12 results for author:"Strina D." in Literature citations
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| RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations. Pangrazio A., Cassani B., Guerrini M.M., Crockett J.C., Marrella V., Zammataro L., Strina D., Schulz A., Schlack C., Kornak U. et al. J. Bone Miner. Res. 27:342-351(2012) · Mapped (6) |
| Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. Cassani B., Poliani P.L., Marrella V., Schena F., Sauer A.V., Ravanini M., Strina D., Busse C.E., Regenass S., Wardemann H. et al. J. Exp. Med. 207:1525-1540(2010) · Mapped (4) |
| V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. Villa A., Sobacchi C., Notarangelo L.D., Bozzi F., Abinun M., Abrahamsen T.G., Arkwright P.D., Baniyash M., Brooks E.G., Conley M.E. et al. Blood 97:81-88(2001) · UniProtKB (1) |
| Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need for tight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndrome. Sacco M.G., Ungari M., Cato E.M., Villa A., Strina D., Notarangelo L.D., Jonkers J., Zecca L., Facchetti F., Vezzoni P. Cancer Gene Ther. 7:1299-1306(2000) · Mapped (2) |
| Structural and functional basis for JAK3-deficient severe combined immunodeficiency. Candotti F., Oakes S.A., Johnston J.A., Giliani S., Schumacher R.F., Mella P., Fiorini M., Ugazio A.G., Badolato R., Notarangelo L.D. et al. Blood 90:3996-4003(1997) · UniProtKB (1) |
| The ZNF75 zinc finger gene subfamily: isolation and mapping of the four members in humans and great apes. Villa A., Strina D., Frattini A., Faranda S., Macchi P., Finelli P., Bozzi F., Susani L., Archidiacono N., Rocchi M. et al. Genomics 35:312-320(1996) · UniProtKB (6) |
| ZNF75: isolation of a cDNA clone of the KRAB zinc finger gene subfamily mapped in YACs 1 Mb telomeric of HPRT. Villa A., Zucchi I., Pilia G., Strina D., Susani L., Morali F., Patrosso C., Frattini A., Lucchini F., Repetto M. et al. Genomics 18:223-229(1993) · UniProtKB (1) |
| Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28. Frattini A., Faranda S., Redolfi E., Zucchi I., Villa A., Patrosso M.C., Strina D., Susani L., Vezzoni P. |
| X-linked thrombocytopenia and Wiskott-Aldrich syndrome are allelic diseases with mutations in the WASP gene. Villa A., Notarangelo L., Macchi P., Mantuano E., Cavagni G., Brugnoni D., Strina D., Patrosso M.C., Ramenghi U., Sacco M.G. et al. Nat. Genet. 9:414-417(1995) · UniProtKB (1) |
| Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry. Macchi P., Villa A., Strina D., Sacco M.G., Morali F., Brugnoni D., Giliani S., Mantuano E., Fasth A., Andersson B. et al. Am. J. Hum. Genet. 56:898-906(1995) · UniProtKB (1) |
| The genomic organization of the human transcription factor 3 (TFE3) gene. Macchi P., Notarangelo L., Giliani S., Strina D., Repetto M., Sacco M.G., Vezzoni P., Villa A. Genomics 28:491-494(1995) · Mapped (7) |
| Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26. Villa A., Patrosso C., Biunno I., Frattini A., Repetto M., Mostardini M., Evans G., Susani L., Strina D., Redolfi E. et al. Genomics 13:1231-1236(1992) · UniProtKB (1) |