نتایج جستجو برای: uromodulin

تعداد نتایج: 340  

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2004
Sigrid Tinschert Nico Ruf Ilenia Bernascone Kai Sacherer Giuseppe Lamorte Hans-Hellmut Neumayer Peter Nürnberg Friedrich C Luft Luca Rampoldi

BACKGROUND Familial juvenile hyperuricaemic nephropathy (FJHN) is an autosomal-dominant disorder featuring hyperuricaemia, low fractional urate excretion, interstitial nephritis and chronic renal failure. The responsible gene UMOD was recently identified. UMOD encodes for uromodulin or Tamm-Horsfall glycoprotein, the most abundant protein in normal urine. We encountered a family with FJHN and i...

Journal: :Journal of the American Society of Nephrology : JASN 2003
Karin Dahan Olivier Devuyst Michèle Smaers Didier Vertommen Guy Loute Jean-Michel Poux Béatrice Viron Christian Jacquot Marie-France Gagnadoux Dominique Chauveau Mathias Büchler Pierre Cochat Jean-Pierre Cosyns Béatrice Mougenot Mark H Rider Corinne Antignac Christine Verellen-Dumoulin Yves Pirson

Familial juvenile hyperuricemic nephropathy (FJHN [MIM 162000]) is an autosomal-dominant disorder characterized by abnormal tubular handling of urate and late development of chronic interstitial nephritis leading to progressive renal failure. A locus for FJHN was previously identified on chromosome 16p12 close to the MCKD2 locus, which is responsible for a variety of autosomal-dominant medullar...

Journal: :Clinical chemistry 2016
Qin Fu Eric Grote Jie Zhu Christine Jelinek Anna Köttgen Josef Coresh Jennifer E Van Eyk

BACKGROUND Many avenues have been proposed for a seamless transition between biomarker discovery data and selected reaction monitoring (SRM) assays for biomarker validation. Unfortunately, studies with the abundant urinary protein uromodulin have shown that these methods do not converge on a consistent set of surrogate peptides for targeted mass spectrometry. As an alternative, we present an em...

Journal: :Human molecular genetics 2003
Luca Rampoldi Gianluca Caridi Daniela Santon Francesca Boaretto Ilenia Bernascone Giuseppe Lamorte Regina Tardanico Monica Dagnino Giacomo Colussi Francesco Scolari Gian Marco Ghiggeri Antonio Amoroso Giorgio Casari

The disease complex medullary cystic disease/familial juvenile hyperuricemic nephropathy (MCKD/FJHN) is characterized by alteration of urinary concentrating ability, frequent hyperuricemia, tubulo-interstitial fibrosis, cysts at the cortico-medullary junction and renal failure. MCKD/FJHN is caused by mutations of the gene encoding uromodulin, the most abundant protein in urine. Here, we describ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
Laura Labriola Kar in Dahan Yves Pirson

Familial juvenile hyperuricaemic nephropathy (FJHN) and medullary cystic kidney disease (MCKD) are rare autosomal-dominant disorders, both characterized by early hyperuricaemia due to reduced urinary excretion of urate and the development of chronic interstitial nephropathy, most often leading to end-stage renal failure (ESRF) in adulthood. Although a history of gout is more frequently reported...

2014
Frank Horsfall

Tamm–Horsfall protein was discovered in 1950 by Igor Tamm and Frank Horsfall, using a salt precipitation procedure to isolate a potent inhibitor of viral hemagglutination from urine. Muchmore and Decker, in 1985, isolated a glycoprotein (calling it uromodulin) with in vitro immunosuppressive properties from urine of pregnant women. In 1987, Pennica et al confirmed by cDNA analysis that uromodul...

Journal: :Hypertension 2014
Sandosh Padmanabhan Lesley Graham Nicholas R Ferreri Delyth Graham Martin McBride Anna F Dominiczak

Tamm–Horsfall protein was discovered in 1950 by Igor Tamm and Frank Horsfall, using a salt precipitation procedure to isolate a potent inhibitor of viral hemagglutination from urine. Muchmore and Decker, in 1985, isolated a glycoprotein (calling it uromodulin) with in vitro immunosuppressive properties from urine of pregnant women. In 1987, Pennica et al confirmed by cDNA analysis that uromodul...

Journal: :American journal of physiology. Renal physiology 2009
Elisabeth Kemter Birgit Rathkolb Jan Rozman Wolfgang Hans Anja Schrewe Christina Landbrecht Matthias Klaften Boris Ivandic Helmut Fuchs Valérie Gailus-Durner Martin Klingenspor Martin Hrabé de Angelis Eckhard Wolf Ruediger Wanke Bernhard Aigner

Uromodulin-associated kidney disease is a heritable renal disease in humans caused by mutations in the uromodulin (UMOD) gene. The pathogenesis of the disease is mostly unknown. In this study, we describe a novel chemically induced mutant mouse line termed Umod(A227T) exhibiting impaired renal function. The A227T amino acid exchange may impair uromodulin trafficking, leading to dysfunction of t...

Journal: :Molecular biology of the cell 2009
Céline Schaeffer Sara Santambrogio Simone Perucca Giorgio Casari Luca Rampoldi

Uromodulin is the most abundant protein secreted in urine, in which it is found as a high-molecular-weight polymer. Polymerization occurs via its zona pellucida (ZP) domain, a conserved module shared by many extracellular eukaryotic proteins that are able to assemble into matrices. In this work, we identified two motifs in uromodulin, mapping in the linker region of the ZP domain and in between...

2010
Sandosh Padmanabhan Olle Melander Toby Johnson Anna Maria Di Blasio Wai K. Lee Davide Gentilini Claire E. Hastie Cristina Menni Maria Cristina Monti Christian Delles Stewart Laing Barbara Corso Gerjan Navis Arjan J. Kwakernaak Pim van der Harst Murielle Bochud Marc Maillard Michel Burnier Thomas Hedner Sverre Kjeldsen Björn Wahlstrand Marketa Sjögren Cristiano Fava Martina Montagnana Elisa Danese Ole Torffvit Bo Hedblad Harold Snieder John M. C. Connell Morris Brown Nilesh J. Samani Martin Farrall Giancarlo Cesana Giuseppe Mancia Stefano Signorini Guido Grassi Susana Eyheramendy H. Erich Wichmann Maris Laan David P. Strachan Peter Sever Denis Colm Shields Alice Stanton Peter Vollenweider Alexander Teumer Henry Völzke Rainer Rettig Christopher Newton-Cheh Pankaj Arora Feng Zhang Nicole Soranzo Timothy D. Spector Gavin Lucas Sekar Kathiresan David S. Siscovick Jian'an Luan Ruth J. F. Loos Nicholas J. Wareham Brenda W. Penninx Ilja M. Nolte Martin McBride William H. Miller Stuart A. Nicklin Andrew H. Baker Delyth Graham Robert A. McDonald Jill P. Pell Naveed Sattar Paul Welsh Patricia Munroe Mark J. Caulfield Alberto Zanchetti Anna F. Dominiczak

Hypertension is a heritable and major contributor to the global burden of disease. The sum of rare and common genetic variants robustly identified so far explain only 1%-2% of the population variation in BP and hypertension. This suggests the existence of more undiscovered common variants. We conducted a genome-wide association study in 1,621 hypertensive cases and 1,699 controls and follow-up ...

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