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10.1080/15384101.2017.1317418 http://scihub22266oqcxt.onion/10.1080/15384101.2017.1317418 C5499842!5499842!28486014     free     free     free Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 229.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Cell+Cycle 2017 ; 16 (12): 1171-4 Nephropedia Template TP {{tp|p=28486014|t=2017. Tissue TGF-? expression following conventional radiotherapy and pulsed low-dose-rate radiation |pdf=|usr=}}{{28486014}} gab.com Text Tissue TGF- expression following conventional radiotherapy and pulsed low-dose-rate radiation JO: Cell Cycle http://www.kidney.de/pget.php?&tw=1&pmid=28486014 #FOAvip The release of inflammatory cytokines has been implicated in the toxicity of conventional radiotherapy (CRT). Transforming growth factor ? (TGF-?) has been suggested to be a risk marker for pulmonary toxicity following radiotherapy. Pulsed low-dose rate radiotherapy (PLDR) is a technique that involves spreading out a conventional radiotherapy dose into short pulses of dose with breaks in between to reduce toxicities. We hypothesized that the more tolerable toxicity profile of PLDR compared with CRT may be related to differential expression of inflammatory cytokines such as TGF-? in normal tissues. To address this, we analyzed tissues from mice that had been subjected to lethal doses of CRT and PLDR by histology and immunohistochemistry (IHC). Equivalent physical doses of CRT triggered more cellular atrophy in the bone marrow, intestine, and pancreas when compared with PLDR as indicated by hematoxylin and eosin staining. IHC data indicates that TGF-? expression is increased in the bone marrow, intestine, and lungs of mice subjected to CRT as compared with tissues from mice subjected to PLDR. Our in vivo data suggest that differential expression of inflammatory cytokines such as TGF-? may play a role in the more favorable normal tissue late response following treatment with PLDR. Twit Text FOAVip Tissue TGF- expression following conventional radiotherapy and pulsed low-dose-rate radiation ????Cell Cycle http://www.kidney.de/pget.php?&tw=1&pmid=28486014 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28486014 #FOAvip English Wikipedia <ref>{{Cite pmid|28486014}}</ref> Tissue TGF-? expression following conventional radiotherapy and pulsed low-dose-rate radiation #MMPMID28486014 Meyer JE; Finnberg NK; Chen L; Cvetkovic D; Wang B; Zhou L; Dong Y; Hallman MA; Ma CMC; El-Deiry WS Cell Cycle 2017[]; 16 (12): 1171-4 PMID28486014show ga The release of inflammatory cytokines has been implicated in the toxicity of conventional radiotherapy (CRT). Transforming growth factor ? (TGF-?) has been suggested to be a risk marker for pulmonary toxicity following radiotherapy. Pulsed low-dose rate radiotherapy (PLDR) is a technique that involves spreading out a conventional radiotherapy dose into short pulses of dose with breaks in between to reduce toxicities. We hypothesized that the more tolerable toxicity profile of PLDR compared with CRT may be related to differential expression of inflammatory cytokines such as TGF-? in normal tissues. To address this, we analyzed tissues from mice that had been subjected to lethal doses of CRT and PLDR by histology and immunohistochemistry (IHC). Equivalent physical doses of CRT triggered more cellular atrophy in the bone marrow, intestine, and pancreas when compared with PLDR as indicated by hematoxylin and eosin staining. IHC data indicates that TGF-? expression is increased in the bone marrow, intestine, and lungs of mice subjected to CRT as compared with tissues from mice subjected to PLDR. Our in vivo data suggest that differential expression of inflammatory cytokines such as TGF-? may play a role in the more favorable normal tissue late response following treatment with PLDR. äTissue TGF-? expression following conventional radiotherapy and pulsed(epmc).pdf DeepDyve Pubget Overpricing