A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family-Reference-Cited by-同舟云学术

A novel single amino acid deletion impairs fibronectin function and causes familial glomerulopathy with fibronectin deposits: case report of a family

Published:2019-08-16 Issue:1 Volume:20 Page:
ISSN:1471-2369
Container-title:BMC Nephrology
language:en
Short-container-title:BMC Nephrol

Author:

dos Reis Monteiro Maria Luíza Gonçalves,Custódio Fabiano Bichuette,de Menezes Neves Precil Diego Miranda,Ferreira Frederico Moraes,Watanabe Elieser Hitoshi,Lerário Antônio Marcondes,de Araújo Liliane Silvano,Balbo Bruno Eduardo Pedroso,Pinto Vívian Christine Dourado,Barbosa Lívia Maria Gruli,de Paiva Marques Vilmar,Machado Juliana Reis,Reis Marlene Antônia,Onuchic Luiz Fernando

Publisher

Springer Science and Business Media LLC

Subject

Nephrology

Link

http://link.springer.com/content/pdf/10.1186/s12882-019-1507-7.pdf

Reference15 articles.

1. Baydar DE, Kutlugun AA, Bresin E, et al. A case of familial Glomerulopathy with fibronectin deposits caused by the Y973C mutation in fibronectin. Am J Kidney Dis. 2013;61(3):514–8.

2. Castelletti F, Donadelli R, Banterla F, et al. Mutations in FN1 cause glomerulopathy with fibronectin deposits. Proc Natl Acad Sci U S A. 2008;105(7):2538–43.

3. Strøm EH, Banfi G, Krapf R, et al. Glomerulopathy associated with predominant fibronectin deposits: a newly recognized hereditary disease. Kidney Int. 1995;48(1):163–70.

4. Nadamuni M, Piras R, Pharm DC, et al. Fibronectin Glomerulopathy: an unusual cause of adult-onset nephrotic syndrome. Am J Kidney Dis. 2012;60(5):839–42.

5. Li WZ, Jaroszewski L, Godzik A. Clustering of highly homologous sequences to reduce the size of large protein databases. Bioinformatics. 2001;17(3):282–3.

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Fibronectin glomerulopathy in a kidney allograft biopsy;BMC Nephrology;2023-12-05

2. Nucleation of fibronectin fibril assembly requires binding between heparin and the 13th type III module of fibronectin;Journal of Biological Chemistry;2023-05

3. A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy;BMC Nephrology;2022-07-14

4. Bortezomib-containing regiment in treating glomerulopathy with fibronectin deposits combined with monoclonal gammopathy of undetermined significance: a case report and literature review;Annals of Translational Medicine;2022-03

5. Clinical case of fibronectin glomerulopathy;Nephrology (Saint-Petersburg);2022-02-18