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10.1038/s41598-018-29240-w http://scihub22266oqcxt.onion/10.1038/s41598-018-29240-w C6056427!6056427!30038331     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       Sci+Rep 2018 ; 8 (ä): ä Nephropedia Template TP {{tp|p=30038331|t=2018. Urine-derived cells: a promising diagnostic tool in Fabry disease patients |pdf=|usr=}}{{30038331}} gab.com Text Urine-derived cells: a promising diagnostic tool in Fabry disease patients JO: Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=30038331 #FOAvip Fabry disease is a lysosomal storage disorder resulting from impaired alpha-galactosidase A (?-Gal A) enzyme activity due to mutations in the GLA gene. Currently, powerful diagnostic tools and in vivo research models to study Fabry disease are missing, which is a major obstacle for further improvements in diagnosis and therapy. Here, we explore the utility of urine-derived primary cells of Fabry disease patients. Viable cells were isolated and cultured from fresh urine void. The obtained cell culture, modeling the renal epithelium, is characterized by patient-specific information. We demonstrate that this non-invasive source of patient cells provides an adequate cellular in vivo model as cells exhibit decreased ?-Gal A enzyme activity and concomitant globotriaosylceramide accumulation. Subsequent quantitative proteomic analyses revealed dysregulation of endosomal and lysosomal proteins indicating an involvement of the Coordinated Lysosomal Expression and Regulation (CLEAR) network in the disease pathology. This proteomic pattern resembled data from our previously described human podocyte model of Fabry disease. Taken together, the employment of urine-derived primary cells of Fabry disease patients might have diagnostic and prognostic implications in the future. Our findings pave the way towards a more detailed understanding of pathophysiological mechanisms and may allow the development of future tailored therapeutic strategies. Twit Text FOAVip Urine-derived cells: a promising diagnostic tool in Fabry disease patients ????Sci Rep http://www.kidney.de/pget.php?&tw=1&pmid=30038331 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=30038331 #FOAvip English Wikipedia <ref>{{Cite pmid|30038331}}</ref> Urine-derived cells: a promising diagnostic tool in Fabry disease patients #MMPMID30038331 Slaats GG; Braun F; Hoehne M; Frech LE; Blomberg L; Benzing T; Schermer B; Rinschen MM; Kurschat CE Sci Rep 2018[]; 8 (ä): ä PMID30038331show ga Fabry disease is a lysosomal storage disorder resulting from impaired alpha-galactosidase A (?-Gal A) enzyme activity due to mutations in the GLA gene. Currently, powerful diagnostic tools and in vivo research models to study Fabry disease are missing, which is a major obstacle for further improvements in diagnosis and therapy. Here, we explore the utility of urine-derived primary cells of Fabry disease patients. Viable cells were isolated and cultured from fresh urine void. The obtained cell culture, modeling the renal epithelium, is characterized by patient-specific information. We demonstrate that this non-invasive source of patient cells provides an adequate cellular in vivo model as cells exhibit decreased ?-Gal A enzyme activity and concomitant globotriaosylceramide accumulation. Subsequent quantitative proteomic analyses revealed dysregulation of endosomal and lysosomal proteins indicating an involvement of the Coordinated Lysosomal Expression and Regulation (CLEAR) network in the disease pathology. This proteomic pattern resembled data from our previously described human podocyte model of Fabry disease. Taken together, the employment of urine-derived primary cells of Fabry disease patients might have diagnostic and prognostic implications in the future. Our findings pave the way towards a more detailed understanding of pathophysiological mechanisms and may allow the development of future tailored therapeutic strategies. äUrine-derived cells: a promising diagnostic tool in Fabry disease pati(epmc).pdf DeepDyve Pubget Overpricing