scholarly journals In vitro formation of cysts derived from a rat model of autosomal dominant polycystic kidney disease

1996 ◽  
Vol 11 (supp6) ◽  
pp. 58-61 ◽  
Author(s):  
R. Pey ◽  
M. Hafner ◽  
G. Schieren ◽  
J. Bach ◽  
N. Gretz
2020 ◽  
Vol 21 (12) ◽  
pp. 4537
Author(s):  
Svenja Koslowski ◽  
Camille Latapy ◽  
Pierrïck Auvray ◽  
Marc Blondel ◽  
Laurent Meijer

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inheritable cause of end stage renal disease and, as of today, only a single moderately effective treatment is available for patients. Even though ADPKD research has made huge progress over the last decades, the precise disease mechanisms remain elusive. However, a wide variety of cellular and animal models have been developed to decipher the pathophysiological mechanisms and related pathways underlying the disease. As none of these models perfectly recapitulates the complexity of the human disease, the aim of this review is to give an overview of the main tools currently available to ADPKD researchers, as well as their main advantages and limitations.


2011 ◽  
Vol 15 (5) ◽  
pp. 676-687 ◽  
Author(s):  
Takafumi Toyohara ◽  
Takehiro Suzuki ◽  
Yasutoshi Akiyama ◽  
Daisuke Yoshihara ◽  
Yoichi Takeuchi ◽  
...  

2018 ◽  
Vol 9 (1) ◽  
pp. 389-396 ◽  
Author(s):  
Yangyang Zhu ◽  
Tian Teng ◽  
Hu Wang ◽  
Hao Guo ◽  
Lei Du ◽  
...  

Autosomal dominant polycystic kidney disease (ADPKD) is a common monogenic disease characterized by massive enlargement of fluid-filled cysts in the kidney.


2017 ◽  
Vol 32 (suppl_3) ◽  
pp. iii104-iii104
Author(s):  
Giuseppina Toteda ◽  
Anna Perri ◽  
Donatella Vizza ◽  
Simona Lupinacci ◽  
Antonella La Russa ◽  
...  

2018 ◽  
Vol 9 (11) ◽  
pp. 5925-5935
Author(s):  
G. Toteda ◽  
D. Vizza ◽  
S. Lupinacci ◽  
A. Perri ◽  
M. F. Scalise ◽  
...  

–Autosomal dominant polycystic kidney disease (ADPKD) is characterized by progressive enlargement of kidney cysts, leading to chronic kidney disease.


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