{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T20:09:12Z","timestamp":1786133352686,"version":"build-2736575974"},"reference-count":22,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2010,8]]},"DOI":"10.1681\/asn.2009101046","type":"journal-article","created":{"date-parts":[[2010,7,8]],"date-time":"2010-07-08T22:24:28Z","timestamp":1278627868000},"page":"1390-1397","source":"Crossref","is-referenced-by-count":7,"title":["A New Locus for Familial FSGS on Chromosome 2P"],"prefix":"10.1681","volume":"21","author":[{"given":"Rasheed","family":"Gbadegesin","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"Lavin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Louis","family":"Janssens","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bartlomiej","family":"Bartkowiak","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alison","family":"Homstad","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guanghong","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Brandy","family":"Bowling","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jason","family":"Eckel","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chris","family":"Potocky","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Diana","family":"Abbott","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peter","family":"Conlon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"William K.","family":"Scott","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Howell","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth","family":"Hauser","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michelle P.","family":"Winn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-27-20230410","doi-asserted-by":"crossref","first-page":"1299","DOI":"10.1016\/S0140-6736(70)91905-7","article-title":"Pathology of the nephrotic syndrome in children: A report for the International Study of Kidney Disease in Children","volume":"760","author":"Churg","year":"1970","journal-title":"Lancet"},{"key":"R2-27-20230410","doi-asserted-by":"crossref","first-page":"172","DOI":"10.1053\/snep.2003.50025","article-title":"Trends in the epidemiology of focal segmental glomerulosclerosis","volume":"23","author":"Kitiyakara","year":"2003","journal-title":"Semin Nephrol"},{"key":"R5-27-20230410","doi-asserted-by":"crossref","first-page":"815","DOI":"10.1016\/S0272-6386(04)01081-9","article-title":"Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States","volume":"44","author":"Kitiyakara","year":"2004","journal-title":"Am J Kidney Dis"},{"key":"R6-27-20230410","doi-asserted-by":"crossref","first-page":"647","DOI":"10.1016\/S0272-6386(96)90098-0","article-title":"The racial prevalence of glomerular lesions in nephrotic adults","volume":"27","author":"Korbet","year":"1996","journal-title":"Am J Kidney Dis"},{"key":"R7-27-20230410","doi-asserted-by":"crossref","first-page":"556","DOI":"10.1016\/S0140-6736(74)91880-7","article-title":"Pathogenesis of lipoid nephrosis: A disorder of T-cell function","volume":"2","author":"Shalhoub","year":"1974","journal-title":"Lancet"},{"key":"R8-27-20230410","doi-asserted-by":"crossref","first-page":"878","DOI":"10.1056\/NEJM199604043341402","article-title":"Circulating factor associated with increased glomerular permeability to albumin in recurrent focal segmental glomerulosclerosis","volume":"334","author":"Savin","year":"1996","journal-title":"N Engl J Med"},{"key":"R9-27-20230410","doi-asserted-by":"crossref","first-page":"575","DOI":"10.1016\/S1097-2765(00)80057-X","article-title":"Positionally cloned gene for a novel glomerular protein\u2014nephrin\u2014is mutated in congenital nephrotic syndrome","volume":"1","author":"Kestila","year":"1998","journal-title":"Mol Cell"},{"key":"R10-27-20230410","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1038\/74166","article-title":"NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome","volume":"24","author":"Boute","year":"2000","journal-title":"Nat Genet"},{"key":"R11-27-20230410","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1038\/73456","article-title":"Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis","volume":"24","author":"Kaplan","year":"2000","journal-title":"Nat Genet"},{"key":"R12-27-20230410","doi-asserted-by":"crossref","first-page":"1801","DOI":"10.1126\/science.1106215","article-title":"A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis","volume":"308","author":"Winn","year":"2005","journal-title":"Science"},{"key":"R13-27-20230410","doi-asserted-by":"crossref","first-page":"1298","DOI":"10.1126\/science.1081068","article-title":"CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility","volume":"300","author":"Kim","year":"2003","journal-title":"Science"},{"key":"R14-27-20230410","doi-asserted-by":"crossref","first-page":"1397","DOI":"10.1038\/ng1918","article-title":"Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible","volume":"38","author":"Hinkes","year":"2006","journal-title":"Nat Genet"},{"key":"R15-27-20230410","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1159\/000052628","article-title":"Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin","volume":"9","author":"Wang","year":"2001","journal-title":"Exp Nephrol"},{"key":"R16-27-20230410","doi-asserted-by":"crossref","first-page":"394","DOI":"10.1097\/00007890-200202150-00013","article-title":"Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: Role of nephrin","volume":"73","author":"Patrakka","year":"2002","journal-title":"Transplantation"},{"key":"R17-27-20230410","doi-asserted-by":"crossref","first-page":"F203","DOI":"10.1152\/ajprenal.2000.279.2.F203","article-title":"Molecular chaperones in the kidney: Distribution, putative roles, and regulation","volume":"279","author":"Beck","year":"2000","journal-title":"Am J Physiol Renal Physiol"},{"key":"R18-27-20230410","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1038\/ncpneph0117","article-title":"Modulation of renal cell injury by heat shock proteins: Lessons learned from the immature kidney","volume":"2","author":"Riordan","year":"2006","journal-title":"Nat Clin Pract Nephrol"},{"key":"R19-27-20230410","doi-asserted-by":"crossref","first-page":"1275","DOI":"10.1111\/j.1523-1755.2005.00205.x","article-title":"Differential proteomic analysis of proteins induced by glucocorticoids in cultured murine podocytes","volume":"67","author":"Ransom","year":"2005","journal-title":"Kidney Int"},{"key":"R20-27-20230410","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1096\/fj.01-0681com","article-title":"Hsp27 regulates podocyte cytoskeletal changes in an in vitro model of podocyte process retraction","volume":"16","author":"Smoyer","year":"2002","journal-title":"FASEB J"},{"key":"R21-27-20230410","doi-asserted-by":"crossref","first-page":"4664","DOI":"10.1046\/j.1432-1327.2001.02393.x","article-title":"Cytosolic chaperonin-containing t-complex polypeptide 1 changes the content of a particular subunit species concomitant with substrate binding and folding activities during the cell cycle","volume":"268","author":"Yokota","year":"2001","journal-title":"Eur J Biochem"},{"key":"R22-27-20230410","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1006\/geno.1999.5828","article-title":"Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity","volume":"58","author":"Winn","year":"1999","journal-title":"Genomics"},{"key":"R23-27-20230410","first-page":"513","article-title":"Estimating the power of a proposed linkage study: a practical computer simulation approach","volume":"39","author":"Boehnke","year":"1986","journal-title":"Am J Hum Genet"},{"key":"R24-27-20230410","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1038\/ng1295-402","article-title":"The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance","volume":"11","author":"O'Connell","year":"1995","journal-title":"Nat Genet"}],"container-title":["Journal of the American Society of Nephrology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/00001751-201008000-00027","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,7]],"date-time":"2026-08-07T19:32:44Z","timestamp":1786131164000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/00001751-201008000-00027"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010,8]]},"references-count":22,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2010]]}},"URL":"https:\/\/doi.org\/10.1681\/asn.2009101046","relation":{},"ISSN":["1046-6673"],"issn-type":[{"value":"1046-6673","type":"print"}],"subject":[],"published":{"date-parts":[[2010,8]]}}}