Pinpointing Podocin Trafficking Defects in Kidney Organoids-Reference-Cited by-同舟云学术

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Pinpointing Podocin Trafficking Defects in Kidney Organoids

Published:2023-01 Issue:1 Volume:34 Page:2-4
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Tian Pinyuan¹,Lennon Rachel¹²

Affiliation:

1. Wellcome Centre for Cell-Matrix Research, Division of Cell-Matrix Biology and Regenerative Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom

2. Department of Paediatric Nephrology, Royal Manchester Children's Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Nephrology,General Medicine

Reference10 articles.

1. Genetic disorders of the glomerular filtration barrier;Li;Clin J Am Soc Nephrol.,2020

2. Positionally cloned gene for a novel glomerular protein—nephrin—is mutated in congenital nephrotic syndrome;Kestilä;Mol Cell.,1998

3. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome;Boute;Nat Genet.,2000

4. Directing human embryonic stem cell differentiation towards a renal lineage generates a self-organizing kidney;Takasato;Nat Cell Biol.,2014

5. Redefining the in vivo origin of metanephric nephron progenitors enables generation of complex kidney structures from pluripotent stem cells;Taguchi;Cell Stem Cell.,2014

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