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Titolo Data di pubblicazione Autore(i) File
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH 1-gen-1999 Berthelsen, J; KILSTRUP-NIELSEN, Charlotte; Blasi, F; Mavilio, F; Zappavigna, V.
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH. 1-gen-1999 Berthelsen, J.; KILSTRUP-NIELSEN, Charlotte; Blasi, F.; Mavilio, F.; Zappavigna, V.
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors 1-gen-2002 Fognani, C; KILSTRUP-NIELSEN, Charlotte; Berthelsen, J; Ferretti, E; Zappavigna, V; Blasi, F.
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome 1-gen-2002 Landsberger, N.; Bergo, A.; Carro, S.; KILSTRUP-NIELSEN, Charlotte; Badaracco, Gianfranco
Identification and characterization of proteins that interacting with MeCP2, could be involved in Rett Syndrome 1-gen-2002 Landsberger, Nicoletta; N., Bergo; Carro, S.; KILSTRUP-NIELSEN, Charlotte; Mengoni, M.; Badaracco, G.
DNA methylation and Rett syndrome 1-gen-2003 A., Bergo; KILSTRUP-NIELSEN, Charlotte; Mengoni, M.; Francois, S.; Bolognese, F.; Badaracco, Gianfranco
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties 1-gen-2003 Segalla, S; Rinaldi, L; KILSTRUP-NIELSEN, Charlotte; Badaracco, Gianfranco; Minucci, S; Pelicci, Pg; Landsberger, Nicoletta
Characterization of a novel MeCP2 interacting protein 1-gen-2003 Bergo, A.; Badaracco, G.; Mengoni, M.; KILSTRUP-NIELSEN, Charlotte; Landsberger, Nicoletta
PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain 1-gen-2003 KILSTRUP-NIELSEN, Charlotte; Alessio, M; Zappavigna, V.
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction 1-gen-2004 S., Carro; Bergo, Anna; M., Mengoni; A., Bachi; Badaracco, Gianfranco; KILSTRUP-NIELSEN, Charlotte; Landsberger, Nicoletta
CDKL5 belongs to the same molecular pathway of MeCP2 and is responsible for the early seizure variant of Rett Syndrome 1-gen-2005 Bertani, I; Azimonti, S; Mari, F; Bolognese, F; Colombo, E; Caselli, R; Scala, E; Longo, I; Pescucci, C; Ariani, F; Bergo, A; Hayek, G; Badaracco, G; Zapella, M; Brocolli, V; Renieri, A; KILSTRUP-NIELSEN, Charlotte; Landsberger, Nicoletta
Genetics and mechanisms of disease in Rett Syndrome 1-gen-2005 Mari, F; KILSTRUP-NIELSEN, Charlotte; Cambi, F; Speciale, C; Mencarelli, Ma; Renieri, A.
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 1-gen-2005 F., Mari; S., Azimonti; I., Bertani; F., Bolognese; E., Colombo; R., Caselli; E., Scala; I., Longo; S., Grosso; C., Pescucci; F., Ariani; G., Hayek; P., Balestri; Bergo, Anna; Badaracco, Gianfranco; M., Zappella; V., Broccoli; A., Renieri; KILSTRUP-NIELSEN, Charlotte; Landsberger, Nicoletta
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome 1-gen-2006 Rusconi, L.; Bertani, I.; Forlani, Greta; Bergo, A.; Conca, B.; Guarda, A.; Badaracco, G.; KILSTRUP-NIELSEN, Charlotte; Landsberger, N.
Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation 1-gen-2006 Bertani, I.; Rusconi, L.; Bolognese, F.; Forlani, Greta; Conca, B.; De Monte, L.; Badaracco, G.; Landsberger, N.; KILSTRUP-NIELSEN, Charlotte
Functional characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams 1-gen-2006 Bertani, I.; Rusconi, L.; Bolognese, F.; Forlani, Greta; Conca, B.; Badaracco, G.; Landsberger, N.; KILSTRUP-NIELSEN, Charlotte
Functional Characterization of CDKL5, a novel gene involved in the onset of Rett syndrome 1-gen-2006 Forlani, Greta; Rusconi, L.; Bertani, I.; Bergo, A.; Conca, B.; Guarda, A.; Badaracco, G.; KILSTRUP-NIELSEN, Charlotte; Landsberger, N.
Functional Characterization of CDKL5, a Novel Gene Involved in The Onset of Rett Syndrome and Infantile Spasms. 1-gen-2006 Bertani, ; Rusconi, Laura; F., Bolognese; Forlani, Greta; B., Conca; G., Badaracco; Landsberger, Nicoletta; KILSTRUP-NIELSEN, Charlotte
Functional characterization of CDKL5, a novel gene involved in the onset of Rett Syndrome 1-gen-2006 Rusconi, L.; Bertani, I.; Forlani, Greta; Bergo, A.; Conca, B.; Guarda, A.; Bolognese, F.; Giudici, L.; Badaracco, G.; KILSTRUP-NIELSEN, Charlotte; Landsberger, N.
Functional characterization of CDKL5, a novel gene involved in Rett syndrome and infantile spams associated with mental retardation 1-gen-2006 Forlani, Greta; Rusconi, L.; Bertani, I.; Bergo, A.; Conca, B.; Guarda, A.; Badaracco, G.; KILSTRUP-NIELSEN, Charlotte; Landsberger, N.
Mostrati risultati da 1 a 20 di 74
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