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10.1016/j.hoc.2014.10.002 http://scihub22266oqcxt.onion/10.1016/j.hoc.2014.10.002 C4385194!4385194!25836928     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25836928&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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25836928.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Hematol+Oncol+Clin+North+Am 2015 ; 29 (2): 191-203 Nephropedia Template TP {{tp|p=25836928|t=2015. Molecular biology of bladder cancer |pdf=|usr=}}{{25836928}} gab.com Text Molecular biology of bladder cancer JO: Hematol Oncol Clin North Am http://www.kidney.de/pget.php?&tw=1&pmid=25836928 #FOAvip Many detailed studies of the molecular pathogenesis of bladder cancer have been published during the past three decades, identifying important roles for many of the classic cancer pathways in bladder cancer development. Nonetheless, recent large scale mutational and expression analyses in bladder cancer made possible by next generation sequencing and other new techniques have uncovered multiple genes and pathways important for bladder cancer development, many of which were previously unknown. Genes involved in cell cycle control, chromatin regulation, and receptor tyrosine and PI 3-kinase-mTOR signaling pathways are commonly mutated in muscle-invasive bladder cancer, and most cancers have involvement of more than one of these pathways. In addition, expression-based analyses have enabled identification of two distinct types of bladder cancer, basal and luminal, that are similar to those same subsets of breast cancer, and have prognostic and therapeutic significance. These observations are leading to a number of novel therapeutic approaches in bladder cancer, providing optimism for therapeutic progress in the near future. Twit Text FOAVip Molecular biology of bladder cancer ????Hematol Oncol Clin North Am http://www.kidney.de/pget.php?&tw=1&pmid=25836928 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25836928 #FOAvip English Wikipedia <ref>{{Cite pmid|25836928}}</ref> Molecular biology of bladder cancer #MMPMID25836928 Martin-Doyle W; Kwiatkowski DJ Hematol Oncol Clin North Am 2015[Apr]; 29 (2): 191-203 PMID25836928show ga Many detailed studies of the molecular pathogenesis of bladder cancer have been published during the past three decades, identifying important roles for many of the classic cancer pathways in bladder cancer development. Nonetheless, recent large scale mutational and expression analyses in bladder cancer made possible by next generation sequencing and other new techniques have uncovered multiple genes and pathways important for bladder cancer development, many of which were previously unknown. Genes involved in cell cycle control, chromatin regulation, and receptor tyrosine and PI 3-kinase-mTOR signaling pathways are commonly mutated in muscle-invasive bladder cancer, and most cancers have involvement of more than one of these pathways. In addition, expression-based analyses have enabled identification of two distinct types of bladder cancer, basal and luminal, that are similar to those same subsets of breast cancer, and have prognostic and therapeutic significance. These observations are leading to a number of novel therapeutic approaches in bladder cancer, providing optimism for therapeutic progress in the near future. äMolecular biology of bladder cancer (epmc).pdf DeepDyve Pubget Overpricing