نتایج جستجو برای: uromodulin

تعداد نتایج: 340  

2017
Céline Schaeffer Stefania Merella Elena Pasqualetto Dejan Lazarevic Luca Rampoldi

Uromodulin is the most abundant urinary protein in physiological conditions. It is exclusively produced by renal epithelial cells lining the thick ascending limb of Henle's loop (TAL) and it plays key roles in kidney function and disease. Mutations in UMOD, the gene encoding uromodulin, cause autosomal dominant tubulointerstitial kidney disease uromodulin-related (ADTKD-UMOD), characterised by ...

2017
Sian E Piret Eric Olinger Anita A C Reed M Andrew Nesbit Tertius A Hough Liz Bentley Olivier Devuyst Roger D Cox Rajesh V Thakker

Renal fibrosis is a common feature of renal failure resulting from multiple etiologies, including diabetic nephropathy, hypertension and inherited renal disorders. However, the mechanisms of renal fibrosis are incompletely understood and we therefore explored these by establishing a mouse model for a renal tubular disorder, referred to as autosomal dominant tubulointerstitial kidney disease (AD...

Journal: :Asian Pacific journal of allergy and immunology 2015
Chia-Yean Hong Nyet-Kui Wong Maha Abdullah

BACKGROUND Tamm-Horsfall glycoprotein (THP) and uromodulin are the most abundant glycoproteins in non-pregnant women's/men's and pregnant women's urine, respectively. However, the bioactivities of these glycoproteins are still unclear. OBJECTIVE To evaluate the immunomodulatory properties of THP and uromodulin on human peripheral blood mononuclear cells (PBMC) METHODS: THP and uromodulin isol...

Journal: :American journal of physiology. Renal physiology 2005
Wenkai Dou Sandra Thompson-Jaeger Stanley J F Laulederkind John W Becker Julia Montgomery Eduardo Ruiz-Bustos David L Hasty Leslie R Ballou P Scott Eastman Betsy Srichai Matthew D Breyer Rajendra Raghow

Mice lacking a functional cyclooxygenase-2 (COX-2) gene develop abnormal kidneys that contain hypoplastic glomeruli and reduced proximal tubular mass, and they often die of renal failure. A comparison of kidney-specific gene expression between wild-type and COX-2-deficient mice by cDNA microarrays revealed that although more than 500 mRNAs were differentially expressed between the two strains o...

Journal: :Human molecular genetics 2010
Ilenia Bernascone Sylvie Janas Masami Ikehata Matteo Trudu Alessandro Corbelli Céline Schaeffer Maria Pia Rastaldi Olivier Devuyst Luca Rampoldi

Uromodulin-associated kidney diseases (UAKD) are autosomal-dominant disorders characterized by alteration of urinary concentrating ability, tubulo-interstitial fibrosis, hyperuricaemia and renal cysts at the cortico-medullary junction. UAKD are caused by mutations in UMOD, the gene encoding uromodulin. Although uromodulin is the most abundant protein secreted in urine, its physiological role re...

2011
Michael G Shlipak Yongmei Li Caroline Fox Josef Coresh Carl Grunfeld Mary Whooley

BACKGROUND A common variant of the UMOD gene was linked with prevalent chronic kidney disease (CKD) in large, genomics consortia. One community-based study found that urine concentrations of the uromodulin protein forecast risk of incident CKD. This study within persons with known coronary artery disease (CAD) evaluated whether uromodulin concentrations could distinguish CKD risk. METHODS In ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2005
Olivier Devuyst Karin Dahan Yves Pirson

More than 50 years ago, Tamm and Horsfall isolated a mucoprotein from the human urine, and showed that the protein was able to interact and inhibit viral haemagglutination [1,2]. Of interest, the protein was found to be heavily glycosylated, containing up to 30% of its mass in carbohydrates [3]. It was then discovered that the Tamm–Horsfall protein (THP), as it was readily named, was the most a...

Journal: :Journal of the American Society of Nephrology : JASN 2005
Sung Won Choi Ok Hee Ryu Sun Jin Choi In Sun Song Anthony J Bleyer Thomas C Hart

As a consequence of uromodulin gene mutations, individuals develop precocious hyperuricemia, gout, and progressive renal failure. In vitro studies suggest that pathologic accumulation of uromodulin/Tamm-Horsfall glycoprotein (THP) occurs in the endoplasmic reticulum (ER), but the pathophysiology of renal damage is unclear. It was hypothesized that programmed cell death triggered by accumulation...

Journal: :Human molecular genetics 2009
Siân E Williams Anita A C Reed Juris Galvanovskis Corinne Antignac Tim Goodship Fiona E Karet Peter Kotanko Karl Lhotta Vincent Morinière Paul Williams William Wong Patrik Rorsman Rajesh V Thakker

Familial juvenile hyperuricaemic nephropathy (FJHN), an autosomal dominant disorder, is caused by mutations in the UMOD gene, which encodes Uromodulin, a glycosylphosphatidylinositol-anchored protein that is expressed in the thick ascending limb of the loop of Henle and excreted in the urine. Uromodulin contains three epidermal growth factor (EGF)-like domains, a cysteine-rich region which incl...

Journal: :BMC Biotechnology 2005
Yue-Jin Huang Nathalie Chretien Annie S Bilodeau Jiang Feng Zhou Anthoula Lazaris Costas N Karatzas

BACKGROUND Uromodulin is the most abundant protein found in the urine of mammals. In an effort to utilize the uromodulin promoter in order to target recombinant proteins in the urine of transgenic animals we have cloned a goat uromodulin gene promoter fragment (GUM promoter) and used it to drive expression of GFP in the kidney of transgenic mice. RESULTS The GUM-GFP cassette was constructed a...

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