Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing-Reference-Cited by-同舟云学术

Frequency of COL4A3/COL4A4 Mutations amongst Families Segregating Glomerular Microscopic Hematuria and Evidence for Activation of the Unfolded Protein Response. Focal and Segmental Glomerulosclerosis Is a Frequent Development during Ageing

Published:2014-12-16 Issue:12 Volume:9 Page:e115015
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Papazachariou Louiza,Demosthenous Panayiota,Pieri Myrtani,Papagregoriou Gregory,Savva Isavella,Stavrou Christoforos,Zavros Michael,Athanasiou Yiannis,Ioannou Kyriakos,Patsias Charalambos,Panagides Alexia,Potamitis Costas,Demetriou Kyproula,Prikis Marios,Hadjigavriel Michael,Kkolou Maria,Loukaidou Panayiota,Pastelli Androulla,Michael Aristos,Lazarou Akis,Arsali Maria,Damianou Loukas,Goutziamani Ioanna,Soloukides Andreas,Yioukas Lakis,Elia Avraam,Zouvani Ioanna,Polycarpou Polycarpos,Pierides Alkis,Voskarides Konstantinos,Deltas Constantinos

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference56 articles.

1. Deltas C, Pierides A, Voskarides K (2013) Molecular genetics of familial hematuric diseases. Nephrol Dial Transplant.

2. Structure and function of basement membranes;VS LeBleu;Exp Biol Med (Maywood),2007

3. Basement membranes and human disease;T Van Agtmael;Cell Tissue Res,2010

4. Inherited diseases of the glomerular basement membrane;MC Gubler;Nat Clin Pract Nephrol,2008

5. Familial hematuria;CE Kashtan;Pediatr Nephrol,2009

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