A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA -> AAUGAA) leads to the IPEX syndrome

      IMMUNOGENETICS
    46. Jones, MD; Williams, ME; Hess, EJ
      Abnormal presynaptic catecholamine regulation in a hyperactive SNAP-25-deficient mouse mutant

      PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
    47. Giese, KP; Peters, M; Vernon, J
      Modulation of excitability as a learning and memory mechanism: A moleculargenetic perspective

      PHYSIOLOGY & BEHAVIOR
    48. Giese, KP; Friedman, E; Telliez, JB; Fedorov, NB; Wines, M; Feig, LA; Silva, AJ
      Hippocampus-dependent learning and memory is impaired in mice lacking the Ras-guanine-nucleotide releasing factor 1 (Ras-GRF1)

      NEUROPHARMACOLOGY
    49. Clarke, G; Collins, RA; Leavitt, BR; Andrews, DF; Hayden, MR; Lumsden, CJ; McInnes, RR
      A one-hit model of cell death in inherited neuronal degenerations (vol 406, pg 195, 2000)

      NATURE
    50. Cohen, MP; Lautenslager, GT; Shearman, CW
      Increased urinary type IV collagen marks the development of glomerular pathology in diabetic d/db mice

      METABOLISM-CLINICAL AND EXPERIMENTAL
    51. Rousset, M; Cens, T; Restituito, S; Barrere, C; Black, JL; McEnery, MW; Charnet, P
      Functional roles of gamma(2), gamma(3) and gamma(4), three new Ca2+ channel subunits, in P/Q-type Ca2+ channel expressed in Xenopus oocytes

      JOURNAL OF PHYSIOLOGY-LONDON
    52. Levy-Labad, E; Wildin, RS
      Neonatal diabetes mellitus, enteropathy, thrombocytopenia, and endocrinopathy: Further evidence for an X-linked lethal syndrome

      JOURNAL OF PEDIATRICS
    53. Armstrong, C; Hawkes, R
      Selective purkinje cell ectopia in the cerebellum of the weaver mouse

      JOURNAL OF COMPARATIVE NEUROLOGY
    54. Armstrong, CL; Krueger-Naug, AMR; Currie, RW; Hawkes, R
      Expression of heat-shock protein Hsp25 in mouse Purkinje cells during development reveals novel features of cerebellar compartmentation

      JOURNAL OF COMPARATIVE NEUROLOGY
    55. Keshvara, L; Benhayon, D; Magdaleno, S; Curran, T
      Identification of reelin-induced sites of tyrosyl phosphorylation on disabled 1

      JOURNAL OF BIOLOGICAL CHEMISTRY
    56. Ren, JC; Stubbs, EB; Matthes, MT; Yasumura, D; Naash, MI; Lavail, MM; Peachey, NS
      Retinal degeneration in the nervous mutant mouse. IV. Inner retinal changes

      EXPERIMENTAL EYE RESEARCH
    57. Machado, AF; Zimmerman, EF; Hovland, DN; Weiss, R; Collins, MD
      Diabetic embryopathy in C57BL/6J mice - Altered fetal sex ratio and impactof the splotch allele

      DIABETES
    58. Mjaatvedt, CH; Nakaoka, T; Moreno-Rodriguez, R; Norris, RA; Kern, MJ; Eisenberg, CA; Turner, D; Markwald, RR
      The outflow tract of the heart is recruited from a novel heart-forming field

      DEVELOPMENTAL BIOLOGY
    59. Colnot, C; Sidhu, SS; Balmain, N; Poirier, F
      Uncoupling of chondrocyte death and vascular invasion in mouse galectin 3 null mutant bones

      DEVELOPMENTAL BIOLOGY
    60. Zeyda, T; Diehl, N; Paylor, R; Brennan, MB; Hochgeschwender, U
      Impairment in motor learning of somatostatin null mutant mice

      BRAIN RESEARCH
    61. Jones, HC; Carter, BJ; Depelteau, JS; Roman, M; Morel, L
      Chromosomal linkage associated with disease severity in the hydrocephalic H-Tx rat

      BEHAVIOR GENETICS
    62. Kwiecien, JM; Blanco, M; Fox, JG; Delaney, KH; Fletch, AL
      Neuropathology of Bouncer Long Evans, a novel dysmyelinated rat

      COMPARATIVE MEDICINE
    63. Rachel, RA; Murdoch, JN; Beermann, F; Copp, AJ; Mason, CA
      Retinal axon misrouting at the optic chiasm in mice with neural tube closure defects

      GENESIS
    64. Kostopoulos, GK
      Spike-and-wave discharges of absence seizures asa transformation of sleep spindles: the continuing development of a hypothesis

      CLINICAL NEUROPHYSIOLOGY
    65. Barr, CL; Feng, Y; Wigg, K; Bloom, S; Roberts, W; Malone, M; Schachar, R; Tannock, R; Kennedy, JL
      Identification of DNA variants in the SNAP-25 gene and linkage study of these polymorphisms and attention-deficit hyperactivity disorder

      MOLECULAR PSYCHIATRY
    66. Rogner, UC; Spyropoulos, DD; Le Novere, N; Changeux, JP; Avner, P
      Control of neurulation by the nucleosome assembly protein-1-like 2

      NATURE GENETICS
    67. Miles, AT; Hawksworth, GM; Beattie, JH; Rodilla, V
      Induction, regulation, degradation, and biological significance of mammalian metallothioneins

      CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY
    68. Lilp, IG; Bizikoeva, FZ; Revishin, AV; Korochkin, LI; Ivanov, VI; Poletaeva, II
      Behavioral, neurochemical, and brain morphology features of the 101/HY mice: A genetic model of some human hereditary diseases

      RUSSIAN JOURNAL OF GENETICS
    69. Yokoi, N; Shimizu, S; Ishibashi, K; Kitada, K; Iwama, H; Namae, M; Sugawara, M; Serikawa, T; Komeda, K
      Genetic mapping of the rat mutation creeping and evaluation of its positional candidate gene reelin

      MAMMALIAN GENOME
    70. Rother, KI; Accili, D
      Role of insulin receptors and IGF receptors in growth and development

      PEDIATRIC NEPHROLOGY
    71. Tong, CK; Cammer, W; Chesler, M
      Activity-dependent pH shifts in hippocampal slices from normal and carbonic anhydrase II-deficient mice

      GLIA
    72. Marcus, J; Dupree, JL; Popko, B
      Effects of galactolipid elimination on oligodendrocyte development and myelination

      GLIA
    73. Bennett, GD; Wlodarczyk, B; Calvin, JA; Craig, JC; Finnell, RH
      Valproic acid-induced alterations in growth and neurotrophic factor gene expression in murine embryos

      REPRODUCTIVE TOXICOLOGY
    74. Saito, Y; Adachi, K; Nezu, A; Deguchi, K; Kimura, S
      Topographical features of the sensory-evoked responses in malformed brains

      PEDIATRIC NEUROLOGY
    75. Armstrong, CL; Hawkes, R
      Pattern formation in the cerebellar cortex

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    76. Fuentealba, IC; Mullins, JE; Aburto, EM; Lau, JC; Cherian, GM
      Effect of age and sex on liver damage due to excess dietary copper in Fischer 344 rats

      JOURNAL OF TOXICOLOGY-CLINICAL TOXICOLOGY
    77. Maeda, T; Haeno, S; Oda, K; Mori, D; Ichinose, H; Nagatsu, T; Suzuki, T
      Studies on the genotype-phenotype relation in the hph-1 mouse mutant deficient in guanosine triphosphate (GTP) cyclohydrolase I activity

      BRAIN & DEVELOPMENT
    78. Alagramam, KN; Zahorsky-Reeves, J; Wright, CG; Pawlowski, KS; Erway, LC; Stubbs, L; Woychik, RP
      Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

      HEARING RESEARCH
    79. Scott, DA; Drury, S; Sundstrom, RA; Bishop, J; Swiderski, RE; Carmi, R; Ramesh, A; Elbedour, K; Srisailapathy, CRS; Keats, BJ; Sheffield, VC; Smith, RJH
      Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms ina novel gene, TMEM2

      GENE
    80. Ait-Ikhlef, A; Hantaz-Ambroise, D; Henderson, CE; Rieger, F
      Influence of factors secreted by wobbler astrocytes on neuronal and motoneuronal survival

      JOURNAL OF NEUROSCIENCE RESEARCH
    81. Konno, R; Ikeda, M; Yamaguchi, K; Ueda, Y; Niwa, A
      Nephrotoxicity of D-propargylglycine in mice

      ARCHIVES OF TOXICOLOGY
    82. Mori, Y; Wakamori, M; Oda, S; Fletcher, CF; Sekiguchi, N; Mori, E; Copeland, NG; Jenkins, NA; Matsushita, K; Matsuyama, Z; Imoto, K
      Reduced voltage sensitivity of activation of P/Q-type Ca2+ channels is associated with the ataxic mouse mutation rolling Nagoya (tg(rol))

      JOURNAL OF NEUROSCIENCE
    83. Kakizawa, S; Yamasaki, M; Watanabe, M; Kano, M
      Critical period for activity-dependent synapse elimination in developing cerebellum

      JOURNAL OF NEUROSCIENCE
    84. Jones, HC; Lopman, BA; Jones, TW; Carter, BJ; Depelteau, JS; Morel, L
      The expression of inherited hydrocephalus in H-Tx rats

      CHILDS NERVOUS SYSTEM
    85. Kojima, T; Nakajima, K; Mikoshiba, K
      The disabled 1 gene is disrupted by a replacement with L1 fragment in yotari mice

      MOLECULAR BRAIN RESEARCH
    86. Ikeda, K; Kobayashi, T; Kumanishi, T; Niki, H; Yano, R
      Involvement of G-protein-activated inwardly rectifying K+ (GIRK) channels in opioid-induced analgesia

      NEUROSCIENCE RESEARCH
    87. Jeong, YG; Hyun, BH; Hawkes, R
      Abnormalities in cerebellar Purkinje cells in the novel ataxic mutant mouse, pogo

      DEVELOPMENTAL BRAIN RESEARCH
    88. Marti, J; Wills, KV; Ghetti, B; Bayer, SA
      The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons

      DEVELOPMENTAL BRAIN RESEARCH
    89. Marti, J; Wills, KV; Ghetti, B; Bayer, SA
      The weaver gene continues to target late-generated dopaminergic neurons inmidbrain areas at P90

      DEVELOPMENTAL BRAIN RESEARCH
    90. Simon, A; Savy, C; Martin-Martinelli, E; Douhou, A; Frederic, F; Verney, C; Nguyen-Legros, J; Raisman-Vozari, R
      Paradoxical increase of tyrosine hydroxylase-immunoreactive retinopetal fibers in the weaver mouse

      DEVELOPMENTAL BRAIN RESEARCH
    91. George, TM; Speer, MC
      Genetic and embryological approaches to studies of neural tube defects: A critical review

      NEUROLOGICAL RESEARCH
    92. Wilson, MC
      Coloboma mouse mutant as an animal model of hyperkinesis and attention deficit hyperactivity disorder

      NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
    93. Nakagawa, T; Sheng, M
      Neurobiology - A stargazer foretells the way to the synapse

      SCIENCE
    94. Abel, RM
      The ontogeny of the peptide innervation of the human pylorus with special reference to understanding the aetiology and pathogenesis of infantile hypertrophic pyloric stenosis

      ANNALS OF THE ROYAL COLLEGE OF SURGEONS OF ENGLAND
    95. Chen, L; Chetkovich, DM; Petralia, RS; Sweeney, NT; Kawasaki, Y; Wenthold, RJ; Bredt, DS; Nicoll, RA
      Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms

      NATURE
    96. Clarke, G; Collins, RA; Leavitt, BR; Andrews, DF; Hayden, MR; Lumsden, CJ; McInnes, RR
      A one-hit model of cell death in inherited neuronal degenerations

      NATURE
    97. Millonig, JH; Millen, KJ; Hatten, ME
      The mouse Dreher gene Lmx1a controls formation of the roof plate in the vertebrate CNS

      NATURE
    98. Rasband, MN; Shrager, P
      Ion channel sequestration in central nervous system axons

      JOURNAL OF PHYSIOLOGY-LONDON
    99. Darmanto, W; Inouye, M; Takagishi, Y; Ogawa, M; Mikoshiba, K; Murata, Y
      Derangement of Purkinje cells in the rat cerebellum following prenatal exposure to X-irradiation: Decreased reelin level is a possible cause

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    100. Chu, T; Hullinger, H; Schilling, K; Oberdick, J
      Spatial and temporal changes in natural and target deprivation-induced cell death in the mouse inferior olive

      JOURNAL OF NEUROBIOLOGY


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Documento generato il 28/05/20 alle ore 18:32:41