Sfoglia per SSD
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
2024 Musolf, A. M.; Justice, C. M.; Erdogan-Yildirim, Z.; Goovaerts, S.; Cuellar, A.; Shaffer, J. R.; Marazita, M. L.; Claes, P.; Weinberg, S. M.; Li, J.; Senders, C.; Zwienenberg, M.; Simeonov, E.; Kaneva, R.; Roscioli, T.; Di Pietro, Lorena; Barba, Marta; Lattanzi, Wanda; Cunningham, M. L.; Romitti, P. A.; Boyadjiev, S. A.
The Wiskott-Aldrich syndrome (WAS) gene is expressed prior to the granulocyte-macrophage colony forming unit (GM-CFU) stage of hematopoietic differentiation
1993 Mantuano, E; Notarangelo, Ld; Candotti, F; Giliani, S; Lusardi, M; Parolini, Ornella; Porta, F; Ugazio, Ag
Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27ß
1992 De Saint Basile, G; Notarangelo, Ld; Bonaiti Pellie, C; Doussau, M; Parolini, Ornella; Craig, Iw; Ugazio, A; Griscelli, C; Fischer, A.
X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty
1994 Buzi, F; Notarangelo, L. D; Plebani, A; Duse, M; Parolini, Ornella; Monteleone, M; Ugazio, A. G.
X-linked agammaglobulinemia: new approaches to old questions based on the identification of the defective gene
1994 Conley, M E; Parolini, Ornella; Rohrer, J; Campana, D
X-linked Wiskott-Aldrich syndrome in a girl
1998 Parolini, Ornella; Ressmann, G; Haas, O. A; Pawlowsky, J; Gadner, H; Knapp, W; Holter, W.
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population
2017 Santonocito, Concetta; Scapaticci, Margherita; Nedovic, Bojan; Annicchiarico, Eleonora B; Guarino, Donatella; Leoncini, Emanuele; Boccia, Stefania; Gasbarrini, Antonio; Capoluongo, Ettore Domenico
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2024 | Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428 | Musolf, A. M.; Justice, C. M.; Erdogan-Yildirim, Z.; Goovaerts, S.; Cuellar, A.; Shaffer, J. R.; Marazita, M. L.; Claes, P.; Weinberg, S. M.; Li, J.; Senders, C.; Zwienenberg, M.; Simeonov, E.; Kaneva, R.; Roscioli, T.; Di Pietro, Lorena; Barba, Marta; Lattanzi, Wanda; Cunningham, M. L.; Romitti, P. A.; Boyadjiev, S. A. | |
| 1-gen-1993 | The Wiskott-Aldrich syndrome (WAS) gene is expressed prior to the granulocyte-macrophage colony forming unit (GM-CFU) stage of hematopoietic differentiation | Mantuano, E; Notarangelo, Ld; Candotti, F; Giliani, S; Lusardi, M; Parolini, Ornella; Porta, F; Ugazio, Ag | |
| 1-gen-1992 | Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27ß | De Saint Basile, G; Notarangelo, Ld; Bonaiti Pellie, C; Doussau, M; Parolini, Ornella; Craig, Iw; Ugazio, A; Griscelli, C; Fischer, A. | |
| 1-gen-1994 | X-linked agammaglobulinemia, growth hormone deficiency and delay of growth and puberty | Buzi, F; Notarangelo, L. D; Plebani, A; Duse, M; Parolini, Ornella; Monteleone, M; Ugazio, A. G. | |
| 1-gen-1994 | X-linked agammaglobulinemia: new approaches to old questions based on the identification of the defective gene | Conley, M E; Parolini, Ornella; Rohrer, J; Campana, D | |
| 1-gen-1998 | X-linked Wiskott-Aldrich syndrome in a girl | Parolini, Ornella; Ressmann, G; Haas, O. A; Pawlowsky, J; Gadner, H; Knapp, W; Holter, W. | |
| 1-gen-2017 | XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population | Santonocito, Concetta; Scapaticci, Margherita; Nedovic, Bojan; Annicchiarico, Eleonora B; Guarino, Donatella; Leoncini, Emanuele; Boccia, Stefania; Gasbarrini, Antonio; Capoluongo, Ettore Domenico |
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