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| DOI | 10.3389/FPHAR.2024.1373507 | ||||
| Año | 2024 | ||||
| Tipo | revisión |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Large Conductance Voltage- and Calcium-activated K+ (BK) channels are transmembrane pore-forming proteins that regulate cell excitability and are also expressed in non-excitable cells. They play a role in regulating vascular tone, neuronal excitability, neurotransmitter release, and muscle contraction. Dysfunction of the BK channel can lead to arterial hypertension, hearing disorders, epilepsy, and ataxia. Here, we provide an overview of BK channel functioning and the implications of its abnormal functioning in various diseases. Understanding the function of BK channels is crucial for comprehending the mechanisms involved in regulating vital physiological processes, both in normal and pathological conditions, controlled by BK. This understanding may lead to the development of therapeutic interventions to address BK channelopathies.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Echeverria, Felipe | - |
Universidad de Valparaíso - Chile
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| 2 | Gonzalez-Sanabria, Naileth | - |
Universidad de Valparaíso - Chile
|
| 3 | Alvarado-Sanchez, Rosangelina | - |
Universidad de Valparaíso - Chile
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| 4 | Fernández, Miguel | Hombre |
Universidad de Valparaíso - Chile
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| 5 | CASTILLO-HUERA, KAREN LORENA | Mujer |
Universidad de Valparaíso - Chile
Universidad Católica del Maule - Chile |
| 6 | LATORRE-DE LA CRUZ, RAMON OSVALDO | Hombre |
Universidad de Valparaíso - Chile
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| Agradecimiento |
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| The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Chilean government through FONDECYT Grants #1230265 (RL) and the National Institutes of Health Award R01GM030376 (RL). FE, NG-S, RA-S, and MF, were supported by a PhD fellowship from ANID #21202097 (FE), #21200592 (NG-S), #21221040 (RA-S) and #21171141 (MF). |