Albumin contributes to kidney disease progression in Alport syndrome. - Wikidata - awgldk - TriplyDB

Albumin contributes to kidney disease progression in Alport syndrome.

Albumin contributes to kidney disease progression in Alport syndrome.

http://www.wikidata.org/entity/Q37139486

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Alport syndrome: facts and opinions.Accelerated podocyte detachment and progressive podocyte loss from glomeruli with age in Alport Syndrome.Role of albumin and its modifications in glomerular injury.Collagen IV diseases: A focus on the glomerular basement membrane in Alport syndrome.Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome.Investigation into the underlying molecular mechanisms of hypertensive nephrosclerosis using bioinformatics analyses.Albumin: innocent bystander or culprit?Osteopontin deficiency ameliorates Alport pathology by preventing tubular metabolic deficits.Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.Tumstatin, a Matrikine Derived from Collagen Type IVα3, is Elevated in Serum from Patients with Non-Small Cell Lung Cancer.

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Albumin contributes to kidney disease progression in Alport syndrome.

http://www.wikidata.org/entity/Q37139486

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 04 May 2016

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Albumin contributes to kidney disease progression in Alport syndrome.

@en

Albumin contributes to kidney disease progression in Alport syndrome.

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type

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Albumin contributes to kidney disease progression in Alport syndrome.

@en

Albumin contributes to kidney disease progression in Alport syndrome.

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prefLabel

Albumin contributes to kidney disease progression in Alport syndrome.

@en

Albumin contributes to kidney disease progression in Alport syndrome.

@nl

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AJPRENAL.00456.2015

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American Journal of Physiology - Renal Physiology

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Albumin contributes to kidney disease progression in Alport syndrome.

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George Jarad

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Robert P Mecham

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Russell H Knutsen

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P2860

The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform

Diet-induced obesity in C57BL/6J mice causes increased renal lipid accumulation and glomerulosclerosis via a sterol regulatory element-binding protein-1c-dependent pathway

Proteinuria precedes podocyte abnormalities inLamb2-/- mice, implicating the glomerular basement membrane as an albumin barrier

Involvement of endoplasmic reticulum stress in albuminuria induced inflammasome activation in renal proximal tubular cells

In response to protein load podocytes reorganize cytoskeleton and modulate endothelin-1 gene: implication for permselective dysfunction of chronic nephropathies

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

Comparative studies on the half-life of I 131-labeled albumins and nonradioactive human serum albumin in a case of analbuminemia.

Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: implications for Pierson syndrome

Endocytosis of albumin by podocytes elicits an inflammatory response and induces apoptotic cell death.

Low TGFβ1 expression prevents and high expression exacerbates diabetic nephropathy in mice.

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F120-30

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scholarly article

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10.1152/AJPRENAL.00456.2015

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1

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311

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Jeffrey H Miner

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2016-05-04T00:00:00Z

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