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mouse kidneys

The Urbach Lab

kidney sem

The Urbach Lab

kidney

The Urbach Lab

brain organoids -sem

The Urbach Lab

Stem cells and Development

Human pluripotent stem cells (hPSCs) are a unique type of cells that can differentiate in vitro into nearly any cell type found in both the embryo and adult. Their ability to differentiate, combined with their unlimited capacity for self-renewal, makes hPSCs an invaluable resource for regenerative medicine and an essential tool for studying embryonic development and disease modeling. Our lab leverages the unique properties of hPSCs to model developmental genetic kidney disorders and diseases caused by mutations in nuclear envelope genes. Additionally, we are working to enhance kidney disease modeling by improving the maturation of kidney organoids derived from hPSCs. As a complementary area of our stem cell-based kidney research, we collaborate with other laboratories to explore novel therapeutic strategies for developmental kidney disorders and pediatric kidney cancers. Alongside our in-vitro studies, we employ transgenic mouse models to gain deeper insights into kidney development.

Research

Disease Modeling by hPSCs

Embryonic Kidney Development

Gene Therapy For Pediatric Tumors

Kidney Organoids

Recent Publications

Nephron-Specific Lin28A Overexpression Triggers Severe Inflammatory Response and Kidney Damage

Futorian A, Armon L, Waldman Ben-Asher H, Shoval I, Hazut I, Munitz A, Urbach A. , 2024

Characterization of Alternative Splicing in High-Risk Wilms' Tumors

Trink Y, Urbach A, Dekel B, Hohenstein P, Goldberger J, Kalisky T. , 2024

Characterization of Continuous Transcriptional Heterogeneity in High-Risk Blastemal-Type Wilms' Tumors Using Unsupervised Machine Learning

Trink Y, Urbach A, Dekel B, Hohenstein P, Goldberger J, Kalisky T. , 2023

Generation and characterization of iPSC lines from two nuclear envelopathy patients with a homozygous nonsense mutation in the TOR1AIP1 gene

Ben-Haim Y, Armon L, Fichtman B, Epshtein I, Spiegel R, Harel A, Urbach A. , 2021

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