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http://purl.uniprot.org/citations/7830863http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/7830863http://www.w3.org/2000/01/rdf-schema#comment"The clinical course of murine hereditary nephrotic syndrome (ICGN strain) was determined by examining 201 animals under different conditions. In the early stage, significant hypoproteinemia and hypoalbuminemia developed (p < 0.001) in parallel with a progressive rise in urinary protein concentration (p < 0.001). In the middle stage, the concentrations of total cholesterol, triglyceride, and beta-lipoprotein markedly increased (p < 0.01, p < 0.001, and p < 0.001, respectively), suggesting that type IIb hyperlipoproteinemia developed as in human nephrotic patients. Systemic edema appeared in 8 of 24 animals. In the terminal stage, both BUN and creatinine values greatly increased (p < 0.001), indicating rapid deterioration of renal function. The present study suggests that ICGN mice could be a useful model to study the pathophysiology of human nephrotic syndrome and its progression to renal failure."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.org/dc/terms/identifier"doi:10.1159/000188264"xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Kawaguchi H."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Suzuki O."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Yamamoto Y."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Yamaguchi Y."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Asano T."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Noguchi Y."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/author"Ogura A."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/date"1994"xsd:gYear
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/name"Nephron"xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/pages"239-244"xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/title"Hereditary nephrotic syndrome with progression to renal failure in a mouse model (ICGN strain): clinical study."xsd:string
http://purl.uniprot.org/citations/7830863http://purl.uniprot.org/core/volume"68"xsd:string
http://purl.uniprot.org/citations/7830863http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/7830863
http://purl.uniprot.org/citations/7830863http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/7830863
http://purl.uniprot.org/uniprot/#_A0A2R8VHQ0-mappedCitation-7830863http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7830863
http://purl.uniprot.org/uniprot/#_A0A2R8W6Z5-mappedCitation-7830863http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7830863
http://purl.uniprot.org/uniprot/#_Q8CGB6-mappedCitation-7830863http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/7830863
http://purl.uniprot.org/uniprot/Q8CGB6http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7830863
http://purl.uniprot.org/uniprot/A0A2R8W6Z5http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7830863
http://purl.uniprot.org/uniprot/A0A2R8VHQ0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/7830863