يعرض 1 - 10 نتائج من 76 نتيجة بحث عن '"oxidation reduction state"', وقت الاستعلام: 0.93s تنقيح النتائج
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    المساهمون: Ege Üniversitesi

    مصطلحات موضوعية: 0301 basic medicine, Embryology, analytical parameters, Organogenesis, medicine.disease_cause, Embryo Culture Techniques, Mice, chemistry.chemical_compound, Bagg albino mouse, 0302 clinical medicine, Pregnancy, Gene expression, oxidative stress, glutathione, gestational age, Lung, Mice, Inbred BALB C, Fetal Growth Retardation, 030219 obstetrics & reproductive medicine, quantitative analysis, catalase, malonaldehyde, Obstetrics and Gynecology, Embryo, gene expression regulation, intrauterine growth retardation, cohort analysis, Malondialdehyde, superoxide dismutase, unclassified drug, 3. Good health, embryo culture, fetus, female, oxidation reduction state, medicine.anatomical_structure, priority journal, real time polymerase chain reaction, validation study, Female, total antioxidant capacity, Lung morphogenesis, Oxidation-Reduction, down regulation, in vitro study, immunoregulation, phenotype, animal experiment, Embryonic Development, embryo, morphogenesis, Fertilization in Vitro, Biology, Article, animal tissue, in vivo study, Andrology, 03 medical and health sciences, male, Genetics, medicine, Animals, C57BL 6 mouse, controlled study, Blastocyst, atmospheric oxygen, Molecular Biology, cell transfer, mouse, lung development, Fetus, nonhuman, blastocyst, animal model, assisted reproduction, embryo development, Embryo culture, Cell Biology, fetus weight, clinical feature, Mice, Inbred C57BL, 030104 developmental biology, Reproductive Medicine, chemistry, exposure, oxygen, Oxidative stress, Developmental Biology

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    المساهمون: Molecular Genetics, Cell biology, Pathology, Sepe, Sara, Milanese, Chiara, Gabriels, Sylvia, Derks, Kasper W. J., Payan Gomez, Cesar, van IJcken, Wilfred F. J., Rijksen, Yvonne M. A., Nigg, Alex L., Moreno, Sandra, Cerri, Silvia, Blandini, Fabio, Hoeijmakers, Jan H. J., Mastroberardino, Pier G.

    المصدر: Cell Reports, Vol 15, Iss 9, Pp 1866-1875 (2016)
    Cell Reports, 15(9), 1866-1875. Cell Press
    Cell Reports
    Ahmad, A., Robinson, A.R., Duensing, A., van Drunen, E., Beverloo, H.B., Weisberg, D.B., Hasty, P., Niedernhofer, L.J., ERCC1-XPF endonuclease facilitates DNA double-strand break repair (2008) Mol. Cell. Biol., 28, pp. 5082-5092
    Repositorio EdocUR-U. Rosario
    Universidad del Rosario
    instacron:Universidad del Rosario

    مصطلحات موضوعية: Genetics and Molecular Biology (all), 0301 basic medicine, Gene Mutation, Aging, Parkinson's disease, Excision Repair Cross Complementing Protein 1, Mouse, Protein Homeostasis, DNA Repair, Protein Expression, Enfermedad de parkinson, Gene Expression, Gene mutation, Biochemistry, Protein Phosphorylation, Edad adulta, Mice, chemistry.chemical_compound, Pathology, Down Regulation, lcsh:QH301-705.5, Neuropathology, Vejez, Cre Recombinase, Genetics, MPTP, Oxidation Reduction State, Parkinson Disease, 3. Good health, DNA-Binding Proteins, Animals, Corpus Striatum, Dopaminergic Neurons, Endonucleases, Fibroblasts, Humans, Biochemistry, Genetics and Molecular Biology (all), Dna Damage, Ultrastructure, Priority Journal, Fibroblast, Histone H2Ax Gamma, Autonomic Innervation, Human, Dopaminergic Nerve Cell, Disease Association, DNA repair, DNA damage, Skin Fibroblast, Dna-Binding Proteins, Biology, Article, General Biochemistry, Genetics and Molecular Biology, Rna Sequence, Dna Repair, Enzyme Activity, Unclassified Drug, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Upregulation, Report, medicine, Controlled Study, Dopaminergic System, Endonuclease, Double Stranded Dna Break, Human Cell, Alpha-synuclein, Histone H2Ax, Excision Repair, Animal, Ercc1 Gene, Alpha Synuclein, Animal Experiment, Nonhuman, medicine.disease, Dna Binding Protein, Enfermedades, Ercc1 Protein, Metabolism, 030104 developmental biology, lcsh:Biology (General), chemistry, Mitochondrial Respiration, Cancer research, Animal Model, ERCC1, Nucleotide excision repair

    وصف الملف: application/pdf

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    المصدر: Oxidative Medicine and Cellular Longevity
    Oxidative Medicine and Cellular Longevity, Vol 2019 (2019)

    مصطلحات موضوعية: Male, dermoepidermal junction, Aging, Antioxidant, cycline, medicine.medical_treatment, Glutathione reductase, animal cell, Biochemistry, aldehyde, fibroblast, Skin Aging, analogs and derivatives, mitochondrion, chemistry.chemical_classification, integumentary system, lcsh:Cytology, Glutathione peroxidase, adult, thioredoxin reductase, lipid peroxidation, General Medicine, postnatal development, mitochondria, aged, cutaneous parameters, oxidation reduction state, Glutathione Reductase, subcutaneous tissue, Collagen, MSRA, medicine.medical_specialty, Article Subject, enzymes, rough endoplasmic reticulum, wistar, keratinocyte, Oxidative phosphorylation, animal tissue, 03 medical and health sciences, lcsh:QH573-671, Rats, Wistar, sebaceous gland, 4 hydroxynonenal, protein expression, Aldehydes, animal model, superoxide dismutases, Fibroblasts, 030104 developmental biology, Endocrinology, peptides, ultrastructural changes, oxidation reduction reaction, 0301 basic medicine, methionine sulfoxide reductase a, Time Factors, Thioredoxin reductase, biomolecules, basal lamina, msra protein, time factor, oxidative stress, rat, animal, oxidoreductase, skin cell, Skin, biology, Chemistry, article, Catalase, ultrastructure, 8-oxo-7-hydrodeoxyguanosine, enzyme activity, 8-Hydroxy-2'-Deoxyguanosine, immunohistochemistry, manganese, Oxidoreductases, damage, Oxidation-Reduction, Research Article, Thioredoxin-Disulfide Reductase, 4-hydroxy-2-nonenal, extracellular matrix, enzymology, animal experiment, amino acids, peptides, glutathione peroxidase, glutathione reductase, methionine sulfoxide reductase, structural alterations, ultrastructural changes, rats, 4 hydroxynonenal, 8 hydroxyguanine, catalase, collagen, glutathione peroxidase, superoxide dismutase, deoxyguanosine, msra protein, rat, thioredoxin reductase, adult, aging, cell proliferation, controlled study, dna damage, erythroid precursor cell, male, nonhuman, metabolism, pathology, skin, wistar rat, aging, capacity, development, peptides, aging, aldehydes, animals, fibroblasts, oxidation-reduction, oxidoreductases, proliferating cell nuclear antigen, rats, wistar, thioredoxin-disulfide reductase, time factors, Superoxide dismutase, Internal medicine, Proliferating Cell Nuclear Antigen, medicine, Animals, Cell Proliferation, Glutathione Peroxidase, 030102 biochemistry & molecular biology, Superoxide Dismutase, Deoxyguanosine, Cell Biology, rats, wistar rat, biology.protein, DNA Damage

    وصف الملف: text/xhtml

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    كتاب إلكتروني

    المؤلفون: Mayevsky, A.Aff6, Nioka, S.Aff7, Chance, B.Aff7

    المساهمون: Mochizuki, Masaji, editorAff1, Honig, Carl R., editorAff2, Koyama, Tomiyasu, editorAff3, Goldstick, Thomas K., editorAff4, Bruley, Duane F., editorAff5

    المصدر: Oxygen Transport to Tissue X. 222:365-374

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