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10.1007/s12551-010-0035-2 http://scihub22266oqcxt.onion/10.1007/s12551-010-0035-2 C5418370!5418370 !28510069     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28510069 &cmd=llinks): Failed to open stream: HTTP request failed! 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Multi-dimensional correlative imaging of subcellular events: combining the strengths of light and electron microscopy |pdf=|usr=}}{{28510069 }} gab.com Text Multi-dimensional correlative imaging of subcellular events: combining the strengths of light and electron microscopy JO: Biophys Rev http://www.kidney.de/pget.php?&tw=1&pmid=28510069 #FOAvip To genuinely understand how complex biological structures function, we must integrate knowledge of their dynamic behavior and of their molecular machinery. The combined use of light or laser microscopy and electron microscopy has become increasingly important to our understanding of the structure and function of cells and tissues at the molecular level. Such a combination of two or more different microscopy techniques, preferably with different spatial- and temporal-resolution limits, is often referred to as 'correlative microscopy'. Correlative imaging allows researchers to gain additional novel structure-function information, and such information provides a greater degree of confidence about the structures of interest because observations from one method can be compared to those from the other method(s). This is the strength of correlative (or 'combined') microscopy, especially when it is combined with combinatorial or non-combinatorial labeling approaches. In this topical review, we provide a brief historical perspective of correlative microscopy and an in-depth overview of correlative sample-preparation and imaging methods presently available, including future perspectives on the trend towards integrative microscopy and microanalysis. Twit Text FOAVip Multi-dimensional correlative imaging of subcellular events: combining the strengths of light and electron microscopy ????Biophys Rev http://www.kidney.de/pget.php?&tw=1&pmid=28510069 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28510069 #FOAvip English Wikipedia <ref>{{Cite pmid|28510069 }}</ref> Multi-dimensional correlative imaging of subcellular events: combining the strengths of light and electron microscopy #MMPMID28510069 Su Y ; Nykanen M ; Jahn KA ; Whan R ; Cantrill L ; Soon LL ; Ratinac KR ; Braet F Biophys Rev 2010[Aug]; 2 (3 ): 121-135 PMID28510069 show ga To genuinely understand how complex biological structures function, we must integrate knowledge of their dynamic behavior and of their molecular machinery. The combined use of light or laser microscopy and electron microscopy has become increasingly important to our understanding of the structure and function of cells and tissues at the molecular level. Such a combination of two or more different microscopy techniques, preferably with different spatial- and temporal-resolution limits, is often referred to as 'correlative microscopy'. Correlative imaging allows researchers to gain additional novel structure-function information, and such information provides a greater degree of confidence about the structures of interest because observations from one method can be compared to those from the other method(s). This is the strength of correlative (or 'combined') microscopy, especially when it is combined with combinatorial or non-combinatorial labeling approaches. In this topical review, we provide a brief historical perspective of correlative microscopy and an in-depth overview of correlative sample-preparation and imaging methods presently available, including future perspectives on the trend towards integrative microscopy and microanalysis. äMulti-dimensional correlative imaging of subcellular events: combining(epmc).pdf DeepDyve Pubget Overpricing