Restoration of hemoglobin A synthesis in erythroid cells from peripheral blood of thalassemic patients G Lacerra, H Sierakowska, C Carestia, S Fucharoen, J Summerton, ...
Proceedings of the National Academy of Sciences 97 (17), 9591-9596, 2000
211 2000 β+ 45 G→ C: a novel silent β‐thalassaemia mutation, the first in the Kozak sequence M De Angioletti, G Lacerra, V Sabato, C Carestia
British journal of haematology 124 (2), 224-231, 2004
108 2004 Restoration of human β-globin gene expression in murine and human IVS2–654 thalassemic erythroid cells by free uptake of antisense oligonucleotides T Suwanmanee, H Sierakowska, G Lacerra, S Svasti, S Kirby, CE Walsh, ...
Molecular pharmacology 62 (3), 545-553, 2002
98 2002 High-level expression of hemoglobin A in human thalassemic erythroid progenitor cells following lentiviral vector delivery of an antisense snRNA MM Vacek, H Ma, F Gemignani, G Lacerra, T Kafri, R Kole
Blood, The Journal of the American Society of Hematology 101 (1), 104-111, 2003
65 2003 A failure mode and effect analysis (FMEA)-based approach for risk assessment of scientific processes in non-regulated research laboratories A Mascia, AM Cirafici, A Bongiovanni, G Colotti, G Lacerra, M Di Carlo, ...
Accreditation and Quality Assurance 25 (5), 311-321, 2020
62 2020 DNA Polymorphisms Associated with HB D-Los Angeles β121 (GH4) GLU→ GLN] in Southern Italy G Fioretti, M De Angioletti, L Paganol, G Lacerra, A Viola, C De Bonis, ...
Hemoglobin 17 (1), 9-17, 1993
46 1993 Genotyping for known Mediterranean α-thalassemia point mutations using a multiplex amplification refractory mutation system G Lacerra, G Musollino, F Di Noce, R Prezioso, C Carestia
Haematologica 92 (2), 254-255, 2007
40 2007 (Alpha) alpha 5.3: a novel alpha (+)-thalassemia deletion with the breakpoints in the alpha 2-globin gene and in close proximity to an Alu family repeat between the psi alpha 2 … G Lacerra, G Fioretti, M De Angioletti, L Pagano, E Guarino, C de Bonis, ...
40 1991 Epidemiology of the delta globin alleles in southern Italy shows complex molecular, genetic, and phenotypic features MD Angioletti, G Lacerra, C Gaudiano, G Mastrolonardo, L Pagano, ...
Human mutation 20 (5), 358-367, 2002
39 2002 Hemoglobin Neapolis, beta 126 (H4) Val----Gly: a novel beta-chain variant associated with a mild beta-thalassemia phenotype and displaying anomalous stability features L Pagano, G Lacerra, L Camardella, M De Angioletti, G Fioretti, ...
39 1991 Sequence variations of the α‐globin genes: Scanning of high CG content genes with DHPLC and DG‐DGGE G Lacerra, M Fiorito, G Musollino, FD Noce, M Esposito, V Nigro, ...
Human mutation 24 (4), 338-349, 2004
37 2004 Applying Quality and Project Management methodologies in biomedical research laboratories: a public research network’s case study A Bongiovanni, G Colotti, GL Liguori, M Di Carlo, FA Digilio, G Lacerra, ...
Accreditation and Quality Assurance 20 (3), 203-213, 2015
36 2015 Hb Foggia or α117 (GH5) Phe→ Ser: a new α2 globin allele affecting the αHb-AHSP interaction G Lacerra, C Scarano, G Musollino, A Flagiello, P Pucci, C Carestia
Haematologica 93 (1), 141-142, 2008
28 2008 Origin heterogeneity of Hb Lepore-Boston gene in Italy G Fioretti, M De Angioletti, F Masciangelo, G Lacerra, A Scarallo, ...
American journal of human genetics 50 (4), 781, 1992
27 1992 Genotype-Phenotype Relationship of the δ-Thalassemia and Hb A2 Variants: Observation of 52 Genotypes G Lacerra, C Scarano, LF Lagona, R Testa, DG Caruso, E Medulla, ...
Hemoglobin 34 (5), 407-423, 2010
24 2010 Quality-based model for Life Sciences research guidelines FA Digilio, A Lanati, A Bongiovanni, A Mascia, M Di Carlo, A Barra, ...
Accreditation and Quality Assurance 21 (3), 221-230, 2016
20 2016 WTAP and BIRC3 are involved in the posttranscriptional mechanisms that impact on the expression and activity of the human lactonase PON2 TM Carusone, G Cardiero, M Cerreta, L Mandrich, O Moran, E Porzio, ...
Cell Death & Disease 11 (5), 324, 2020
15 2020 Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2‐Globin Gene, Associated with a Mild α+ ‐Thalassemia Phenotype G Lacerra, R Testa, M De Angioletti, G Schilirò, C Carestia
Hemoglobin 27 (3), 149-159, 2003
15 2003 &': A novel a'-thalassemia deletion with the breakpoint in the az-globin gene and in close proximity to an Alu family repeat between the G Lacerra, G Fioretti, M De Angioletti, L Pagano, E Guarino, C de Bonis, ...
Blood 78, 2740, 1991
15 1991 Hb O-Arab [β121 (GH4) Glu→ Lys]: association with DNA polymorphisms of African ancestry in two Mediterranean families G Lacerra, G Fioretti, A Hani, D Duka, MD Angioletti, L Pagano, A Viola, ...
Hemoglobin 17 (6), 523-535, 1993
14 1993 