نتایج جستجو برای: polycystic kidney diseases pkd

تعداد نتایج: 1000149  

2017
Shih-Ting Huang Ya-Wen Chuang Tung-Min Yu Cheng-Li Lin Long-Bin Jeng

Background The objective of this study was to determine the incidence of major hepatointestinal complications in patients with polycystic kidney disease (PKD). Methods We analyzed the Taiwan National Health Insurance claims data (2000-2010) of 6031 patients with PKD and 23,976 non-PKD hospitalized controls. The control cohort was propensity score matched with the PKD cohort at a 1:4 ratio. Al...

Journal: :American journal of physiology. Regulatory, integrative and comparative physiology 2000
S M Ali V Y Wong K Kikly T A Fredrickson P M Keller W E DeWolf D Lee D P Brooks

Polycystic kidney disease (PKD) is characterized by the development of large renal cysts and progressive loss of renal function. Although the cause of the development of renal cysts is unknown, recent evidence suggests that excessive apoptosis occurs in PKD. With the use of terminal deoxynucleotidyl transferase dUTP nick-end labeling staining, we have confirmed the presence of apoptotic bodies ...

2011
Mukta Rani Manas R. Dikhit Ganesh C Sahoo Pradeep Das

EMR2 is an EGF-like module containing mucin-like hormone receptor-2 precursor, a G-protein coupled receptor (G-PCR). Mutation in EMR2 causes complicated disorders like polycystic kidney disease (PKD). The structure of EMR2 shows that the fifth domain is comprised of EGF-TM7 helices. Functional assignment of EMR2 by support vector machine (SVM) revealed that along with transporter activity, seve...

Journal: :Molecular biology of the cell 2005
Jinghua Hu Maureen M Barr

Caenorhabditis elegans is a powerful model to study the molecular basis of autosomal dominant polycystic kidney disease (ADPKD). ADPKD is caused by mutations in the polycystic kidney disease (PKD)1 or PKD2 gene, encoding polycystin (PC)-1 or PC-2, respectively. The C. elegans polycystins LOV-1 and PKD-2 are required for male mating behaviors and are localized to sensory cilia. The function of t...

Journal: :QJM : monthly journal of the Association of Physicians 2013
K M Thong A C M Ong

BACKGROUND AND AIM Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease. The major objective of this study was to analyse the natural history of disease progression in all patients with ADPKD seen at the Sheffield Kidney Institute between 1978 and 2012. METHODS A retrospective analysis was performed based on recorded renal function up to 30 years pr...

Journal: :Journal of the American Society of Nephrology : JASN 1998
G A Tanner

Polycystic kidney disease (PKD) has been shown to be exacerbated by acidosis or a low potassium intake, and there is evidence that administration of alkali might have a beneficial effect. This study determined whether ingestion of potassium citrate and citric acid would ameliorate PKD. Healthy normal and heterozygous littermate Han:SPRD rats with autosomal dominant PKD were provided with either...

Journal: :Kidney international 2000
J T Hjelle M A Miller-Hjelle I R Poxton E O Kajander N Ciftcioglu M L Jones R C Caughey R Brown P D Millikin F S Darras

BACKGROUND Microbes have been suspected as provocateurs of polycystic kidney disease (PKD), but attempts to isolate viable organisms have failed. Bacterial endotoxin is the most often reported microbial product found in PKD fluids. We assessed potential microbial origins of endotoxin in cyst fluids from 13 PKD patients and urines of PKD and control individuals. METHODS Fluids were probed for ...

2017
Carsten Bergmann

Autosomal recessive polycystic kidney disease (ARPKD) is a hepatorenal fibrocystic disorder that is characterized by enlarged kidneys with progressive loss of renal function and biliary duct dilatation and congenital hepatic fibrosis that leads to portal hypertension in some patients. Mutations in the PKHD1 gene are the primary cause of ARPKD; however, the disease is genetically not as homogene...

2013
Katherine I. Swenson-Fields Carolyn J. Vivian Sally M. Salah Jacqueline D. Peda Bradley M. Davis Nico van Rooijen Darren P. Wallace Timothy A. Fields

Renal M2-like macrophages have critical roles in tissue repair, stimulating tubule cell proliferation and, if they remain, fibrosis. M2-like macrophages have also been implicated in promoting cyst expansion in mouse models of autosomal dominant polycystic kidney disease (ADPKD). While renal macrophages have been documented in human ADPKD, there are no studies in autosomal recessive polycystic k...

2017
Yeoungjee Cho Benedicte Sautenet Gopala Rangan Jonathan C Craig Albert C M Ong Arlene Chapman Curie Ahn Dongping Chen Helen Coolican Juliana Tze-Wah Kao Ron Gansevoort Ronald Perrone Tess Harris Vicente Torres York Pei Peter G Kerr Jessica Ryan Talia Gutman Martin Howell Angela Ju Karine E Manera Armando Teixeira-Pinto Lorraine A Hamiwka Allison Tong

BACKGROUND Autosomal dominant polycystic kidney disease (ADPKD) is the most common potentially life threatening inherited kidney disease and is responsible for 5-10% of cases of end-stage kidney disease (ESKD). Cystic kidneys may enlarge up to 20 times the weight of a normal kidney due to the growth of renal cysts, and patients with ADPKD have an increased risk of morbidity, premature mortality...

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