CNR Institutional Research Information System

PREZIOSO, ROMEO

PREZIOSO, ROMEO  

Istituto di genetica e biofisica "Adriano Buzzati Traverso"- IGB - Sede Napoli  

Mostra records
Risultati 1 - 12 di 12 (tempo di esecuzione: 0.075 secondi).
Titolo Data di pubblicazione Autore(i) File
Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster 1-gen-2023 Cardiero, Giovanna; Musollino, Gennaro; Prezioso, Romeo; Nigro, Vincenzo; Lacerra, Giuseppina
Functional analysis of three new alpha-thalassemia deletions involving MCS-R2 reveals the presence of an additional enhancer element in the 5' boundary region 1-gen-2023 Serena Capasso; Giovanna Cardiero; Gennaro Musollino; Romeo Prezioso;Rosario Testa; Sabrina Dembech; Giulio Piluso; Vincenzo Nigro; F. Anna Digilio;Giuseppina LacerraID
mRNA analysis of frameshift mutations with stop codon in the last exon: The case of hemoglobins Campania [alpha1 cod95 (-C)] and Sciacca [alpha1 cod109 (-C)] 1-gen-2021 Cardiero G.; Musollino G.; Prezioso R.; Lacerra G.
Identification and molecular characterization of a novel 163 kb deletion the Italian (epsilongammadeltabeta)0-thalassemia. 1-gen-2016 Cardiero G; Prezioso R; Dembech S; Del Vecchio Blanco F; Scarano C; Lacerra G
alpha-Thalassemia Associated with Hb Instability: A Tale of Two Features. The Case of Hb Rogliano or alpha1 Cod 108(G15)Thr->Asn and Hb Policoro or alpha2 Cod 124(H7)Ser->Pro. 1-gen-2015 Bisconte Maria Grazia; Caldora Mercedes; Musollino Gennaro; Cardiero Giovanna; Flagiello Angela; La Porta Gaetana; Lagona Laura; Prezioso Romeo; Qualtieri Gabriele; Gaudiano Carlo; Medulla Emilia; Merlino Antonello; Pucci Piero; Lacerra Giuseppina
Identification and molecular characterization of a novel 55 kb deletion recurrent in Southern Italy: the Italian Ggamma(Agamma delta beta)°-thalassemia. 1-gen-2013 Lacerra, Giuseppina; Prezioso, Romeo; Musollino, Gennaro; Mastrullo, Lucia; Piluso, Giulio; DE ANGIOLETTI, Maria
South-Italy beta°-thalassemia: a novel deletion not removing the gamma-globin silencing element and with 3' breakpoint in a hsRTVL-H element, associated with beta°-thalassemia and high levels of HbF. 1-gen-2013 De Angioletti, M; Sabato, V; Musollino, G; Prezioso, R; Carestia, C; Lacerra, G
Molecular mechanisms of a novel beta-thalassaemia mutation due to the duplication of tetranucleotide 'AGCT' at the junction IVS-II/exon 3. 1-gen-2012 Musollino G; Mastrolonardo G; Prezioso R; Pagano L; Primignani P; Carestia C; Lacerra G.
Genotype-phenotype relationship of the delta-thalassemia and Hb A(2) variants: observation of 52 genotypes 1-gen-2010 Lacerra, G; Scarano, C; Lagona, Lf; Testa, R; Caruso, Dg; Medulla, E; Friscia, Mg; Mastrullo, L; Caldora, M; Prezioso, R; Gaudiano, C; Magnano, C; Romeo, Ma; Musollino, G; Di Noce, F; Carestia, C
HbA2-Partinico or delta(A2)Pro-->Thr, a new genetic variation in the delta-globin gene in cis to the beta(+) thal IVS-I-110 G>A, and the heterogeneity of delta-globin alleles in double heterozygotes for beta- and delta-globin gene defects. 1-gen-2010 Lacerra, G; Scarano, C; Musollino, G; Testa, R; Prezioso, R; Caruso, Dg; Lagona, Lf; Medulla, E; Friscia, Mg; Gaudiano, C; Carestia, C
Molecular evidences of single mutational events followed by recurrent crossing-overs in the common delta-globin alleles in the Mediterranean area 1-gen-2008 Lacerra, G; Musollino, G; Scarano, C; Lagona, Lf; Caruso, Dg; Testa, R; Prezioso, R; Di Noce, F; Medulla, E; Friscia, Mg; Mastrullo, L; Caldora, M; Nota, L; Gaudiano, C; Magnano, C; Ciaccio, C; Romeo, Ma; Carestia, C
Genotyping for known Mediterranean alpha-thalassemia point mutations using a multiplex amplification refractory mutation 1-gen-2007 Lacerra G.; Musollino G.; Di Noce F.; Prezioso R.; Carestia C.