Roberta Asci

Missense mutations in the ABCB6 transporter cause dominant familialpseudohyperkalemia

Immacolata Andolfo, Seth L. Alper, J. Delaunay et al. · American Journal of Hematology · 2012 · 82 citations · Full text

Missense Mutations, Mendelian Disorder, Genetic Disorder +13

Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in <i>SEC23B</i> gene

Roberta Russo, Maria Rosaria Esposito, Roberta Asci et al. · American Journal of Hematology · 2010 · 42 citations · Full text

Novel Variants, Cda Ii, Genetic Disorder +13

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 et al. · Journal of Cancer Research and Clinical Oncology · 2009 · 32 citations · Full text

Southern Italian Population, Significant Association, Genetics +12

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 et al. · Neuroscience Research · 2013 · 31 citations

Sh-sy5y Cells, Systems Biology, Synaptic Signaling +6