Mutations in FN1 cause glomerulopathy with fibronectin deposits.
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Fibronectins, their fibrillogenesis, and in vivo functions.Assembly of fibronectin extracellular matrix.Genetic analysis of albuminuria in aging mice and concordance with loci for human diabetic nephropathy found in a genome-wide association scanExtracellular matrix molecules: potential targets in pharmacotherapy.A comprehensive analysis and annotation of human normal urinary proteome.Emerging roles of fibronectin in thrombosis.Characterization of glomerular diseases using proteomic analysis of laser capture microdissected glomeruli.A quantitative proteomic workflow for characterization of frozen clinical biopsies: laser capture microdissection coupled with label-free mass spectrometryExploring the genetic basis of early-onset chronic kidney disease.Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageingThe polyphenols (-)-epigallocatechin-3-gallate and luteolin synergistically inhibit TGF-β-induced myofibroblast phenotypes through RhoA and ERK inhibitionSpecific macrophage subtypes influence the progression of rhabdomyolysis-induced kidney injuryGIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment.New insights into form and function of fibronectin splice variants.Molecular Mechanism Responsible for Fibronectin-controlled Alterations in Matrix Stiffness in Advanced Chronic Liver Fibrogenesis.Musculocontractural Ehlers-Danlos syndrome and neurocristopathies: dermatan sulfate is required for Xenopus neural crest cells to migrate and adhere to fibronectinHaemodynamics Regulate Fibronectin Assembly via PECAM.Fibronectin splice variants: understanding their multiple roles in health and disease using engineered mouse models.The renal biopsy in the genomic era.Molecular genetics of familial hematuric diseases.Protein conformation as a regulator of cell-matrix adhesion.Stressed podocytes-mechanical forces, sensors, signaling and response.Kidney development and perspectives for organ engineering.Fibronectin glomerulopathy complicated with persistent cloaca and congenital esophageal atresia: a case report and literature review.Fibronectin glomerulopathy.Fibronectin Glomerulopathy: A Rare Autosomal Dominant Glomerular Disease.Deficiency of liver sinusoidal scavenger receptors stabilin-1 and -2 in mice causes glomerulofibrotic nephropathy via impaired hepatic clearance of noxious blood factors.Hypertension and proteinuria-the needle in the haystack?: Answers.Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures".De Novo Coding Variants Are Strongly Associated with Tourette Disorder.A Case of Fibronectin Glomerulopathy Caused by Missense Mutations in the Fibronectin 1 Gene.Fibronectin Conformation and Assembly: Analysis of Fibronectin Deletion Mutants and Fibronectin Glomerulopathy (GFND) Mutants.Frequent COL4 mutations in familial microhematuria accompanied by later-onset Alport nephropathy due to focal segmental glomerulosclerosis.Basement Membrane Defects in Genetic Kidney Diseases.A recurrent fibronectin glomerulopathy in a renal transplant patient: a case report.Extracellular Matrix as a Regulator of Epidermal Stem Cell Fate.Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits.Identification of mutations in FN1 leading to glomerulopathy with fibronectin deposits.
P2860
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P2860
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@ast
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@en
type
label
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@ast
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@en
prefLabel
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@ast
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
@en
P2093
P2860
P50
P356
P1476
Mutations in FN1 cause glomerulopathy with fibronectin deposits
@en
P2093
Christine Skerka
Elena Bresin
Federica Banterla
Federica Castelletti
Friedhelm Hildebrandt
Jessica Caprioli
Marina Noris
Marta Todeschini
Roberta Donadelli
Rosa Maria Caruso
P2860
P304
P356
10.1073/PNAS.0707730105
P407
P577
2008-02-11T00:00:00Z