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10.1016/j.ceb.2013.02.006 http://scihub22266oqcxt.onion/10.1016/j.ceb.2013.02.006 C5614462!5614462 !23478217     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=23478217 &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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\23478217 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Curr+Opin+Cell+Biol 2013 ; 25 (4 ): 428-33 Nephropedia Template TP {{tp|p=23478217 |t=2013. ER structure and function |pdf=|usr=}}{{23478217 }} gab.com Text ER structure and function JO: Curr Opin Cell Biol http://www.kidney.de/pget.php?&tw=1&pmid=23478217 #FOAvip The ER forms a contiguous structure of interconnected sheets and tubules that spreads from the nuclear envelope to the cell cortex. Through its attachment to the cytoskeleton, the ER undergoes dynamic rearrangements, such as tubule extension and movement. ER shaping proteins (reticulons and DP1/Yop1p) play key roles in generating and maintaining the unique reticular morphology of the ER. Atlastin and its yeast homologue, Sey1p, mediate homotypic ER membrane fusion, which leads to the formation of new three-way junctions within the polygonal network. At these junctions, the Lunapark protein, Lnp1p, works in conjunction with the reticulons, DP1/Yop1p, and in antagonism to atlastin/Sey1p to maintain the network in a dynamic equilibrium. Defects in ER morphology have been linked to certain neurological disorders. Twit Text FOAVip ER structure and function ????Curr Opin Cell Biol http://www.kidney.de/pget.php?&tw=1&pmid=23478217 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=23478217 #FOAvip English Wikipedia <ref>{{Cite pmid|23478217 }}</ref> ER structure and function #MMPMID23478217 Chen S ; Novick P ; Ferro-Novick S Curr Opin Cell Biol 2013[Aug]; 25 (4 ): 428-33 PMID23478217 show ga The ER forms a contiguous structure of interconnected sheets and tubules that spreads from the nuclear envelope to the cell cortex. Through its attachment to the cytoskeleton, the ER undergoes dynamic rearrangements, such as tubule extension and movement. ER shaping proteins (reticulons and DP1/Yop1p) play key roles in generating and maintaining the unique reticular morphology of the ER. Atlastin and its yeast homologue, Sey1p, mediate homotypic ER membrane fusion, which leads to the formation of new three-way junctions within the polygonal network. At these junctions, the Lunapark protein, Lnp1p, works in conjunction with the reticulons, DP1/Yop1p, and in antagonism to atlastin/Sey1p to maintain the network in a dynamic equilibrium. Defects in ER morphology have been linked to certain neurological disorders. |Animals [MESH] |Cytoskeleton/metabolism [MESH] |Endoplasmic Reticulum/*chemistry/*metabolism [MESH] |Humans [MESH] |Membrane Fusion [MESH] |Membrane Proteins/metabolism [MESH] |Microtubules/metabolism [MESH] |Nuclear Envelope/metabolism [MESH]ER structure and function (epmc).pdf DeepDyve Pubget Overpricing