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Developmental Biology|January 15, 2008
Distribution of RNA binding protein MOEP19 in the oocyte cortex and early embryo indicates pre-patterning related to blastomere polarity and trophectoderm specificationJohn C Herr, Olga Chertihin, Laura Digilio, et al.
The Journal of Organic Chemistry|October 19, 2019
Lanthionine Peptides by <i>S</i>-Alkylation with Substituted Cyclic Sulfamidates Promoted by Activated Molecular Sieves: Effects of the Sulfamidate Structure on the YieldStefania De Luca, Giuseppe Digilio, Valentina Verdoliva, et al.
Annales De Genetique|January 1, 1992
Deletion 11q23-->qter (Jacobsen syndrome). Report of three new patientsM G Obregon, R Mingarelli, M C Digilio, et al.
Developmental Biology|June 29, 2005
Mouse SLLP1, a sperm lysozyme-like protein involved in sperm-egg binding and fertilizationMaría Belén Herrero, Arabinda Mandal, Laura C Digilio, et al.
Chemical Communications (Cambridge, England)|February 14, 2009
Targeting exofacial protein thiols with Gd(III) complexes. An efficient procedure for MRI cell labellingGiuseppe Digilio, Valeria Catanzaro, Franco Fedeli, et al.
Journal of Medicinal Chemistry|June 11, 2010
Exofacial protein thiols as a route for the internalization of Gd(III)-based complexes for magnetic resonance imaging cell labelingGiuseppe Digilio, Valeria Menchise, Eliana Gianolio, et al.
Congenital Heart Disease|February 6, 2018
Analysis of DICER1 in familial and sporadic cases of transposition of the great arteriesNelly Sabbaghian, Maria C Digilio, Gillian M Blue, et al.
Genes|November 27, 2021
SARS-CoV-2 and Pre-Tamponade Pericardial Effusion. Could Sotos Syndrome Be a Major Risk Factor?Barbara Citoni, Maria Cristina Digilio, Rossella Capolino, et al.
Autism Research : Official Journal of the International Society for Autism Research|December 14, 2020
Comparison of Adaptive Functioning in Children with Williams Beuren Syndrome and Autism Spectrum Disorder: A Cross-Syndrome StudyPaolo Alfieri, Francesco Scibelli, Maria C Digilio, et al.
Clinical Genetics|April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomaliesM C Digilio, A Angioni, M De Santis, et al.
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