Contribution of theTTC21Bgene to glomerular and cystic kidney diseases-Reference-Cited by-同舟云学术

Contribution of theTTC21Bgene to glomerular and cystic kidney diseases

Published:2016-03-02 Issue: Volume: Page:gfv453
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrol. Dial. Transplant.

Author:

Bullich Gemma,Vargas Iván,Trujillano Daniel,Mendizábal Santiago,Piñero-Fernández Juan Alberto,Fraga Gloria,García-Solano José,Ballarín José,Estivill Xavier,Torra Roser,Ars Elisabet

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/32/1/151/9675098/gfv453.pdf

Reference12 articles.

1. A Homozygous Missense Mutation in the Ciliary GeneTTC21BCauses Familial FSGS

2. TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

3. THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia

4. Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short-rib thoracic dystrophies

5. Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy

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