Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
BACKGROUND: Glomerular sieving coefficients (GSCs) of proteins have been measured extensively in animals but not humans. We have studied the proteinuria of Fanconi syndrome, a "knock-out" of renal tubular protein reabsorption, to estimate GSCs and detect potential contributors to developm...
Prif Awduron: | Norden, A, Lapsley, M, Lee, P, Pusey, C, Scheinman, S, Tam, F, Thakker, R, Unwin, R, Wrong, O |
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Fformat: | Conference item |
Cyhoeddwyd: |
2001
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Eitemau Tebyg
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Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
gan: Norden, A, et al.
Cyhoeddwyd: (2002) -
Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
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Cyhoeddwyd: (2002) -
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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Cyhoeddwyd: (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.
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Cyhoeddwyd: (1993) -
Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.
gan: Norden, A, et al.
Cyhoeddwyd: (1999)