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Human Mutation|May 12, 2017
Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathyTojo Nakayama, Jiang Wu, Patricia Galvin-Parton, et al.
Biomacromolecules|May 17, 2025
Intracellular Nanodelivery of DNA with Enzyme-Degradable and pH-Responsive Peptide DendronsM A Urello, H J Vaughan, L T Dockery, et al.
Journal of Molecular Biology|December 21, 2010
Engineering a high-affinity anti-IL-15 antibody: crystal structure reveals an α-helix in VH CDR3 as key component of paratopeDavid C Lowe, Stefan Gerhardt, Alison Ward, et al.
Environmental Science & Technology|March 4, 2010
Optimizing Cr(VI) and Tc(VII) remediation through nanoscale biomineral engineeringRichard S Cutting, Victoria S Coker, Neil D Telling, et al.
Biomaterials|April 27, 2019
Cancer-selective nanoparticles for combinatorial siRNA delivery to primary human GBM in vitro and in vivoKristen L Kozielski, Alejandro Ruiz-Valls, Stephany Y Tzeng, et al.
Science Advances|July 20, 2022
Polymeric nanoparticles for dual-targeted theranostic gene delivery to hepatocellular carcinomaHannah J Vaughan, Camila G Zamboni, Laboni F Hassan, et al.
The Journal of Cell Biology|April 25, 2020
A direct role for SNX9 in the biogenesis of filopodiaIris K Jarsch, Jonathan R Gadsby, Annalisa Nuccitelli, et al.
Neurology. Clinical Practice|December 20, 2018
Review process for IVIg treatment: Lessons learned from INSIGHTS neuropathy studyTodd D Levine, Jonathan S Katz, Richard Barohn, et al.
Annals of Neurology|August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Vaughan, A Durr, J Tassin, et al.
Journal of Biomolecular Screening|December 5, 2012
Development of a homogeneous high-throughput screening assay for biological inhibitors of human rhinovirus infectionPhilip Newton, Desmond O'Shea, Edward Wells, et al.
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