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Human Molecular Genetics|December 12, 2018
Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter traffickingStefano Gabriele, Marco Canali, Carla Lintas, et al.Nutrients|April 3, 2021
The Role of Resveratrol in Liver Disease: A Comprehensive Review from In Vitro to Clinical TrialsCarmine Izzo, Monica Annunziata, Giuseppe Melara, et al.Molecular Syndromology|March 22, 2016
Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial FeaturesCarla Lintas, Chiara Picinelli, Ignazio S Piras, et al.Journal of Hepatology|June 1, 1988
Sex steroid modulation of the hepatic uptake of organic anions in ratM Persico, S Bellentani, P Marchegiano, et al.Oncology Reports|December 21, 2018
Chitosan-coated liposomes loaded with butyric acid demonstrate anticancer and anti-inflammatory activity in human hepatoma HepG2 cellsVincenzo Quagliariello, Mario Masarone, Emilia Armenia, et al.Prenatal Diagnosis|March 12, 2021
Cell-free DNA analysis of maternal blood in prenatal screening for chromosomal microdeletions and microduplications: a systematic reviewAlessandra Familiari, Simona Boito, Georgios Rembouskos, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 20, 2016
First trimester combined screening test in pregnancies derived from blastocyst transferPaolo Cavoretto, Chiara Dallagiovanna, Paola Viganò, et al.Journal of the American Geriatrics Society|September 22, 2018
Frailty and Delirium in Older Adults: A Systematic Review and Meta-Analysis of the LiteratureIlaria Persico, Matteo Cesari, Alessandro Morandi, et al.American Journal of Obstetrics and Gynecology|February 7, 2006
Uterine dehiscence in term pregnant patients with one previous cesarean delivery: growth factor immunoexpression and collagen content in the scarred lower uterine segmentFabrizio Pollio, Stefania Staibano, Massimo Mascolo, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 28, 2016
Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disordersChiara Picinelli, Carla Lintas, Ignazio Stefano Piras, et al.Pageof 120