Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys
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Podocin localizes in the kidney to the slit diaphragm areaA mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.VP23R of infectious spleen and kidney necrosis virus mediates formation of virus-mock basement membrane to provide attaching sites for lymphatic endothelial cells.Alport disease: a review of the diagnostic difficulties.Association of a polymorphism of the interleukin 6 receptor gene with chronic kidney disease in Japanese individuals.Bone-marrow-derived stem cells repair basement membrane collagen defects and reverse genetic kidney disease.Learning cell biology as a team: a project-based approach to upper-division cell biologyThe LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes.A human-mouse chimera of the alpha3alpha4alpha5(IV) collagen protomer rescues the renal phenotype in Col4a3-/- Alport mice.Protective effects of leukemia inhibitory factor against oxidative stress during high glucose-induced apoptosis in podocytes.COL4A2 mutation associated with familial porencephaly and small-vessel disease.Glomerular basement membrane and related glomerular diseasePrognostic value of glomerular collagen IV immunofluorescence studies in male patients with X-linked Alport syndrome.Nanoscale protein architecture of the kidney glomerular basement membrane.Cellular origins of type IV collagen networks in developing glomeruli.Stem cell therapy for Alport syndrome: the hope beyond the hype.Alport syndrome: facts and opinions.Feasibility of repairing glomerular basement membrane defects in Alport syndrome.Glomerular cell cross-talk influences composition and assembly of extracellular matrixMolecular genetics of familial hematuric diseases.Evidence for activation of the unfolded protein response in collagen IV nephropathiesAccumulation of worn-out GBM material substantially contributes to mesangial matrix expansion in diabetic nephropathy.Quaternary organization of the goodpasture autoantigen, the alpha 3(IV) collagen chain. Sequestration of two cryptic autoepitopes by intrapromoter interactions with the alpha4 and alpha5 NC1 domains.Regulation of the paired type IV collagen genes COL4A5 and COL4A6. Role of the proximal promoter region.Pathological features of proteinuric nephropathy resembling Alport syndrome in a young Pyrenean Mountain dogInfluence of C-peptide on early glomerular changes in diabetic mice.The Chemical Chaperone, PBA, Reduces ER Stress and Autophagy and Increases Collagen IV α5 Expression in Cultured Fibroblasts From Men With X-Linked Alport Syndrome and Missense Mutations.Genetic cause of X-linked Alport syndrome in a family of domestic dogs.Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.
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P2860
Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
2000年论文
@zh
2000年论文
@zh-cn
name
Glomerular expression of type ...... linked Alport syndrome kidneys
@ast
Glomerular expression of type ...... linked Alport syndrome kidneys
@en
type
label
Glomerular expression of type ...... linked Alport syndrome kidneys
@ast
Glomerular expression of type ...... linked Alport syndrome kidneys
@en
prefLabel
Glomerular expression of type ...... linked Alport syndrome kidneys
@ast
Glomerular expression of type ...... linked Alport syndrome kidneys
@en
P2860
P50
P1476
Glomerular expression of type ...... linked Alport syndrome kidneys
@en
P2093
P2860
P304
P356
10.1016/S0002-9440(10)65063-8
P407
P577
2000-06-01T00:00:00Z