Sfoglia per Autore
Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome
2005 Tabolacci, Elisabetta; Zollino, Marcella; Lecce, Rosetta; Sangiorgi, Eugenio; Gurrieri, Fiorella; Leuzzi, Vincenzo; M Opitz, John; Neri, Giovanni
Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments
2005 Tabolacci, Elisabetta; Pietrobono, Roberta; Moscato, Umberto; A Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni
Molecular dissection of the events leading to inactivation of the FMR1 gene
2005 Pietrobono, Roberta; Tabolacci, Elisabetta; Zalfa, Francesca; Zito, Ilaria; Terracciano, Alessandra; Moscato, Umberto; Bagni, Claudia; Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni
X-linked mental retardation (XLMR): from clinical conditions to cloned genes
2004 Chiurazzi, Pietro; Tabolacci, Elisabetta; Neri, Giovanni
Assisted reproductive technology and congenital overgrowth:some speculations on a case of Pallister-Killian syndrome
2004 Chiurazzi, Pietro; Bajer, Jolanta Alina; Tabolacci, Elisabetta; Pomponi, Maria Grazia; Lecce, Rosetta; Zollino, Marcella; Neri, Giovanni
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine
2002 Pietrobono, Roberta; Pomponi, Maria Grazia; Tabolacci, Elisabetta; Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni
L-acetylcarnitine treatment on fragile X patients hyperactive behaviour
2001 Calvani, M; D'Iddio, S; De Gaetano, A; Mariotti, Paolo; Mosconi, Luigi; Pomponi, Maria Grazia; Tabolacci, Elisabetta; Torrioli, Maria Giulia; Vernacotola, Silvia; Neri, Giovanni
Telomeric associations and chromosome instability in ataxia telangiectasia T cells characterized by TCL1 expression
2001 Petrinelli, P; Elli, R; Marcucci, L; Tabolacci, Elisabetta; Barbieri, C; Antonelli, A
| Data di pubblicazione | Titolo | Autore(i) | File |
|---|---|---|---|
| 1-gen-2005 | Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome | Tabolacci, Elisabetta; Zollino, Marcella; Lecce, Rosetta; Sangiorgi, Eugenio; Gurrieri, Fiorella; Leuzzi, Vincenzo; M Opitz, John; Neri, Giovanni | |
| 1-gen-2005 | Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments | Tabolacci, Elisabetta; Pietrobono, Roberta; Moscato, Umberto; A Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni | |
| 1-gen-2005 | Molecular dissection of the events leading to inactivation of the FMR1 gene | Pietrobono, Roberta; Tabolacci, Elisabetta; Zalfa, Francesca; Zito, Ilaria; Terracciano, Alessandra; Moscato, Umberto; Bagni, Claudia; Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni | |
| 1-gen-2004 | X-linked mental retardation (XLMR): from clinical conditions to cloned genes | Chiurazzi, Pietro; Tabolacci, Elisabetta; Neri, Giovanni | |
| 1-gen-2004 | Assisted reproductive technology and congenital overgrowth:some speculations on a case of Pallister-Killian syndrome | Chiurazzi, Pietro; Bajer, Jolanta Alina; Tabolacci, Elisabetta; Pomponi, Maria Grazia; Lecce, Rosetta; Zollino, Marcella; Neri, Giovanni | |
| 1-gen-2002 | Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine | Pietrobono, Roberta; Pomponi, Maria Grazia; Tabolacci, Elisabetta; Oostra, Ben; Chiurazzi, Pietro; Neri, Giovanni | |
| 1-gen-2001 | L-acetylcarnitine treatment on fragile X patients hyperactive behaviour | Calvani, M; D'Iddio, S; De Gaetano, A; Mariotti, Paolo; Mosconi, Luigi; Pomponi, Maria Grazia; Tabolacci, Elisabetta; Torrioli, Maria Giulia; Vernacotola, Silvia; Neri, Giovanni | |
| 1-gen-2001 | Telomeric associations and chromosome instability in ataxia telangiectasia T cells characterized by TCL1 expression | Petrinelli, P; Elli, R; Marcucci, L; Tabolacci, Elisabetta; Barbieri, C; Antonelli, A |
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