Lambertus van den Heuvel

No ORCID on file · 3 papers in corpus · active 2022-2026

Study types

  • other 1
  • review 1
2026
Journal of the American Society of Nephrology : JASN ·doi:10.1681/asn.0000001159

BACKGROUND: The mechanisms by which apolipoprotein L1 (APOL1) risk variants, G1 and G2, induce kidney disease in individuals of African ancestry remain contentious. METHODS: In this study, we utilized a heterologous expression system of HE…

review 2025
BMC nephrology ·doi:10.1186/s12882-025-04687-y

Fifteen years have elapsed since the publication of the seminal work establishing the association between risk variants in the Apolipoprotein L1 (APOL1) gene and kidney disease in individuals of African ancestry. During this period, substan…

other 2022
Cells ·doi:10.3390/cells11071245

Nephropathic cystinosis is an inherited lysosomal storage disorder caused by pathogenic variants in the cystinosin (CTNS) gene and is characterized by the excessive shedding of proximal tubular epithelial cells (PTECs) and podocytes into ur…