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10.1186/s13045-017-0472-5 http://scihub22266oqcxt.onion/10.1186/s13045-017-0472-5 C5414291!5414291 !28464892     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 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\28464892 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       J+Hematol+Oncol 2017 ; 10 (1 ): 99 Nephropedia Template TP {{tp|p=28464892 |t=2017. Non-driver mutations in myeloproliferative neoplasm-associated myelofibrosis |pdf=|usr=}}{{28464892 }} gab.com Text Non-driver mutations in myeloproliferative neoplasm-associated myelofibrosis JO: J Hematol Oncol http://www.kidney.de/pget.php?&tw=1&pmid=28464892 #FOAvip We studied non-driver mutations in 62 subjects with myeloproliferative neoplasm (MPN)-associated myelofibrosis upon diagnosis, including 45 subjects with primary myelofibrosis (PMF) and 17 with post-polycythemia vera or post-essential thrombocythemia myelofibrosis (post-PV/ET MF). Fifty-eight subjects had ?1 non-driver mutation upon diagnosis. Mutations in mRNA splicing genes, especially in U2AF1, were significantly more frequent in PMF than in post-PV/ET MF (33 vs. 6%; P?=?0.015). There were also striking differences in clonal architecture. These data indicate different genomic spectrums between PMF and post-PV/ET MF. Twit Text FOAVip Non-driver mutations in myeloproliferative neoplasm-associated myelofibrosis ????J Hematol Oncol http://www.kidney.de/pget.php?&tw=1&pmid=28464892 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28464892 #FOAvip English Wikipedia <ref>{{Cite pmid|28464892 }}</ref> Non-driver mutations in myeloproliferative neoplasm-associated myelofibrosis #MMPMID28464892 Li B ; Gale RP ; Xu Z ; Qin T ; Song Z ; Zhang P ; Bai J ; Zhang L ; Zhang Y ; Liu J ; Huang G ; Xiao Z J Hematol Oncol 2017[May]; 10 (1 ): 99 PMID28464892 show ga We studied non-driver mutations in 62 subjects with myeloproliferative neoplasm (MPN)-associated myelofibrosis upon diagnosis, including 45 subjects with primary myelofibrosis (PMF) and 17 with post-polycythemia vera or post-essential thrombocythemia myelofibrosis (post-PV/ET MF). Fifty-eight subjects had ?1 non-driver mutation upon diagnosis. Mutations in mRNA splicing genes, especially in U2AF1, were significantly more frequent in PMF than in post-PV/ET MF (33 vs. 6%; P?=?0.015). There were also striking differences in clonal architecture. These data indicate different genomic spectrums between PMF and post-PV/ET MF. |*Mutation [MESH] |Adult [MESH] |Aged [MESH] |Aged, 80 and over [MESH] |Apoptosis/genetics [MESH] |Cell Adhesion/genetics [MESH] |Cell Cycle/genetics [MESH] |Chromatin Assembly and Disassembly/genetics [MESH] |Clone Cells [MESH] |DNA Methylation/genetics [MESH] |DNA Repair/genetics [MESH] |Female [MESH] |Humans [MESH] |Male [MESH] |Middle Aged [MESH] |Polycythemia Vera/complications/*genetics [MESH] |Primary Myelofibrosis/etiology/*genetics [MESH] |RNA Splicing/genetics [MESH] |Signal Transduction/genetics [MESH] |Splicing Factor U2AF/genetics [MESH] |Thrombocythemia, Essential/complications/genetics [MESH]Non-driver mutations in myeloproliferative neoplasm-associated myelofi(epmc).pdf DeepDyve Pubget Overpricing