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The EMBO Journal|February 4, 2006
A unique set of SH3-SH3 interactions controls IB1 homodimerizationOle Kristensen, Sylvie Guenat, Imran Dar, et al.
Journal of Biomolecular Screening|November 10, 2006
Homogeneous and nonradioactive high-throughput screening platform for the characterization of kinase inhibitors in cell lysatesSylvie Guenat, Nathalie Rouleau, Christelle Bielmann, et al.
Molecular and Cellular Biology|October 18, 2017
Loss of Extracellular Signal-Regulated Kinase 1/2 in the Retinal Pigment Epithelium Leads to RPE65 Decrease and Retinal DegenerationAswin Pyakurel, Delphine Balmer, Marc K Saba-El-Leil, et al.
Human Mutation|November 14, 2008
Mutations in NR2E3 can cause dominant or recessive retinal degenerations in the same familyPascal Escher, Peter Gouras, Raphaël Roduit, et al.
International Journal of Molecular Sciences|November 27, 2021
CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh CattleIrene M Häfliger, Emma Marchionatti, Michele Stengård, et al.
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