Gennaro Musollino

发表

Sequence variations of the α‐globin genes: Scanning of high CG content genes with DHPLC and DG‐DGGE

V. Nigro, G. Lacerra, M. Fiorito, 2004, Human mutation.

Genotype-Phenotype Relationship of the δ-Thalassemia and Hb A2 Variants: Observation of 52 Genotypes

L. Mastrullo, M. Romeo, G. Lacerra, 2010, Hemoglobin.

South-Italy β°-thalassemia: a novel deletion not removing the γ-globin silencing element and with 3′ breakpoint in a hsRTVL-H element, associated with β°-thalassemia and high levels of HbF

G. Lacerra, Gennaro Musollino, C. Carestia, 2013, Haematologica.

Identification and molecular characterization of a novel 55‐kb deletion recurrent in southern Italy: the Italian Gγ(Aγδβ)°‐thalassemia

G. Piluso, L. Mastrullo, G. Lacerra, 2013, European journal of haematology.

mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)]

G. Lacerra, Gennaro Musollino, Romeo Prezioso, 2021, Biomedicines.

Role of nonsense-mediated decay and nonsense-associated altered splicing in the mRNA pattern of two new α-thalassemia mutants.

G. Lacerra, Gennaro Musollino, Maria Grazia Bisconte, 2017, The international journal of biochemistry & cell biology.

Molecular evidences of single mutational events followed by recurrent crossing-overs in the common delta-globin alleles in the Mediterranean area.

L. Mastrullo, M. Romeo, G. Lacerra, 2008, Gene.

Genotyping for known Mediterranean alpha-thalassemia point mutations using a multiplex amplification refractory mutation system.

G. Lacerra, Gennaro Musollino, C. Carestia, 2007, Haematologica.

Hb Foggia or α117(GH5)Phe → Ser : a new α2 globin allele affecting the αHb-AHSP interaction

P. Pucci, G. Lacerra, Gennaro Musollino, 2008, Haematologica.

Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy

G. Manco, G. Lacerra, Gennaro Musollino, 2020, Genes.

α-Thalassemia Associated with Hb Instability: A Tale of Two Features. The Case of Hb Rogliano or α1 Cod 108(G15)Thr→Asn and Hb Policoro or α2 Cod 124(H7)Ser→Pro.

A. Merlino, P. Pucci, G. Lacerra, 2015, PloS one.

Molecular mechanisms of a novel β-thalassaemia mutation due to the duplication of tetranucleotide ‘AGCT’ at the junction IVS-II/exon 3

G. Lacerra, Gennaro Musollino, C. Carestia, 2012, Annals of Hematology.

Functional analysis of three new alpha-thalassemia deletions involving MCS-R2 reveals the presence of an additional enhancer element in the 5’ boundary region

G. Piluso, V. Nigro, Serena Capasso, 2023, PLoS genetics.

Alpha-Thalassemia in Southern Italy: Characterization of Five New Deletions Removing the Alpha-Globin Gene Cluster

V. Nigro, G. Lacerra, Gennaro Musollino, 2023, International journal of molecular sciences.

HbA2-Partinico or δ(A2)Pro→Thr, a new genetic variation in the δ-globin gene in cis to the β+ thal IVS-I-110 G>A, and the heterogeneity of δ-globin alleles in double heterozygotes for β- and δ-globin gene defects

G. Lacerra, Gennaro Musollino, C. Gaudiano, 2010, Annals of Hematology.