{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T14:40:55Z","timestamp":1791816055677,"version":"4.3.4"},"reference-count":61,"publisher":"Elsevier BV","issue":"7","license":[{"start":{"date-parts":[[2016,7,1]],"date-time":"2016-07-01T00:00:00Z","timestamp":1467331200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation","doi-asserted-by":"publisher","award":["0388015"],"award-info":[{"award-number":["0388015"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation","doi-asserted-by":"publisher","award":["39870747"],"award-info":[{"award-number":["39870747"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation","doi-asserted-by":"publisher","award":["81370807"],"award-info":[{"award-number":["81370807"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100013286","name":"Specialized Research Fund for the Doctoral Program of Higher Education","doi-asserted-by":"crossref","award":["20130181110055"],"award-info":[{"award-number":["20130181110055"]}],"id":[{"id":"10.13039\/501100013286","id-type":"DOI","asserted-by":"crossref"}]},{"name":"Scientific Research Foundation of Ministry of Health","award":["98-1-213"],"award-info":[{"award-number":["98-1-213"]}]}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Autoimmunity Reviews"],"published-print":{"date-parts":[[2016,7]]},"DOI":"10.1016\/j.autrev.2016.02.007","type":"journal-article","created":{"date-parts":[[2016,2,11]],"date-time":"2016-02-11T14:03:08Z","timestamp":1455199388000},"page":"632-637","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":21,"title":["New insight into the pathogenesis of minimal change nephrotic syndrome: Role of the persistence of respiratory tract virus in immune disorders"],"prefix":"10.1016","volume":"15","author":[{"given":"Hui","family":"Zhang","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zheng","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Liqun","family":"Dong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yannan","family":"Guo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jin","family":"Wu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Songhui","family":"Zhai","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"issue":"10","key":"10.1016\/j.autrev.2016.02.007_bb0005","first-page":"853","article-title":"Minimal change nephrotic syndrome: new insights into disease pathogenesis","volume":"24","author":"Audard","year":"2008","journal-title":"Med Sci"},{"issue":"2","key":"10.1016\/j.autrev.2016.02.007_bb0010","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1089\/vim.2007.0110","article-title":"Regulation of immunity to respiratory syncytial virus by dendritic cells, toll-like receptors, and notch","volume":"21","author":"Lukacs","year":"2008","journal-title":"Viral Immunol"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0015","doi-asserted-by":"crossref","first-page":"1181","DOI":"10.1007\/s00467-009-1119-8","article-title":"Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome","volume":"24","author":"Hashimura","year":"2009","journal-title":"Pediatr Nephrol"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0020","first-page":"969","article-title":"Respiratory virus expression in renal tissues and urine of children with steroid responsive simple nephrotic syndrome","volume":"38","author":"Wu","year":"2007","journal-title":"Sichuan Da Xue Xue Bao Yi Xue Ban"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0025","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1590\/S0041-87812004000500009","article-title":"Influence of nephrotic state on the infectious profile in childhood idiopathic nephrotic syndrome","volume":"59","author":"Soeiro","year":"2004","journal-title":"Rev Hosp Clin Fac Med Sao Paulo"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0030","doi-asserted-by":"crossref","first-page":"378","DOI":"10.1016\/S0022-3476(86)80876-9","article-title":"Role of respiratory viruses in exacerbations of primary nephrotic syndrome","volume":"108","author":"MacDonald","year":"1986","journal-title":"J Pediatr"},{"issue":"2","key":"10.1016\/j.autrev.2016.02.007_bb0035","first-page":"230","article-title":"Regulatory effect of IkappaBalpha on NF-kappaB activity during viral gene transactivation in patients with steroid responsive simple nephrotic syndrome","volume":"38","author":"Tao","year":"2007","journal-title":"Sichuan Da Xue Xue Bao Yi Xue Ban"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0040","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1038\/sj.ki.5002030","article-title":"Respiratory syncytial virus nephropathy in rats","volume":"71","author":"Liu","year":"2007","journal-title":"Kidney Int"},{"issue":"2","key":"10.1016\/j.autrev.2016.02.007_bb0045","first-page":"183","article-title":"Viral transactivation of transcription by NF-kappaB in steroid-responsive simple nephrotic syndrome","volume":"37","author":"Liu","year":"2006","journal-title":"Sichuan Da Xue Xue Bao Yi Xue Ban"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0050","first-page":"559","article-title":"A study on the relationship between respiratory tract viruses antigen in peripheral blood mononuclear cells and their antibody from children with steroid-sensitive and simple nephrotic syndrome","volume":"32","author":"Wang","year":"2001","journal-title":"Hua Xi Yi Ke Da Xue Xue Bao"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0055","first-page":"315","article-title":"Study of the carrying of respiratory tract viruses in steroid-responsive and simple nephrotic syndrome","volume":"30","author":"Wang","year":"1999","journal-title":"Hua Xi Yi Ke Da Xue Xue Bao"},{"issue":"12","key":"10.1016\/j.autrev.2016.02.007_bb0060","doi-asserted-by":"crossref","first-page":"3270","DOI":"10.3390\/v4123270","article-title":"Respiratory syncytial virus persistence in macrophages alters the profile of cellular gene expression","volume":"4","author":"Rivera-Toledo","year":"2012","journal-title":"Viruses"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0065","doi-asserted-by":"crossref","first-page":"111","DOI":"10.1016\/j.virol.2005.09.028","article-title":"Viral persistence: parameters, mechanisms and future predictions","volume":"344","author":"Oldstone","year":"2006","journal-title":"Virology"},{"issue":"12","key":"10.1016\/j.autrev.2016.02.007_bb0070","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0051485","article-title":"Combination therapy using monoclonal antibodies against respiratory syncytial virus (RSV) G glycoprotein protects from RSV disease in BALB\/c mice","volume":"7","author":"Caidi","year":"2012","journal-title":"PLoS One"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0075","doi-asserted-by":"crossref","first-page":"672","DOI":"10.1111\/j.1365-2222.2005.02244.x","article-title":"Persistence of rhinovirus RNA after asthma exacerbation in children","volume":"35","author":"Kling","year":"2005","journal-title":"Clin Exp Allergy"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0080","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1093\/infdis\/jir790","article-title":"Natural polymorphisms and resistance-associated mutations in the fusion protein of respiratory syncytial virus (RSV): effects on RSV susceptibility to palivizumab","volume":"205","author":"Zhu","year":"2012","journal-title":"J Infect Dis"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0085","doi-asserted-by":"crossref","first-page":"1339","DOI":"10.1128\/JVI.06096-11","article-title":"Respiratory syncytial virus glycoprotein G interacts with DC-SIGN and L-SIGN to activate ERK1 and ERK2","volume":"86","author":"Johnson","year":"2012","journal-title":"J Virol"},{"issue":"10","key":"10.1016\/j.autrev.2016.02.007_bb0090","doi-asserted-by":"crossref","first-page":"S60","DOI":"10.1097\/INF.0b013e3181684d52","article-title":"Respiratory syncytial virus persistence: evidence in the mouse model","volume":"27","author":"Mej\u00edas","year":"2008","journal-title":"Pediatr Infect Dis J"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0095","doi-asserted-by":"crossref","first-page":"2123","DOI":"10.1073\/pnas.0710333105","article-title":"Superinfection as a driver of genomic diversification in antigenically variant pathogens","volume":"105","author":"Futse","year":"2008","journal-title":"Proc Natl Acad Sci"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0100","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1016\/j.mehy.2004.02.061","article-title":"Dendritic cells and the immunity\/tolerance decision","volume":"64","author":"Usharauli","year":"2005","journal-title":"Med Hypotheses"},{"issue":"10","key":"10.1016\/j.autrev.2016.02.007_bb0105","doi-asserted-by":"crossref","first-page":"S63","DOI":"10.1097\/INF.0b013e3181684d67","article-title":"Respiratory syncytial virus persistence in chronic obstructive pulmonary disease","volume":"27","author":"Sikkel","year":"2008","journal-title":"Pediatr Infect Dis J"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0110","doi-asserted-by":"crossref","first-page":"279","DOI":"10.2217\/fmb.09.1","article-title":"The host response and molecular pathogenesis associated with respiratory syncytial virus infection","volume":"4","author":"Oshansky","year":"2009","journal-title":"Future Microbiol"},{"issue":"12","key":"10.1016\/j.autrev.2016.02.007_bb0115","doi-asserted-by":"crossref","DOI":"10.1371\/journal.ppat.1002377","article-title":"Neonatal CD8 T-cell hierarchy is distinct from adults and is influenced by intrinsic T cell properties in respiratory syncytial virus infected mice","volume":"7","author":"Ruckwardt","year":"2011","journal-title":"PLoS Pathog"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0120","first-page":"386","article-title":"Minimal-change disease with mesangial IgA deposits associated with Sjogren syndrome","volume":"22","author":"Mon","year":"2001","journal-title":"Nefrologia"},{"issue":"11","key":"10.1016\/j.autrev.2016.02.007_bb0125","doi-asserted-by":"crossref","first-page":"3229","DOI":"10.1099\/vir.0.80219-0","article-title":"Shifting immunodominance pattern of two cytotoxic T-lymphocyte epitopes in the F glycoprotein of the long strain of respiratory syncytial virus","volume":"85","author":"Johnstone","year":"2004","journal-title":"J Gen Virol"},{"issue":"12","key":"10.1016\/j.autrev.2016.02.007_bb0130","doi-asserted-by":"crossref","first-page":"3973","DOI":"10.4049\/jimmunol.137.12.3973","article-title":"Human and murine cytotoxic T cells specific to respiratory syncytial virus recognize the viral nucleoprotein (N), but not the major glycoprotein (G), expressed by vaccinia virus recombinants","volume":"137","author":"Bangham","year":"1986","journal-title":"J Immunol"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0135","doi-asserted-by":"crossref","first-page":"79","DOI":"10.1099\/0022-1317-70-1-79","article-title":"Recognition of respiratory syncytial virus fusion protein by mouse cytotoxic T cell clones and a human cytotoxic T cell line","volume":"70","author":"Cannon","year":"1989","journal-title":"J Gen Virol"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0140","doi-asserted-by":"crossref","first-page":"211","DOI":"10.1016\/S0165-2427(96)05686-3","article-title":"Identification of potential CTL epitopes of bovine RSV using allele-specific peptide motifs from bovine MHC class I molecules","volume":"54","author":"Gaddum","year":"1996","journal-title":"Vet Immunol Immunopathol"},{"issue":"9","key":"10.1016\/j.autrev.2016.02.007_bb0145","doi-asserted-by":"crossref","DOI":"10.1371\/journal.pone.0025500","article-title":"Immunoprotectivity of HLA-A2 CTL peptides derived from respiratory syncytial virus fusion protein in HLA-A2 transgenic mouse","volume":"6","author":"Shao","year":"2011","journal-title":"PLoS One"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0150","doi-asserted-by":"crossref","first-page":"531","DOI":"10.1615\/CritRevImmunol.v29.i6.40","article-title":"The role of Toll-like receptors in regulating the immune response against respiratory syncytial virus","volume":"29","author":"Klouwenberg","year":"2009","journal-title":"Crit Rev Immunol"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0155","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1177\/1753425908095957","article-title":"Host species-specific usage of the TLR4-LPS receptor complex","volume":"14","author":"Lizundia","year":"2008","journal-title":"Innate Immun"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0160","doi-asserted-by":"crossref","first-page":"1937","DOI":"10.4049\/jimmunol.176.3.1937","article-title":"Deletion of TLR3 alters the pulmonary immune environment and mucus production during respiratory syncytial virus infection","volume":"176","author":"Rudd","year":"2006","journal-title":"J Immunol"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0165","doi-asserted-by":"crossref","first-page":"3350","DOI":"10.1128\/JVI.79.6.3350-3357.2005","article-title":"Differential role for TLR3 in respiratory syncytial virus-induced chemokine expression","volume":"79","author":"Rudd","year":"2005","journal-title":"J Virol"},{"issue":"10","key":"10.1016\/j.autrev.2016.02.007_bb0170","doi-asserted-by":"crossref","first-page":"1525","DOI":"10.1038\/nm.2896","article-title":"Early infection with respiratory syncytial virus impairs regulatory T cell function and increases susceptibility to allergic asthma","volume":"18","author":"Krishnamoorthy","year":"2012","journal-title":"Nat Med"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0175","doi-asserted-by":"crossref","first-page":"627","DOI":"10.1002\/1521-4141(200203)32:3<627::AID-IMMU627>3.0.CO;2-1","article-title":"Pathogenic autoantibody production requires loss of tolerance against desmoglein 3 in both T and B cells in experimental pemphigus vulgaris","volume":"32","author":"Tsunoda","year":"2002","journal-title":"Eur J Immunol"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0180","doi-asserted-by":"crossref","first-page":"303","DOI":"10.1080\/08916930500124429","article-title":"The role of T cells in cutaneous autoimmune disease","volume":"38","author":"Chow","year":"2005","journal-title":"Autoimmunity"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0185","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":"Kestil\u00e4","year":"1998","journal-title":"Mol Cell"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0190","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"},{"issue":"2","key":"10.1016\/j.autrev.2016.02.007_bb0195","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1016\/0092-8674(91)90194-4","article-title":"Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys\u2013Drash syndrome","volume":"67","author":"Pelletier","year":"1991","journal-title":"Cell"},{"issue":"5623","key":"10.1016\/j.autrev.2016.02.007_bb0200","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"},{"issue":"14","key":"10.1016\/j.autrev.2016.02.007_bb0205","doi-asserted-by":"crossref","first-page":"4829","DOI":"10.1128\/MCB.21.14.4829-4836.2001","article-title":"Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN","volume":"21","author":"Donoviel","year":"2001","journal-title":"Mol Cell Biol"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0210","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1038\/73456","article-title":"Mutations in ACTN4, encoding \u03b1-actinin-4, cause familial focal segmental glomerulosclerosis","volume":"24","author":"Kaplan","year":"2000","journal-title":"Nat Genet"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0215","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1038\/ng.505","article-title":"Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis","volume":"42","author":"Brown","year":"2010","journal-title":"Nat Genet"},{"issue":"5729","key":"10.1016\/j.autrev.2016.02.007_bb0220","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"},{"issue":"8","key":"10.1016\/j.autrev.2016.02.007_bb0225","doi-asserted-by":"crossref","first-page":"1073","DOI":"10.1016\/j.metabol.2011.12.003","article-title":"Impact of high glucose and transforming growth factor-\u03b2 on bioenergetic profiles in podocytes","volume":"61","author":"Stieger","year":"2012","journal-title":"Metabolism"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0230","doi-asserted-by":"crossref","first-page":"1856","DOI":"10.1111\/j.1523-1755.2004.00583.x","article-title":"Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS)","volume":"65","author":"Lahdenkari","year":"2004","journal-title":"Kidney Int"},{"issue":"12","key":"10.1016\/j.autrev.2016.02.007_bb0235","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"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0240","doi-asserted-by":"crossref","first-page":"139","DOI":"10.1016\/j.ajhg.2011.05.026","article-title":"Disruption of PTPRO causes childhood-onset nephrotic syndrome","volume":"89","author":"Ozaltin","year":"2011","journal-title":"Am J Hum Genet"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0245","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1038\/ng0598-47","article-title":"Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome","volume":"19","author":"Dreyer","year":"1998","journal-title":"Nat Genet"},{"issue":"2","key":"10.1016\/j.autrev.2016.02.007_bb0250","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1038\/ng821","article-title":"Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia","volume":"30","author":"Boerkoel","year":"2002","journal-title":"Nat Genet"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0255","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1016\/j.ajhg.2014.10.011","article-title":"Loss-of-function mutations in WDR73 are responsible for microcephaly and steroid-resistant nephrotic syndrome: Galloway\u2013Mowat syndrome","volume":"95","author":"Colin","year":"2014","journal-title":"Am J Hum Genet"},{"issue":"5993","key":"10.1016\/j.autrev.2016.02.007_bb0260","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1126\/science.1193032","article-title":"Association of trypanolytic ApoL1 variants with kidney disease in African Americans","volume":"329","author":"Genovese","year":"2010","journal-title":"Science"},{"issue":"4","key":"10.1016\/j.autrev.2016.02.007_bb0265","doi-asserted-by":"crossref","first-page":"295","DOI":"10.1056\/NEJMoa1101273","article-title":"MYO1E mutations and childhood familial focal segmental glomerulosclerosis","volume":"365","author":"Mele","year":"2011","journal-title":"N Engl J Med"},{"issue":"10","key":"10.1016\/j.autrev.2016.02.007_bb0270","doi-asserted-by":"crossref","first-page":"4127","DOI":"10.1172\/JCI46458","article-title":"Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis","volume":"121","author":"Shreeram","year":"2011","journal-title":"J Clin Invest"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0275","doi-asserted-by":"crossref","first-page":"330","DOI":"10.1136\/jmedgenet-2012-101442","article-title":"ARHGDIA: a novel gene implicated in nephrotic syndrome","volume":"50","author":"Gupta","year":"2013","journal-title":"J Med Genet"},{"issue":"9","key":"10.1016\/j.autrev.2016.02.007_bb0280","doi-asserted-by":"crossref","first-page":"1991","DOI":"10.1681\/ASN.2013090976","article-title":"Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS","volume":"25","author":"Gbadegesin","year":"2014","journal-title":"J Am Soc Nephrol"},{"issue":"5","key":"10.1016\/j.autrev.2016.02.007_bb0285","doi-asserted-by":"crossref","first-page":"2013","DOI":"10.1172\/JCI45693","article-title":"COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness","volume":"121","author":"Heeringa","year":"2011","journal-title":"J Clin Invest"},{"issue":"21","key":"10.1016\/j.autrev.2016.02.007_bb0290","doi-asserted-by":"crossref","DOI":"10.1093\/hmg\/ddh284","article-title":"Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities","volume":"13","author":"Zenker","year":"2004","journal-title":"Hum Mol Genet"},{"issue":"1","key":"10.1016\/j.autrev.2016.02.007_bb0295","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1053\/ajkd.2000.8293","article-title":"Congenital focal segmental glomerulosclerosis associated with beta 4 integrin mutation and epidermolysis bullosa","volume":"36","author":"Kambham","year":"2000","journal-title":"Am J Kidney Dis"},{"issue":"6","key":"10.1016\/j.autrev.2016.02.007_bb0300","doi-asserted-by":"crossref","first-page":"1253","DOI":"10.1038\/ki.2014.305","article-title":"Rare hereditary COL4A3\/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis","volume":"86","author":"Malone","year":"2014","journal-title":"Kidney Int"},{"issue":"3","key":"10.1016\/j.autrev.2016.02.007_bb0305","doi-asserted-by":"crossref","first-page":"673","DOI":"10.1016\/j.ajhg.2007.12.019","article-title":"Array-based gene discovery with three unrelated subjects shows SCARB2\/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis","volume":"82","author":"Berkovic","year":"2008","journal-title":"Am J Hum Genet"}],"container-title":["Autoimmunity Reviews"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1568997216300337?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1568997216300337?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,6,14]],"date-time":"2024-06-14T05:09:42Z","timestamp":1718341782000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1568997216300337"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,7]]},"references-count":61,"journal-issue":{"issue":"7","published-print":{"date-parts":[[2016,7]]}},"alternative-id":["S1568997216300337"],"URL":"https:\/\/doi.org\/10.1016\/j.autrev.2016.02.007","relation":{},"ISSN":["1568-9972"],"issn-type":[{"value":"1568-9972","type":"print"}],"subject":[],"published":{"date-parts":[[2016,7]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"New insight into the pathogenesis of minimal change nephrotic syndrome: Role of the persistence of respiratory tract virus in immune disorders","name":"articletitle","label":"Article Title"},{"value":"Autoimmunity Reviews","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.autrev.2016.02.007","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}