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10.3390/genes6020267 http://scihub22266oqcxt.onion/10.3390/genes6020267 C4488665!4488665!26010955     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Genes+(Basel) 2015 ; 6 (2): 267-98 Nephropedia Template TP {{tp|p=26010955|t=2015. Replication Stress in Mammalian Cells and Its Consequences for Mitosis |pdf=|usr=}}{{26010955}} gab.com Text Replication Stress in Mammalian Cells and Its Consequences for Mitosis JO: Genes (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=26010955 #FOAvip The faithful transmission of genetic information to daughter cells is central to maintaining genomic stability and relies on the accurate and complete duplication of genetic material during each cell cycle. However, the genome is routinely exposed to endogenous and exogenous stresses that can impede the progression of replication. Such replication stress can be an early cause of cancer or initiate senescence. Replication stress, which primarily occurs during S phase, results in consequences during mitosis, jeopardizing chromosome segregation and, in turn, genomic stability. The traces of replication stress can be detected in the daughter cells during G1 phase. Alterations in mitosis occur in two types: 1) local alterations that correspond to breaks, rearrangements, intertwined DNA molecules or non-separated sister chromatids that are confined to the region of the replication dysfunction; 2) genome-wide chromosome segregation resulting from centrosome amplification (although centrosomes do not contain DNA), which amplifies the local replication stress to the entire genome. Here, we discuss the endogenous causes of replication perturbations, the mechanisms of replication fork restart and the consequences for mitosis, chromosome segregation and genomic stability. Twit Text FOAVip Replication Stress in Mammalian Cells and Its Consequences for Mitosis ????Genes (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=26010955 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26010955 #FOAvip English Wikipedia <ref>{{Cite pmid|26010955}}</ref> Replication Stress in Mammalian Cells and Its Consequences for Mitosis #MMPMID26010955 Gelot C; Magdalou I; Lopez BS Genes (Basel) 2015[Jun]; 6 (2): 267-98 PMID26010955show ga The faithful transmission of genetic information to daughter cells is central to maintaining genomic stability and relies on the accurate and complete duplication of genetic material during each cell cycle. However, the genome is routinely exposed to endogenous and exogenous stresses that can impede the progression of replication. Such replication stress can be an early cause of cancer or initiate senescence. Replication stress, which primarily occurs during S phase, results in consequences during mitosis, jeopardizing chromosome segregation and, in turn, genomic stability. The traces of replication stress can be detected in the daughter cells during G1 phase. Alterations in mitosis occur in two types: 1) local alterations that correspond to breaks, rearrangements, intertwined DNA molecules or non-separated sister chromatids that are confined to the region of the replication dysfunction; 2) genome-wide chromosome segregation resulting from centrosome amplification (although centrosomes do not contain DNA), which amplifies the local replication stress to the entire genome. Here, we discuss the endogenous causes of replication perturbations, the mechanisms of replication fork restart and the consequences for mitosis, chromosome segregation and genomic stability. äReplication Stress in Mammalian Cells and Its Consequences for Mitosis(epmc).pdf DeepDyve Pubget Overpricing