Fundamental insights into autosomal dominant polycystic kidney disease from human-based cell models-Reference-Cited by-同舟云学术

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Fundamental insights into autosomal dominant polycystic kidney disease from human-based cell models

Published:2018-09-13 Issue:10 Volume:34 Page:1697-1715
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Weydert Caroline,Decuypere Jean-Paul,De Smedt Humbert,Janssens Peter,Vennekens Rudi,Mekahli Djalila

Funder

Agentschap Innoveren en Ondernemen

Clinical research fund, UZ Leuven

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-018-4057-5.pdf

Reference114 articles.

1. Cornec-Le Gall E, Torres VE, Harris PC (2017) Genetic complexity of autosomal dominant polycystic kidney and liver diseases. J Am Soc Nephrol. https://doi.org/10.1681/ASN.2017050483

2. Gabow PA, Johnson AM, Kaehny WD, Kimberling WJ, Lezotte DC, Duley IT, Jones RH (1992) Factors affecting the progression of renal disease in autosomal-dominant polycystic kidney disease. Kidney Int 41:1311–1319

3. Cornec-Le Gall E, Audrezet MP, Chen JM, Hourmant M, Morin MP, Perrichot R, Charasse C, Whebe B, Renaudineau E, Jousset P, Guillodo MP, Grall-Jezequel A, Saliou P, Ferec C, Le Meur Y (2013) Type of PKD1 mutation influences renal outcome in ADPKD. J Am Soc Nephrol 24:1006–1013. https://doi.org/10.1681/ASN.2012070650

4. Hanaoka K, Qian F, Boletta A, Bhunia AK, Piontek K, Tsiokas L, Sukhatme VP, Guggino WB, Germino GG (2000) Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents. Nature 408:990–994. https://doi.org/10.1038/35050128

5. Calvet JP (2015) The role of calcium and cyclic AMP in PKD. In: Li X (ed) Polycystic kidney disease. Codon Publications, Brisbane (AU). https://doi.org/10.15586/codon.pkd.2015.ch8

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1. Revisiting the gene mutations and protein profile of WT 9‐12: An autosomal dominant polycystic kidney disease cell line;Genes to Cells;2024-05-23

2. Comparative analysis of SEC61A1 mutant R236C in two patient-derived cellular platforms;Scientific Reports;2024-04-25

3. Polycystin-2 Ion Channel Function and Pathogenesis in Autosomal Dominant Polycystic Kidney;PROG BIOCHEM BIOPHYS;2024

4. Molecular determinants of SEC61A1 mutant R236C in two patient-derived cellular platforms;2023-12-07

5. Experimental Models of Polycystic Kidney Disease: Applications and Therapeutic Testing;Kidney360;2023-07-07

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