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.

Bibliografski detalji
Glavni autori:	Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O
Format:	Journal article
Jezik:	English
Izdano:	2002

Slični predmeti

Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
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Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
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THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
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Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
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Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.
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P-proteins in Arabidopsis are heteromeric structures involved in rapid sieve tube sealing
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Nanoscale protein architecture of the kidney glomerular basement membrane
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Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and HypertriglyceridemiaSummary
od: Abdul Elkadri, i dr.
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od: Narasaiah Kovuru, i dr.
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od: Browning, TD, i dr.
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