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1.
Predicting the protein composition of human urine in normal and pathological states: Quantitative description based on Dent1 disease (CLCN5 mutation).
J Physiol
; 599(1): 323-341, 2021 01.
Article
in English
| MEDLINE | ID: mdl-33107589
2.
Exploration of a panel of urine biomarkers of kidney disease in two paediatric cohorts with Type 1 diabetes mellitus of differing duration.
Diabetol Metab Syndr
; 14(1): 71, 2022 May 12.
Article
in English
| MEDLINE | ID: mdl-35550634
3.
Lysosomal enzymuria is a feature of hereditary Fanconi syndrome and is related to elevated CI-mannose-6-P-receptor excretion.
Nephrol Dial Transplant
; 23(9): 2795-803, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18174267
4.
Signalling through phospholipase C interferes with clathrin-mediated endocytosis.
Cell Signal
; 19(1): 42-51, 2007 Jan.
Article
in English
| MEDLINE | ID: mdl-16843639
5.
Is the albumin retrieval hypothesis a paradigm shift for nephrology?
J Am Soc Nephrol
; 23(4): 569-71, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22423012
6.
In memoriam: Oliver M. Wrong.
Kidney Int
; 82(2): 121-2, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22743559
7.
A more tubulocentric view of diabetic kidney disease.
J Nephrol
; 30(6): 701-717, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-28840540
8.
Obesity-Related Glomerulopathy: Hyperfiltration May Contribute to Early Proteinuria.
Kidney Int Rep
; 6(3): 867, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-33733005
9.
Urine retinol-binding protein 4: a functional biomarker of the proximal renal tubule.
Adv Clin Chem
; 63: 85-122, 2014.
Article
in English
| MEDLINE | ID: mdl-24783352
10.
A New Estimate of the Glomerular Sieving Coefficient for Retinol-Binding Protein 4 Suggests It Is Not Freely Filtered.
Kidney Int Rep
; 4(7): 1017-1018, 2019 Jul.
Article
in English
| MEDLINE | ID: mdl-31384698
11.
Analysis of molecular forms of urine Retinol-Binding Protein in Fanconi Syndrome and design of an accurate immunoassay.
Clin Chim Acta
; 413(3-4): 483-9, 2012 Feb 18.
Article
in English
| MEDLINE | ID: mdl-22120727
12.
Characterization of a recurrent in-frame UMOD indel mutation causing late-onset autosomal dominant end-stage renal failure.
Clin J Am Soc Nephrol
; 6(12): 2766-74, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-22034507
13.
Quantitative amino acid and proteomic analysis: very low excretion of polypeptides >750 Da in normal urine.
Kidney Int
; 66(5): 1994-2003, 2004 Nov.
Article
in English
| MEDLINE | ID: mdl-15496171
14.
Detection and analysis of urinary peptides by on-line liquid chromatography and mass spectrometry: application to patients with renal Fanconi syndrome.
Clin Sci (Lond)
; 104(5): 483-90, 2003 May.
Article
in English
| MEDLINE | ID: mdl-12529166
15.
The urinary proteome in Fanconi syndrome implies specificity in the reabsorption of proteins by renal proximal tubule cells.
Am J Physiol Renal Physiol
; 287(3): F353-64, 2004 Sep.
Article
in English
| MEDLINE | ID: mdl-15140760
16.
Megalin is essential for renal proximal tubule reabsorption and accumulation of transcobalamin-B(12).
Am J Physiol Renal Physiol
; 282(3): F408-16, 2002 Mar.
Article
in English
| MEDLINE | ID: mdl-11832420
17.
Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
J Am Soc Nephrol
; 13(1): 125-133, 2002 Jan.
Article
in English
| MEDLINE | ID: mdl-11752029
18.
Clinical urinary peptidomics: learning to walk before we can run.
Clin Chem
; 53(3): 375-6, 2007 Mar.
Article
in English
| MEDLINE | ID: mdl-17327502
19.
Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.
Kidney Int
; 62(1): 349, 2002 Jul.
Article
in English
| MEDLINE | ID: mdl-12081599
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