Literature DB >> 9761542

Exclusion of the uteroglobin gene as a candidate for fibronectin glomerulopathy (GFND)

M Vollmer, R Krapf, F Hildebrandt.   

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Year:  1998        PMID： 9761542     DOI： 10.1093/ndt/13.9.2417

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  3 in total

1.  The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.

Authors:  M Vollmer; M Jung; F Rüschendorf; R Ruf; T Wienker; A Reis; R Krapf; F Hildebrandt
Journal:  Am J Hum Genet       Date:  1998-12       Impact factor: 11.025

2.  Mutations in FN1 cause glomerulopathy with fibronectin deposits.

Authors:  Federica Castelletti; Roberta Donadelli; Federica Banterla; Friedhelm Hildebrandt; Peter F Zipfel; Elena Bresin; Edgar Otto; Christine Skerka; Alessandra Renieri; Marta Todeschini; Jessica Caprioli; Rosa Maria Caruso; Rosangela Artuso; Giuseppe Remuzzi; Marina Noris
Journal:  Proc Natl Acad Sci U S A       Date:  2008-02-11       Impact factor: 11.205

3.  Fibronectin glomerulopathy: an uncommon cause of nephrotic syndrome in systemic lupus erythematosus.

Authors:  Antonella Stoppacciaro; Angelo Pietrucci; Claudia Fofi; Salvatore Raffa; Maria Rosaria Torrisi; Paolo Menè
Journal:  NDT Plus       Date:  2008-04-14
  3 in total

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