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We subjected human podocytes with and without alpha-Galactosidase knockdown to proteomic analysis.
ORGANISM(S): Homo sapiens (Human) 
2018-10-17 | PXD007080 | Pride
Fabry disease is an X-linked condition caused by variants of the GLA gene that result in the absence or enzymatic deficiency of alpha-galactosidase A (AGAL). This enzyme defect leads to lysosomal storage of globotriaosylceramide (Gb3Cer) in a variety of cell types throughout the body and manifests a...
ORGANISM(S): Homo sapiens (Human) 
2025-11-06 | PXD033936 | Pride
Genomics
Alpha-galactosidase gene of Rhopalosiphum padi L. sequencing
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