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10.1016/B978-0-12-800223-0.00011-6 http://scihub22266oqcxt.onion/10.1016/B978-0-12-800223-0.00011-6 24745990!�!24745990 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24745990&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\24745990.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Curr+Top+Membr 2014 ; 73 (�): 383-410 Nephropedia Template TP {{tp|p=24745990|t=2014. SLC41 transporters--molecular identification and functional role |pdf=|usr=}}{{24745990}} gab.com Text SLC41 transporters--molecular identification and functional role JO: Curr Top Membr http://www.kidney.de/pget.php?&tw=1&pmid=24745990 #FOAvip The solute carrier family 41 (SLC41) encompasses three members A1, A2, and A3. Based on their distant homology to the bacterial Mg(2)(+) channel MgtE, all have been linked to Mg(2)(+) transport. There is only very limited knowledge on the molecular biology and exact functions of SLC41A2 and SLC41A3. SLC41A1 is ubiquitously expressed and data on its functional and molecular properties, regulation, complex-forming ability, and spectrum of binding partners are available. SLC41A1 was recently identified as being the Na(+)/Mg(2)(+) exchanger (NME)-a predominant Mg(2)(+) efflux system. Mg(2)(+)-dependent and hormonal regulation of NME activity is now known to depend on the intracellular N terminus of SLC41A1 that is involved in Mg(2)(+) sensing and contains phosphorylation sites for protein kinase (PK) A and PKC. Data showing a link between SLC41A1 and human disorders such as Parkinson's disease, nephronophthisis (induced by the null mutation c.698G>T in renal SLC41A1), and preeclampsia make the protein a candidate therapeutic target. Twit Text FOAVip SLC41 transporters--molecular identification and functional role ????Curr Top Membr http://www.kidney.de/pget.php?&tw=1&pmid=24745990 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24745990 #FOAvip English Wikipedia <ref>{{Cite pmid|24745990}}</ref> SLC41 transporters--molecular identification and functional role #MMPMID24745990 Schweigel-Rontgen M; Kolisek M Curr Top Membr 2014[]; 73 (�): 383-410 PMID24745990show ga The solute carrier family 41 (SLC41) encompasses three members A1, A2, and A3. Based on their distant homology to the bacterial Mg(2)(+) channel MgtE, all have been linked to Mg(2)(+) transport. There is only very limited knowledge on the molecular biology and exact functions of SLC41A2 and SLC41A3. SLC41A1 is ubiquitously expressed and data on its functional and molecular properties, regulation, complex-forming ability, and spectrum of binding partners are available. SLC41A1 was recently identified as being the Na(+)/Mg(2)(+) exchanger (NME)-a predominant Mg(2)(+) efflux system. Mg(2)(+)-dependent and hormonal regulation of NME activity is now known to depend on the intracellular N terminus of SLC41A1 that is involved in Mg(2)(+) sensing and contains phosphorylation sites for protein kinase (PK) A and PKC. Data showing a link between SLC41A1 and human disorders such as Parkinson's disease, nephronophthisis (induced by the null mutation c.698G>T in renal SLC41A1), and preeclampsia make the protein a candidate therapeutic target. |Animals[MESH] |Cation Transport Proteins/*chemistry/*metabolism[MESH] |Disease[MESH] |Humans[MESH] |Magnesium/metabolism[MESH] |Protein Transport[MESH]SLC41 transporters--molecular identification and functional role (epmc).pdf DeepDyve Pubget Overpricing