end stage renal disease

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Summary

Literature (2)

Literature for DOID 783: end stage renal disease

Xenbase Articles Publications associated with this Disease Ontology entry or its descendants

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A homozygous human WNT11 variant is associated with laterality, heart and renal defects., Berns H,Weber D,Haas M,Bakey Z,Brislinger-Engelhardt MM,Schmidts M,Walentek P, Dis Model Mech. April 9, 2025; :1754-8411.
Differential modulation of polycystin-2 gain-of-function channels by cysteine-reactive compounds, amphiphilic substances, and S4-S5 linker mutations., Geiges L,Staudner T,Khamseekaew J,Korbmacher C,Ilyaskin AV, J Biol Chem. November 24, 2025; 301(11):1083-351X.

A homozygous human WNT11 variant is associated with laterality, heart and renal defects., Berns H,Weber D,Haas M,Bakey Z,Brislinger-Engelhardt MM,Schmidts M,Walentek P, Dis Model Mech. April 9, 2025; :1754-8411.

Differential modulation of polycystin-2 gain-of-function channels by cysteine-reactive compounds, amphiphilic substances, and S4-S5 linker mutations., Geiges L,Staudner T,Khamseekaew J,Korbmacher C,Ilyaskin AV, J Biol Chem. November 24, 2025; 301(11):1083-351X.