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10.1097/MNH.0b013e32832f125e http://scihub22266oqcxt.onion/10.1097/MNH.0b013e32832f125e 19584721!2883450!19584721     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Curr+Opin+Nephrol+Hypertens 2009 ; 18 (5): 439-48 Nephropedia Template TP {{tp|p=19584721|t=2009. The physiological impact of the serum and glucocorticoid-inducible kinase SGK1 |pdf=|usr=}}{{19584721}} gab.com Text The physiological impact of the serum and glucocorticoid-inducible kinase SGK1 JO: Curr Opin Nephrol Hypertens http://www.kidney.de/pget.php?&tw=1&pmid=19584721 #FOAvip PURPOSE OF REVIEW: The role of serum and glucocorticoid-inducible kinase 1 (SGK1) in renal physiology and pathophysiology is reviewed with particular emphasis on recent advances. RECENT FINDINGS: The mammalian target of rapamycin complex 2 has been shown to phosphorylate SGK1 at Ser422 (the so-called hydrophobic motif). Ser397 and Ser401 are two additional SGK1-phosphorylation sites required for maximal SGK1 activity. A 5' variant alternate transcript of human Sgk1 has been identified that is widely expressed and shows improved stability, enhanced membrane association, and greater stimulation of epithelial Na+ transport. SGK1 is essential for optimal processing of the epithelial sodium channel and also regulates the expression of the Na+-Cl- cotransporter. With regard to pathophysiology, SGK1 participates in the stimulation of renal tubular glucose transport in diabetes, the renal profibrotic effect of both angiotensin II and aldosterone, and in fetal programing of arterial hypertension. SUMMARY: The outlined recent findings advanced our understanding of the molecular regulation of SGK1 as well as the role of the kinase in renal physiology and the pathophysiology of renal disease and hypertension. Future studies using pharmacological inhibitors of SGK1 will reveal the utility of the kinase as a new therapeutic target. Twit Text FOAVip The physiological impact of the serum and glucocorticoid-inducible kinase SGK1 ????Curr Opin Nephrol Hypertens http://www.kidney.de/pget.php?&tw=1&pmid=19584721 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=19584721 #FOAvip English Wikipedia <ref>{{Cite pmid|19584721}}</ref> The physiological impact of the serum and glucocorticoid-inducible kinase SGK1 #MMPMID19584721 Lang F; Artunc F; Vallon V Curr Opin Nephrol Hypertens 2009[Sep]; 18 (5): 439-48 PMID19584721show ga PURPOSE OF REVIEW: The role of serum and glucocorticoid-inducible kinase 1 (SGK1) in renal physiology and pathophysiology is reviewed with particular emphasis on recent advances. RECENT FINDINGS: The mammalian target of rapamycin complex 2 has been shown to phosphorylate SGK1 at Ser422 (the so-called hydrophobic motif). Ser397 and Ser401 are two additional SGK1-phosphorylation sites required for maximal SGK1 activity. A 5' variant alternate transcript of human Sgk1 has been identified that is widely expressed and shows improved stability, enhanced membrane association, and greater stimulation of epithelial Na+ transport. SGK1 is essential for optimal processing of the epithelial sodium channel and also regulates the expression of the Na+-Cl- cotransporter. With regard to pathophysiology, SGK1 participates in the stimulation of renal tubular glucose transport in diabetes, the renal profibrotic effect of both angiotensin II and aldosterone, and in fetal programing of arterial hypertension. SUMMARY: The outlined recent findings advanced our understanding of the molecular regulation of SGK1 as well as the role of the kinase in renal physiology and the pathophysiology of renal disease and hypertension. Future studies using pharmacological inhibitors of SGK1 will reveal the utility of the kinase as a new therapeutic target. |Animals[MESH] |Appetite/genetics/physiology[MESH] |Gene Expression Regulation, Enzymologic/physiology[MESH] |Humans[MESH] |Hypertension/enzymology/genetics[MESH] |Immediate-Early Proteins/biosynthesis/*blood/genetics/*physiology[MESH] |Kidney/physiology[MESH] |Metabolic Syndrome/enzymology/genetics[MESH] |Obesity/enzymology/genetics[MESH]The physiological impact of the serum and glucocorticoid-inducible kin(epmc).pdf DeepDyve Pubget Overpricing