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10.1007/s00467-013-2684-4 http://scihub22266oqcxt.onion/10.1007/s00467-013-2684-4 C4676405!4676405!24398540     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 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 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Pediatr+Nephrol 2014 ; 29 (4): 695-704 Nephropedia Template TP {{tp|p=24398540|t=2014. Single-Gene Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in Humans |pdf=|usr=}}{{24398540}} gab.com Text Single-Gene Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in Humans JO: Pediatr Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=24398540 #FOAvip Congenital anomalies of the kidney and urinary tract (CAKUT) cover a wide range of structural malformations that result from defects in the morphogenesis of the kidney and/or urinary tract. These anomalies account for about 40?50% of children with chronic kidney disease worldwide. Knowledge from genetically modified mouse models suggests that single gene mutations in renal developmental genes may lead to CAKUT in humans. However, until recently only a handful of CAKUT-causing genes were reported, most of them in familial syndromic cases. Recent findings suggest that CAKUT may arise from mutations in a multitude of different single gene causes. We focus here on single gene causes of CAKUT and their developmental origin. Currently more than 20 monogenic CAKUT-causing genes have been identified. High-throughput sequencing techniques make it likely that additional CAKUT-causing genes will be identified in the near future. Twit Text FOAVip Single-Gene Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in Humans ????Pediatr Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=24398540 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24398540 #FOAvip English Wikipedia <ref>{{Cite pmid|24398540}}</ref> Single-Gene Causes of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) in Humans #MMPMID24398540 Vivante A; Kohl S; Hwang DY; Dworschak GC; Hildebrandt F Pediatr Nephrol 2014[Apr]; 29 (4): 695-704 PMID24398540show ga Congenital anomalies of the kidney and urinary tract (CAKUT) cover a wide range of structural malformations that result from defects in the morphogenesis of the kidney and/or urinary tract. These anomalies account for about 40?50% of children with chronic kidney disease worldwide. Knowledge from genetically modified mouse models suggests that single gene mutations in renal developmental genes may lead to CAKUT in humans. However, until recently only a handful of CAKUT-causing genes were reported, most of them in familial syndromic cases. Recent findings suggest that CAKUT may arise from mutations in a multitude of different single gene causes. We focus here on single gene causes of CAKUT and their developmental origin. Currently more than 20 monogenic CAKUT-causing genes have been identified. High-throughput sequencing techniques make it likely that additional CAKUT-causing genes will be identified in the near future. äSingle-Gene Causes of Congenital Anomalies of the Kidney and Urinary T(epmc).pdf DeepDyve Pubget Overpricing