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Journal of Clinical Medicine|December 8, 2019
FAD/NADH Dependent Oxidoreductases: From Different Amino Acid Sequences to Similar Protein Shapes for Playing an Ancient FunctionLucia Trisolini, Nicola Gambacorta, Ruggiero Gorgoglione, et al.The EPMA Journal|January 11, 2022
Modeling SARS-CoV-2 spike/ACE2 protein-protein interactions for predicting the binding affinity of new spike variants for ACE2, and novel ACE2 structurally related human protein targets, for COVID-19 handling in the 3PM contextVincenzo Tragni, Francesca Preziusi, Luna Laera, et al.Sleep & Breathing = Schlaf & Atmung|May 1, 2020
Different barbed pharyngoplasty techniques for retropalatal collapse in obstructive sleep apnea patients: a systematic reviewAntonio Moffa, Vittorio Rinaldi, Mario Mantovani, et al.American Journal of Medical Genetics|December 31, 1997
X-linked recessive chondrodysplasia punctata due to a new point mutation of the ARSE geneG Parenti, P Buttitta, G Meroni, et al.Journal of Child Neurology|January 11, 2008
Brain proton magnetic resonance spectroscopy and neuromuscular pathology in a patient with GM1 gangliosidosisNicola Brunetti-Pierri, Meenakshi B Bhattacharjee, Zhiyue J Wang, et al.Italian Heart Journal : Official Journal of the Italian Federation of Cardiology|June 10, 2004
Aortic valve-sparing surgery for aortic root aneurysmGiuseppe Di Eusanio, Andrea Quarti, Marco Di Eusanio, et al.Haematologica|May 1, 1994
Fludarabine in untreated and previously treated B-CLL patients: a report on efficacy and toxicityM Spriano, M Clavio, P Carrara, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 8, 2005
Interaction between human NK cells and bone marrow stromal cells induces NK cell triggering: role of NKp30 and NKG2D receptorsAlessandro Poggi, Claudia Prevosto, Anna-Maria Massaro, et al.European Journal of Human Genetics : EJHG|January 9, 2014
SMAD4 mutations causing Myhre syndrome result in disorganization of extracellular matrix improved by losartanPasquale Piccolo, Pratibha Mithbaokar, Valeria Sabatino, et al.Human Gene Therapy|July 7, 2012
Sustained reduction of hyperbilirubinemia in Gunn rats after adeno-associated virus-mediated gene transfer of bilirubin UDP-glucuronosyltransferase isozyme 1A1 to skeletal muscleNunzia Pastore, Edoardo Nusco, Jana Vaníkova, et al.Pageof 93