Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Hypoxia results in increased expression of some genes. This can compensate effects of hypoxia on the organism, and adapt cells and tissues to the environment with low oxygen tension. Mechanisms of cell and tissue responses to hypoxia have been extensively studied last years. The first identified mediator of cell response to hypoxia was hypoxia-inducible factor (HIF-1), which is being up regulated during hypoxic conditions. It binds to regulatory regions of sensitive genes and increases their transcription rate. Other key elements of cell response to hypoxia have been described recently--von Hippel-Lindau protein and prolyl hydroxylases, that allow degradation of alpha-subunit of HIF-1 during normal oxygen tension. This can ensure low level of HIF-1 in cells under physiological oxygen tension thus the expression of target genes is maintained on basal level. These new findings are starting points for further research and possible therapeutic use.
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