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10.3390/ijms161126023 http://scihub22266oqcxt.onion/10.3390/ijms161126023 C4661881!4661881!26580600     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       Int+J+Mol+Sci 2015 ; 16 (11): 27208-27 Nephropedia Template TP {{tp|p=26580600|t=2015. Developing Potential Candidates of Preclinical Preeclampsia |pdf=|usr=}}{{26580600}} gab.com Text Developing Potential Candidates of Preclinical Preeclampsia JO: Int J Mol Sci http://www.kidney.de/pget.php?&tw=1&pmid=26580600 #FOAvip The potential for developing molecules of interest in preclinical preeclampsia from candidate genes that were discovered on gene expression microarray analysis has been challenged by limited access to additional first trimester trophoblast and decidual tissues. The question of whether these candidates encode secreted proteins that may be detected in maternal circulation early in pregnancy has been investigated using various proteomic methods. Pilot studies utilizing mass spectrometry based proteomic assays, along with enzyme linked immunosorbent assays (ELISAs), and Western immunoblotting in first trimester samples are reported. The novel targeted mass spectrometry methods led to robust multiple reaction monitoring assays. Despite detection of several candidates in early gestation, challenges persist. Future antibody-based studies may lead to a novel multiplex protein panel for screening or detection to prevent or mitigate preeclampsia. Twit Text FOAVip Developing Potential Candidates of Preclinical Preeclampsia ????Int J Mol Sci http://www.kidney.de/pget.php?&tw=1&pmid=26580600 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26580600 #FOAvip English Wikipedia <ref>{{Cite pmid|26580600}}</ref> Developing Potential Candidates of Preclinical Preeclampsia #MMPMID26580600 Founds S; Zeng X; Lykins D; Roberts JM Int J Mol Sci 2015[Nov]; 16 (11): 27208-27 PMID26580600show ga The potential for developing molecules of interest in preclinical preeclampsia from candidate genes that were discovered on gene expression microarray analysis has been challenged by limited access to additional first trimester trophoblast and decidual tissues. The question of whether these candidates encode secreted proteins that may be detected in maternal circulation early in pregnancy has been investigated using various proteomic methods. Pilot studies utilizing mass spectrometry based proteomic assays, along with enzyme linked immunosorbent assays (ELISAs), and Western immunoblotting in first trimester samples are reported. The novel targeted mass spectrometry methods led to robust multiple reaction monitoring assays. Despite detection of several candidates in early gestation, challenges persist. Future antibody-based studies may lead to a novel multiplex protein panel for screening or detection to prevent or mitigate preeclampsia. äDeveloping Potential Candidates of Preclinical Preeclampsia (epmc).pdf DeepDyve Pubget Overpricing