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
The development of Schwann cells, the principal glial cell in the peripheral nervous system, occurs through a series of transitional embryonic and postnatal phases, which are tightly regulated by a number of axonal signals. During the axon ensheathment and myelin growth, the diameter of the axon play an important role in the maturation of Schwann cells. Because of electrospun fibers similar to protein fibers within the native extracellular matrix, the scaffolds are being developed as neural tissue engineering scaffolds. Until now, the correlation between varying diameter of aligned electrospun fibers and Schwann cells maturation has not been investigated. We hypothesize that the different diameter of aligned electrospun fibers may influence the maturation of Schwann cells and may help improve the outcome of cell-based approaches to cure demyelinated lesions or peripheral nerve regeneration.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1016/j.mehy.2013.07.038 | DOI Listing |
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