9
results
for author:"Belloni E."
in Literature Citations
| Overexpression of sPRDM16 coupled with loss of p53 induces myeloid leukemias in mice. Shing D.C., Trubia M., Marchesi F., Radaelli E., Belloni E., Tapinassi C., Scanziani E., Mecucci C., Crescenzi B., Lahortiga I. et al. J. Clin. Invest. 117:3696-3707(2007) · Mapped (26) |
| A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene. Gorello P., La Starza R., Brandimarte L., Trisolini S.M., Pierini V., Crescenzi B., Limongi M.Z., Nanni M., Belloni E., Tapinassi C. et al. Leukemia 22:216-218(2008) · Mapped (3) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
| Involvement of the HLXB9 homeobox gene in Currarino syndrome. Belloni E., Martucciello G., Verderio D., Ponti E., Seri M., Jasonni V., Torre M., Ferrari M., Tsui L.-C., Scherer S.W. Am. J. Hum. Genet. 66:312-319(2000) · UniProtKB (1) |
| Mutations in the C-terminal domain of Sonic hedgehog cause holoprosencephaly. Roessler E., Belloni E., Gaudenz K., Vargas F., Scherer S.W., Tsui L.-C., Muenke M. Hum. Mol. Genet. 6:1847-1853(1997) · UniProtKB (1) |
| Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotype. Mackay M., Fantes J., Scherer S., Boyle S., West K., Tsui L.-C., Belloni E., Lutz E., van Heyningen V., Harmar A.J. |
| Mutations in the human Sonic hedgehog gene cause holoprosencephaly. Roessler E., Belloni E., Gaudenz K., Jay P., Berta P., Scherer S.W., Tsui L.-C., Muenke M. |
| Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly. Belloni E., Muenke M., Roessler E., Traverso G., Siegel-Bartelt J., Frumkin A., Mitchell H.F., Donis-Keller H., Helms C., Hing A.V. et al. Nat. Genet. 14:353-356(1996) · Mapped (2) |
| Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations. Brancolini V., Cremonesi L., Belloni E., Pappalardo E., Bordoni R., Seia M., Russo S., Padoan R., Giunta A., Ferrari M. Hum. Genet. 96:312-318(1995) · UniProtKB (1) |
