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http://scihub22266oqcxt.onion/ C4058302!4058302!24936213     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Transl+Res 2014 ; 6 (3): 179-87 Nephropedia Template TP {{tp|p=24936213|t=2014. In vivo optical imaging of cancer metastasis using multiphoton microscopy: a short review |pdf=|usr=}}{{24936213}} gab.com Text In vivo optical imaging of cancer metastasis using multiphoton microscopy: a short review JO: Am J Transl Res http://www.kidney.de/pget.php?&tw=1&pmid=24936213 #FOAvip Intravital (in vivo) microscopy using fluorescently-tagged proteins is a valuable tool for imaging the expression of a specific protein, its subcellular location and the dynamics of specific cell populations in living animals. Recently, multiphoton microscopy including two-photon laser scanning microscopy (TPLSM) has been used in the field of tumor biology due to its ability to image target organs at higher magnification and at deeper depths from the tissue surface for longer time periods. We developed a method of in vivo real-time imaging for tumor metastasis using TPLSM with an organ stabilizing system, which allow us to observe not only a single tumor cell and its microenvironment for a long time, but also to observe the same organ of the same mouse at multiple time points in preclinical models. Here, we presented in vivo real-time images of 1) tumor cell arrest, 2) tumor cell-platelet interaction, 3) tumor cell-leukocyte interaction, and 4) metastatic colonization at the secondary organs as representative steps of metastatic process of experimental liver metastasis models using TPLSM. Twit Text FOAVip In vivo optical imaging of cancer metastasis using multiphoton microscopy: a short review ????Am J Transl Res http://www.kidney.de/pget.php?&tw=1&pmid=24936213 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24936213 #FOAvip English Wikipedia <ref>{{Cite pmid|24936213}}</ref> In vivo optical imaging of cancer metastasis using multiphoton microscopy: a short review #MMPMID24936213 Tanaka K; Toiyama Y; Okugawa Y; Okigami M; Inoue Y; Uchida K; Araki T; Mohri Y; Mizoguchi A; Kusunoki M Am J Transl Res 2014[]; 6 (3): 179-87 PMID24936213show ga Intravital (in vivo) microscopy using fluorescently-tagged proteins is a valuable tool for imaging the expression of a specific protein, its subcellular location and the dynamics of specific cell populations in living animals. Recently, multiphoton microscopy including two-photon laser scanning microscopy (TPLSM) has been used in the field of tumor biology due to its ability to image target organs at higher magnification and at deeper depths from the tissue surface for longer time periods. We developed a method of in vivo real-time imaging for tumor metastasis using TPLSM with an organ stabilizing system, which allow us to observe not only a single tumor cell and its microenvironment for a long time, but also to observe the same organ of the same mouse at multiple time points in preclinical models. Here, we presented in vivo real-time images of 1) tumor cell arrest, 2) tumor cell-platelet interaction, 3) tumor cell-leukocyte interaction, and 4) metastatic colonization at the secondary organs as representative steps of metastatic process of experimental liver metastasis models using TPLSM. äIn vivo optical imaging of cancer metastasis using multiphoton microsc(epmc).pdf DeepDyve Pubget Overpricing