Sfoglia per Autore
The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH
1999-01-01 Berthelsen, J.; KILSTRUP-NIELSEN, Charlotte; Blasi, F.; Mavilio, F.; Zappavigna, V.
Identification and Characterization of proteins that, interacting with MeCP2, could be involved in Rett Syndrome
2002-01-01 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
2002-01-01 Landsberger, Nicoletta; N., Bergo; Carro, S.; KILSTRUP-NIELSEN, Charlotte; Mengoni, M.; Badaracco, G.
Characterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factors
2002-01-01 Fognani, C; KILSTRUP-NIELSEN, Charlotte; Berthelsen, J; Ferretti, E; Zappavigna, V; Blasi, F.
DNA methylation and Rett syndrome
2003-01-01 A., Bergo; KILSTRUP-NIELSEN, Charlotte; Mengoni, M.; Francois, S.; Bolognese, F.; Badaracco, Gianfranco
Characterization of a novel MeCP2 interacting protein
2003-01-01 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
2003-01-01 KILSTRUP-NIELSEN, Charlotte; Alessio, M; Zappavigna, V.
Retinoic acid receptor a fusion to PML affects its transcriptional and chromatin-remodeling properties
2003-01-01 Segalla, S; Rinaldi, L; KILSTRUP-NIELSEN, Charlotte; Badaracco, Gianfranco; Minucci, S; Pelicci, Pg; Landsberger, Nicoletta
A novel protein, Xenopus p20, influences the stability of MeCP2 through direct interaction
2004-01-01 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
2005-01-01 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
2005-01-01 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
2005-01-01 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 characterization of CDKL5, a novel gene involved in Rett Syndrome and infantile spams
2006-01-01 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 and Infantile Spasms.
2006-01-01 Bertani, ; Rusconi, Laura; F., Bolognese; Forlani, Greta; B., Conca; G., Badaracco; Landsberger, Nicoletta; KILSTRUP-NIELSEN, Charlotte
Functional characterizationof CDKL5, a novel gene involved in the onset of Rett Syndrome
2006-01-01 Rusconi, L.; Bertani, I.; Forlani, Greta; 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
2006-01-01 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
2006-01-01 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
2006-01-01 Forlani, Greta; Rusconi, L.; Bertani, I.; 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
2006-01-01 Bertani, I.; Rusconi, L.; Bolognese, F.; Forlani, Greta; Conca, B.; De Monte, L.; Badaracco, G.; Landsberger, N.; KILSTRUP-NIELSEN, Charlotte
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells
2007-01-01 Marchi, M; Guarda, A; Landsberger, Nicoletta; KILSTRUP-NIELSEN, Charlotte; Ratto, Gm; Costa, M.
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. | |
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. | |
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. | |
DNA methylation and Rett syndrome | 1-gen-2003 | A., Bergo; KILSTRUP-NIELSEN, Charlotte; Mengoni, M.; Francois, S.; Bolognese, F.; Badaracco, Gianfranco | |
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. | |
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 | |
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 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 and Infantile Spasms. | 1-gen-2006 | Bertani, ; Rusconi, Laura; F., Bolognese; Forlani, Greta; B., Conca; G., Badaracco; Landsberger, Nicoletta; KILSTRUP-NIELSEN, Charlotte | |
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 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. | |
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 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 | |
Spatio-temporal dynamics and localization of MeCP2 and pathological mutants in living cells | 1-gen-2007 | Marchi, M; Guarda, A; Landsberger, Nicoletta; KILSTRUP-NIELSEN, Charlotte; Ratto, Gm; Costa, M. |
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