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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 4, 2026
Late Endosome Transport by RILP-RAB7A Promotes Dendrite Arborization Independently of DegradationChan Choo Yap, Laura Digilio, Lloyd P McMahon, et al.
Chemical Communications (Cambridge, England)|March 17, 2011
Gadolinium-doped LipoCEST agents: a potential novel class of dual 1H-MRI probesEnzo Terreno, Cinzia Boffa, Valeria Menchise, et al.
Bioinformatics (Oxford, England)|July 13, 2004
A computational search for box C/D snoRNA genes in the Drosophila melanogaster genomeM C Accardo, E Giordano, S Riccardo, et al.
The Journal of Biological Chemistry|October 7, 2018
A dominant dendrite phenotype caused by the disease-associated G253D mutation in doublecortin (DCX) is not due to its endocytosis defectChan Choo Yap, Laura Digilio, Kamil Kruczek, et al.
Expert Review of Molecular Diagnostics|July 27, 2017
Congenital heart disease and genetic syndromes: new insights into molecular mechanismsGiulio Calcagni, Marta Unolt, Maria Cristina Digilio, et al.
The Journal of Pain|April 14, 2024
Impact of Shared Decision-Making on Opioid Prescribing Among Patients With Chronic Pain: A Retrospective Cohort StudyJohn C Licciardone, Braden Van Alfen, Michaela N Digilio, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2012
Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutationsAdriana Lo-Castro, Francesco Brancati, Maria Cristina Digilio, et al.
International Journal of Pediatric Otorhinolaryngology|December 12, 2017
Audiological findings in a de novo mutation of ANKRD11 gene in KBG syndrome: Report of a case and review of the literaturePier Marco Bianchi, Alessandra Bianchi, Maria Cristina Digilio, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|April 5, 2003
The role of segment 32-47 of cholecystokinin receptor type A in CCK8 binding: synthesis, nuclear magnetic resonance, circular dichroism and fluorescence studiesStefania De Luca, Raffaele Ragone, Chiara Bracco, et al.
Journal of Medical Genetics|March 1, 1994
Trisomy 8 syndrome owing to isodicentric 8p chromosomes: regional assignment of a presumptive gene involved in corpus callosum developmentM C Digilio, A Giannotti, G Floridia, et al.
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