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10.1080/15476286.2015.1094596 http://scihub22266oqcxt.onion/10.1080/15476286.2015.1094596 C4993306!4993306!26400640     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       RNA+Biol 2016 ; 13 (8): 696-706 Nephropedia Template TP {{tp|p=26400640|t=2016. The molecular genetics of the telomere biology disorders |pdf=|usr=}}{{26400640}} gab.com Text The molecular genetics of the telomere biology disorders JO: RNA Biol http://www.kidney.de/pget.php?&tw=1&pmid=26400640 #FOAvip The importance of telomere function for human health is exemplified by a collection of Mendelian disorders referred to as the telomere biology disorders (TBDs), telomeropathies, or syndromes of telomere shortening. Collectively, the TBDs cover a spectrum of conditions from multisystem disease presenting in infancy to isolated disease presentations in adulthood, most notably idiopathic pulmonary fibrosis. Eleven genes have been found mutated in the TBDs to date, each of which is linked to some aspect of telomere maintenance. This review summarizes the molecular defects that result from mutations in these genes, highlighting recent advances, including the addition of PARN to the TBD gene family and the discovery of heterozygous mutations in RTEL1 as a cause of familial pulmonary fibrosis. Twit Text FOAVip The molecular genetics of the telomere biology disorders ????RNA Biol http://www.kidney.de/pget.php?&tw=1&pmid=26400640 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26400640 #FOAvip English Wikipedia <ref>{{Cite pmid|26400640}}</ref> The molecular genetics of the telomere biology disorders #MMPMID26400640 Bertuch AA RNA Biol 2016[Aug]; 13 (8): 696-706 PMID26400640show ga The importance of telomere function for human health is exemplified by a collection of Mendelian disorders referred to as the telomere biology disorders (TBDs), telomeropathies, or syndromes of telomere shortening. Collectively, the TBDs cover a spectrum of conditions from multisystem disease presenting in infancy to isolated disease presentations in adulthood, most notably idiopathic pulmonary fibrosis. Eleven genes have been found mutated in the TBDs to date, each of which is linked to some aspect of telomere maintenance. This review summarizes the molecular defects that result from mutations in these genes, highlighting recent advances, including the addition of PARN to the TBD gene family and the discovery of heterozygous mutations in RTEL1 as a cause of familial pulmonary fibrosis. äThe molecular genetics of the telomere biology disorders (epmc).pdf DeepDyve Pubget Overpricing