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
Previous studies have described a primary afferent vestibular projection to second-order cochlear neurons originating from the saccular maculae. As could be shown in the guinea pig by means of anterograde transport of horseradish peroxidase and immuno-cytochemistry, these saccular afferents terminated at cells immunoreactive to glutamate and aspartate but not to gamma-aminobutyric acid (GABA). These were intermingled among the fibers of the acoustic striae and situated between the dorsal cochlear nucleus and the octopus cell area. Within the acoustic striae, these saccular afferents appear to have a close relationship to GABA-immunoreactive structures, such as boutons en passant and terminal boutons. This striking relationship, along with cytoarchitectural criteria and the saccular input to these second-order cochlear neurons, gave reason to discern them as a separate cell group.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1007/BF00627628 | DOI Listing |
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