{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,30]],"date-time":"2025-10-30T22:16:17Z","timestamp":1761862577373},"reference-count":31,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2006,9,1]],"date-time":"2006-09-01T00:00:00Z","timestamp":1157068800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Biochemical and Biophysical Research Communications"],"published-print":{"date-parts":[[2006,9]]},"DOI":"10.1016\/j.bbrc.2006.07.097","type":"journal-article","created":{"date-parts":[[2006,7,30]],"date-time":"2006-07-30T05:24:37Z","timestamp":1154237077000},"page":"507-513","source":"Crossref","is-referenced-by-count":10,"title":["Genetic variations of the NR3C1 gene in children with sporadic nephrotic syndrome"],"prefix":"10.1016","volume":"348","author":[{"given":"Jianwei","family":"Ye","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zihua","family":"Yu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jie","family":"Ding","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yan","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jianping","family":"Huang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yong","family":"Yao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Huijie","family":"Xiao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jiyun","family":"Yang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying","family":"Shen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Qun","family":"Meng","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.bbrc.2006.07.097_bib1","doi-asserted-by":"crossref","first-page":"571","DOI":"10.1111\/j.1523-1755.2004.00776.x","article-title":"NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence","volume":"66","author":"Weber","year":"2004","journal-title":"Kidney Int."},{"key":"10.1016\/j.bbrc.2006.07.097_bib2","doi-asserted-by":"crossref","first-page":"722","DOI":"10.1097\/01.ASN.0000113552.59155.72","article-title":"Arbeitsgemeinschaft Fur Padiatrische Nephrologie Study Group, Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome","volume":"15","author":"Ruf","year":"2004","journal-title":"J. Am. Soc. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib3","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-nephrin-is mutated in congenital nephrotic syndrome","volume":"1","author":"Kestila","year":"1998","journal-title":"Mol. Cell"},{"key":"10.1016\/j.bbrc.2006.07.097_bib4","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":"10.1016\/j.bbrc.2006.07.097_bib5","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":"10.1016\/j.bbrc.2006.07.097_bib6","doi-asserted-by":"crossref","first-page":"447","DOI":"10.1172\/JCI0215094","article-title":"Genetic models: clues for understanding the pathogenesis of idiopathic nephrotic syndrome","volume":"109","author":"Antignac","year":"2002","journal-title":"J. Clin. Invest."},{"key":"10.1016\/j.bbrc.2006.07.097_bib7","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1681\/ASN.V132388","article-title":"Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome","volume":"13","author":"Karle","year":"2002","journal-title":"J. Am. Soc. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib8","doi-asserted-by":"crossref","first-page":"1278","DOI":"10.1097\/01.ASN.0000060578.79050.E0","article-title":"Broadening the spectrum of diseases related to podocin mutations","volume":"14","author":"Caridi","year":"2003","journal-title":"J. Am. Soc. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib9","doi-asserted-by":"crossref","first-page":"470","DOI":"10.1007\/BF00869822","article-title":"Pharmacokinetics of prednisolone in children with the nephrotic syndrome","volume":"4","author":"Rostin","year":"1990","journal-title":"Pediatr. Nephro. l"},{"key":"10.1016\/j.bbrc.2006.07.097_bib10","doi-asserted-by":"crossref","first-page":"653","DOI":"10.1007\/s004670050675","article-title":"Glucocorticoid receptors in idiopathic nephrotic syndrome","volume":"13","author":"Haack","year":"1999","journal-title":"Pediatr. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib11","doi-asserted-by":"crossref","first-page":"403","DOI":"10.1111\/j.1523-1755.2004.00392.x","article-title":"Glucocorticoid receptors, in vitro steroid sensitivity, and cytokine secretion in idiopathic nephrotic syndrome","volume":"65","author":"Carlotti","year":"2004","journal-title":"Kidney Int."},{"key":"10.1016\/j.bbrc.2006.07.097_bib12","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1016\/S0960-0760(02)00062-6","article-title":"Glucocorticoid receptor variants: clinical implications","volume":"81","author":"DeRijk","year":"2002","journal-title":"J. Steroid Biochem. Mol. Biol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib13","doi-asserted-by":"crossref","first-page":"635","DOI":"10.1038\/318635a0","article-title":"Primary structure and expression of a functional human glucocorticoid receptor cDNA","volume":"318","author":"Hollenberg","year":"1985","journal-title":"Nature"},{"key":"10.1016\/j.bbrc.2006.07.097_bib14","doi-asserted-by":"crossref","first-page":"7182","DOI":"10.1016\/S0021-9258(20)89627-6","article-title":"The genomic structure of the human glucocorticoid receptor","volume":"266","author":"Encio","year":"1991","journal-title":"J. Biol. Chem."},{"key":"10.1016\/j.bbrc.2006.07.097_bib15","doi-asserted-by":"crossref","first-page":"678","DOI":"10.1007\/s00439-001-0615-0","article-title":"The HUGO Gene Nomenclature Committee (HGNC)","volume":"109","author":"Povey","year":"2001","journal-title":"Hum. Genet."},{"key":"10.1016\/j.bbrc.2006.07.097_bib16","first-page":"144","article-title":"A polymorphism in the glucocorticoid receptor gene may be associated with and increased sensitivity to glucocorticoids in vivo","volume":"83","author":"Huizenga","year":"1998","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.bbrc.2006.07.097_bib17","doi-asserted-by":"crossref","first-page":"892","DOI":"10.1210\/jc.2003-031235","article-title":"Glucocorticoid sensitivity is determined by a specific glucocorticoid receptor haplotype","volume":"89","author":"Stevens","year":"2004","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.bbrc.2006.07.097_bib18","doi-asserted-by":"crossref","first-page":"557","DOI":"10.1002\/humu.10213","article-title":"Variations of the human glucocorticoid receptor gene (NR3C1): pathological and in vitro mutations and polymorphisms","volume":"21","author":"Bray","year":"2003","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.bbrc.2006.07.097_bib19","first-page":"296","article-title":"Cushing\u2019s disease preceded by generalized glucocorticoid resistance: clinical consequences of a novel, dominant-negative glucocorticoid receptor mutation","volume":"108","author":"Karl","year":"1996","journal-title":"Proc. Assoc. Am. Physicians"},{"key":"10.1016\/j.bbrc.2006.07.097_bib20","first-page":"2056","article-title":"Glucocorticoid receptor gene mutations in leukemic cells acquired in vitro and in vivo","volume":"60","author":"Hillmann","year":"2000","journal-title":"Cancer Res."},{"key":"10.1016\/j.bbrc.2006.07.097_bib21","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/S0009-8981(01)00661-1","article-title":"The phase-shift mutation in the glucocorticoid receptor gene: potential etiologic significance of neuroendocrine mechanisms in lupus nephritis","volume":"313","author":"Jiang","year":"2001","journal-title":"Clin. Chim. Acta"},{"key":"10.1016\/j.bbrc.2006.07.097_bib22","doi-asserted-by":"crossref","first-page":"1805","DOI":"10.1210\/jcem.87.4.8379","article-title":"Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene","volume":"87","author":"Mendonca","year":"2002","journal-title":"J. Clin. Endocrinol. Metab."},{"key":"10.1016\/j.bbrc.2006.07.097_bib23","doi-asserted-by":"crossref","unstructured":"International Study of Kidney Disease in Children. The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone, J. Pediatr. 98 (1981) 561\u2013564.","DOI":"10.1016\/S0022-3476(81)80760-3"},{"key":"10.1016\/j.bbrc.2006.07.097_bib24","doi-asserted-by":"crossref","first-page":"1013","DOI":"10.1007\/s00467-002-0972-5","article-title":"Phenotypic and genotypic features of Alport syndrome in Chinese children","volume":"17","author":"Wang","year":"2002","journal-title":"Pediatr. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib25","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1007\/s004390050425","article-title":"Lack of association between five polymorphisms in the human glucocorticoid receptor gene and glucocorticoid resistance","volume":"99","author":"Koper","year":"1997","journal-title":"Hum. Genet."},{"key":"10.1016\/j.bbrc.2006.07.097_bib26","doi-asserted-by":"crossref","first-page":"1285","DOI":"10.1007\/s00467-004-1585-y","article-title":"A novel mutation of NPHS2 identified in a Chinese family","volume":"19","author":"Yu","year":"2004","journal-title":"Pediatr. Nephrol."},{"key":"10.1016\/j.bbrc.2006.07.097_bib27","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1007\/s004390100505","article-title":"Nomenclature for the description of human sequence variations","volume":"109","author":"den Dunnen","year":"2001","journal-title":"Hum. Genet."},{"key":"10.1016\/j.bbrc.2006.07.097_bib28","doi-asserted-by":"crossref","first-page":"404","DOI":"10.1161\/01.HYP.0000055342.40301.DC","article-title":"Association of coronary artery disease with glucocorticoid receptor N363S variant","volume":"41","author":"Lin","year":"2003","journal-title":"Hypertension"},{"key":"10.1016\/j.bbrc.2006.07.097_bib29","doi-asserted-by":"crossref","first-page":"802","DOI":"10.1038\/oby.2003.111","article-title":"Association of obesity, but not diabetes or hypertension, with glucocorticoid receptor N363S variant","volume":"11","author":"Lin","year":"2003","journal-title":"Obes. Res."},{"key":"10.1016\/j.bbrc.2006.07.097_bib30","doi-asserted-by":"crossref","first-page":"7871","DOI":"10.1073\/pnas.96.14.7871","article-title":"Single-nucleotide polymorphisms can cause different structural folds of mRNA","volume":"96","author":"Shen","year":"1999","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"10.1016\/j.bbrc.2006.07.097_bib31","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1038\/nrg775","article-title":"Listening to silence and understanding nonsense: exonic mutations that affect splicing","volume":"3","author":"Cartegni","year":"2002","journal-title":"Nat. Rev. Genet."}],"container-title":["Biochemical and Biophysical Research Communications"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0006291X06016299?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0006291X06016299?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2021,7,30]],"date-time":"2021-07-30T20:32:43Z","timestamp":1627677163000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0006291X06016299"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2006,9]]},"references-count":31,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2006,9]]}},"alternative-id":["S0006291X06016299"],"URL":"https:\/\/doi.org\/10.1016\/j.bbrc.2006.07.097","relation":{},"ISSN":["0006-291X"],"issn-type":[{"value":"0006-291X","type":"print"}],"subject":[],"published":{"date-parts":[[2006,9]]}}}