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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Trypanosomatids are protozoan parasites that cause deadly infectious diseases. Despite the unique characteristics of their cAMP signaling pathways, little is known about the mechanisms driving signal specificity in these early divergent eukaryotes. From the activation of adenylate cyclases in response to environmental cues to the downstream regulation of gene expression, the signaling mechanisms triggering developmental transformations in trypanosomes are poorly understood. In this review we integrate previous and new evidence supporting the existence of membrane microdomains that assemble cAMP signaling proteins in different subcellular compartments of Trypanosoma cruzi, the etiologic agent of Chagas disease. We also discuss the main cellular processes regulated by cAMP compartments in this parasite. Advances in this field are crucial to identifying new targets for antiparasitic interventions.
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http://dx.doi.org/10.1016/j.pt.2025.06.013 | DOI Listing |