Art
J-GLOBAL ID:201302200241572505
Reference number:13A0035010
Nonfunction of the ECT2 gene may cause renal tubulointerstitial injury leading to focal segmental glomerulosclerosis
ECT2遺伝子の非機能は腎尿細管間質損傷を生じ,巣状分節性糸球体硬化症を生じる
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Material:
Volume:
16
Issue:
6
Page:
875-882
Publication year:
Dec. 2012
JST Material Number:
L3173A
ISSN:
1342-1751
Document type:
Article
Article type:
原著論文
Country of issue:
Germany, Federal Republic of (DEU)
Language:
ENGLISH (EN)
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Semi thesaurus term:
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
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JST classification (2):
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Category name(code) classified by JST.
Clinical medicine on urogenital system in general
, Molecular genetics in general
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Reference (23):
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KIFFEL, J. Focal segmental glomerulosclerosis and chronic kidney disease in pediatric patients. Adv Chronic Kidney Dis. 2011, 18, 332-338
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GBADEGESIN, R. Pathogenesis and therapy of focal segmental glomerulosclerosis : an update. Pediatr Nephrol. 2011, 26, 1001-1015
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COPELOVITCH, L. Hpothesis : Dent disease is an underrecognized cause of focal glomerulosclerosis. Clin J Am Soc Nephrol. 2007, 2, 914-918
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KANEKO, K. Focal segmental glomerulosclerosis in a boy wish Dent-2 disease. Pediatr Nephrol. 2010, 25, 781-782
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TADA, M. Histopathological evidence of poor prognosis in patients with vesicoureteral reflux. Pediatr Nephrol. 2001, 16, 482-487
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