Showing results (21-30 of 38) with videos related to
Sort By:
Pageof 4
Biomedicines|December 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse ModelsHamid Meziane, Marie-Christine Birling, Olivia Wendling, et al.Archives of Cardiovascular Diseases|November 9, 2017
Nox4 genetic inhibition in experimental hypertension and metabolic syndromeGhina Bouabout, Estelle Ayme-Dietrich, Hugues Jacob, et al.Journal of Lipid Research|May 11, 2010
PCSK9 is not involved in the degradation of LDL receptors and BACE1 in the adult mouse brainMali Liu, Guoxin Wu, Jennifer Baysarowich, et al.Plos Genetics|September 29, 2021
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndromeVéronique Brault, Thu Lan Nguyen, Javier Flores-Gutiérrez, et al.Human Molecular Genetics|April 17, 2018
A new mouse model of ARX dup24 recapitulates the patients' behavioral and fine motor alterationsAline Dubos, Hamid Meziane, Giovanni Iacono, et al.BMC Cell Biology|August 7, 2016
Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reactionGemma F Codner, Loic Lindner, Adam Caulder, et al.Scientific Reports|August 31, 2017
Atp6ap2 ablation in adult mice impairs viability through multiple organ deficienciesOlivia Wendling, Marie-France Champy, Solène Jaubert, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 11, 2012
Absence of TI-VAMP/Vamp7 leads to increased anxiety in miceLydia Danglot, Kathleen Zylbersztejn, Maja Petkovic, et al.Proceedings of the National Academy of Sciences of the United States of America|September 14, 2016
E4F1-mediated control of pyruvate dehydrogenase activity is essential for skin homeostasisPerrine Goguet-Rubio, Berfin Seyran, Laurie Gayte, et al.The Journal of Biological Chemistry|September 14, 2016
Physiological Expression of AMPKγ2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in MiceXiaodong Yang, John Mudgett, Ghina Bou-About, et al.Pageof 4