Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 197
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 197
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 271
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3165
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 597
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 511
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 317
Function: require_once
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The KCNE gene family is crucial for physiological and pathological processes in the body and encodes small transmembrane proteins that function as auxiliary subunits to regulate voltage-gated potassium channels (K channels). This family includes five members, KCNE1, KCNE2, KCNE3, KCNE4, and KCNE5, whose encoded proteins are referred to as MinK and MinK-related peptides (MiRPs), which influence the properties and localization of K. When KCNE is coexpressed with Kv, it can alter the conductance, gating kinetics, and pharmacology of the channel. Therefore, these genes are particularly important for action potentials in excitable cells, and mutations in these genes can lead to significant diseases. In this paper, we review the functional roles of KCNE genes and their effects on Kv α subunits to further understand the regulatory effects of KCNE in modulating ion channels.
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http://dx.doi.org/10.1007/s10528-025-11202-3 | DOI Listing |