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Annals of the New York Academy of Sciences|November 16, 2022
Antibodies as drugs-a Keystone Symposia reportJennifer Cable, Erica Ollmann Saphire, Adrian C Hayday, et al.
The Journal of Biological Chemistry|June 16, 2012
Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle diseaseEloisa Carta, Seo-Kyung Chung, Victoria M James, et al.
JCI Insight|February 23, 2026
Structural modeling and functional characterization of a novel gain-of-function TLR8 variant causing severe inflammatory syndromeNikolaos T Skenteris, Elisa Luttermann, Sanjana Nair, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|May 5, 2024
Ultrapotent Broadly Neutralizing Human-llama Bispecific Antibodies against HIV-1Jianliang Xu, Tongqing Zhou, Krisha McKee, et al.
Proteins|October 9, 2025
Protein Target Highlights in CASP16: Insights From the Structure ProvidersLeila T Alexander, Océane M Follonier, Andriy Kryshtafovych, et al.
Cell Host & Microbe|March 5, 2020
VRC34-Antibody Lineage Development Reveals How a Required Rare Mutation Shapes the Maturation of a Broad HIV-Neutralizing LineageChen-Hsiang Shen, Brandon J DeKosky, Yicheng Guo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 25, 2022
MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe DystoniaKimberley M Reid, Robert Spaull, Smrithi Salian, et al.
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