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10.1007/s13238-015-0177-x http://scihub22266oqcxt.onion/10.1007/s13238-015-0177-x C4491053!4491053!26081469     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26081469&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Protein+Cell 2015 ; 6 (7): 472-5 Nephropedia Template TP {{tp|p=26081469|t=2015. Eliminate mitochondrial diseases by gene editing in germ-line cells and embryos |pdf=|usr=}}{{26081469}} gab.com Text Eliminate mitochondrial diseases by gene editing in germ-line cells and embryos JO: Protein Cell http://www.kidney.de/pget.php?&tw=1&pmid=26081469 #FOAvip Nuclease-based gene editing technologies have opened up opportunities for correcting human genetic diseases. For the first time, scientists achieved targeted gene editing of mitochondrial DNA in mouse oocytes fused with patient cells. This fascinating progression may encourage the development of novel therapy for human maternally inherent mitochondrial diseases. Twit Text FOAVip Eliminate mitochondrial diseases by gene editing in germ-line cells and embryos ????Protein Cell http://www.kidney.de/pget.php?&tw=1&pmid=26081469 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26081469 #FOAvip English Wikipedia <ref>{{Cite pmid|26081469}}</ref> Eliminate mitochondrial diseases by gene editing in germ-line cells and embryos #MMPMID26081469 Wang S; Yi F; Qu J Protein Cell 2015[Jul]; 6 (7): 472-5 PMID26081469show ga Nuclease-based gene editing technologies have opened up opportunities for correcting human genetic diseases. For the first time, scientists achieved targeted gene editing of mitochondrial DNA in mouse oocytes fused with patient cells. This fascinating progression may encourage the development of novel therapy for human maternally inherent mitochondrial diseases. äEliminate mitochondrial diseases by gene editing in germ-line cells an(epmc).pdf DeepDyve Pubget Overpricing