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10.3233/ACP-130075 http://scihub22266oqcxt.onion/10.3233/ACP-130075 C4605645!4605645 !23579249     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 245.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\23579249 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Anal+Cell+Pathol+(Amst) 2013 ; 36 (1-2 ): 27-35 Nephropedia Template TP {{tp|p=23579249 |t=2013. Structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications |pdf=|usr=}}{{23579249 }} gab.com Text Structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications JO: Anal Cell Pathol (Amst) http://www.kidney.de/pget.php?&tw=1&pmid=23579249 #FOAvip Structured illumination fluorescence microscopy utilizes interfering light and the moiré effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of resolution in the z- direction by the same factor of two (to approximately 220 nm), making it a powerful tool for 3-D morphology studies of fluorescently labeled cells or thin tissue sections. In this report, we applied this technique to several types of blood cells that are commonly seen in hematopathology. Compared with standard brightfield and ordinary fluorescence microscopy images, the 3-D morphology results clearly reveal the morphological features of different types of normal blood cells. We have also used this technique to evaluate morphologies of abnormal erythrocytes and compare them with those recorded on normal cells. The results give a very intuitive presentation of morphological structures of erythrocytes with great details. This research illustrates the potential of this technique to be used in hematology and cyto-pathology studies aimed at identifying nanometer-sized features that cannot be distinguished otherwise with conventional optical microscopy. Twit Text FOAVip Structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications ????Anal Cell Pathol (Amst) http://www.kidney.de/pget.php?&tw=1&pmid=23579249 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=23579249 #FOAvip English Wikipedia <ref>{{Cite pmid|23579249 }}</ref> Structured illumination-based super-resolution optical microscopy for hemato- and cyto-pathology applications #MMPMID23579249 Zhang T ; Osborn S ; Brandow C ; Dwyre D ; Green R ; Lane S ; Wachsmann-Hogiu S Anal Cell Pathol (Amst) 2013[]; 36 (1-2 ): 27-35 PMID23579249 show ga Structured illumination fluorescence microscopy utilizes interfering light and the moiré effect to enhance spatial resolution to about a half of that of conventional light microscopy, i.e. approximately 90 nm. In addition to the enhancement in the x and y directions, it also allows enhancement of resolution in the z- direction by the same factor of two (to approximately 220 nm), making it a powerful tool for 3-D morphology studies of fluorescently labeled cells or thin tissue sections. In this report, we applied this technique to several types of blood cells that are commonly seen in hematopathology. Compared with standard brightfield and ordinary fluorescence microscopy images, the 3-D morphology results clearly reveal the morphological features of different types of normal blood cells. We have also used this technique to evaluate morphologies of abnormal erythrocytes and compare them with those recorded on normal cells. The results give a very intuitive presentation of morphological structures of erythrocytes with great details. This research illustrates the potential of this technique to be used in hematology and cyto-pathology studies aimed at identifying nanometer-sized features that cannot be distinguished otherwise with conventional optical microscopy. |*Cytological Techniques [MESH] |*Lighting [MESH] |Azure Stains [MESH] |Blood Cells/*pathology [MESH] |Hematology/*methods [MESH] |Humans [MESH] |Imaging, Three-Dimensional [MESH] |Microscopy, Fluorescence/*methods [MESH] |Pathology/*methods [MESH] |Predictive Value of Tests [MESH]Structured illumination-based super-resolution optical microscopy for (epmc).pdf DeepDyve Pubget Overpricing