Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.

Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.

Bibliografiske detaljer
Main Authors:	Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O
Format:	Journal article
Sprog:	English
Udgivet:	2002

Lignende værker

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
af: Norden, A, et al.
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af: Norden, A, et al.
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Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
af: Norden, A, et al.
Udgivet: (2000)

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af: Thakker, R, et al.
Udgivet: (1993)

Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
af: Pook, M, et al.
Udgivet: (1993)

Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.
af: Norden, A, et al.
Udgivet: (1999)

In memoriam: Oliver M. Wrong.
af: Scheinman, S, et al.
Udgivet: (2012)

Multifunctional Fanconi proteins, inflammation and the Fanconi phenotype
af: Grover C. Bagby
Udgivet: (2016-06-01)

Dent's disease.
af: Neild, G, et al.
Udgivet: (2005)

MAPPING OF 2 HEREDITARY RENAL TUBULAR DISORDERS ASSOCIATED WITH KIDNEY-STONES, AND REFERRED TO AS DENT-DISEASE AND X-LINKED RECESSIVE NEPHROLITHIASIS, TO CHROMOSOME-XP11
af: Thakker, R, et al.
Udgivet: (1994)

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis.
af: Reinhart, S, et al.
Udgivet: (1995)

Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
af: Scheinman, S, et al.
Udgivet: (2000)

Uncovering roles of proteins in the Fanconi Anemia DNA repair pathway
af: Xu, H
Udgivet: (2024)

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af: Tagrid Kaddar, et al.
Udgivet: (2012-01-01)

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af: Stephen Benedict Walsh, et al.
Udgivet: (2017-07-01)

HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
af: Lloyd, S, et al.
Udgivet: (1995)

Effects of plasma proteins on the sieving of macromolecular tracers in the kidney
af: Lazzara, Matthew J
Udgivet: (2007)

The Fanconi Anemia C Protein Binds to and Regulates Stathmin-1 Phosphorylation.
af: Audrey Magron, et al.
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Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
af: Lloyd, SE, et al.
Udgivet: (1996)

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af: Hiroaki Hanafusa, et al.
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Late Diagnosis of Fanconi-Bickel Syndrome
af: Nirupama Gupta MD, et al.
Udgivet: (2016-11-01)

Ifosfamide-Induced Fanconi's Syndrome
af: Lin-Kun Lee, et al.
Udgivet: (2014-06-01)

Supramolecular framework membrane for precise sieving of small molecules, nanoparticles and proteins
af: Guohua Zhang, et al.
Udgivet: (2023-02-01)

A Pst I restriction fragment length polymorphism near the MAO locus on Xp.
af: Salenger, P, et al.
Udgivet: (1996)

A UAF1-containing multisubunit protein complex regulates the Fanconi anemia pathway.
af: Cohn, M, et al.
Udgivet: (2007)

The Fanconi anemia group C protein interacts with uncoordinated 5A and delays apoptosis.
af: FengFei Huang, et al.
Udgivet: (2014-01-01)

Direct inhibition of TNF-α promoter activity by Fanconi anemia protein FANCD2.
af: Nobuko Matsushita, et al.
Udgivet: (2011-01-01)

The Fanconi syndrome of cystinosis: insights into the pathophysiology
af: Abdullah Sakarcan
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Glycine amidinotransferase (GATM), renal Fanconi syndrome, and kidney failure
af: Reichold, M, et al.
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MUSTANG-MR structural sieving server: applications in protein structural analysis and crystallography.
af: Arun S Konagurthu, et al.
Udgivet: (2010-01-01)

P-proteins in Arabidopsis are heteromeric structures involved in rapid sieve tube sealing
af: Stephan B Jekat, et al.
Udgivet: (2013-07-01)

Nanoscale protein architecture of the kidney glomerular basement membrane
af: Hani Suleiman, et al.
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af: Abdul Elkadri, et al.
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af: Socha, A
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af: Narasaiah Kovuru, et al.
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af: Browning, TD, et al.
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OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability.
af: Shrimpton, A, et al.
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af: Satoshi Takashima, et al.
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af: Philip S. Rosenberg, et al.
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