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The Journal of Biological Chemistry|April 8, 2021
PIKfyve activity is required for lysosomal trafficking of tau aggregates and tau seedingAlberto Carpinteiro Soares, Andreia Ferreira, Jonas Mariën, et al.
The Journal of Cell Biology|September 10, 2003
NuSAP, a novel microtubule-associated protein involved in mitotic spindle organizationTim Raemaekers, Katharina Ribbeck, Joel Beaudouin, et al.
Molecular Neurodegeneration|April 25, 2025
Spectrum of γ-Secretase dysfunction as a unifying predictor of ADAD age at onset across PSEN1, PSEN2 and APP causal genesSara Gutiérrez Fernández, Cristina Gan Oria, Dieter Petit, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 10, 2010
Genetically encoded dendritic marker sheds light on neuronal connectivity in DrosophilaLaura J J Nicolaï, Ariane Ramaekers, Tim Raemaekers, et al.
Stem Cells Translational Medicine|April 15, 2016
Using miRNA-mRNA Interaction Analysis to Link Biologically Relevant miRNAs to Stem Cell Identity Testing for Next-Generation Culturing DevelopmentMarian A E Crabbé, Kristel Gijbels, Aline Visser, et al.
The Journal of Biological Chemistry|November 14, 2014
Sequence-dependent internalization of aggregating peptidesJosé R Couceiro, Rodrigo Gallardo, Frederik De Smet, et al.
Plos One|June 16, 2012
Impaired LDL receptor-related protein 1 translocation correlates with improved dyslipidemia and atherosclerosis in apoE-deficient micePhilip L S M Gordts, Alexander Bartelt, Stefan K Nilsson, et al.
The Journal of Cell Biology|September 29, 2004
Presenilin 1 mediates the turnover of telencephalin in hippocampal neurons via an autophagic degradative pathwayCary Esselens, Viola Oorschot, Veerle Baert, et al.
The Journal of Biological Chemistry|July 30, 2003
Presenilins mutated at Asp-257 or Asp-385 restore Pen-2 expression and Nicastrin glycosylation but remain catalytically inactive in the absence of wild type PresenilinOmar Nyabi, Mostafa Bentahir, Katrien Horré, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type IIFrançois Foulquier, Eliza Vasile, Els Schollen, et al.
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