Page last updated: 2024-08-21

2-tert-butylhydroquinone and Neuroblastoma

2-tert-butylhydroquinone has been researched along with Neuroblastoma in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (11.11)18.2507
2000's7 (77.78)29.6817
2010's1 (11.11)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Citron, BA; Hatic, H; Pick, CG; Rachmany, L; Rubovitch, V; Saykally, JN; Shaer, A1
Adachi, T; Hara, H; Kuno, S; Ohta, K; Ohta, M1
Calkins, M; Johnson, D; Johnson, J; Li, J; Svendsen, C; Wright, L1
Johnson, JA; Moehlenkamp, JD1
Hanson, JM; Johnson, JA; Lee, JM; Moehlenkamp, JD1
Honey, CR; Johnson, DA; Johnson, JA; Murphy, TH; Ng, R; Shen, H; Yu, J1
Chu, WA; Hanson, JM; Johnson, JA; Lee, JM1
Johnson, JA; Lee, JM; Li, J1
Johnson, JA; Li, J1

Other Studies

9 other study(ies) available for 2-tert-butylhydroquinone and Neuroblastoma

ArticleYear
The nuclear factor erythroid 2-like 2 activator, tert-butylhydroquinone, improves cognitive performance in mice after mild traumatic brain injury.
    Neuroscience, 2012, Oct-25, Volume: 223

    Topics: Analysis of Variance; Animals; Antioxidants; Avoidance Learning; Brain; Brain Injuries; Caspase 3; Cell Line, Tumor; Cell Survival; Cognition Disorders; Disease Models, Animal; Gene Expression Regulation; Glial Fibrillary Acidic Protein; HSP70 Heat-Shock Proteins; Humans; Hydroquinones; Male; Maze Learning; Mice; Mice, Inbred ICR; Motor Activity; Neuroblastoma; NF-E2-Related Factor 2; Proto-Oncogene Proteins c-jun; Purine Nucleosides; Recognition, Psychology; RNA, Messenger; Rotarod Performance Test; Time Factors

2012
Increase of antioxidative potential by tert-butylhydroquinone protects against cell death associated with 6-hydroxydopamine-induced oxidative stress in neuroblastoma SH-SY5Y cells.
    Brain research. Molecular brain research, 2003, Nov-26, Volume: 119, Issue:2

    Topics: Antioxidants; Cell Death; Cell Line, Tumor; Dose-Response Relationship, Drug; Glutathione; Humans; Hydroquinones; JNK Mitogen-Activated Protein Kinases; Mitogen-Activated Protein Kinases; Models, Neurological; NAD(P)H Dehydrogenase (Quinone); Neuroblastoma; Neurons; Neuroprotective Agents; Oxidative Stress; Oxidopamine; Parkinson Disease; Reactive Oxygen Species; RNA, Messenger; Transcriptional Activation

2003
Stabilization of Nrf2 by tBHQ confers protection against oxidative stress-induced cell death in human neural stem cells.
    Toxicological sciences : an official journal of the Society of Toxicology, 2005, Volume: 83, Issue:2

    Topics: Adenoviridae; Antioxidants; Apoptosis; Cell Line, Tumor; Cell Survival; DNA-Binding Proteins; Humans; Hydroquinones; Leucine Zippers; Microarray Analysis; Necrosis; Neuroblastoma; Neurons; NF-E2-Related Factor 2; Oxidative Stress; Stem Cells; Trans-Activators; Transfection; Ubiquitin-Protein Ligase Complexes; Up-Regulation

2005
Activation of antioxidant/electrophile-responsive elements in IMR-32 human neuroblastoma cells.
    Archives of biochemistry and biophysics, 1999, Mar-01, Volume: 363, Issue:1

    Topics: Antioxidants; Butylated Hydroxyanisole; Dose-Response Relationship, Drug; Down-Regulation; Enzyme Induction; Gene Expression Regulation, Neoplastic; Genes, Reporter; Humans; Hydroquinones; NAD(P)H Dehydrogenase (Quinone); Neuroblastoma; Neurons; Protein Kinase C; Regulatory Sequences, Nucleic Acid; Signal Transduction; Tetradecanoylphorbol Acetate; Transcriptional Activation; Tumor Cells, Cultured

1999
Nrf2-dependent activation of the antioxidant responsive element by tert-butylhydroquinone is independent of oxidative stress in IMR-32 human neuroblastoma cells.
    Biochemical and biophysical research communications, 2001, Jan-12, Volume: 280, Issue:1

    Topics: Antioxidants; DNA-Binding Proteins; Gene Expression Regulation; Genes, jun; Genes, Reporter; Humans; Hydroquinones; Kinetics; Leucine Zippers; Maleates; NAD(P)H Dehydrogenase (Quinone); Neuroblastoma; NF-E2-Related Factor 2; Oxidative Stress; Recombinant Fusion Proteins; Trans-Activators; Transfection; Tumor Cells, Cultured

2001
Preferential expression of antioxidant response element mediated gene expression in astrocytes.
    Journal of neurochemistry, 2001, Volume: 76, Issue:6

    Topics: Animals; Antioxidants; Astrocytes; Base Sequence; Biolistics; Cells, Cultured; Cerebral Cortex; Dimethyl Fumarate; Fumarates; Gene Expression Regulation, Enzymologic; Genes, Reporter; Glioma; Glutamate-Cysteine Ligase; Glutathione Transferase; Humans; Hybridomas; Hydroquinones; In Vitro Techniques; Molecular Sequence Data; Neuroblastoma; Neuroglia; Promoter Regions, Genetic; Quinone Reductases; Rats; Recombinant Fusion Proteins; Transfection

2001
Phosphatidylinositol 3-kinase, not extracellular signal-regulated kinase, regulates activation of the antioxidant-responsive element in IMR-32 human neuroblastoma cells.
    The Journal of biological chemistry, 2001, Jun-08, Volume: 276, Issue:23

    Topics: Antioxidants; Base Sequence; Chromones; DNA Primers; Enzyme Activation; Enzyme Inhibitors; Humans; Hydroquinones; Mitogen-Activated Protein Kinases; Morpholines; Neuroblastoma; Phosphatidylinositol 3-Kinases; Phosphorylation; Tumor Cells, Cultured

2001
Microarray analysis reveals an antioxidant responsive element-driven gene set involved in conferring protection from an oxidative stress-induced apoptosis in IMR-32 cells.
    The Journal of biological chemistry, 2002, Jan-04, Volume: 277, Issue:1

    Topics: Antioxidants; Apoptosis; Chromones; Humans; Hydrogen Peroxide; Hydroquinones; Morpholines; Neuroblastoma; Oligonucleotide Array Sequence Analysis; Oxidative Stress; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Response Elements; Tumor Cells, Cultured

2002
Time-dependent changes in ARE-driven gene expression by use of a noise-filtering process for microarray data.
    Physiological genomics, 2002, Volume: 9, Issue:3

    Topics: Animals; Antioxidants; Cluster Analysis; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; Hydroquinones; Mice; Neuroblastoma; Oligonucleotide Array Sequence Analysis; Rats; Response Elements; Time Factors; Tumor Cells, Cultured

2002