Publications by authors named "Roberta Asci"

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Trasferrin receptor 2 gene regulation by microRNA 221 in SH-SY5Y cells treated with MPP⁺ as Parkinson's disease cellular model.
Roberta Asci, Fara Vallefuoco, Immacolata Andolfo, Mariasole Bruno, Luigia De Falco

Neurosci Res· November 2013

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Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.
Immacolata Andolfo, Seth L Alper, Jean Delaunay, Carla Auriemma, Roberta Russo, Roberta Asci

Am J Hematol· January 2013

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New understandings of the genetic basis of isolated idiopathic central hypogonadism.
Marco Bonomi, Domenico Vladimiro Libri, Fabiana Guizzardi, Elena Guarducci, Elisabetta Maiolo, Roberta Asci

Asian J Androl· January 2012

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

Blood Transfus· July 2011

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Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.
Roberta Russo, Maria Rosaria Esposito, Roberta Asci, Antonella Gambale, Silverio Perrotta

Am J Hematol· December 2010

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Regulation of divalent metal transporter 1 (DMT1) non-IRE isoform by the microRNA Let-7d in erythroid cells.
Immacolata Andolfo, Luigia De Falco, Roberta Asci, Roberta Russo, Simona Colucci

Haematologica· August 2010

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Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.
Achille Iolascon, Roberta Russo, Maria Rosaria Esposito, Roberta Asci, Carmelo Piscopo

Haematologica· May 2010

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A predicted functional single-nucleotide polymorphism of bone morphogenetic protein-4 gene affects mRNA expression and shows a significant association with cutaneous melanoma in Southern Italian population.
Mario Capasso, Fabrizio Ayala, Roberta Russo, Rosa Anna Avvisati, Roberta Asci

J Cancer Res Clin Oncol· December 2009

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Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: case report.
Antonio Agostino Sinisi, Roberta Asci, Giuseppe Bellastella, Luigi Maione, Dario Esposito

Hum Reprod· October 2008

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