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10.1088/1361-648X/aa7185 http://scihub22266oqcxt.onion/10.1088/1361-648X/aa7185 C5952331!5952331!28481213     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Phys+Condens+Matter 2017 ; 29 (27): ä Nephropedia Template TP {{tp|p=28481213|t=2017. Super-resolution optical microscopy for studying membrane structure and dynamics |pdf=|usr=}}{{28481213}} gab.com Text Super-resolution optical microscopy for studying membrane structure and dynamics JO: J Phys Condens Matter http://www.kidney.de/pget.php?&tw=1&pmid=28481213 #FOAvip Investigation of cell membrane structure and dynamics requires high spatial and temporal resolution. The spatial resolution of conventional light microscopy is limited due to the diffraction of light. However, recent developments in microscopy enabled us to access the nano-scale regime spatially, thus to elucidate the nanoscopic structures in the cellular membranes. In this review, we will explain the resolution limit, address the working principles of the most commonly used super-resolution microscopy techniques and summarise their recent applications in the biomembrane field. Twit Text FOAVip Super-resolution optical microscopy for studying membrane structure and dynamics ????J Phys Condens Matter http://www.kidney.de/pget.php?&tw=1&pmid=28481213 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28481213 #FOAvip English Wikipedia <ref>{{Cite pmid|28481213}}</ref> Super-resolution optical microscopy for studying membrane structure and dynamics #MMPMID28481213 Sezgin E J Phys Condens Matter 2017[Jul]; 29 (27): ä PMID28481213show ga Investigation of cell membrane structure and dynamics requires high spatial and temporal resolution. The spatial resolution of conventional light microscopy is limited due to the diffraction of light. However, recent developments in microscopy enabled us to access the nano-scale regime spatially, thus to elucidate the nanoscopic structures in the cellular membranes. In this review, we will explain the resolution limit, address the working principles of the most commonly used super-resolution microscopy techniques and summarise their recent applications in the biomembrane field. äSuper-resolution optical microscopy for studying membrane structure an(epmc).pdf DeepDyve Pubget Overpricing