Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?
about
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 geneRenal manifestations of patients with MYH9-related disorders.Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A.The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.Polymorphisms in the non-muscle myosin heavy chain gene (MYH9) are associated with lower glomerular filtration rate in mixed ancestry diabetic subjects from South Africa.Pathogenesis of glomerular haematuria.African origins and chronic kidney disease susceptibility in the human immunodeficiency virus era.Advances in our understanding of the pathogenesis of HIV-1 associated nephropathy in children.How benign is hematuria? Using genetics to predict prognosis.Cellular force assay detects altered contractility caused by a nephritis-associated mutation in nonmuscle myosin IIA.
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P2860
Glomerular pathology in autosomal dominant MYH9 spectrum disorders: what are the clues telling us about disease mechanism?
description
2010 nî lūn-bûn
@nan
2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年學術文章
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name
Glomerular pathology in autoso ...... ng us about disease mechanism?
@ast
Glomerular pathology in autoso ...... ng us about disease mechanism?
@en
type
label
Glomerular pathology in autoso ...... ng us about disease mechanism?
@ast
Glomerular pathology in autoso ...... ng us about disease mechanism?
@en
prefLabel
Glomerular pathology in autoso ...... ng us about disease mechanism?
@ast
Glomerular pathology in autoso ...... ng us about disease mechanism?
@en
P2860
P356
P1433
P1476
Glomerular pathology in autoso ...... ng us about disease mechanism?
@en
P2860
P2888
P304
P356
10.1038/KI.2010.82
P407
P577
2010-07-01T00:00:00Z