Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
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: | Journal article |
Iaith: | English |
Cyhoeddwyd: |
2002
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Eitemau Tebyg
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Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
gan: Norden, A, et al.
Cyhoeddwyd: (2001) -
Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
gan: Norden, A, et al.
Cyhoeddwyd: (2002) -
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
gan: Norden, A, et al.
Cyhoeddwyd: (2000) -
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)
gan: Thakker, R, et al.
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.
gan: Pook, M, et al.
Cyhoeddwyd: (1993)