Works matching DE "OXIDOREDUCTASE genetics"
Results: 20
Vascular-targeted therapies for Duchenne muscular dystrophy.
- Published in:
- Skeletal Muscle, 2013, v. 3, n. 1, p. 1, doi. 10.1186/2044-5040-3-9
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- Publication type:
- Article
Hypermethylation in the promoter of the MTHFR gene is associated with diabetic complications and biochemical indicators.
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- Diabetology & Metabolic Syndrome, 2017, v. 9, p. 1, doi. 10.1186/s13098-017-0284-3
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- Publication type:
- Article
RNA sequencing analysis of transcriptional change in the freshwater mussel Elliptio complanata after environmentally relevant sodium chloride exposure.
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- Environmental Toxicology & Chemistry, 2017, v. 36, n. 9, p. 2352, doi. 10.1002/etc.3774
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- Publication type:
- Article
Disulfide Bonds: A Key Modification in Bacterial Extracytoplasmic Proteins.
- Published in:
- 2017
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- Publication type:
- journal article
Genome analysis of the freshwater planktonic <italic>Vulcanococcus limneticus</italic> sp. nov. reveals horizontal transfer of nitrogenase operon and alternative pathways of nitrogen utilization.
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- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-4648-3
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- Publication type:
- Article
Development of quantitative competitive PCR for determination of copy number and expression level of the synthetic glyphosate oxidoreductase gene in transgenic canola plants.
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- Electronic Journal of Biotechnology, 2012, v. 15, n. 4, p. 1, doi. 10.2225/vol15-issue4-fulltext-5
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- Publication type:
- Article
Novel Sequence Features of DNA Repair Genes/Proteins from Deinococcus Species Implicated in Protection from Oxidatively Generated Damage.
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- Genes, 2018, v. 9, n. 3, p. 149, doi. 10.3390/genes9030149
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- Publication type:
- Article
Complete genome sequence of ΦCP51, a temperate bacteriophage of Clostridium perfringens.
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- Archives of Virology, 2013, v. 158, n. 9, p. 2015, doi. 10.1007/s00705-013-1647-1
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- Publication type:
- Article
Identification of genes specifically required for the anaerobic metabolism of benzene in Geobacter metallireducens.
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- Frontiers in Microbiology, 2014, v. 5, p. 1, doi. 10.3389/fmicb.2014.00245
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- Publication type:
- Article
Genetic variation in dihydropyrimidine dehydrogenase ( DPYD) gene in a healthy adult Indian population.
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- Annals of Human Biology, 2015, v. 42, n. 1, p. 97, doi. 10.3109/03014460.2014.942365
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- Publication type:
- Article
Mutations in MICAL-1cause autosomal-dominant lateral temporal epilepsy.
- Published in:
- 2018
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- Publication type:
- journal article
Synthesis, Molecular Docking and Potential Antioxidant Activity of Di/Trisubstituted Pyridazinone Derivatives.
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- Journal of the Chinese Chemical Society, 2016, v. 63, n. 9, p. 739, doi. 10.1002/jccs.201600051
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- Publication type:
- Article
Optimization of heme precursors for the expression of human cytochrome P450 2A13 and its co-expression with oxidoreductase in baculovirus/sf9 system.
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- Journal of Biochemistry, 2013, v. 153, n. 6, p. 555
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- Publication type:
- Article
Light-Dependent Expression of Protochlorophyllide Oxidoreductase Gene in the Liverwort, Marchantia paleacea var. diptera.
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- Plant & Cell Physiology, 1998, v. 39, n. 6, p. 665, doi. 10.1093/oxfordjournals.pcp.a029420
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- Publication type:
- Article
Does the MTHFR A1298C Polymorphism Modulate the Cardiorespiratory Response to Training?
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- Journal of Human Kinetics, 2016, v. 54, n. 1, p. 43, doi. 10.1515/hukin-2016-0055
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- Publication type:
- Article
Identification and characterization of oxidoreductase component (NdmD) of methylxanthine oxygenase system in Pseudomonas sp. NCIM 5235.
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- Applied Microbiology & Biotechnology, 2018, v. 102, n. 18, p. 7913, doi. 10.1007/s00253-018-9224-x
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- Publication type:
- Article
Targeted knock-in mice expressing the oxidase-fixed form of xanthine oxidoreductase favor tumor growth.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-12565-z
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- Publication type:
- Article
Sulfolobus solfataricus thiol redox puzzle: characterization of an atypical protein disulfide oxidoreductase.
- Published in:
- Extremophiles, 2014, v. 18, n. 2, p. 219, doi. 10.1007/s00792-013-0607-8
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- Publication type:
- Article
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.
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- Brain: A Journal of Neurology, 2014, v. 137, n. 2, p. 411, doi. 10.1093/brain/awt338
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- Publication type:
- Article
W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case report.
- Published in:
- 2016
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- Publication type:
- Case Study