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Proceedings of the National Academy of Sciences of the United States of America|January 11, 2003
WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epitheliaKeith A Choate, Kristopher T Kahle, Frederick H Wilson, et al.
NPJ Precision Oncology|January 5, 2024
A destabilizing Y891D mutation in activated EGFR impairs sensitivity to kinase inhibitionDaniel S Lenchner, Zaritza O Petrova, Lisa Hunihan, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
An SGK1 site in WNK4 regulates Na+ channel and K+ channel activity and has implications for aldosterone signaling and K+ homeostasisAaron M Ring, Qiang Leng, Jesse Rinehart, et al.
NPJ Precision Oncology|July 4, 2025
Genetic and oncogenic features of RASGRF fusionsSreya Das, Daniel S Lenchner, Ellen Jaeger, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 11, 2004
WNK4 regulates apical and basolateral Cl- flux in extrarenal epitheliaKristopher T Kahle, Ignacio Gimenez, Hatim Hassan, et al.
The Journal of Physiology|December 17, 2005
WNK3, a kinase related to genes mutated in hereditary hypertension with hyperkalaemia, regulates the K+ channel ROMK1 (Kir1.1)Qiang Leng, Kristopher T Kahle, Jesse Rinehart, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 8, 2003
Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4Frederick H Wilson, Kristopher T Kahle, Ernesto Sabath, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2005
WNK3 kinase is a positive regulator of NKCC2 and NCC, renal cation-Cl- cotransporters required for normal blood pressure homeostasisJesse Rinehart, Kristopher T Kahle, Paola de Los Heros, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
WNK4 regulates activity of the epithelial Na+ channel in vitro and in vivoAaron M Ring, Sam X Cheng, Qiang Leng, et al.
Blood|November 12, 2010
Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cellsShilpee Dutt, Anupama Narla, Katherine Lin, et al.
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