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Results:
1-18
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Results: 18
Authors:
Botta, A
Tandoi, C
Fini, G
Calabrese, G
Dallapiccola, B
Novelli, G
Citation: A. Botta et al., Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L), GENE, 275(1), 2001, pp. 39-46
Authors:
Ratti, A
Amati, F
Bozzali, M
Conti, E
Sangiuolo, F
Berloco, M
Palumbo, G
Botta, A
Pizzuti, A
Novelli, G
Dallapiccola, B
Citation: A. Ratti et al., Cloning and molecular characterization of three Ubiquitin Fusion Degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster, CYTOG C GEN, 92(3-4), 2001, pp. 279-282
Authors:
Botta, A
Amati, F
Novelli, G
Citation: A. Botta et al., Causes of the phenotype-genotype dissociation in DiGeorge syndrome: clues from mouse models, TRENDS GEN, 17(10), 2001, pp. 551-554
Authors:
Tandoi, C
Botta, A
Fini, G
Sangiuolo, F
Novelli, G
Ricci, R
Zampino, G
Anichini, C
Dallapiccola, B
Citation: C. Tandoi et al., Exclusion of the elastin gene in the pathogenesis of Costello syndrome, AM J MED G, 98(3), 2001, pp. 286-287
Authors:
De Luca, A
Pasini, A
Amati, F
Botta, A
Spalletta, G
Alimenti, S
Caccamo, F
Conti, E
Trakalo, J
Macciardi, F
Dallapiccola, B
Novelli, G
Citation: A. De Luca et al., Association study of a promoter polymorphism of UFD1L gene with schizophrenia, AM J MED G, 105(6), 2001, pp. 529-533
Authors:
Pozzato, C
Botta, A
Melgara, C
Fiori, L
Gianni, ML
Riva, E
Citation: C. Pozzato et al., Sonographic findings in type I glycogen storage disease, J CLIN ULTR, 29(8), 2001, pp. 456-461
Authors:
Dellgren, G
Koirala, B
Sakopoulus, A
Botta, A
Joseph, J
Benson, L
McCrindle, B
Dipchand, A
Cardella, C
Lee, KJ
West, L
Poirier, N
Van Arsdell, GS
Williams, WG
Coles, JG
Citation: G. Dellgren et al., Pediatric heart transplantation: Improving results in high-risk patients, J THOR SURG, 121(4), 2001, pp. 782-791
Authors:
Fellay-Reynier, I
Orsiere, T
Sari-Minodier, I
Auquier, P
Zattara-Cannoni, H
Capodano, AM
Coze, C
De Meo, M
Bernard, JL
Botta, A
Citation: I. Fellay-reynier et al., Evaluation of micronucleated lymphocytes, constitutional karyotypes and anti-p53 antibodies in 21 children with various malignancies, MUT RES-GTE, 467(1), 2000, pp. 31-39
Authors:
Botta, A
Viovy, N
Ciais, P
Friedlingstein, P
Monfray, P
Citation: A. Botta et al., A global prognostic scheme of leaf onset using satellite data, GL CHANGE B, 6(7), 2000, pp. 709-725
Authors:
Botta, A
Lu, MJ
Zhen, X
Kemper, T
Roggendorf, M
Citation: A. Botta et al., Naturally occurring woodchuck hepatitis virus (WHV) deletion mutants in chronically WHV-infected woodchucks, VIROLOGY, 277(2), 2000, pp. 226-234
Authors:
Daffaud, F
Orsiere, T
Villani, P
Volot, F
Favre, R
Botta, A
Citation: F. Daffaud et al., Micronucleated lymphocyte rates from head-and-neck cancer patients, MUT RES-GTE, 439(2), 1999, pp. 259-266
Authors:
Digue, L
Orsiere, T
De Meo, M
Mattei, MG
Depetris, D
Duffaud, F
Favre, R
Botta, A
Citation: L. Digue et al., Evaluation of the genotoxic activity of paclitaxel by the in vitro micronucleus test in combination with fluorescent in situ hybridization of a DNA centromeric probe and the alkaline single cell gel electrophoresis technique(comet assay) in human T-lymphocytes, ENV MOL MUT, 34(4), 1999, pp. 269-278
Authors:
Botta, A
Sangiuolo, F
Calza, L
Giardino, L
Potenza, S
Novelli, G
Dallapiccola, B
Citation: A. Botta et al., Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome, GENOMICS, 62(3), 1999, pp. 525-528
Authors:
Pelissier-Alicot, AL
Leonetti, G
Champsaur, P
Allain, P
Mauras, Y
Botta, A
Citation: Al. Pelissier-alicot et al., Fatal poisoning due to intravasation after oral administration of barium sulfate for contrast radiography, FOREN SCI I, 106(2), 1999, pp. 109-113
Authors:
Lindsay, EA
Botta, A
Jurecic, V
Carattini-Rivera, S
Cheah, YC
Rosenblatt, HM
Bradley, A
Baldini, A
Citation: Ea. Lindsay et al., Congenital heart disease in mice deficient for the DiGeorge syndrome region, NATURE, 401(6751), 1999, pp. 379-383
Authors:
Botta, A
Novelli, G
Mari, A
Novelli, A
Sabani, M
Korenberg, J
Osborne, LR
Digilio, MC
Giannotti, A
Dallapiccola, B
Citation: A. Botta et al., Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes, J MED GENET, 36(6), 1999, pp. 478-480
Authors:
Capon, F
Novelli, G
Semprini, S
Clementi, M
Nudo, M
Vultaggio, P
Mazzanti, C
Gobello, T
Botta, A
Fabrizi, G
Dallapiccola, B
Citation: F. Capon et al., Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1, J INVES DER, 112(1), 1999, pp. 32-35
Authors:
Villani, P
Orsiere, T
Duffaud, F
Digue, L
Bouvenot, G
Botta, A
Citation: P. Villani et al., Genotoxic and clastogenic effects of doxorubicin, THERAPIE, 53(4), 1998, pp. 391-395
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1-18
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