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DNA damage in Fabry patients: An investigation of oxidative damage and repair

  • Published:2015-06 Issue: Volume:784-785 Page:31-36
  • ISSN:1383-5718
  • Container-title:Mutation Research/Genetic Toxicology and Environmental Mutagenesis
  • language:en
  • Short-container-title:Mutation Research/Genetic Toxicology and Environmental Mutagenesis

Author:

Biancini Giovana Brondani,Moura Dinara Jaqueline,Manini Paula Regina,Faverzani Jéssica Lamberty,Netto Cristina Brinckmann Oliveira,Deon Marion,Giugliani Roberto,Saffi Jenifer,Vargas Carmen Regla

Funder

CNPq

CAPES

FIPE/HCPA

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference32 articles.

1. α-Galactosidase A. deficiency: Fabry disease;Desnick,2001

2. Enzyme replacement therapy for Anderson–Fabry disease;El Dib;Cochrane Database Syst. Rev.,2010

3. Globotriaosylceramide is correlated with oxidative stress and inflammation in Fabry patients treated with enzyme replacement therapy;Biancini;Biochim. Biophys. Acta,2012

4. Fabry disease peripheral blood immune cells release inflammatory cytokines: role of globotriaosylceramide;De Francesco;Mol. Genet. Metab.,2013

5. Invariant natural killer T cells are phenotypically and functionally altered in Fabry disease;Pereira;Mol. Genet. Metab.,2013

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