Taurine treatment prevents derangement of the hepatic γ‐glutamyl cycle and methylglyoxal metabolism in a mouse model of classical homocystinuria: regulatory crosstalk between thiol and sulfinic acid metabolism-Reference-Cited by-同舟云学术

Taurine treatment prevents derangement of the hepatic γ‐glutamyl cycle and methylglyoxal metabolism in a mouse model of classical homocystinuria: regulatory crosstalk between thiol and sulfinic acid metabolism

Published:2018-01-03 Issue:3 Volume:32 Page:1265-1280
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:FASEB j.

Author:

Maclean Kenneth N.¹,Jiang Hua¹,Aivazidis Stefanos²,Kim Eugene¹,Shearn Colin T.²,Harris Peter S.²,Petersen Dennis R.²,Allen Robert H.³,Stabler Sally P.³,Roede James R.²

Affiliation:

1. Department of Pediatrics Aurora Colorado USA

2. Department of Pharmaceutical Sciences Aurora Colorado USA

3. Department of Medicine University of Colorado Health Sciences Center Aurora Colorado USA

Funder

Skaggs School of Pharmacy and Pharmaceutical Sciences

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1096/fj.201700586R

Reference95 articles.

1. The natural history of homocystinuria due to cystathionine β‐synthase deficiency;Mudd S. H.;Am. J. Hum. Genet.,1985

2. Glutathione metabolism and its selective modification;Meister A.;J. Biol. Chem.,1988

3. [5] Diversity of glutathione peroxidases

4. Glutathione synthesis

5. Glyoxalase I – structure, function and a critical role in the enzymatic defence against glycation

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