Cargando…
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism
Adrenal aldosterone-producing adenomas (APAs) constitutively produce the salt-retaining hormone aldosterone and are a common cause of severe hypertension. Recurrent mutations in the potassium channel KCNJ5 that result in cell depolarization and Ca(2+) influx cause ~40% of these tumors(1). We found f...
Autores principales: | Scholl, Ute I., Goh, Gerald, Stölting, Gabriel, de Oliveira, Regina Campos, Choi, Murim, Overton, John D., Fonseca, Annabelle L., Korah, Reju, Starker, Lee F., Kunstman, John W., Prasad, Manju L., Hartung, Erum A., Mauras, Nelly, Benson, Matthew R., Brady, Tammy, Shapiro, Jay R., Loring, Erin, Nelson-Williams, Carol, Libutti, Steven K., Mane, Shrikant, Hellman, Per, Westin, Gunnar, Åkerström, Göran, Björklund, Peyman, Carling, Tobias, Fahlke, Christoph, Hidalgo, Patricia, Lifton, Richard P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876926/ https://www.ncbi.nlm.nih.gov/pubmed/23913001 http://dx.doi.org/10.1038/ng.2695 |
Ejemplares similares
-
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
por: Scholl, Ute I, et al.
Publicado: (2015) -
CACNA1H Calcium Channel Mutations in Primary Aldosteronism – Is Sodium the Culprit?
por: Stölting, Gabriel, et al.
Publicado: (2020) -
Isradipine therapy in Cacna1d(Ile772Met/+) mice ameliorates primary aldosteronism and neurologic abnormalities
por: Stölting, Gabriel, et al.
Publicado: (2023) -
Enhanced Ca(2+) signaling, mild primary aldosteronism, and hypertension in a familial hyperaldosteronism mouse model (Cacna1h(M1560V/+))
por: Seidel, Eric, et al.
Publicado: (2021) -
Elevated aldosterone and blood pressure in a mouse model of familial hyperaldosteronism with ClC-2 mutation
por: Schewe, Julia, et al.
Publicado: (2019)