 Peroxiredoxins
"Peroxiredoxins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A family of ubiquitously-expressed peroxidases that play a role in the reduction of a broad spectrum of PEROXIDES like HYDROGEN PEROXIDE; LIPID PEROXIDES and peroxinitrite. They are found in a wide range of organisms, such as BACTERIA; PLANTS; and MAMMALS. The enzyme requires the presence of a thiol-containing intermediate such as THIOREDOXIN as a reducing cofactor.
| Descriptor ID |
D054464
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| MeSH Number(s) |
D08.811.682.732.850
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| Concept/Terms |
Peroxiredoxins- Peroxiredoxins
- Alkylhydroperoxide Reductase
- Peroxidoxin
- Thioredoxin Peroxidase
- Protector Protein (Mixed-Function Oxidase Systems)
- Thiol-Specific Antioxidant Protein
- Thiol Specific Antioxidant Protein
- Alkyl Hydroperoxide Reductase
- Hydroperoxide Reductase, Alkyl
- Peroxiredoxin
Peroxiredoxin II- Peroxiredoxin II
- Thioredoxin Peroxidase 1
- Thioredoxin-Dependent Peroxide Reductase 1
- Thioredoxin Dependent Peroxide Reductase 1
- Peroxiredoxin 2
Peroxiredoxin I- Peroxiredoxin I
- Thioredoxin Peroxidase 2
- Thioredoxin-Dependent Peroxide Reductase 2
- Thioredoxin Dependent Peroxide Reductase 2
- Peroxiredoxin 1
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Below are MeSH descriptors whose meaning is more general than "Peroxiredoxins".
Below are MeSH descriptors whose meaning is more specific than "Peroxiredoxins".
This graph shows the total number of publications written about "Peroxiredoxins" by people in this website by year, and whether "Peroxiredoxins" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Peroxiredoxins" by people in Profiles.
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Gu?ant JL, Ch?ry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, Montpetit A, Hariri F, Tregou?t D, Raby BA, Chung WK, Morange PE, Froese DS, Baumgartner MR, Benoist JF, Ficicioglu C, Marchand V, Motorin Y, Bonnemains C, Feillet F, Majewski J, Rosenblatt DS. APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nat Commun. 2018 01 04; 9(1):67.
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