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[Lysosomes and lysosomal storage diseases].
Journal de la Societe de biologie, 2002Lysosomal storage disorders (LSDs) are monogenic inborn errors of metabolism. Various groups have been delineated according to the affected pathway and the accumulated substrate, and new entities are still being identified. They are severe disorders with a heterogeneous clinical spectrum encompassing visceral, skeletal and neurologic involvement, and ...
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Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology
Nature Reviews Molecular Cell Biology, 2023Rushika M Perera
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Targeting lysosomes in human disease: from basic research to clinical applications
Signal Transduction and Targeted Therapy, 2021XiangYuan Luo, Xing-Xing He
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CLN3 is required for the clearance of glycerophosphodiesters from lysosomes
Nature, 2022Christian Grimm +2 more
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Organelle-level precision with next-generation targeting technologies
Nature Reviews Materials, 2021Anand Saminathan +2 more
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