Ontology highlight
ABSTRACT:
SUBMITTER: Luciani A
PROVIDER: S-EPMC8204406 | biostudies-literature | 2020 Jul
REPOSITORIES: biostudies-literature
Luciani Alessandro A Freedman Benjamin S BS
Kidney international 20200701 1
Rare mutations in the LRP2 gene encoding for the endocytic receptor megalin cause developmental abnormalities and kidney disease. However, the mechanisms governing the dysfunction of mutant megalin remain unclear. A new study utilizing patient-derived induced pluripotent stem cells is now putting the endolysosomal system into the spotlight, as it is proposed to play a central role in the regulation of megalin in health and disease. ...[more]