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10.1111/j.1582-4934.2009.00748.x http://scihub22266oqcxt.onion/10.1111/j.1582-4934.2009.00748.x C4496136!4496136!19382915     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Cell+Mol+Med 2009 ; 13 (7): 1221-7 Nephropedia Template TP {{tp|p=19382915|t=2009. Apoptosis pathways and their therapeutic exploitation in pancreatic cancer |pdf=|usr=}}{{19382915}} gab.com Text Apoptosis pathways and their therapeutic exploitation in pancreatic cancer JO: J Cell Mol Med http://www.kidney.de/pget.php?&tw=1&pmid=19382915 #FOAvip Resistance to apoptosis (programmed cell death) is a characteristic feature of human malignancies including pancreatic cancer, which is one of the leading causes of cancer deaths in the western world. Defects in this intrinsic cell death program can contribute to the multistep process of tumorigenesis, because too little cell death can disturb tissue homeostasis. Further, blockade of apoptosis pathways can cause treatment failure, because intact apoptosis signalling cascades largely mediate therapy-induced cytotoxicity. The elucidation of apoptosis pathways in pancreatic carcinoma over the last decade has resulted in the identification of various molecular defects. How apoptosis pathways can be exploited for the treatment of pancreatic cancer will be discussed in this review. Twit Text FOAVip Apoptosis pathways and their therapeutic exploitation in pancreatic cancer ????J Cell Mol Med http://www.kidney.de/pget.php?&tw=1&pmid=19382915 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=19382915 #FOAvip English Wikipedia <ref>{{Cite pmid|19382915}}</ref> Apoptosis pathways and their therapeutic exploitation in pancreatic cancer #MMPMID19382915 Fulda S J Cell Mol Med 2009[Jul]; 13 (7): 1221-7 PMID19382915show ga Resistance to apoptosis (programmed cell death) is a characteristic feature of human malignancies including pancreatic cancer, which is one of the leading causes of cancer deaths in the western world. Defects in this intrinsic cell death program can contribute to the multistep process of tumorigenesis, because too little cell death can disturb tissue homeostasis. Further, blockade of apoptosis pathways can cause treatment failure, because intact apoptosis signalling cascades largely mediate therapy-induced cytotoxicity. The elucidation of apoptosis pathways in pancreatic carcinoma over the last decade has resulted in the identification of various molecular defects. How apoptosis pathways can be exploited for the treatment of pancreatic cancer will be discussed in this review. äApoptosis pathways and their therapeutic exploitation in pancreatic ca(epmc).pdf DeepDyve Pubget Overpricing