Sfoglia per Autore
DiGeorge anomaly associated with 10p deletion.
1991-01-01 Monaco, G; Pignata, C; Rossi, Elena; Mascellaro, O; Cocozza, S; Ciccimarra, F.
Trisomy 10qter confirmed by in siyu hybridization
1993-01-01 Briscioli, V; Floridia, G; Rossi, Elena; Selicorni, A; Lalatta, F; Zuffardi, Orsetta
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.
1993-01-01 Rossi, Elena; Floridia, G; Casali, M; Danesino, Cesare; Chiumello, G; Bernardi, F; Magnani, I; Papi, L; Mura, M; Zuffardi, Orsetta
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1
1993-01-01 Rossi, Elena; Zarrilli, R; Zuffardi, Orsetta
D8S7 is consistently deleted in inverted duplication of the short arm of chromosome 8 ( inv dup 8p)
1993-01-01 Minelli, Antonella; G., Floridia; Rossi, Elena; M., Clementi; R., Tencon; L., Camurri; F., Bernardi
Molecular cloning of cDNA encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1
1994-01-01 Corti, O; Finochiaro, G; Rossi, Elena; Zuffardi, Orsetta; Di Donato, S.
order of six loci at 2q24-q31 and orientation of the HOXD locus
1994-01-01 Rossi, Elena; Faiella, A; Zeviani, M; Labeit, S; Floridia, G; Brunelli, S; Cammarata, M; Boncinelli, E; Zuffardi, Orsetta
Activation of the galectin-1 (L-14-I) gene from nonexpressing differentiated cells by fusion with undifferentiated and tumorigenic cells.
1994-01-01 Chiariotti, L; Benvenuto, G; Zarrilli, R; Rossi, Elena; Salvatore, P; Colantuoni, V; Bruni, C. B.
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2
1994-01-01 Pezzolo, A; Gimelli, G; Sposito, M; Giusani, U; Rossi, Elena; Zuffardi, Orsetta
Colocalization of (TTAGGG)n telomeric sequences and ribosomal genes in Atlantic eels.
1995-01-01 Salvadori, S; Deiana, Am; Coluccia, E; Floridia, G; Rossi, Elena; Zuffardi, Orsetta
Chromosomal localization of mitochondrial transcription factr A (TCF6), single-straned DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis
1995-01-01 Tiranti, V; Rossi, Elena; Ruiz carrillo, A; Rossi, G; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M.
The gene (NFE2L1) for human NRF-1, an activator involved in nuclear mitochondrial interaction, maps to 7q32
1995-01-01 Tiranti, V; Rossi, Elena; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M.
A novel mechnaism for the origin of supernumerary marker chromosomes
1996-01-01 Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein.
1996-01-01 Nigro, V; Piluso, G; Belsito, A; Politano, L; Puca, Aa; Papparella, S; Rossi, Elena; Viglietto, G; Esposito, Mg; Abbondanza, C; Medici, N; Molinari, Am; Nigro, G; Puca, G. A.
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
1996-01-01 Banfi, S.; Borsani, G.; Rossi, Elena; Bernard, L.; Guffanti, A.; Rubboli, F.; Marchitiello, A.; Giglio, S.; Coluccia, E.; Zollo, M.; Zuffardi, Orsetta; Ballabio, A.
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications
1996-01-01 Floridia, G.; Piantanida, M.; Minelli, Antonella; Dellavecchia, C.; Bonaglia, C.; Rossi, Elena; Gimelli, G.; Croci, G.; Franchi, F.; Gilgenkrantz, S.; Grammatico, P.; Dalpra', L.; Wood, S.; Danesino, Cesare; Zuffardi, Orsetta
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome
1997-01-01 Carrozzo, R.; Rossi, Elena; Christian, S. L.; Kittikamron, K.; Livieri, C.; Corrias, A.; Pucci, L.; Fois, A.; Simi, P.; Bosio, L.; Beccaria, L.; Zuffardi, Orsetta; Ledbetter, D. H.
A novel zinc finger-containing RNA-binding protein conserved from fruitflies to humans.
1997-01-01 Jackson, Fr; Banfi, S; Guffanti, A; Rossi, Elena
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(x)(pter-->q24::q21.32-->qter) and random X inactivation
1997-01-01 Carrozzo, R; Arrigo, G; Rossi, Elena; Bardoni, B; Cammarata, M; Gandullia, P; Gatti, R; Zuffardi, Orsetta
Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern.
1998-01-01 Canevini, Mp; Sgro, V; Zuffardi, Orsetta; Canger, R; Carrozzo, R; Rossi, Elena; Ledbetter, D; Minicucci, F; Vignoli, A; Piazzini, A; Guidolin, L; Saltarelli, A; DALLA BERNARDINA, B.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
DiGeorge anomaly associated with 10p deletion. | 1-gen-1991 | Monaco, G; Pignata, C; Rossi, Elena; Mascellaro, O; Cocozza, S; Ciccimarra, F. | |
Trisomy 10qter confirmed by in siyu hybridization | 1-gen-1993 | Briscioli, V; Floridia, G; Rossi, Elena; Selicorni, A; Lalatta, F; Zuffardi, Orsetta | |
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. | 1-gen-1993 | Rossi, Elena; Floridia, G; Casali, M; Danesino, Cesare; Chiumello, G; Bernardi, F; Magnani, I; Papi, L; Mura, M; Zuffardi, Orsetta | |
Regional assignment of the gene coding for a human Graves' disease autoantigen to 10q21.3-q22.1 | 1-gen-1993 | Rossi, Elena; Zarrilli, R; Zuffardi, Orsetta | |
D8S7 is consistently deleted in inverted duplication of the short arm of chromosome 8 ( inv dup 8p) | 1-gen-1993 | Minelli, Antonella; G., Floridia; Rossi, Elena; M., Clementi; R., Tencon; L., Camurri; F., Bernardi | |
Molecular cloning of cDNA encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1 | 1-gen-1994 | Corti, O; Finochiaro, G; Rossi, Elena; Zuffardi, Orsetta; Di Donato, S. | |
order of six loci at 2q24-q31 and orientation of the HOXD locus | 1-gen-1994 | Rossi, Elena; Faiella, A; Zeviani, M; Labeit, S; Floridia, G; Brunelli, S; Cammarata, M; Boncinelli, E; Zuffardi, Orsetta | |
Activation of the galectin-1 (L-14-I) gene from nonexpressing differentiated cells by fusion with undifferentiated and tumorigenic cells. | 1-gen-1994 | Chiariotti, L; Benvenuto, G; Zarrilli, R; Rossi, Elena; Salvatore, P; Colantuoni, V; Bruni, C. B. | |
Definitive assignment of the growth hormone-releasing factor gene to 20q11.2 | 1-gen-1994 | Pezzolo, A; Gimelli, G; Sposito, M; Giusani, U; Rossi, Elena; Zuffardi, Orsetta | |
Colocalization of (TTAGGG)n telomeric sequences and ribosomal genes in Atlantic eels. | 1-gen-1995 | Salvadori, S; Deiana, Am; Coluccia, E; Floridia, G; Rossi, Elena; Zuffardi, Orsetta | |
Chromosomal localization of mitochondrial transcription factr A (TCF6), single-straned DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis | 1-gen-1995 | Tiranti, V; Rossi, Elena; Ruiz carrillo, A; Rossi, G; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M. | |
The gene (NFE2L1) for human NRF-1, an activator involved in nuclear mitochondrial interaction, maps to 7q32 | 1-gen-1995 | Tiranti, V; Rossi, Elena; Rocchi, M; Di Donato, S; Zuffardi, Orsetta; Zeviani, M. | |
A novel mechnaism for the origin of supernumerary marker chromosomes | 1-gen-1996 | Maraschio, Paola; Tupler, R; Rossi, Elena; Barbierato, L; Uccellatore, F; Rocchi, M; Zuffardi, Orsetta; Fraccaro, Marco | |
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein. | 1-gen-1996 | Nigro, V; Piluso, G; Belsito, A; Politano, L; Puca, Aa; Papparella, S; Rossi, Elena; Viglietto, G; Esposito, Mg; Abbondanza, C; Medici, N; Molinari, Am; Nigro, G; Puca, G. A. | |
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching | 1-gen-1996 | Banfi, S.; Borsani, G.; Rossi, Elena; Bernard, L.; Guffanti, A.; Rubboli, F.; Marchitiello, A.; Giglio, S.; Coluccia, E.; Zollo, M.; Zuffardi, Orsetta; Ballabio, A. | |
The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications | 1-gen-1996 | Floridia, G.; Piantanida, M.; Minelli, Antonella; Dellavecchia, C.; Bonaglia, C.; Rossi, Elena; Gimelli, G.; Croci, G.; Franchi, F.; Gilgenkrantz, S.; Grammatico, P.; Dalpra', L.; Wood, S.; Danesino, Cesare; Zuffardi, Orsetta | |
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome | 1-gen-1997 | Carrozzo, R.; Rossi, Elena; Christian, S. L.; Kittikamron, K.; Livieri, C.; Corrias, A.; Pucci, L.; Fois, A.; Simi, P.; Bosio, L.; Beccaria, L.; Zuffardi, Orsetta; Ledbetter, D. H. | |
A novel zinc finger-containing RNA-binding protein conserved from fruitflies to humans. | 1-gen-1997 | Jackson, Fr; Banfi, S; Guffanti, A; Rossi, Elena | |
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(x)(pter-->q24::q21.32-->qter) and random X inactivation | 1-gen-1997 | Carrozzo, R; Arrigo, G; Rossi, Elena; Bardoni, B; Cammarata, M; Gandullia, P; Gatti, R; Zuffardi, Orsetta | |
Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern. | 1-gen-1998 | Canevini, Mp; Sgro, V; Zuffardi, Orsetta; Canger, R; Carrozzo, R; Rossi, Elena; Ledbetter, D; Minicucci, F; Vignoli, A; Piazzini, A; Guidolin, L; Saltarelli, A; DALLA BERNARDINA, B. |
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