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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2001 1
2002 1
2003 1
2004 5
2005 1
2007 6
2008 2
2009 4
2010 6
2011 4
2012 5
2013 6
2014 6
2015 3
2016 3
2017 2
2018 2
2020 3
2021 2
2022 3
2023 3
2024 1

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62 results

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Page 1
Somatic SLC30A1 mutations altering zinc transporter ZnT1 cause aldosterone-producing adenomas and primary aldosteronism.
Rege J, Bandulik S, Nanba K, Kosmann C, Blinder AR, Plain A, Vats P, Kumar-Sinha C, Lerario AM, Else T, Yamazaki Y, Satoh F, Sasano H, Giordano TJ, Williams TA, Reincke M, Turcu AF, Udager AM, Warth R, Rainey WE. Rege J, et al. Among authors: warth r. Nat Genet. 2023 Oct;55(10):1623-1631. doi: 10.1038/s41588-023-01498-5. Epub 2023 Sep 14. Nat Genet. 2023. PMID: 37709865
Local Control of Aldosterone Production and Primary Aldosteronism.
Lalli E, Barhanin J, Zennaro MC, Warth R. Lalli E, et al. Among authors: warth r. Trends Endocrinol Metab. 2016 Mar;27(3):123-131. doi: 10.1016/j.tem.2016.01.003. Epub 2016 Jan 20. Trends Endocrinol Metab. 2016. PMID: 26803728 Review.
Two-pore domain potassium channels in the adrenal cortex.
Bandulik S, Tauber P, Lalli E, Barhanin J, Warth R. Bandulik S, et al. Among authors: warth r. Pflugers Arch. 2015 May;467(5):1027-42. doi: 10.1007/s00424-014-1628-6. Epub 2014 Oct 23. Pflugers Arch. 2015. PMID: 25339223 Free PMC article. Review.
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.
Schlingmann KP, Renigunta A, Hoorn EJ, Forst AL, Renigunta V, Atanasov V, Mahendran S, Barakat TS, Gillion V, Godefroid N, Brooks AS, Lugtenberg D, Lake J, Debaix H, Rudin C, Knebelmann B, Tellier S, Rousset-Rouvière C, Viering D, de Baaij JHF, Weber S, Palygin O, Staruschenko A, Kleta R, Houillier P, Bockenhauer D, Devuyst O, Vargas-Poussou R, Warth R, Zdebik AA, Konrad M. Schlingmann KP, et al. Among authors: warth r. J Am Soc Nephrol. 2021 Jun 1;32(6):1498-1512. doi: 10.1681/ASN.2020111587. Epub 2021 Apr 2. J Am Soc Nephrol. 2021. PMID: 33811157 Free PMC article.
A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.
Meindl K, Issler N, Afonso S, Cebrian-Serrano A, Müller K, Sterner C, Othmen H, Tegtmeier I, Witzgall R, Klootwijk E, Davies B, Kleta R, Warth R. Meindl K, et al. Among authors: warth r. Front Cell Dev Biol. 2023 Oct 12;11:1240558. doi: 10.3389/fcell.2023.1240558. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37900275 Free PMC article.
Renal Fanconi syndrome: taking a proximal look at the nephron.
Klootwijk ED, Reichold M, Unwin RJ, Kleta R, Warth R, Bockenhauer D. Klootwijk ED, et al. Among authors: warth r. Nephrol Dial Transplant. 2015 Sep;30(9):1456-60. doi: 10.1093/ndt/gfu377. Epub 2014 Dec 9. Nephrol Dial Transplant. 2015. PMID: 25492894 Review.
62 results