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: 3122
Function: getPubMedXML
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
A study of the adhesion of embryonic chicken heart muscle cells was conducted with a newly developed time-resolved acoustic microscope, which operates in the GHz-frequency range. The interpretation of the acoustical images of the heart muscle cells was done in combination with the fluorescence optical microscopy. A comparison between the acoustical images of chicken heart muscle cells and optical images of the same cells after staining showed that the actin fibers end inside the dark streaks in the acoustical images and thus represent the focal contacts (FCs). For cell biology applications, this demonstrates (a) the use of SAM as a tool for studying the dynamics of the FCs of living cells without any chemical staining and (b) that the combination of acoustic and optical microscopes allows interpretation of the acoustical images by using the wide variety of techniques available in optical microscopy.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.ultrasmedbio.2007.01.016 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!