نتایج جستجو برای: polycystic kidneys

تعداد نتایج: 39226  

2004
Irma S. Lantinga-van Leeuwen Johannes G. Dauwerse Hans J. Baelde Wouter N. Leonhard Annemieke van de Wal Christopher J. Ward Sjef Verbeek Marco C. DeRuiter Martijn H. Breuning Emile de Heer Dorien J.M. Peters

Autosomal dominant polycystic kidney disease (ADPKD) is a major cause of renal failure and is characterized by the formation of many fluid-filled cysts in the kidneys. It is a systemic disorder that is caused by mutations in PKD1 or PKD2. Homozygous inactivation of these genes at the cellular level, by a ‘two-hit’ mechanism, has been implicated in cyst formation but does not seem to be the sole...

Journal: :The FASEB Journal 2021

Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the development of bilateral renal cysts which enlarge continuously, leading to compression adjacent intact nephrons. The growing lead a progressive decline in function. Cyst growth driven enhanced cell proliferation and chloride secretion into cyst lumen. Chloride believed occur mainly cAMP-activated cystic fibrosis trans...

Journal: :Human molecular genetics 2004
Irma S Lantinga-van Leeuwen Johannes G Dauwerse Hans J Baelde Wouter N Leonhard Annemieke van de Wal Christopher J Ward Sjef Verbeek Marco C Deruiter Martijn H Breuning Emile de Heer Dorien J M Peters

Autosomal dominant polycystic kidney disease (ADPKD) is a major cause of renal failure and is characterized by the formation of many fluid-filled cysts in the kidneys. It is a systemic disorder that is caused by mutations in PKD1 or PKD2. Homozygous inactivation of these genes at the cellular level, by a 'two-hit' mechanism, has been implicated in cyst formation but does not seem to be the sole...

2004
Johannes G. Dauwerse Hans J. Baelde Wouter N. Leonhard Annemieke van de Wal Christopher J. Ward Sjef Verbeek Marco C. DeRuiter Martijn H. Breuning Emile de Heer Dorien J.M. Peters

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a major cause of renal failure and is characterized by the formation of many fluid-filled cysts in the kidneys. It is a systemic disorder that is caused by mutations in PKD1 or PKD2. Homozygous inactivation of these genes at the cellular level, by a 'two-hit' mechanism, has been implicated in cyst formation but does not seem to be the sole...

Journal: :Kidney & blood pressure research 2016
Sarika Kapoor Daniel Rodriguez Katharyn Mitchell Rudolf P Wüthrich

BACKGROUND/AIMS The PCK rat model of polycystic kidney disease is characterized by the progressive development of renal medullary cysts. Here, we evaluated the suitability of high resolution ultrasonography (HRU) to assess the kidney and cyst volume in PCK rats, testing three different ultrasound image analysis methods, and correlating them with kidneys weights and histological examinations. ...

Journal: :American journal of physiology. Renal physiology 2011
Kirti Bhatt Qing-Sheng Mi Zheng Dong

MicroRNAs (miRNA) are endogenously produced, short RNAs that repress and thus regulate the expression of almost half of known protein-coding genes. miRNA-mediated gene repression is an important regulatory mechanism to modulate fundamental cellular processes such as the cell cycle, growth, proliferation, phenotype, and death, which in turn have major influences on pathophysiological outcomes. I...

Journal: :Internal medicine 2011
Isamu Hoshino Tetsuro Maruyama Toru Fukunaga Hisahiro Matsubara

A 46-year-old man presented with abdominal pain. A CAT scan showed the presence of cysts in both the liver and kidneys. Moreover, a cystic mass was also observed in the middle of the small intestine and the typical appearance of small bowel intussusceptions was identified (Picture 1). The density was clearly the same as that of the cysts in the liver and kidneys, indicating that a cyst may have...

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