Maria Luisa Tenchini

Missense mutations in the human β fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion

Stefano Duga, Rosanna Asselta, Elena Santagostino et al. · Blood · 2000 · 111 citations

Life Sciences, Genetics, Molecular Genetics +14

Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs

Rosanna Asselta, Stefano Duga, Silvia Spena et al. · Blood · 2001 · 78 citations · Full text

Life Sciences, Genetics, Molecular Biology +9

Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aα-chain gene

Silvia Spena, Stefano Duga, Rosanna Asselta et al. · European Journal of Human Genetics · 2004 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Frontal lobe epilepsy and mutations of the corticotropin‐releasing hormone gene

Romina Combi, Leda Dalprà, Luigi Ferini‐Strambi et al. · Annals of Neurology · 2005 · 65 citations

Life Sciences, Genetics, Molecular Genetics +17

Activation of NF-κB by IL-1β blocks IL-6-induced sustained STAT3 activation and STAT3-dependent gene expression of the human γ-fibrinogen gene

Ute Albrecht, Xiang‐Ping Yang, Rosanna Asselta et al. · Cellular Signalling · 2007 · 50 citations

Life Sciences, Immunology, Molecular Biology +13