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The Journal of Biological Chemistry|December 14, 2020
ATP13A3 is a major component of the enigmatic mammalian polyamine transport systemNorin Nabil Hamouda, Chris Van den Haute, Roeland Vanhoutte, et al.
Science (New York, N.Y.)|April 26, 2008
Efficient inhibition of the Alzheimer's disease beta-secretase by membrane targetingLawrence Rajendran, Anja Schneider, Georg Schlechtingen, et al.
The Journal of Cell Biology|March 13, 2013
Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levelsNathalie Jurisch-Yaksi, Applonia J Rose, Huiqi Lu, et al.
Acta Neuropathologica Communications|February 13, 2021
Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's diseaseStefanie Smolders, Stéphanie Philtjens, David Crosiers, et al.
Nature Genetics|December 25, 2007
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2Uwe Kornak, Ellen Reynders, Aikaterini Dimopoulou, et al.
Nature Communications|August 8, 2019
Lysosomal integral membrane protein-2 (LIMP-2/SCARB2) is involved in lysosomal cholesterol exportSaskia Heybrock, Kristiina Kanerva, Ying Meng, et al.
Scientific Reports|January 31, 2017
A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiencyArun Kumar Tharkeshwar, Jesse Trekker, Wendy Vermeire, et al.
Molecular Cell|February 28, 2017
The ER Stress Sensor PERK Coordinates ER-Plasma Membrane Contact Site Formation through Interaction with Filamin-A and F-Actin RemodelingAlexander R van Vliet, Francesca Giordano, Sarah Gerlo, et al.
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