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Genomics|June 5, 2012
Genome-scale analysis of human mRNA 5' coding sequences based on expressed sequence tag (EST) databaseRaffaella Casadei, Allison Piovesan, Lorenza Vitale, et al.
Journal of Cellular Physiology|January 23, 2019
Human trisomy 21 fibroblasts rescue methotrexate toxic effect after treatment with 5-methyl-tetrahydrofolate and 5-formyl-tetrahydrofolateLorenza Vitale, Valentina Serpieri, Mattia Lauriola, et al.
Clinical Colorectal Cancer|January 21, 2018
LGALS4, CEACAM6, TSPAN8, and COL1A2: Blood Markers for Colorectal Cancer-Validation in a Cohort of Subjects With Positive Fecal Immunochemical Test ResultMaria Teresa Rodia, Rossella Solmi, Francesco Pasini, et al.
Plos One|October 1, 2011
Complexity of bidirectional transcription and alternative splicing at human RCAN3 locusFederica Facchin, Lorenza Vitale, Eva Bianconi, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 8, 2014
Improving mRNA 5' coding sequence determination in the mouse genomeAllison Piovesan, Maria Caracausi, Maria Chiara Pelleri, et al.
Gene|November 26, 2003
mRNA 5' region sequence incompleteness: a potential source of systematic errors in translation initiation codon assignment in human mRNAsRaffaella Casadei, Pierluigi Strippoli, Pietro D'Addabbo, et al.
Theoretical Biology & Medical Modelling|October 4, 2005
Uncertainty principle of genetic information in a living cellPierluigi Strippoli, Silvia Canaider, Francesco Noferini, et al.
Gene|March 7, 2006
Proteins encoded by human Down syndrome critical region gene 1-like 2 (DSCR1L2) mRNA and by a novel DSCR1L2 mRNA isoform interact with cardiac troponin I (TNNI3)Silvia Canaider, Federica Facchin, Cristiana Griffoni, et al.
Gene|June 7, 2005
Expression of T cell receptor alpha gene (TCRA) in human rhabdomyosarcoma and other musculo-skeletal sarcomasStefania Croci, Pierluigi Strippoli, Laura Bonsi, et al.
Human Molecular Genetics|April 24, 2016
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotypeMaria Chiara Pelleri, Elena Cicchini, Chiara Locatelli, et al.
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