Results: 1-23 |
Results: 23

Authors: Sacco, MG Cato, EM Ceruti, R Soldati, S Indraccolo, S Caniatti, M Scanziani, E Vezzoni, P
Citation: Mg. Sacco et al., Systemic gene therapy with anti-angiogenic factors inhibits spontaneous breast tumor growth and metastasis in MMTVneu transgenic mice, GENE THER, 8(1), 2001, pp. 67-70

Authors: Sobacchi, C Frattini, A Orchard, P Porras, O Tezcan, I Andolina, M Babul-Hirji, R Baric, I Canham, N Chitayat, D Dupuis-Girod, S Ellis, I Etzioni, A Fasth, A Fisher, A Gerritsen, B Gulino, V Horwitz, E Klamroth, V Lanino, E Mirolo, M Musio, A Matthijs, G Nonomaya, S Notarangelo, LD Ochs, HD Furga, AS Valiaho, J van Hove, JLK Vihinen, M Vujic, D Vezzoni, P Villa, A
Citation: C. Sobacchi et al., The mutational spectrum of human malignant autosomal recessive osteopetrosis, HUM MOL GEN, 10(17), 2001, pp. 1767-1773

Authors: Rodolfo, M Cato, EM Soldati, S Ceruti, R Asioli, M Scanziani, E Vezzoni, P Parmiani, G Sacco, MG
Citation: M. Rodolfo et al., Growth of human melanoma xenografts is suppressed by systemic angiostatin gene therapy, CANC GENE T, 8(7), 2001, pp. 491-496

Authors: Richter, BWM Mir, SS Eiben, LJ Lewis, J Reffey, SB Frattini, A Tian, L Frank, S Youle, RJ Nelson, DL Notarangelo, LD Vezzoni, P Fearnhead, HO Duckett, CS
Citation: Bwm. Richter et al., Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family, MOL CELL B, 21(13), 2001, pp. 4292-4301

Authors: Zucchi, I Bini, L Valaperta, R Ginestra, A Albani, D Susani, L Sanchez, JC Liberatori, S Magi, B Raggiaschi, R Hochstrasser, DF Pallini, V Vezzoni, P Dulbecco, R
Citation: I. Zucchi et al., Proteomic dissection of dome formation in a mammary cell line: Role of tropomyosin-5b and maspin, P NAS US, 98(10), 2001, pp. 5608-5613

Authors: Zecca, L Gallorini, M Schunemann, V Trautwein, AX Gerlach, M Riederer, P Vezzoni, P Tampellini, D
Citation: L. Zecca et al., Iron, neuromelanin and ferritin content in the substantia nigra of normal subjects at different ages: consequences for iron storage and neurodegenerative processes, J NEUROCHEM, 76(6), 2001, pp. 1766-1773

Authors: Villa, A Sobacchi, C Notarangelo, LD Bozzi, F Abinun, M Abrahamsen, TG Arkwright, PD Baniyash, M Brooks, EG Conley, ME Cortes, P Duse, M Fasth, A Filipovich, AM Infante, AJ Jones, A Mazzolari, E Muller, SM Pasic, S Rechavi, G Sacco, MG Santagata, S Schroeder, ML Seger, R Strina, D Ugazio, A Valiaho, J Vihinen, M Vogler, LB Ochs, H Vezzoni, P Friedrich, W Schwarz, K
Citation: A. Villa et al., V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations, BLOOD, 97(1), 2001, pp. 81-88

Authors: Frattini, A Orchard, PJ Sobacchi, C Giliani, S Abinun, M Mattsson, JP Keeling, DJ Andersson, AK Wallbrandt, P Zecca, L Notarangelo, LD Vezzoni, P Villa, A
Citation: A. Frattini et al., Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis, NAT GENET, 25(3), 2000, pp. 343-346

Authors: Albertazzi, E Zanchetta, D Barbier, P Faranda, S Frattini, A Vezzoni, P Procaccio, M Bettinelli, A Guzzi, F Parenti, M Chini, B
Citation: E. Albertazzi et al., Nephrogenic diabetes insipidus: Functional analysis of new AVPR2 mutationsidentified in Italian families, J AM S NEPH, 11(6), 2000, pp. 1033-1043

Authors: Sacco, MG Ungari, M Cato, EM Villa, A Strina, D Notarangelo, LD Jonkers, J Zecca, L Facchetti, F Vezzoni, P
Citation: Mg. Sacco et al., Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need fortight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndrome, CANC GENE T, 7(10), 2000, pp. 1299-1306

Authors: Hol, FA Schepens, MT van Beersum, SEC Redolfi, E Affer, M Vezzoni, P Hamel, BCJ Karnes, PS Mariman, ECM Zucchi, I
Citation: Fa. Hol et al., Identification and characterization of an Xq26-q27 duplication in a familywith spina bifida and panhypopituitarism suggests the involvement of two distinct genes, GENOMICS, 69(2), 2000, pp. 174-181

Authors: Gomez, CA Ptaszek, LM Villa, A Bozzi, F Sobacchi, C Brooks, EG Notarangelo, LD Spanopoulou, E Pan, ZQ Vezzoni, P Cortes, P Santagata, S
Citation: Ca. Gomez et al., Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficiencies, MOL CELL B, 20(15), 2000, pp. 5653-5664

Authors: Villa, A Bozzi, F Sobacchi, C Strina, D Fasth, A Pasic, S Notarangelo, LD Vezzoni, P
Citation: A. Villa et al., Prenatal diagnosis of RAG-deficient Omenn syndrome, PRENAT DIAG, 20(1), 2000, pp. 56-59

Authors: Santagata, S Villa, A Sobacchi, C Cortes, P Vezzoni, P
Citation: S. Santagata et al., The genetic and biochemical basis of Omenn syndrome, IMMUNOL REV, 178, 2000, pp. 64-74

Authors: Santagata, S Gomez, CA Sobacchi, C Bozzi, F Abinun, M Pasic, S Cortes, P Vezzoni, P Villa, A
Citation: S. Santagata et al., N-terminal RAG1 frameshift mutations in Omenn's syndrome: Internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domains, P NAS US, 97(26), 2000, pp. 14572-14577

Authors: Sacco, MG Caniatti, M Cato, EM Frattini, A Chiesa, G Ceruti, R Adorni, F Zecca, L Scanziani, E Vezzoni, P
Citation: Mg. Sacco et al., Liposome-delivered angiostatin strongly inhibits tumor growth and metastatization in a transgenic model of spontaneous breast cancer, CANCER RES, 60(10), 2000, pp. 2660-2665

Authors: Santagata, S Besmer, E Villa, A Bozzi, F Allingham, JS Sobacchi, C Haniford, DB Vezzoni, P Nussenzweig, MC Pan, ZQ Cortes, P
Citation: S. Santagata et al., The RAG1/RAG2 complex constitutes a 3 ' flap endonuclease: Implications for junctional diversity in V(D)J and transpositional recombination, MOL CELL, 4(6), 1999, pp. 935-947

Authors: Sacco, MG Benedetti, S Cato, EM Caniatti, M Ceruti, R Scanziani, E Pirola, B Villa, A Finocchiaro, G Vezzoni, P
Citation: Mg. Sacco et al., Retrovirus-mediated IL-4 gene therapy in spontaneous adenocarcinomas from MMTV-neu transgenic mice, GENE THER, 6(11), 1999, pp. 1893-1897

Authors: Zucchi, I Jones, J Affer, M Montagna, C Redolfi, E Susani, L Vezzoni, P Parvari, R Schlessinger, D Whyte, MP Mumm, S
Citation: I. Zucchi et al., Transcription map of Xq27: Candidates for several X-linked diseases, GENOMICS, 57(2), 1999, pp. 209-218

Authors: Zucchi, I Montagna, C Susani, L Montesano, R Affer, M Zanotti, S Redolfi, E Vezzoni, P Dulbecco, R
Citation: I. Zucchi et al., Genetic dissection of dome formation in a mammary cell line: Identification of two genes with opposing action, P NAS US, 96(24), 1999, pp. 13766-13770

Authors: Redolfi, E Pizzuti, A Di Bacco, A Susani, L Labella, T Affer, M Montagna, C Reinbold, R Mumm, S Vezzoni, P Zucchi, I
Citation: E. Redolfi et al., Mapping of the MYCL2 processed gene to Xq22-23 and identification of an additional L MYC-related sequence in Xq27.2, FEBS LETTER, 446(2-3), 1999, pp. 273-277

Authors: Signorini, S Imberti, L Pirovano, S Villa, A Facchetti, F Ungari, M Bozzi, F Albertini, A Ugazio, AG Vezzoni, P Notarangelo, LD
Citation: S. Signorini et al., Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome, BLOOD, 94(10), 1999, pp. 3468-3478

Authors: Redolfi, E Montagna, C Mumm, S Affer, M Susani, L Reinbold, R Hol, F Vezzoni, P Cimino, M Zucchi, I
Citation: E. Redolfi et al., Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampus, DNA CELL B, 17(12), 1998, pp. 1009-1016
Risultati: 1-23 |