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International Journal of Molecular Sciences|December 10, 2021
CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 IsoformsKévin Mairot, Vasily Smirnov, Béatrice Bocquet, et al.Ophthalmology Science|October 17, 2022
Retinitis Punctata Albescens and RLBP1-Allied Phenotypes: Phenotype-Genotype Correlation and Natural History in the Aim of Gene TherapyBéatrice Bocquet, Hicham El Alami Trebki, Anne Françoise Roux, et al.Science Advances|January 24, 2025
Cryo-EM structure and regulation of human NAD kinasePrakash P Praharaj, Yang Li, Charline Mary, et al.Human Molecular Genetics|January 9, 2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epitheliumIsabelle Meunier, Guy Lenaers, Béatrice Bocquet, et al.Proteins|December 31, 2024
Integrative Modeling in the Age of Machine Learning: A Summary of HADDOCK Strategies in CAPRI Rounds 47-55Victor Reys, Marco Giulini, Vlad Cojocaru, et al.Scientific Reports|September 8, 2016
A new autosomal dominant eye and lung syndrome linked to mutations in TIMP3 geneIsabelle Meunier, Béatrice Bocquet, Gilles Labesse, et al.Nature Protocols|June 17, 2024
The HADDOCK2.4 web server for integrative modeling of biomolecular complexesRodrigo V Honorato, Mikael E Trellet, Brian Jiménez-García, et al.American Journal of Human Genetics|September 3, 2013
Mutations in IMPG1 cause vitelliform macular dystrophiesGaël Manes, Isabelle Meunier, Almudena Avila-Fernández, et al.Pageof 11