Transgenic zebrafish modeling low-molecular-weight proteinuria and lysosomal storage diseases-Reference-Cited by-同舟云学术

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Transgenic zebrafish modeling low-molecular-weight proteinuria and lysosomal storage diseases

Published:2020-06 Issue:6 Volume:97 Page:1150-1163
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Chen Zhiyong,Luciani Alessandro,Mateos José María,Barmettler Gery,Giles Rachel H.,Neuhauss Stephan C.F.,Devuyst Olivier

Funder

European Union's Seventh Framework Programme

Swiss National Science Foundation

UZH

Cystinosis Research Foundation

Dutch Kidney Foundation

Publisher

Elsevier BV

Subject

Nephrology

Reference51 articles.

1. Endocytic receptors in the renal proximal tubule;Christensen;Physiology,2012

2. Learning physiology from inherited kidney disorders;van der Wijst;Physiol Rev,2019

3. Chloride transporters and receptor-mediated endocytosis in the renal proximal tubule;Devuyst;J Physiol,2015

4. Low-molecular-weight proteins as markers of organ toxicity with special reference to Clara cell protein;Bernard;Toxicol Lett,1995

5. Renal Fanconi syndrome, Dent disease, and Bartter syndrome;Devuyst,2018

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1. Piplartine attenuates aminoglycoside-induced TRPV1 activity and protects from hearing loss in mice;Science Translational Medicine;2024-08-07

2. In Vivo Assessment of Individual and Total Proteinuria in Zebrafish Larvae Using the Solvatochromic Compound ZMB741;Chemical & Biomedical Imaging;2024-05-31

3. The Cl− transporter ClC-7 is essential for phagocytic clearance by microglia;Journal of Cell Science;2024-02-15

4. Drug discovery and therapeutic perspectives for proximal tubulopathies;Kidney International;2023-12

5. Lysosomal cystine export regulates mTORC1 signaling to guide kidney epithelial cell fate specialization;Nature Communications;2023-07-14

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