Ontology highlight
ABSTRACT:
SUBMITTER: Freedman BI
PROVIDER: S-EPMC7056919 | biostudies-literature | 2020 Mar
REPOSITORIES: biostudies-literature
Freedman Barry I BI Moxey-Mims Marva M MM Alexander Amir A AA Astor Brad C BC Birdwell Kelly A KA Bowden Donald W DW Bowen Gordon G Bromberg Jonathan J Craven Timothy E TE Dadhania Darshana M DM Divers Jasmin J Doshi Mona D MD Eidbo Elling E Fornoni Alessia A Gautreaux Michael D MD Gbadegesin Rasheed A RA Gee Patrick O PO Guerra Giselle G Hsu Chi-Yuan CY Iltis Ana S AS Jefferson Nichole N Julian Bruce A BA Klassen David K DK Koty Patrick P PP Langefeld Carl D CD Lentine Krista L KL Ma Lijun L Mannon Roslyn B RB Menon Madhav C MC Mohan Sumit S Moore J Brian JB Murphy Barbara B Newell Kenneth A KA Odim Jonah J Ortigosa-Goggins Mariella M Palmer Nicholette D ND Park Meyeon M Parsa Afshin A Pastan Stephen O SO Poggio Emilio D ED Rajapakse Nishadi N Reeves-Daniel Amber M AM Rosas Sylvia E SE Russell Laurie P LP Sawinski Deirdre D Smith S Carrie SC Spainhour Mitzie M Stratta Robert J RJ Weir Matthew R MR Reboussin David M DM Kimmel Paul L PL Brennan Daniel C DC
Kidney international reports 20191213 3
<h4>Introduction</h4>Much of the higher risk for end-stage kidney disease (ESKD) in African American individuals relates to ancestry-specific variation in the apolipoprotein L1 gene (<i>APOL1</i>). Relative to kidneys from European American deceased-donors, kidneys from African American deceased-donors have shorter allograft survival and African American living-kidney donors more often develop ESKD. The National Institutes of Health (NIH)-sponsored <i>APOL1</i> Long-term Kidney Transplantation O ...[more]