Sfoglia per Autore TARAMELLI, ROBERTO
beta-Like globin RNA sequences in hemoglobin Lepore disease
1979-01-01 Giglioni, B; Comi, P; Taramelli, Roberto; Pozzoli, M; Zanollo, A; Ottolenghi, S; Gianni, Am
Organization of alpha-globin genes in Hb Hasharon(alpha 47 asp replaced by his) carriers
1980-01-01 Giglioni, B; Comi, P; Taramelli, Roberto; Ottolenghi, S; Ciocca Vasino, Ma; Anè, C; Cappellini, Md; Gianni, Am
Prenatal diagnosis of hemoglobinopathies on the DNA of amniotic fluid fibroblasts
1981-01-01 Ottolenghi, S; Taramelli, Roberto; Giglioni, B; Comi, P; Gianni, Am
Molecularcomparison of delta beta-thalassemia and hereditary persistence of fetalhemoglobin DNAs: evidence of a regulatory area?
1982-01-01 Ottolenghi, S; Giglioni, B; Taramelli, Roberto; Comi, P; Mazza, U; Saglio, G; Camaschella, C; Izzo, P; Cao, A; Galanello, R; Gimferrer, E; Baiget, M; Gianni, Am
deltabeta-Thalassemia and HPFH.
1982-01-01 Ottolenghi, S; Giglioni, B; Taramelli, Roberto; Comi, P; Gianni, Am
A gene controlling fetal hemoglobin expression in adults is not linked to the non-alpha globin cluster
1983-01-01 : Gianni, Am; Bregni, M; Cappellini, Md; Fiorelli, G; Taramelli, Roberto; Giglioni, B; Comi, P; Ottolenghi, S.
Delta thalassemia: a non-deletion defect
1983-01-01 Taramelli, Roberto; Giglioni, B; Comi, P; Ottolenghi, S; Brancati, C; Tagarelli, A; Polli, E; Gianni, Am
The human beta-globin genes
1985-01-01 Taramelli, Roberto; Grosveld, F; Wright, S.
DNA sequences required forregulated expression of the human beta-globin gene.
1985-01-01 : Wright, S; Taramelli, Roberto; Rosenthal, A; Deboer, E; Antoniou, M; Kioussis, D; Wilson, F; Hurst, J; Bartram, C; Athanassiadou, A.
Gamma delta beta-thalassaemias 1 and 2 are the result of a 100 kbp deletion inthe human beta-globin cluster
1986-01-01 Taramelli, Roberto; Kioussis, D; Vanin, E; Bartram, K; Groffen, J; Hurst, J; Grosveld, Fg
Sardinian G gamma-HPFH: aT----C substitution in a conserved "octamer" sequence in the G gamma-globinpromoter.
1988-01-01 Ottolenghi, S; Nicolis, S; Taramelli, Roberto; Malgaretti, N; Mantovani, R; Comi, P; Giglioni, B; Longinotti, M; Dore, F; Oggiano, L.
A TaqI RFLP of the human plasminogen gene.
1989-01-01 Candiani, G; Cremonesi, L; Bruno, L; Tenan, M; Ferrari, M; Camerino, G; Taramelli, Roberto
The homozygous state of G toA--117A gamma hereditary persistence of fetal hemoglobin.
1989-01-01 Camaschella, C; Oggiano, L; Sampietro, M; Gottardi, E; Alfarano, A; Pistidda, P; Dore, F; Taramelli, Roberto; Ottolenghi, S; Longinotti, M.
Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele
1990-01-01 Taramelli, Roberto; Pontoglio, M; Candiani, G; Ottolenghi, S; Dieplinger, H; Catapano, A; Albers, J; Vergani, C; Mclean, J.
Nucleotide sequence of thecDNA for lecithin-cholesterol acyl transferase (LCAT) from the rat.
1990-01-01 Meroni, G; Malgaretti, N; Magnaghi, P; Taramelli, Roberto
A new constitutivelyactivating mutation of the Gs protein alpha subunit-gsp oncogene is found inhuman pituitary tumours
1990-01-01 Clementi, E; Malgaretti, N; Meldolesi, J; Taramelli, Roberto
Definition of the transcription initiation site of human plasminogengene in liver and non hepatic cell lines
1990-01-01 Malgaretti, N; Bruno, L; Pontoglio, M; Candiani, G; Meroni, G; Ottolenghi, S; Taramelli, Roberto
Functionalanalysis of the human lecithin cholesterol acyl transferase gene promoter.
1991-01-01 Meroni, G; Malgaretti, N; Pontoglio, M; Ottolenghi, S; Taramelli, Roberto
Identification of the 5' end ofthe gene encoding a human insulin-responsive glucose transporter
1993-01-01 Chiaramonte, R; Martini, R; Taramelli, Roberto; Comi, P.
Substitution of Leu for Pro-193in the insulin receptor in a patient with a genetic form of severe insulinresistance.
1993-01-01 Carrera, P; Cordera, R; Ferrari, M; Cremonesi, L; Taramelli, Roberto; Andraghetti, G; Carducci, C; Dozio, N; Pozza, G; Taylor, Si
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| beta-Like globin RNA sequences in hemoglobin Lepore disease | 1-gen-1979 | Giglioni, B; Comi, P; Taramelli, Roberto; Pozzoli, M; Zanollo, A; Ottolenghi, S; Gianni, Am | |
| Organization of alpha-globin genes in Hb Hasharon(alpha 47 asp replaced by his) carriers | 1-gen-1980 | Giglioni, B; Comi, P; Taramelli, Roberto; Ottolenghi, S; Ciocca Vasino, Ma; Anè, C; Cappellini, Md; Gianni, Am | |
| Prenatal diagnosis of hemoglobinopathies on the DNA of amniotic fluid fibroblasts | 1-gen-1981 | Ottolenghi, S; Taramelli, Roberto; Giglioni, B; Comi, P; Gianni, Am | |
| Molecularcomparison of delta beta-thalassemia and hereditary persistence of fetalhemoglobin DNAs: evidence of a regulatory area? | 1-gen-1982 | Ottolenghi, S; Giglioni, B; Taramelli, Roberto; Comi, P; Mazza, U; Saglio, G; Camaschella, C; Izzo, P; Cao, A; Galanello, R; Gimferrer, E; Baiget, M; Gianni, Am | |
| deltabeta-Thalassemia and HPFH. | 1-gen-1982 | Ottolenghi, S; Giglioni, B; Taramelli, Roberto; Comi, P; Gianni, Am | |
| A gene controlling fetal hemoglobin expression in adults is not linked to the non-alpha globin cluster | 1-gen-1983 | : Gianni, Am; Bregni, M; Cappellini, Md; Fiorelli, G; Taramelli, Roberto; Giglioni, B; Comi, P; Ottolenghi, S. | |
| Delta thalassemia: a non-deletion defect | 1-gen-1983 | Taramelli, Roberto; Giglioni, B; Comi, P; Ottolenghi, S; Brancati, C; Tagarelli, A; Polli, E; Gianni, Am | |
| The human beta-globin genes | 1-gen-1985 | Taramelli, Roberto; Grosveld, F; Wright, S. | |
| DNA sequences required forregulated expression of the human beta-globin gene. | 1-gen-1985 | : Wright, S; Taramelli, Roberto; Rosenthal, A; Deboer, E; Antoniou, M; Kioussis, D; Wilson, F; Hurst, J; Bartram, C; Athanassiadou, A. | |
| Gamma delta beta-thalassaemias 1 and 2 are the result of a 100 kbp deletion inthe human beta-globin cluster | 1-gen-1986 | Taramelli, Roberto; Kioussis, D; Vanin, E; Bartram, K; Groffen, J; Hurst, J; Grosveld, Fg | |
| Sardinian G gamma-HPFH: aT----C substitution in a conserved "octamer" sequence in the G gamma-globinpromoter. | 1-gen-1988 | Ottolenghi, S; Nicolis, S; Taramelli, Roberto; Malgaretti, N; Mantovani, R; Comi, P; Giglioni, B; Longinotti, M; Dore, F; Oggiano, L. | |
| A TaqI RFLP of the human plasminogen gene. | 1-gen-1989 | Candiani, G; Cremonesi, L; Bruno, L; Tenan, M; Ferrari, M; Camerino, G; Taramelli, Roberto | |
| The homozygous state of G toA--117A gamma hereditary persistence of fetal hemoglobin. | 1-gen-1989 | Camaschella, C; Oggiano, L; Sampietro, M; Gottardi, E; Alfarano, A; Pistidda, P; Dore, F; Taramelli, Roberto; Ottolenghi, S; Longinotti, M. | |
| Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele | 1-gen-1990 | Taramelli, Roberto; Pontoglio, M; Candiani, G; Ottolenghi, S; Dieplinger, H; Catapano, A; Albers, J; Vergani, C; Mclean, J. | |
| Nucleotide sequence of thecDNA for lecithin-cholesterol acyl transferase (LCAT) from the rat. | 1-gen-1990 | Meroni, G; Malgaretti, N; Magnaghi, P; Taramelli, Roberto | |
| A new constitutivelyactivating mutation of the Gs protein alpha subunit-gsp oncogene is found inhuman pituitary tumours | 1-gen-1990 | Clementi, E; Malgaretti, N; Meldolesi, J; Taramelli, Roberto | |
| Definition of the transcription initiation site of human plasminogengene in liver and non hepatic cell lines | 1-gen-1990 | Malgaretti, N; Bruno, L; Pontoglio, M; Candiani, G; Meroni, G; Ottolenghi, S; Taramelli, Roberto | |
| Functionalanalysis of the human lecithin cholesterol acyl transferase gene promoter. | 1-gen-1991 | Meroni, G; Malgaretti, N; Pontoglio, M; Ottolenghi, S; Taramelli, Roberto | |
| Identification of the 5' end ofthe gene encoding a human insulin-responsive glucose transporter | 1-gen-1993 | Chiaramonte, R; Martini, R; Taramelli, Roberto; Comi, P. | |
| Substitution of Leu for Pro-193in the insulin receptor in a patient with a genetic form of severe insulinresistance. | 1-gen-1993 | Carrera, P; Cordera, R; Ferrari, M; Cremonesi, L; Taramelli, Roberto; Andraghetti, G; Carducci, C; Dozio, N; Pozza, G; Taylor, Si |
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