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10.1364/OE.23.013833 http://scihub22266oqcxt.onion/10.1364/OE.23.013833 C4523368!4523368 !26072755     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26072755 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26072755 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Opt+Express 2015 ; 23 (11 ): 13833-47 Nephropedia Template TP {{tp|p=26072755 |t=2015. Ultra-large field-of-view two-photon microscopy |pdf=|usr=}}{{26072755 }} gab.com Text Ultra-large field-of-view two-photon microscopy JO: Opt Express http://www.kidney.de/pget.php?&tw=1&pmid=26072755 #FOAvip We present a two-photon microscope that images the full extent of murine cortex with an objective-limited spatial resolution across an 8 mm by 10 mm field. The lateral resolution is approximately 1 µm and the maximum scan speed is 5 mm/ms. The scan pathway employs large diameter compound lenses to minimize aberrations and performs near theoretical limits. We demonstrate the special utility of the microscope by recording resting-state vasomotion across both hemispheres of the murine brain through a transcranial window and by imaging histological sections without the need to stitch. Twit Text FOAVip Ultra-large field-of-view two-photon microscopy ????Opt Express http://www.kidney.de/pget.php?&tw=1&pmid=26072755 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26072755 #FOAvip English Wikipedia <ref>{{Cite pmid|26072755 }}</ref> Ultra-large field-of-view two-photon microscopy #MMPMID26072755 Tsai PS ; Mateo C ; Field JJ ; Schaffer CB ; Anderson ME ; Kleinfeld D Opt Express 2015[Jun]; 23 (11 ): 13833-47 PMID26072755 show ga We present a two-photon microscope that images the full extent of murine cortex with an objective-limited spatial resolution across an 8 mm by 10 mm field. The lateral resolution is approximately 1 µm and the maximum scan speed is 5 mm/ms. The scan pathway employs large diameter compound lenses to minimize aberrations and performs near theoretical limits. We demonstrate the special utility of the microscope by recording resting-state vasomotion across both hemispheres of the murine brain through a transcranial window and by imaging histological sections without the need to stitch. |Animals [MESH] |Cerebral Cortex/blood supply [MESH] |Equipment Design [MESH] |Imaging, Three-Dimensional [MESH] |Mice [MESH] |Microscopy, Fluorescence, Multiphoton/instrumentation/*methods [MESH] |Optical Phenomena [MESH]Ultra-large field-of-view two-photon microscopy (epmc).pdf DeepDyve Pubget Overpricing