Publications by authors named "Francesca Di Noce"

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Role of nonsense-mediated decay and nonsense-associated altered splicing in the mRNA pattern of two new α-thalassemia mutants.
Giovanna Cardiero, Clelia Scarano, Gennaro Musollino, Francesca Di Noce, Romeo Prezioso

Int J Biochem Cell Biol· October 2017

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Identification and characterization of the first SLC11A2 isoform 1a mutation causing a defect in splicing process and an hypomorphic allele expression of the SLC11A2 gene.
Luigia De Falco, Mariasole Bruno, Immacolata Andolfo, Beneitez Pastor David, Domenico Girelli, Francesca Di Noce

Br J Haematol· November 2012

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Congenital dyserythropoietic anaemias: new acquisitions.
Achille Iolascon, Roberta Russo, Maria Rosaria Esposito, Carmelo Piscopo, Roberta Asci, Francesca Di Noce

Blood Transfus· July 2011

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Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes.
Giuseppina Lacerra, Clelia Scarano, Laura F Lagona, Rosario Testa, Daniela G Caruso, Francesca Di Noce

Hemoglobin· March 2011

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Molecular evidences of single mutational events followed by recurrent crossing-overs in the common delta-globin alleles in the Mediterranean area.
Giuseppina Lacerra, Gennaro Musollino, Clelia Scarano, Laura F Lagona, Daniela G Caruso, Francesca Di Noce

Gene· February 2008

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Genotyping for known Mediterranean alpha-thalassemia point mutations using a multiplex amplification refractory mutation system.
Giuseppina Lacerra, Gennaro Musollino, Francesca Di Noce, Romeo Prezioso, Clementina Carestia

Haematologica· February 2007

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Sequence variations of the alpha-globin genes: scanning of high CG content genes with DHPLC and DG-DGGE.
Giuseppina Lacerra, Mirella Fiorito, Gennaro Musollino, Francesca Di Noce, Maria Esposito

Hum Mutat· October 2004

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Beta- and alpha-globin genotypes in Albanian patients affected by beta-globin gene disorders.
Maria De Angioletti, Giuseppina Lacerra, Enis Boletinio, Francesca Di Noce, Gennaro Musollino

Haematologica· September 2002

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