Glomerular proteinuria: a complex interplay between unique players. - Wikidata - wikimedia - TriplyDB

Glomerular proteinuria: a complex interplay between unique players.

Glomerular proteinuria: a complex interplay between unique players.

http://www.wikidata.org/entity/Q35131205

about

Membrane trafficking in podocyte health and disease Proteinuria is associated with neurocognitive impairment in antiretroviral therapy treated HIV-infected individuals Integrin Ligation Results in Nephrin Tyrosine Phosphorylation In Vitro.The Role of Endothelin System in Renal Structure and Function during the Postnatal Development of the Rat Kidney.The Prediction of Key Cytoskeleton Components Involved in Glomerular Diseases Based on a Protein-Protein Interaction Network.Podocyte-specific knockout of myosin 1e disrupts glomerular filtration Endothelin-1 and the kidney: new perspectives and recent findings.Shp2 Associates with and Enhances Nephrin Tyrosine Phosphorylation and Is Necessary for Foot Process Spreading in Mouse Models of Podocyte Injury.The glomerular filtration barrier: components and crosstalk Chronic kidney disease: a new look at pathogenetic mechanisms and treatment options.Sickle cell disease: renal manifestations and mechanisms The Players: Cells Involved in Glomerular Disease.Chrysin ameliorates podocyte injury and slit diaphragm protein loss via inhibition of the PERK-eIF2α-ATF-CHOP pathway in diabetic mice.

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Glomerular proteinuria: a complex interplay between unique players.

http://www.wikidata.org/entity/Q35131205

description

2011 nî lūn-bûn

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2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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name

Glomerular proteinuria: a complex interplay between unique players.

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Glomerular proteinuria: a complex interplay between unique players.

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J.ACKD.2011.06.001

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Advances in Chronic Kidney Disease

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Glomerular proteinuria: a complex interplay between unique players.

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P2860

WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Synaptopodin regulates the actin-bundling activity of alpha-actinin in an isoform-specific manner

Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN

Cubilin is an albumin binding protein important for renal tubular albumin reabsorption

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

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233-242

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10.1053/J.ACKD.2011.06.001

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