Unpacking the Tumor Protein D52-like Family: Roles in Intracellular Trafficking and Cancer Progression. [PDF]
Dorward EL +7 more
europepmc +1 more source
Characterizing KIF16B in Neurons Reveals a Novel Intramolecular “Stalk Inhibition” Mechanism That Regulates Its Capacity to Potentiate the Selective Somatodendritic Localization of Early Endosomes [PDF]
Atena Farkhondeh +3 more
openalex +1 more source
LRRK2 as a Potential Disease‐Modifying Target in Sporadic Parkinson's Disease
Abstract A growing understanding of the role that leucine‐rich repeat kinase 2 (LRRK2) plays in Parkinson's disease (PD) supports continued focus on this enzyme as a therapeutic target for PD. Accumulating evidence suggests that there are phenotypic, neuropathologic, and biological similarities between sporadic PD (sPD) and familial forms in which ...
Anthony E. Lang +12 more
wiley +1 more source
Intracellular Transport of PD-L1 by Rab10-Positive Tubular Endosomes Originated from Macropinocytic Cups in RAW264 Macrophage-Like Cells. [PDF]
Kawai K, Ishikawa Y, Egami Y, Araki N.
europepmc +1 more source
pH-responsive bond as a linker for the release of chemical drugs from RNA–drug complexes in endosome or lysosome [PDF]
Piotr Rychahou +7 more
openalex +1 more source
Abstract Background Peripheral disease mechanisms such as immune dysregulation may contribute to Parkinson's disease (PD). To investigate interactions between common PD mutations and immune responses to environmental pathogens, we studied responses to Pseudomonas aeruginosa (P.
Julian R. Mark +8 more
wiley +1 more source
Deacidification of the Endolysosomal System by the Vesicular Proton Pump V-ATPase Inhibitor Bafilomycin A1 Affects EGF Receptor Endocytosis Differently in Endometrial MSC and HeLa Cells. [PDF]
Salova AV +4 more
europepmc +1 more source
A Selective Transport Route from Golgi to Late Endosomes That Requires the Yeast Gga Proteins [PDF]
Michael W. Black, Hugh R.B. Pelham
openalex +1 more source
Abstract Background Membrane contact sites are crucial for the exchange of ions or lipids and thus are critical for the function and maintenance of organelles. VPS13A is a membrane‐residing, bridge‐like protein connecting two membranes to enable bulk lipid transfer. Loss‐of‐function mutations in the VPS13A gene cause VPS13A disease.
Dajana Grossmann +10 more
wiley +1 more source

