Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Massimo Malcovati

Congenital Afibrinogenemia: First Identification of Splicing Mutations in the Fibrinogen Bbeta -Chain Gene Causing Activation of Cryptic Splice Sites

English

Related publications

Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?

Seminars in Thrombosis and Hemostasis

Cardiovascular Medicine

English

Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia

Seminars in Thrombosis and Hemostasis

Cardiovascular Medicine

English

Mechanism for Cryptic Splice Site Activation During Pre-mRNA Splicing.

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Congenital Afibrinogenemia

Annals of Saudi Medicine

English

Myosin Light-Chain 1/3 Gene Alternative Splicing: Cis Regulation Is Based Upon a Hierarchical Compatibility Between Splice Sites.

Molecular and Cellular Biology

Molecular Biology

English

New POMT2 Mutations Causing Congenital Muscular Dystrophy: Identification of a Founder Mutation

English

Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans

Biophysical Journal

English

Differential Regulation of Fibrinogen Γ Chain Splice Isoforms by Interleukin-6

Thrombosis Research

English

Identification of a Bidirectional Splicing Enhancer: Differential Involvement of SR Proteins in 5′ or 3′ Splice Site Activation

Molecular and Cellular Biology

Molecular Biology

English