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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 9, 2021
Juvenile amyotrophic lateral sclerosis associated with biallelic c.757delG mutation of sorbitol dehydrogenase geneEmilien Bernard, Antoine Pegat, Anne-Evelyne Vallet, et al.
Cells|December 9, 2023
Spatial Transcriptomics Reveals Signatures of Histopathological Changes in Muscular SarcoidosisHippolyte Lequain, Cyril Dégletagne, Nathalie Streichenberger, et al.
The EMBO Journal|May 26, 2006
Retrovirus infection strongly enhances scrapie infectivity release in cell culturePascal Leblanc, Sandrine Alais, Isabel Porto-Carreiro, et al.
Nature Structural & Molecular Biology|April 10, 2012
Human prion protein binds Argonaute and promotes accumulation of microRNA effector complexesDerrick Gibbings, Pascal Leblanc, Florence Jay, et al.
Cellular and Molecular Life Sciences : CMLS|September 18, 2014
Prion strains are differentially released through the exosomal pathwayZaira E Arellano-Anaya, Alvina Huor, Pascal Leblanc, et al.
Genes|December 24, 2021
Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous MutationsJulian Theuriet, Antoine Pegat, Pascal Leblanc, et al.
International Journal of Molecular Sciences|September 19, 2020
Clinical and Molecular Landscape of ALS Patients with SOD1 Mutations: Novel Pathogenic Variants and Novel Phenotypes. A Single ALS Center StudyEmilien Bernard, Antoine Pegat, Juliette Svahn, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 13, 2016
Isolation of Exosomes and Microvesicles from Cell Culture Systems to Study Prion TransmissionPascal Leblanc, Zaira E Arellano-Anaya, Emilien Bernard, et al.
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