Sfoglia per Autore
Expression cloning of a cDNA for the major Fanconi anemia gene, FAA
1996-01-01 LO TEN FOE, J; Rooimans, Ma; BOSNOYAN-COLLINS, L; Alon, N; Wijker, M; Parker, L; Lightfoot, J; Carreau, M; Callen, Df; Savoia, A.; Cheng, Nc; VAN BERKEL, Cgm; Strunk, Mhp; Gille, Jjp; Pals, G; Kruyt, Fae; Pronk, Jc; Arwert, F; Buchwald, M; Joenje, H
Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria (PNH) patients
1996-01-01 Savoia, A.; Ianzano, L; Lunardi, C; DE SANDRE, G; Carotenuto, M; Musto, P; Zelante, L.
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene
1996-01-01 Savoia, Anna; Piemontese, Mr; Savino, M; Zatterale, A; Pronk, J; Arwert, F; Joenje, H; Ramenghi, U; DAGNA BRICARELLI, F; Dallapiccola, B; Zelante, L.
Identification of the gene encoding the human mitochondrial RNA polymerase by cyberscreening of the expressed sequence tags database
1997-01-01 Tiranti, V; Savoia, A.; Forti, F; D' APOLITO, M; Centra, M; Rocchi, M; Zeviani, M
p53 activates Fanconi anemia group C gene expression
1997-01-01 Liebetrau, W; Budde, A; Savoia, A.; Grummt, F; Hoehn, H
The genomic organization of the Fanconi anaemia group A (FAA) gene
1997-01-01 Ianzanol, ; D'Apolito, M; Centra, M; Savino, M; Levran, O; Auerbach, Ad; CLETON-JANSEN, A-M; Doggett, N; Pronk, Jc; Tipping, Aj; Gibson, Ra; Mathew, Cg; Whitmore, Sa; Apostolou, S; Callen, Df; Zelante, L; Savoia, A.
Mutations of the Fanconi anemia group A gene (FAA) in Italian patients
1997-01-01 Savino, M; Ianzano, L; Strippoli, P; Ramenghi, U; Arslanian, A; Bagnara, Gp; Joenje, H; Zelante, L; Savoia, Anna
Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions
1998-01-01 Centra, M; Memeo, E; D'Apolito, M; Savino, M; Ianzano, L; Notarangelo, A; Liu, J; Doggett, Na; Zelante, L; Savoia, A.
Construction of a high-resolution physical and transcriptional map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer
1998-01-01 Whitmore, Sa; Crawford, J; Apostolou, S; Eyre, H; Baker, E; Lower, Km; Settsatian, C; Golup, S; Seshari, R; Gibson, Ra; Mathew, Cg; CLETON-JANSEN, A-M; Savoia, A.; Pronk, Jc; Auerbach, Ad; Doggett, Na; Sutherland, Gr; Callen, Df
. Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopaenia and absent radii (TAR)
1998-01-01 Strippoli, P; Savoia, A.; Iolascon, A; Tonelli, R; Savino, M; Giordano, P; D'Avanzo, M; Massolo, F; Locatelli, F; Borgna, C; DE MATTIA, D; Zelante, L; Paolucci, G; Bagnara, Gb
Molecular basis of Fanconi anemia
1998-01-01 D'Apolito, M; Zelante, L; Savoia, A.
Characterization and screening for mutations in breast cancer of the growth arrest specific 11 (GAS11) and C16orf3 genes at 16q24.3
1998-01-01 Whitmore, Sa; Settasatian, C; Crawford, J; Lower, Km; Cornelisse, Cj; Moerland, Ew; CLETON-JANSEN, A-M; Tipping, Aj; Matthew, Cj; Savino, M; Savoia, A.; Verlander, P; Auerbach, Ad; Vanberkel, C; Pronk, Jc; Doggett, Na; AND CALLEN, Df.
Nuclear localization of FANCC is required for functional activity
1999-01-01 Savoia, A.; GARCIA-HIGUERA, I; D\'Andrea, Ad
The PISSLRE gene: structure, exon skipping and exclusion as tumor suppressor in breast cancer
1999-01-01 Crawford, J; Ianzano, L; Savino, M; Whitmore, M; CLETON-JANSEN, Am; Settasatian, C; D'Apolito, ; M, ; Seshadri, R; Pronk, Jc; Auerbach, Ad; Verlander, Pc; Mathew, Cg; Tipping, Aj; Doggett, Na; Zelante, L; Callen, Df; Savoia, A.
Spontaneous functional correction of homozygous Fanconi anemia alleles reveals novel mechanistic basis for reverse mosaicism
1999-01-01 Waisfisz, Q; Morgan, Nv; Savino, M; DE WINTER, Jp; VAN BERKEL, Cgm; Ianzano, L; Gibson, Ra; Arwert, F; Savoia, A.; Mathew, Cg; Pronk, Jc; Joenje, H
Nevoid basal cell carcinoma syndrome. Clinical finding in 37 Italian affected individuals
1999-01-01 LO MUZIO, L; Nocini, Pf; Savoia, A.; Zelante, L; Consolo, U; Pannone, G; Bucci, P; Dolci, M; Favia, Gf; Solda, P; Procaccini, M
An autosomal dominant thrombocytopenia gene maps to chromosomal region 10p
1999-01-01 Savoia, Anna; DEL VECCHIO, M; Totaro, A; Perrotta, S; Amendola, G; Moretti, A; Zelante, L; Iolascon, A.
Familial dominnat thrombocytopenia: Clinical, Biological, and Molecular Studies
1999-01-01 Iolascon, A; Perrotta, S; Amendola, G; Altomare, A; Bagnara, Gp; DEL VECCHIO, Me; Savoia, A.
Heterogeneous stectrum of mutations in the Fanconi anaemia group A gene
1999-01-01 Wijker, M; Morgan, Nv; Herterich, S; VAN BERKEL, Cgm; Tipping, Aj; Schndler, D; Gille, Jjp; Pals, G; Savino, M; Altay, C; Mohan, Sp; Dokal, I; Cavenagh, J; Marsh, J; VAN WEEL, M; Ortega, Jj; Sculer, D; Samochatova, E; Karwacki, M; Berkassy, A; Abecasis, M; Ebell, W; Kwee, Ml; Gibson, Ra; Gluckman, E; Arwert, F; Joenje, H; Savoia, A.; Hoehn, H; Pronk, Jc; Mathew, Cg
Muatation analysis of the Fanconi A gene in breast tumours with loss of heterozygosity at 16q24.3
1999-01-01 CLETON-JANSEN, A-M; Moerland, Ew; Pronk, J; VAN BERKEL, C; Apostolou, S; Crawford, J; Savoia, A.; Auerbach, Ad; Mathew, Cg; Callen, Df; Cornelisse, Cj.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Expression cloning of a cDNA for the major Fanconi anemia gene, FAA | 1-gen-1996 | LO TEN FOE, J; Rooimans, Ma; BOSNOYAN-COLLINS, L; Alon, N; Wijker, M; Parker, L; Lightfoot, J; Carreau, M; Callen, Df; Savoia, A.; Cheng, Nc; VAN BERKEL, Cgm; Strunk, Mhp; Gille, Jjp; Pals, G; Kruyt, Fae; Pronk, Jc; Arwert, F; Buchwald, M; Joenje, H | |
Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria (PNH) patients | 1-gen-1996 | Savoia, A.; Ianzano, L; Lunardi, C; DE SANDRE, G; Carotenuto, M; Musto, P; Zelante, L. | |
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene | 1-gen-1996 | Savoia, Anna; Piemontese, Mr; Savino, M; Zatterale, A; Pronk, J; Arwert, F; Joenje, H; Ramenghi, U; DAGNA BRICARELLI, F; Dallapiccola, B; Zelante, L. | |
Identification of the gene encoding the human mitochondrial RNA polymerase by cyberscreening of the expressed sequence tags database | 1-gen-1997 | Tiranti, V; Savoia, A.; Forti, F; D' APOLITO, M; Centra, M; Rocchi, M; Zeviani, M | |
p53 activates Fanconi anemia group C gene expression | 1-gen-1997 | Liebetrau, W; Budde, A; Savoia, A.; Grummt, F; Hoehn, H | |
The genomic organization of the Fanconi anaemia group A (FAA) gene | 1-gen-1997 | Ianzanol, ; D'Apolito, M; Centra, M; Savino, M; Levran, O; Auerbach, Ad; CLETON-JANSEN, A-M; Doggett, N; Pronk, Jc; Tipping, Aj; Gibson, Ra; Mathew, Cg; Whitmore, Sa; Apostolou, S; Callen, Df; Zelante, L; Savoia, A. | |
Mutations of the Fanconi anemia group A gene (FAA) in Italian patients | 1-gen-1997 | Savino, M; Ianzano, L; Strippoli, P; Ramenghi, U; Arslanian, A; Bagnara, Gp; Joenje, H; Zelante, L; Savoia, Anna | |
Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions | 1-gen-1998 | Centra, M; Memeo, E; D'Apolito, M; Savino, M; Ianzano, L; Notarangelo, A; Liu, J; Doggett, Na; Zelante, L; Savoia, A. | |
Construction of a high-resolution physical and transcriptional map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer | 1-gen-1998 | Whitmore, Sa; Crawford, J; Apostolou, S; Eyre, H; Baker, E; Lower, Km; Settsatian, C; Golup, S; Seshari, R; Gibson, Ra; Mathew, Cg; CLETON-JANSEN, A-M; Savoia, A.; Pronk, Jc; Auerbach, Ad; Doggett, Na; Sutherland, Gr; Callen, Df | |
. Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopaenia and absent radii (TAR) | 1-gen-1998 | Strippoli, P; Savoia, A.; Iolascon, A; Tonelli, R; Savino, M; Giordano, P; D'Avanzo, M; Massolo, F; Locatelli, F; Borgna, C; DE MATTIA, D; Zelante, L; Paolucci, G; Bagnara, Gb | |
Molecular basis of Fanconi anemia | 1-gen-1998 | D'Apolito, M; Zelante, L; Savoia, A. | |
Characterization and screening for mutations in breast cancer of the growth arrest specific 11 (GAS11) and C16orf3 genes at 16q24.3 | 1-gen-1998 | Whitmore, Sa; Settasatian, C; Crawford, J; Lower, Km; Cornelisse, Cj; Moerland, Ew; CLETON-JANSEN, A-M; Tipping, Aj; Matthew, Cj; Savino, M; Savoia, A.; Verlander, P; Auerbach, Ad; Vanberkel, C; Pronk, Jc; Doggett, Na; AND CALLEN, Df. | |
Nuclear localization of FANCC is required for functional activity | 1-gen-1999 | Savoia, A.; GARCIA-HIGUERA, I; D\'Andrea, Ad | |
The PISSLRE gene: structure, exon skipping and exclusion as tumor suppressor in breast cancer | 1-gen-1999 | Crawford, J; Ianzano, L; Savino, M; Whitmore, M; CLETON-JANSEN, Am; Settasatian, C; D'Apolito, ; M, ; Seshadri, R; Pronk, Jc; Auerbach, Ad; Verlander, Pc; Mathew, Cg; Tipping, Aj; Doggett, Na; Zelante, L; Callen, Df; Savoia, A. | |
Spontaneous functional correction of homozygous Fanconi anemia alleles reveals novel mechanistic basis for reverse mosaicism | 1-gen-1999 | Waisfisz, Q; Morgan, Nv; Savino, M; DE WINTER, Jp; VAN BERKEL, Cgm; Ianzano, L; Gibson, Ra; Arwert, F; Savoia, A.; Mathew, Cg; Pronk, Jc; Joenje, H | |
Nevoid basal cell carcinoma syndrome. Clinical finding in 37 Italian affected individuals | 1-gen-1999 | LO MUZIO, L; Nocini, Pf; Savoia, A.; Zelante, L; Consolo, U; Pannone, G; Bucci, P; Dolci, M; Favia, Gf; Solda, P; Procaccini, M | |
An autosomal dominant thrombocytopenia gene maps to chromosomal region 10p | 1-gen-1999 | Savoia, Anna; DEL VECCHIO, M; Totaro, A; Perrotta, S; Amendola, G; Moretti, A; Zelante, L; Iolascon, A. | |
Familial dominnat thrombocytopenia: Clinical, Biological, and Molecular Studies | 1-gen-1999 | Iolascon, A; Perrotta, S; Amendola, G; Altomare, A; Bagnara, Gp; DEL VECCHIO, Me; Savoia, A. | |
Heterogeneous stectrum of mutations in the Fanconi anaemia group A gene | 1-gen-1999 | Wijker, M; Morgan, Nv; Herterich, S; VAN BERKEL, Cgm; Tipping, Aj; Schndler, D; Gille, Jjp; Pals, G; Savino, M; Altay, C; Mohan, Sp; Dokal, I; Cavenagh, J; Marsh, J; VAN WEEL, M; Ortega, Jj; Sculer, D; Samochatova, E; Karwacki, M; Berkassy, A; Abecasis, M; Ebell, W; Kwee, Ml; Gibson, Ra; Gluckman, E; Arwert, F; Joenje, H; Savoia, A.; Hoehn, H; Pronk, Jc; Mathew, Cg | |
Muatation analysis of the Fanconi A gene in breast tumours with loss of heterozygosity at 16q24.3 | 1-gen-1999 | CLETON-JANSEN, A-M; Moerland, Ew; Pronk, J; VAN BERKEL, C; Apostolou, S; Crawford, J; Savoia, A.; Auerbach, Ad; Mathew, Cg; Callen, Df; Cornelisse, Cj. |
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