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Oncogene|April 1, 1993
Two alternative mRNAs coding for the angiogenic factor, placenta growth factor (PlGF), are transcribed from a single gene of chromosome 14D Maglione, V Guerriero, G Viglietto, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 21, 2021
Percutaneous fetoscopic spina bifida repair: effect on ambulation and need for postnatal cerebrospinal fluid diversion and bladder catheterizationD A Lapa, R H Chmait, Y Gielchinsky, et al.Viruses|October 29, 2025
A Novel Municipal-Level Approach to Uncover the Hidden Burden of Hepatitis C: A Replicable Model for National Elimination StrategiesPietro Torre, Silvana Mirella Aliberti, Tommaso Sarcina, et al.Reviews on Recent Clinical Trials|June 3, 2022
Alcoholic Consumption of Young Italians During the SARS-CoV-2 PandemicAlessandro Federico, Chiara Mazzarella, Annamaria Spina, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|July 12, 2002
Increased hippocampal DNA oxidation in serotonin transporter deficient miceR Mössner, R Dringen, A M Persico, et al.Cytogenetics and Cell Genetics|July 7, 1999
Assignment of human teratocarcinoma derived growth factor (TDGF) sequences to chromosomes 2q37, 3q22, 6p25 and 19q13.1B Scognamiglio, G Baldassarre, C Cassano, et al.Journal of Medicinal Chemistry|March 23, 2011
Oxime amides as a novel zinc binding group in histone deacetylase inhibitors: synthesis, biological activity, and computational evaluationCinzia B Botta, Walter Cabri, Elena Cini, et al.Advances in Therapy|August 6, 2020
Real-World Clinical Practice Use of 8-Week Glecaprevir/Pibrentasvir in Treatment-Naïve Patients with Compensated CirrhosisPietro Lampertico, Stefan Mauss, Marcello Persico, et al.Autism Research : Official Journal of the International Society for Autism Research|October 7, 2015
Slow intestinal transit contributes to elevate urinary p-cresol level in Italian autistic childrenStefano Gabriele, Roberto Sacco, Laura Altieri, et al.Clinical Genetics|February 6, 2018
Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndromeA Angius, S Cossu, P Uva, et al.Pageof 120