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10.1101/gad.278952.116 http://scihub22266oqcxt.onion/10.1101/gad.278952.116 C4782042!4782042 !26944674     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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26944674 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Genes+Dev 2016 ; 30 (5 ): 485-6 Nephropedia Template TP {{tp|p=26944674 |t=2016. Making choices-how stochastic decisions determine disease progression |pdf=|usr=}}{{26944674 }} gab.com Text Making choices-how stochastic decisions determine disease progression JO: Genes Dev http://www.kidney.de/pget.php?&tw=1&pmid=26944674 #FOAvip In this issue of Genes & Development, Ginart and colleagues (pp. 567-578) study a mouse model for Russell-Silver syndrome (RSS) and show that similar cells within one individual can display distinct gene expression patterns because of epigenetic marks that are established stochastically during early development. Their results provide an excellent explanation for phenotypes seen in RSS and other imprinting disorders and especially help us understand how patients with similar or even identical genetic mutations can display distinct disease profiles. Twit Text FOAVip Making choices-how stochastic decisions determine disease progression ????Genes Dev http://www.kidney.de/pget.php?&tw=1&pmid=26944674 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26944674 #FOAvip English Wikipedia <ref>{{Cite pmid|26944674 }}</ref> Making choices-how stochastic decisions determine disease progression #MMPMID26944674 Park KS ; Pfeifer K Genes Dev 2016[Mar]; 30 (5 ): 485-6 PMID26944674 show ga In this issue of Genes & Development, Ginart and colleagues (pp. 567-578) study a mouse model for Russell-Silver syndrome (RSS) and show that similar cells within one individual can display distinct gene expression patterns because of epigenetic marks that are established stochastically during early development. Their results provide an excellent explanation for phenotypes seen in RSS and other imprinting disorders and especially help us understand how patients with similar or even identical genetic mutations can display distinct disease profiles. |*Disease Progression [MESH] |*Gene Expression Regulation, Developmental [MESH] |Alleles [MESH] |Animals [MESH] |DNA Methylation [MESH] |Gene Dosage [MESH] |Genomic Imprinting/*genetics [MESH] |Humans [MESH] |Mice [MESH] |Models, Animal [MESH]Making choices-how stochastic decisions determine disease progression (epmc).pdf DeepDyve Pubget Overpricing