LACERRA, GIUSEPPINA

LACERRA, GIUSEPPINA  

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

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Risultati 1 - 20 di 43 (tempo di esecuzione: 0.133 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
ADP-Ribosylation Post-Translational Modification: An Overview with a Focus on RNA Biology and New Pharmacological Perspectives 1-gen-2022 Manco, Giuseppe; Lacerra, Giuseppina; Porzio, Elena; Catara, Giuliana
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.
A failure mode and effect analysis (FMEA)-based approach for risk assessment of scientific processes in non-regulated research laboratories 1-gen-2020 Mascia, A; Cirafici, Am; Bongiovanni, A; Colotti, G; Lacerra, G; Di Carlo, M; Digilio, Fa; Liguori, Gl; Lanati, A; Kisslinger, A
Effect of mutations on mRNA and globin stability: The cases of Hb Bernalda/Groene hart and Hb Southern Italy 1-gen-2020 Cardiero, Giovanna; Musollino, Gennaro; Friscia Maria, Grazia; Testa, Rosario; Virruso, Lucrezia; Di Girgenti, Caterina; Caldora, Mercedes; Bisogno Rosario, Colella; Gaudiano, Carlo; Manco, Giuseppe; Lacerra, Giuseppina
WTAP and BIRC3 are involved in the posttranscriptional mechanisms that impact on the expression and activity of the human lactonase PON2 1-gen-2020 Carusone, TERESA MARIA; Cardiero, Giovanna; Cerreta, Mariangela; Mandrich, Luigi; Moran, Oscar; Porzio, Elena; Catara, Giuliana; Lacerra, Giuseppina; Manco, Giuseppe
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
Quality-based model for Life Sciences research guidelines 1-gen-2016 Digilio, F Anna; Lanati, Antonella; Bongiovanni, Antonella; Mascia, Anna; DI CARLO, Marta; Barra, Adriano; Cirafici, ANNA MARIA; Colotti, Gianni; Kisslinger, Annamaria; Lacerra, Giuseppina; Liguori Giovanna, L
The qPMO network: quality management tools to improve research efficiency, reproducibility, data management and dissemination 1-gen-2016 Bongiovanni, A; Liguori, Gl; Colotti, G; Cirafici, Am; Di Carlo, M; Digilio, Fa; Lacerra, G; Lanati, A; Mascia, A; Kisslinger, A
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
Applying Quality principles and Project Management methodologies in biomedical research: a public research network's case study. 1-gen-2015 Bongiovanni A.; Colotti G.; Liguori G.L.; Di Carlo M.; Digilio F.A.; Lacerra G.; Mascia A.; Cirafici A.M.; Barra A.; Lanati A.;Kisslinger A.
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
Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala > Pro and Hb Caserta alpha2 26 Ala > Thr) in a single HBA2 gene 1-gen-2009 Lacerra, G; Carestia, C
Hb Foggia or alpha 117(GH5)Phe -> Ser: a new alpha 2 globin allele affecting the alpha Hb-AHSP interaction 1-gen-2008 Lacerra G.; Scarano C.; Musollino G.; Flagiello A.; Pucci P.; 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.