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10.3389/fcell.2021.648024 http://scihub22266oqcxt.onion/10.3389/fcell.2021.648024 33748141!7970000!33748141     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       Front+Cell+Dev+Biol 2021 ; 9 (ä): 648024 Nephropedia Template TP {{tp|p=33748141|t=2021. Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens |pdf=|usr=}}{{33748141}} gab.com Text Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens JO: Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=33748141 #FOAvip Endosomes are essential cellular stations where endocytic and secretory trafficking routes converge. Proteins transiting at endosomes can be degraded via lysosome, or recycled to the plasma membrane, trans-Golgi network (TGN), or other cellular destinations. Pathways regulating endosomal recycling are tightly regulated in order to preserve organelle identity, to maintain lipid homeostasis, and to support other essential cellular functions. Recent studies have revealed that both pathogenic bacteria and viruses subvert host endosomal recycling pathways for their survival and replication. Several host factors that are frequently targeted by pathogens are being identified, including retromer, TBC1D5, SNX-BARs, and the WASH complex. In this review, we will focus on the recent advances in understanding how intracellular bacteria, human papillomavirus (HPV), and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) hijack host endosomal recycling pathways. This exciting work not only reveals distinct mechanisms employed by pathogens to manipulate host signaling pathways, but also deepens our understanding of the molecular intricacies regulating endosomal receptor trafficking. Twit Text FOAVip Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens ????Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=33748141 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33748141 #FOAvip English Wikipedia <ref>{{Cite pmid|33748141}}</ref> Targeting Endosomal Recycling Pathways by Bacterial and Viral Pathogens #MMPMID33748141 Yong X; Mao L; Shen X; Zhang Z; Billadeau DD; Jia D Front Cell Dev Biol 2021[]; 9 (ä): 648024 PMID33748141show ga Endosomes are essential cellular stations where endocytic and secretory trafficking routes converge. Proteins transiting at endosomes can be degraded via lysosome, or recycled to the plasma membrane, trans-Golgi network (TGN), or other cellular destinations. Pathways regulating endosomal recycling are tightly regulated in order to preserve organelle identity, to maintain lipid homeostasis, and to support other essential cellular functions. Recent studies have revealed that both pathogenic bacteria and viruses subvert host endosomal recycling pathways for their survival and replication. Several host factors that are frequently targeted by pathogens are being identified, including retromer, TBC1D5, SNX-BARs, and the WASH complex. In this review, we will focus on the recent advances in understanding how intracellular bacteria, human papillomavirus (HPV), and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) hijack host endosomal recycling pathways. This exciting work not only reveals distinct mechanisms employed by pathogens to manipulate host signaling pathways, but also deepens our understanding of the molecular intricacies regulating endosomal receptor trafficking. äTargeting Endosomal Recycling Pathways by Bacterial and Viral Pathogen(epmc).pdf DeepDyve Pubget Overpricing