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10.5056/jnm15096 http://scihub22266oqcxt.onion/10.5056/jnm15096 C4496899!4496899!26130630     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       J+Neurogastroenterol+Motil 2015 ; 21 (3): 337-51 Nephropedia Template TP {{tp|p=26130630|t=2015. Optical Tools to Investigate Cellular Activity in the Intestinal Wall |pdf=|usr=}}{{26130630}} gab.com Text Optical Tools to Investigate Cellular Activity in the Intestinal Wall JO: J Neurogastroenterol Motil http://www.kidney.de/pget.php?&tw=1&pmid=26130630 #FOAvip Live imaging has become an essential tool to investigate the coordinated activity and output of cellular networks. Within the last decade, 2 Nobel prizes have been awarded to recognize innovations in the field of imaging: one for the discovery, use, and optimization of the green fluorescent protein (2008) and the second for the development of super-resolved fluorescence microscopy (2014). New advances in both optogenetics and microscopy now enable researchers to record and manipulate activity from specific populations of cells with better contrast and resolution, at higher speeds, and deeper into live tissues. In this review, we will discuss some of the recent developments in microscope technology and in the synthesis of fluorescent probes, both synthetic and genetically encoded. We focus on how live imaging of cellular physiology has progressed our understanding of the control of gastrointestinal motility, and we discuss the hurdles to overcome in order to apply the novel tools in the field of neurogastroenterology and motility. Twit Text FOAVip Optical Tools to Investigate Cellular Activity in the Intestinal Wall ????J Neurogastroenterol Motil http://www.kidney.de/pget.php?&tw=1&pmid=26130630 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26130630 #FOAvip English Wikipedia <ref>{{Cite pmid|26130630}}</ref> Optical Tools to Investigate Cellular Activity in the Intestinal Wall #MMPMID26130630 Boesmans W; Hao MM; Berghe PV J Neurogastroenterol Motil 2015[Jul]; 21 (3): 337-51 PMID26130630show ga Live imaging has become an essential tool to investigate the coordinated activity and output of cellular networks. Within the last decade, 2 Nobel prizes have been awarded to recognize innovations in the field of imaging: one for the discovery, use, and optimization of the green fluorescent protein (2008) and the second for the development of super-resolved fluorescence microscopy (2014). New advances in both optogenetics and microscopy now enable researchers to record and manipulate activity from specific populations of cells with better contrast and resolution, at higher speeds, and deeper into live tissues. In this review, we will discuss some of the recent developments in microscope technology and in the synthesis of fluorescent probes, both synthetic and genetically encoded. We focus on how live imaging of cellular physiology has progressed our understanding of the control of gastrointestinal motility, and we discuss the hurdles to overcome in order to apply the novel tools in the field of neurogastroenterology and motility. äOptical Tools to Investigate Cellular Activity in the Intestinal Wall (epmc).pdf DeepDyve Pubget Overpricing