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Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatment

  • Published:2008-03 Issue:3 Volume:93 Page:306-313
  • ISSN:1096-7192
  • Container-title:Molecular Genetics and Metabolism
  • language:en
  • Short-container-title:Molecular Genetics and Metabolism

Author:

Langlois Chantale,Jorquera Rossana,Orejuela Diana,Bergeron Anne,Finegold Milton J.,Rhead William J.,Tanguay Robert M.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference37 articles.

1. Tyrosinemia: a review;Russo;Pediatr. Dev. Pathol.,2001

2. Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean;De Braekeleer;Am. J. Hum. Genet.,1990

3. A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type I;Grompe;N. Engl. J. Med.,1994

4. The occurrence of hepatoma in the chronic form of hereditary tyrosinemia;Weinberg;J. Pediatr.,1976

5. Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase;Lindstedt;Lancet,1992

Cited by 7 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. Evaluation of dynamic thiol/disulfide homeostasis in hereditary tyrosinemia type 1 patients;Pediatric Research;2021-10-09

2. Hereditary tyrosinemia type 1 in children;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2019-11-16

3. GSTZ1 deficiency promotes hepatocellular carcinoma proliferation via activation of the KEAP1/NRF2 pathway;Journal of Experimental & Clinical Cancer Research;2019-10-30

4. Remaining Challenges in the Treatment of Tyrosinemia from the Clinician’s Viewpoint;Advances in Experimental Medicine and Biology;2017

5. Biochemical and Clinical Aspects of Hereditary Tyrosinemia Type 1;Advances in Experimental Medicine and Biology;2017
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