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10.1016/j.ajhg.2015.04.014 http://scihub22266oqcxt.onion/10.1016/j.ajhg.2015.04.014 C4457946!4457946!26004201     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Am+J+Hum+Genet 2015 ; 96 (6): 955-61 Nephropedia Template TP {{tp|p=26004201|t=2015. Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita |pdf=|usr=}}{{26004201}} gab.com Text Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita JO: Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=26004201 #FOAvip Arthrogryposis multiplex congenita is defined by the presence of contractures across two or more major joints and results from reduced or absent fetal movement. Here, we present three consanguineous families affected by lethal arthrogryposis multiplex congenita. By whole-exome or targeted exome sequencing, it was shown that the probands each harbored a different homozygous mutation (one missense, one nonsense, and one frameshift mutation) in GPR126. GPR126 encodes G-protein-coupled receptor 126, which has been shown to be essential for myelination of axons in the peripheral nervous system in fish and mice. A previous study reported that Gpr126?/? mice have a lethal arthrogryposis phenotype. We have shown that the peripheral nerves in affected individuals from one family lack myelin basic protein, suggesting that this disease in affected individuals is due to defective myelination of the peripheral axons during fetal development. Previous work has suggested that autoproteolytic cleavage is important for activating GPR126 signaling, and our biochemical assays indicated that the missense substitution (p.Val769Glu [c.2306T>A]) impairs autoproteolytic cleavage of GPR126. Our data indicate that GPR126 is critical for myelination of peripheral nerves in humans. This study adds to the literature implicating defective axoglial function as a key cause of severe arthrogryposis multiplex congenita and suggests that GPR126 mutations should be investigated in individuals affected by this disorder. Twit Text FOAVip Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita ????Am J Hum Genet http://www.kidney.de/pget.php?&tw=1&pmid=26004201 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26004201 #FOAvip English Wikipedia <ref>{{Cite pmid|26004201}}</ref> Mutations of GPR126 Are Responsible for Severe Arthrogryposis Multiplex Congenita #MMPMID26004201 Ravenscroft G; Nolent F; Rajagopalan S; Meireles A; Paavola K; Gaillard D; Alanio E; Buckland M; Arbuckle S; Krivanek M; Maluenda J; Pannell S; Gooding R; Ong R; Allcock R; Carvalho E; Carvalho M; Kok F; Talbot W; Melki J; Laing N Am J Hum Genet 2015[Jun]; 96 (6): 955-61 PMID26004201show ga Arthrogryposis multiplex congenita is defined by the presence of contractures across two or more major joints and results from reduced or absent fetal movement. Here, we present three consanguineous families affected by lethal arthrogryposis multiplex congenita. By whole-exome or targeted exome sequencing, it was shown that the probands each harbored a different homozygous mutation (one missense, one nonsense, and one frameshift mutation) in GPR126. GPR126 encodes G-protein-coupled receptor 126, which has been shown to be essential for myelination of axons in the peripheral nervous system in fish and mice. A previous study reported that Gpr126?/? mice have a lethal arthrogryposis phenotype. We have shown that the peripheral nerves in affected individuals from one family lack myelin basic protein, suggesting that this disease in affected individuals is due to defective myelination of the peripheral axons during fetal development. Previous work has suggested that autoproteolytic cleavage is important for activating GPR126 signaling, and our biochemical assays indicated that the missense substitution (p.Val769Glu [c.2306T>A]) impairs autoproteolytic cleavage of GPR126. Our data indicate that GPR126 is critical for myelination of peripheral nerves in humans. This study adds to the literature implicating defective axoglial function as a key cause of severe arthrogryposis multiplex congenita and suggests that GPR126 mutations should be investigated in individuals affected by this disorder. äMutations of GPR126 Are Responsible for Severe Arthrogryposis Multiple(epmc).pdf DeepDyve Pubget Overpricing