Sfoglia per Autore
Construction of a YAC contig spanning human chromosome 6p22.
1996 Malaspina, P; Roetto, A; Trettel, Flavia; Jodice, C; Blasi, P; Frontali, M; Carella, M; Franco, B; Camaschella, C. AND NOVELLETTO A.
Ordering of 44 genetic markers in the 6p22 cytogenetic band
1996 Trettel, Flavia; P., Malaspina; P., Blasi; C., Jodice; A., Novelletto; G., Sabbadini; L., Veneziano; M., Frontali; L., Terrenato
Human succinic semialdehyde dehydrogenase molecula cloning and chromosomal localization.
1997 Trettel, Flavia; Malaspina, P; Jodice, C; Novelletto, A; SLAUGHTER C., A; CAUDLE D., L; HINSON D., D; Chambliss, K. L. AND GIBSON K. M.
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13
1997 L., Calandriello; L., Veneziano; Francia, Ada; G., Sabbadini; Colonnese, Claudio; E., Mantuano; C., Jodice; Trettel, Flavia; P., Viviani; Manfredi, Mario; M., Frontali
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
1997 C., Jodice; E., Mantuano; L., Veneziano; Trettel, Flavia; G., Sabbadini; L., Calandriello; Francia, Ada; Spadaro, Maria; Pierelli, Francesco; F., Salvi; R. A., Ophoff; R. R., Frants; M., Frontali
Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1
1998 Elide, Mantuano; Trettel, Flavia; Anne S., Olsen; Greg, Lennon; Marina, Frontali; Carla, Jodice
Two exon skipping mutations as molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)
1998 CHAMBLISS K., L; HINSON D., D; Trettel, Flavia; Malaspina, P; Novelletto, A; Jakobs, C. AND GIBSON K. M.
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformation of the polyglutamine segment.
1999 Persichetti, F; Trettel, Flavia; HUANG C., C; Fraefel, C; TIMMERS H., M; Gusella, J. AND MACDONALD E. M.
Dominant phenotypes produces by HD mutation in StHdh111 striatal cells.
2000 Trettel, Flavia; Rigamonti, D; HILDTICH MAGUIRE, P; WHEELER V., C; SHARP A., H; Persichetti, F; Cattaneo, E. AND MACDONALD M. E.
A fine physical mapping map of the CACNA1A gene region on 19p13.1-p13.2 chromosome. Gene 241: 45-50.
2000 Trettel, Flavia; Mantuano, E; Calabresi, V; Veneziano, L; Olsen, A; Georgescu, A; Gordon, L; Sabbadini, G; Frontali, M. AND JODICE C.
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles
2000 HILDTICH MAGUIRE, P; Trettel, Flavia; PASSANI L., A; Auerbach, A; Persichetti, F. AND MACDONALD M. E.
Complete loss of P/Q calcium channel activity caused by CACNA1A missense mutation carried by episodic ataxia type 2 patients.
2001 Guida, S; Trettel, Flavia; Pagnutti, S; Mantuano, E; Tottene, A; Veneziano, L; Fellin, T; Spadaro, Maria; STAUDERMAN K., A; WILLIAMS M., E; Volsen, S; OPHOFF R., A; FRANTS R., R; Jodice, C; Frontali, M. AND PIETROBON D.
TBX-3, the gene mutated in Ulnar-Mammary Syndrome, is a negative regulator of p19ARF and inhibits senescence.
2002 Brummelkamp, T. R.; Kortlever, R. M.; Lingbeek, M; Trettel, Flavia; Macdonald, M. E.; VAN LOHUIZEN, M. AND BERNARDS R.
Expression of human epileptic temporal lobe neurotransmitter receptors in Xenopus oocytes: An innovative approach to study epilepsy
2002 Palma, Eleonora; Esposito, Vincenzo; A. M., Mileo; G., Di Gennaro; P., Quarato; Giangaspero, Felice; Scoppetta, Ciriaco; Onorati, Paolo; Trettel, Flavia; R., Miledi; Eusebi, Fabrizio
Chemokine receptor CXCR2 regulates the functional properties of AMPA-type glutamate receptor GluR1 in HEK cells.
2002 Lax, P; Limatola, Cristina; Fucile, Sergio; Trettel, Flavia; Di Bartolomeo, S; Renzi, Massimiliano; Ragozzino, Davide Antonio; Eusebi, Fabrizio
Expression of functional neurotransmitter receptors in Xenopus oocytes after injection of human brain membranes
2002 R., Miledi; Eusebi, Fabrizio; A., Martinez Torres; Palma, Eleonora; Trettel, Flavia
Ligand-independent CXCR2 dimerization
2003 Trettel, Flavia; S., Di Bartolomeo; Lauro, Clotilde; Catalano, Myriam; M. T., Ciotti; Limatola, Cristina
Specific progressive cA mp reduction implicates energy deficit in presymptomatic Huntington’s disease knock-in mice
2003 Gines, S; SEONG I., S; Fossale, E; Ivanova, E; Trettel, Flavia; GUSELLA J., F; WHEELER V., C; Persichetti, F. AND MACDONALD M. E.
Microtransplantation of membranes from cultured cells to Xenopus oocytes: A method to study neurotransmitter receptors embedded in native lipids
2003 Palma, Eleonora; Trettel, Flavia; Fucile, Sergio; Renzi, Massimiliano; R., Miledi; Eusebi, Fabrizio
Expression of AMPA-type glutamate receptors in HEK cells and cerebellar granule neurons impairs CXCL2-mediated chemotaxis
2003 Limatola, Cristina; Sabrina Di, Bartolomeo; Trettel, Flavia; Lauro, Clotilde; Maria T., Ciotti; Delio, Mercanti; Loriana, Castellani; Eusebi, Fabrizio
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Construction of a YAC contig spanning human chromosome 6p22. | 1996 | Malaspina, P; Roetto, A; Trettel, Flavia; Jodice, C; Blasi, P; Frontali, M; Carella, M; Franco, B; Camaschella, C. AND NOVELLETTO A. | |
| Ordering of 44 genetic markers in the 6p22 cytogenetic band | 1996 | Trettel, Flavia; P., Malaspina; P., Blasi; C., Jodice; A., Novelletto; G., Sabbadini; L., Veneziano; M., Frontali; L., Terrenato | |
| Human succinic semialdehyde dehydrogenase molecula cloning and chromosomal localization. | 1997 | Trettel, Flavia; Malaspina, P; Jodice, C; Novelletto, A; SLAUGHTER C., A; CAUDLE D., L; HINSON D., D; Chambliss, K. L. AND GIBSON K. M. | |
| Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13 | 1997 | L., Calandriello; L., Veneziano; Francia, Ada; G., Sabbadini; Colonnese, Claudio; E., Mantuano; C., Jodice; Trettel, Flavia; P., Viviani; Manfredi, Mario; M., Frontali | |
| Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p | 1997 | C., Jodice; E., Mantuano; L., Veneziano; Trettel, Flavia; G., Sabbadini; L., Calandriello; Francia, Ada; Spadaro, Maria; Pierelli, Francesco; F., Salvi; R. A., Ophoff; R. R., Frants; M., Frontali | |
| Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1 | 1998 | Elide, Mantuano; Trettel, Flavia; Anne S., Olsen; Greg, Lennon; Marina, Frontali; Carla, Jodice | |
| Two exon skipping mutations as molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria) | 1998 | CHAMBLISS K., L; HINSON D., D; Trettel, Flavia; Malaspina, P; Novelletto, A; Jakobs, C. AND GIBSON K. M. | |
| Mutant huntingtin forms in vivo complexes with distinct context-dependent conformation of the polyglutamine segment. | 1999 | Persichetti, F; Trettel, Flavia; HUANG C., C; Fraefel, C; TIMMERS H., M; Gusella, J. AND MACDONALD E. M. | |
| Dominant phenotypes produces by HD mutation in StHdh111 striatal cells. | 2000 | Trettel, Flavia; Rigamonti, D; HILDTICH MAGUIRE, P; WHEELER V., C; SHARP A., H; Persichetti, F; Cattaneo, E. AND MACDONALD M. E. | |
| A fine physical mapping map of the CACNA1A gene region on 19p13.1-p13.2 chromosome. Gene 241: 45-50. | 2000 | Trettel, Flavia; Mantuano, E; Calabresi, V; Veneziano, L; Olsen, A; Georgescu, A; Gordon, L; Sabbadini, G; Frontali, M. AND JODICE C. | |
| Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles | 2000 | HILDTICH MAGUIRE, P; Trettel, Flavia; PASSANI L., A; Auerbach, A; Persichetti, F. AND MACDONALD M. E. | |
| Complete loss of P/Q calcium channel activity caused by CACNA1A missense mutation carried by episodic ataxia type 2 patients. | 2001 | Guida, S; Trettel, Flavia; Pagnutti, S; Mantuano, E; Tottene, A; Veneziano, L; Fellin, T; Spadaro, Maria; STAUDERMAN K., A; WILLIAMS M., E; Volsen, S; OPHOFF R., A; FRANTS R., R; Jodice, C; Frontali, M. AND PIETROBON D. | |
| TBX-3, the gene mutated in Ulnar-Mammary Syndrome, is a negative regulator of p19ARF and inhibits senescence. | 2002 | Brummelkamp, T. R.; Kortlever, R. M.; Lingbeek, M; Trettel, Flavia; Macdonald, M. E.; VAN LOHUIZEN, M. AND BERNARDS R. | |
| Expression of human epileptic temporal lobe neurotransmitter receptors in Xenopus oocytes: An innovative approach to study epilepsy | 2002 | Palma, Eleonora; Esposito, Vincenzo; A. M., Mileo; G., Di Gennaro; P., Quarato; Giangaspero, Felice; Scoppetta, Ciriaco; Onorati, Paolo; Trettel, Flavia; R., Miledi; Eusebi, Fabrizio | |
| Chemokine receptor CXCR2 regulates the functional properties of AMPA-type glutamate receptor GluR1 in HEK cells. | 2002 | Lax, P; Limatola, Cristina; Fucile, Sergio; Trettel, Flavia; Di Bartolomeo, S; Renzi, Massimiliano; Ragozzino, Davide Antonio; Eusebi, Fabrizio | |
| Expression of functional neurotransmitter receptors in Xenopus oocytes after injection of human brain membranes | 2002 | R., Miledi; Eusebi, Fabrizio; A., Martinez Torres; Palma, Eleonora; Trettel, Flavia | |
| Ligand-independent CXCR2 dimerization | 2003 | Trettel, Flavia; S., Di Bartolomeo; Lauro, Clotilde; Catalano, Myriam; M. T., Ciotti; Limatola, Cristina | |
| Specific progressive cA mp reduction implicates energy deficit in presymptomatic Huntington’s disease knock-in mice | 2003 | Gines, S; SEONG I., S; Fossale, E; Ivanova, E; Trettel, Flavia; GUSELLA J., F; WHEELER V., C; Persichetti, F. AND MACDONALD M. E. | |
| Microtransplantation of membranes from cultured cells to Xenopus oocytes: A method to study neurotransmitter receptors embedded in native lipids | 2003 | Palma, Eleonora; Trettel, Flavia; Fucile, Sergio; Renzi, Massimiliano; R., Miledi; Eusebi, Fabrizio | |
| Expression of AMPA-type glutamate receptors in HEK cells and cerebellar granule neurons impairs CXCL2-mediated chemotaxis | 2003 | Limatola, Cristina; Sabrina Di, Bartolomeo; Trettel, Flavia; Lauro, Clotilde; Maria T., Ciotti; Delio, Mercanti; Loriana, Castellani; Eusebi, Fabrizio |
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