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Loss of function mutations in the lysosomal channel TRPML-1 cause Mucolipidosis type IV, a rare lysosomal storage disease (LSD) characterized by neurological defects, progressive vision loss and achlorhydria.1–4 Recent reports described kidney disease and renal failure in MLIV patients in the secon...
ORGANISM(S): Mus musculus (Mouse) 
2026-04-06 | PXD049984 | Pride
Using diamagnetic levitation, we have exposed A. thaliana in vitro callus cultures to five environments with different levels of effective gravity (from levitation i.e. simulated mg* to 2g*) and magnetic fields (10.1 to 16.5 Tesla) and we have compared the results with those of similar experiments d...
ORGANISM(S): Arabidopsis thaliana 
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