about
Anti-microRNA-21 oligonucleotides prevent Alport nephropathy progression by stimulating metabolic pathwaysVentricular septal defect in a child with Alport syndrome: a case report.A novel COL4A5 mutation identified in a Chinese Han family using exome sequencingThe effect of progressive glomerular disease on megalin-mediated endocytosis in the kidneyMolecular diagnostics for autosomal dominant polycystic kidney diseaseReduction of tumstatin in asthmatic airways contributes to angiogenesis, inflammation, and hyperresponsiveness.Novel X-linked glomerulopathy is associated with a COL4A5 missense mutation in a non-collagenous interruptionThe Accumulation of VEGFA in the Glomerular Basement Membrane and Its Relationship with Podocyte Injury and Proteinuria in Alport Syndrome.Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.The role of RANK ligand/osteoprotegerin in rheumatoid arthritis.Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis.Reducing Hepatocyte Injury and Necrosis in Response to Paracetamol Using Noncoding RNAs.Temporal macular thinning associated with X-linked Alport syndrome.Alport syndrome: a rare cause of uraemia.Alport syndrome: facts and opinions.Glomerular diseases: genetic causes and future therapeutics.Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options.Renal diseases associated with hematuria in children and adolescents: a brief tutorial.Alport syndrome--insights from basic and clinical research.Podocyturia: A Clue for the Rational Use of Amiloride in Alport Renal Disease.KDIGO Clinical Practice Guideline on the Evaluation and Care of Living Kidney Donors.Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome.Plasma leakage through glomerular basement membrane ruptures triggers the proliferation of parietal epithelial cells and crescent formation in non-inflammatory glomerular injury.The interface of genetics with pathology in alport nephritis.A case of mild phenotype Alport syndrome caused by COL4A3 mutations.Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.Tumour necrosis factor-α drives Alport glomerulosclerosis in mice by promoting podocyte apoptosis.
P2860
Q30405346-F2FDDCE1-088E-4A37-8606-57E03918F2C6Q33710267-3376810F-EE88-42BB-B676-6D65A95993DBQ33943303-167D6783-C716-488C-AD56-28A0EDC44F1AQ34021381-0AADC2FB-0C3C-485F-AFBE-F1AEB6F6F87EQ34100184-F9DB5DFC-2922-485B-B8AC-2A4CCE5728CAQ35010424-8DAF933C-CDC0-49D6-8B58-81AA260E889FQ35642498-B3F7D32A-D447-4B80-A6BF-F9F9E956D718Q35746380-F1DDB0E8-AE77-4749-A03F-EB0B902AEDCEQ35952630-77347E85-4373-48FF-990F-53D092D92C79Q36111285-B0A5A70E-58DF-4278-88BA-8192C628915DQ36556406-BBEF8CD4-F94B-423A-BC7C-BCDC56D667ACQ36930476-EF0BB76A-0DBE-4E61-8F18-A0EDE485DDDFQ37101426-333892AD-F1DE-4A36-AE40-9961D19FC6EAQ37588428-76CFBCBC-2EAA-4443-90AB-C9BD810AC197Q37595448-49872E97-A077-445F-80E1-FA20C12232E7Q37774243-51737B74-B6E9-4D7A-BED3-193FEC85526EQ37795641-0D518FC2-BC91-45BB-9CE6-C92CE8962AE5Q37980204-1A4E46F3-6B71-4FA3-98BE-BF22534D5F53Q38061008-4D9A5F39-0471-4BCB-A2FC-5AD30E0A7596Q38362602-CD9DE4AB-D509-4928-9DD0-C1BF4A034D40Q38652031-88EB01F2-DB81-420D-ABF7-A7847B6C329CQ38941236-EA12E01C-6322-4E64-836D-5FBA5EF5D014Q39354612-DB880A67-EC94-4274-87C3-51FF815F25EAQ42870018-E5E2C7A8-C30C-415A-8AFA-2314B9B0AEB2Q45943243-CDC7EBA8-3F38-47F5-AE32-6F0A4F5E2F95Q52718217-4C707709-FB03-4DC6-89E0-B00458591C61Q54346289-F7E6275C-0672-46D9-94EB-F1C2A7B6C1B3
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 21 May 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The renal lesions of Alport syndrome.
@en
The renal lesions of Alport syndrome.
@nl
type
label
The renal lesions of Alport syndrome.
@en
The renal lesions of Alport syndrome.
@nl
prefLabel
The renal lesions of Alport syndrome.
@en
The renal lesions of Alport syndrome.
@nl
P356
P1476
The renal lesions of Alport syndrome.
@en
P304
P356
10.1681/ASN.2008090984
P577
2009-05-21T00:00:00Z