The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
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Citations
Cites
Lifton, R. P., Dluhy, R. G., Powers, M., Rich, G. M., Cook, S., Ulick, S., & Lalouel, J.-M. (1992) · Nature · doi:10.1038/355262a0 · Cited by 1,158
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Molecular Mechanisms of Human Hypertension
Lifton, R. P., Gharavi, A. G., & Geller, D. S. (2001) · Cell · doi:10.1016/s0092-8674(01)00241-0 · Cited by 1,686
Self-citationChang, S. S., Grunder, S., Hanukoglu, A., Rösler, A., Mathew, P. M., Hanukoglu, I., Schild, L., Lu, Y., Shimkets, R. A., Nelson-Williams, C., et al. (1996) · Nature Genetics · doi:10.1038/ng0396-248 · Cited by 808
Self-citationPhosphorylation of Nedd4‐2 by Sgk1 regulates epithelial Na+ channel cell surface expression
Debonneville, C., Flores, S. Y., Kamynina, E., Plant, P. J., Tauxe, C., Thomas, M. A., Münster, C., Chraïbi, A., Pratt, J. H., Horisberger, J., et al. (2001) · The EMBO Journal · doi:10.1093/emboj/20.24.7052 · Cited by 711
Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase
Mune, T., Rogerson, F. M., Nikkilä, H., Agarwal, A. K., & White, P. C. (1995) · Nature Genetics · doi:10.1038/ng0895-394 · Cited by 619
Regulation of stability and function of the epithelial Na+ channel (ENaC) by ubiquitination
Staub, O., Gautschi, I., Ishikawa, T., Breitschopf, K., Ciechanover, A., Schild, L., & Rotin, D. (1997) · The EMBO Journal · doi:10.1093/emboj/16.21.6325 · Cited by 601
11β-Hydroxysteroid Dehydrogenase and the Syndrome of Apparent Mineralocorticoid Excess*
White, P. C., Mune, T., & Agarwal, A. K. (1997) · Endocrine Reviews · doi:10.1210/edrv.18.1.0288 · Cited by 517
Salt Sensitivity of Blood Pressure: A Scientific Statement From the American Heart Association
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Nabel, E. G. (2003) · New England Journal of Medicine · doi:10.1056/nejmra035098 · Cited by 431
Geller, D. S., Rodriguez-Soriano, J., Boado, A. V., Schifter, S., Bayer, M., Chang, S. S., & Lifton, R. P. (1998) · Nature Genetics · doi:10.1038/966 · Cited by 417
Self-citationMechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel
Snyder, P. M., Price, M. P., McDonald, F. J., Adams, C. M., Volk, K. A., Zeiher, B. G., Stokes, J. B., & Welsh, M. J. (1995) · Cell · doi:10.1016/0092-8674(95)90212-0 · Cited by 350
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism
Geller, D. S., Zhang, J., Wisgerhof, M. V., Shackleton, C., Kashgarian, M., & Lifton, R. P. (2008) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2008-0594 · Cited by 296
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Sudol, M. (1996) · Progress in Biophysics and Molecular Biology · doi:10.1016/s0079-6107(96)00008-9 · Cited by 296
Schild, L., Canessa, C. M., Shimkets, R. A., Gautschi, I., Lifton, R. P., & Rossier, B. C. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.12.5699 · Cited by 244
Self-citationEarly Aldosterone-Induced Gene Product Regulates the Epithelial Sodium Channel by Deubiquitylation
Fakitsas, P., Adam, G., Daidie[Combining Acute Accent], D. A. A., van Bemmelen, M. X., Fouladkou, F., Patrignani, A., Wagner, U., Warth, R., Camargo, S. M. R., Staub, O., et al. (2007) · Journal of the American Society of Nephrology · doi:10.1681/asn.2006080902 · Cited by 136
Lavoie, J. L., Lake-Bruse, K. D., & Sigmund, C. D. (2004) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00402.2003 · Cited by 94
Protein trafficking defects in inherited kidney diseases
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Self-citationPathophysiologic approach in genetic hypokalemia: An update
Blanchard, A. (2023) · Annales d'Endocrinologie · doi:10.1016/j.ando.2022.11.005 · Cited by 8
Bertholf, R. L., Jialal, I., & Winter, W. E. (2012) · Tietz Textbook of Clinical Chemistry and Molecular Diagnostics · doi:10.1016/b978-1-4160-6164-9.00054-8 · Cited by 5
The Genetics of Blood Pressure Regulation
Lin, H. J., Guo, X., & Rotter, J. I. (2020) · Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics · doi:10.1016/b978-0-12-812532-8.00006-9 · Cited by 3
Metadata
- Authors
- Shimkets, R. A., Warnock, D. G., Bositis, C. M., Nelson-Williams, C., Hansson, J. H., Schambelan, M., Gill, J. R., Ulick, S., Milora, R. V., Findling, J. W., Canessa, C. M., Rossier, B. C., & Lifton, R. P.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1994-11
- Volume
- 79
- Issue
- 3
- Pages
- 407-414
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2140853270
- Cited by
- 1,259
- References
- 1
- FWCI
- 16.42
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
