Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome-Reference-Cited by-同舟云学术

Glomerular Basement Membrane Protein Expression and the Diagnosis and Prognosis of Autosomal Dominant Alport Syndrome

Published:2019-11 Issue:6 Volume:1 Page:391-396
ISSN:2590-0595
Container-title:Kidney Medicine
language:en
Short-container-title:Kidney Medicine

Author:

Akihisa Taro,Sato Masayo,Wakayama Yoshie,Taneda Sekiko,Horita Shigeru,Hirose Orie,Makabe Shiho,Kataoka Hiroshi,Mori Takayasu,Sohara Eisei,Uchida Shinichi,Nitta Kosaku,Mochizuki Toshio^ORCID

Publisher

Elsevier BV

Subject

Nephrology,Internal Medicine

Reference20 articles.

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3. 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;Papazachariou;PloS One,2014

4. COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy;Voskarides;J Am Soc Nephrol,2007

5. Alport syndrome: a unified classification of genetic disorders of collagen IV alpha345: a position paper of the Alport Syndrome Classification Working Group;Kashtan;Kidney Int,2018

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3. The basement membrane in the cross-roads between the lung and kidney;Matrix Biology;2022-01

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