1. Wilson, Parker C, Wu, Haojia, Kirita, Yuhei, Waikar, Sushrut S, Humphreys, Benjamin D. 2019. The single-cell transcriptomic landscape of early human diabetic nephropathy. In Proceedings of the National Academy of Sciences of the United States of America, 116, 19619-19625. doi:10.1073/pnas.1908706116. https://pubmed.ncbi.nlm.nih.gov/31506348/
2. Gallolu Kankanamalage, Sachith, Lee, A-Young, Wichaidit, Chonlarat, Whitehurst, Angelique W, Cobb, Melanie H. 2017. WNK1 is an unexpected autophagy inhibitor. In Autophagy, 13, 969-970. doi:10.1080/15548627.2017.1286431. https://pubmed.ncbi.nlm.nih.gov/28282258/
3. Quelquejay, Helene, Al-Rifai, Rida, Silvestro, Michele, Jeunemaitre, Xavier, Ait-Oufella, Hafid. 2024. L-Wnk1 Deletion in Smooth Muscle Cells Causes Aortitis and Inflammatory Shift. In Circulation research, 135, 488-502. doi:10.1161/CIRCRESAHA.124.324366. https://pubmed.ncbi.nlm.nih.gov/38979610/
4. Sun, Qi, Lei, Xianli, Meng, Xiangrong, Yan, Lei, Zhang, Wenjing. 2024. Bioinformatics analysis identifies WNK1 gene as a potential biomarker for cholangiocarcinoma diagnosis and immune infiltration. In Journal, genetic engineering & biotechnology, 22, 100426. doi:10.1016/j.jgeb.2024.100426. https://pubmed.ncbi.nlm.nih.gov/39674642/
5. Bergaya, Sonia, Vidal-Petiot, Emmanuelle, Jeunemaitre, Xavier, Hadchouel, Juliette. . Pathogenesis of pseudohypoaldosteronism type 2 by WNK1 mutations. In Current opinion in nephrology and hypertension, 21, 39-45. doi:10.1097/MNH.0b013e32834d2fde. https://pubmed.ncbi.nlm.nih.gov/22080857/
6. Jaykumar, Ankita B, Plumber, Sakina, Barry, David M, Cleaver, Ondine, Cobb, Melanie H. 2022. WNK1 collaborates with TGF-β in endothelial cell junction turnover and angiogenesis. In Proceedings of the National Academy of Sciences of the United States of America, 119, e2203743119. doi:10.1073/pnas.2203743119. https://pubmed.ncbi.nlm.nih.gov/35867836/
7. Sapio, Matthew R, King, Diana M, Staedtler, Ellen S, Mannes, Andrew J, Iadarola, Michael J. 2023. Expression pattern analysis and characterization of the hereditary sensory and autonomic neuropathy 2 A (HSAN2A) gene with no lysine kinase (WNK1) in human dorsal root ganglion. In Experimental neurology, 370, 114552. doi:10.1016/j.expneurol.2023.114552. https://pubmed.ncbi.nlm.nih.gov/37793538/
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