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http://scihub22266oqcxt.onion/ C4565794!4565794!25974523     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Phys+Rev+E+Stat+Nonlin+Soft+Matter+Phys 2015 ; 91 (4): 042703 Nephropedia Template TP {{tp|p=25974523|t=2015. Super-resolution two-photon microscopy via scanning patterned illumination |pdf=|usr=}}{{25974523}} gab.com Text Super-resolution two-photon microscopy via scanning patterned illumination JO: Phys Rev E Stat Nonlin Soft Matter Phys http://www.kidney.de/pget.php?&tw=1&pmid=25974523 #FOAvip We developed two-photon scanning patterned illumination microscopy (2P-SPIM) for super-resolution two-photon imaging. Our approach used a traditional two-photon microscopy setup with temporally modulated excitation to create patterned illumination fields. Combing nine different illuminations and structured illumination reconstruction, super-resolution imaging was achieved in two-photon microscopy. Using 2P-SPIM we achieved a lateral resolution of 141 nm, which represents an improvement by a factor of 1.9 over the corresponding diffraction limit. We further demonstrated super-resolution cellular imaging by 2P-SPIM to image actin cytoskeleton in mammalian cells and three-dimensional imaging in highly scattering retinal tissue. Twit Text FOAVip Super-resolution two-photon microscopy via scanning patterned illumination ????Phys Rev E Stat Nonlin Soft Matter Phys http://www.kidney.de/pget.php?&tw=1&pmid=25974523 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25974523 #FOAvip English Wikipedia <ref>{{Cite pmid|25974523}}</ref> Super-resolution two-photon microscopy via scanning patterned illumination #MMPMID25974523 Urban BE; Yi J; Chen S; Dong B; Zhu Y; DeVries SH; Backman V; Zhang HF Phys Rev E Stat Nonlin Soft Matter Phys 2015[Apr]; 91 (4): 042703 PMID25974523show ga We developed two-photon scanning patterned illumination microscopy (2P-SPIM) for super-resolution two-photon imaging. Our approach used a traditional two-photon microscopy setup with temporally modulated excitation to create patterned illumination fields. Combing nine different illuminations and structured illumination reconstruction, super-resolution imaging was achieved in two-photon microscopy. Using 2P-SPIM we achieved a lateral resolution of 141 nm, which represents an improvement by a factor of 1.9 over the corresponding diffraction limit. We further demonstrated super-resolution cellular imaging by 2P-SPIM to image actin cytoskeleton in mammalian cells and three-dimensional imaging in highly scattering retinal tissue. äSuper-resolution two-photon microscopy via scanning patterned illumina(epmc).pdf DeepDyve Pubget Overpricing