scholarly article | Q13442814 |
P2093 | author name string | Bender K | |
Angel P | |||
Wilhelm D | |||
Knebel A | |||
P2860 | cites work | Signal transduction by tumor necrosis factor mediated by JNK protein kinases | Q24308037 |
JNK1: a protein kinase stimulated by UV light and Ha-Ras that binds and phosphorylates the c-Jun activation domain | Q24308838 | ||
Independent human MAP-kinase signal transduction pathways defined by MEK and MKK isoforms | Q24312029 | ||
Identification of a dual specificity kinase that activates the Jun kinases and p38-Mpk2 | Q24313872 | ||
Selective interaction of JNK protein kinase isoforms with transcription factors | Q24317346 | ||
Activation of Pyk2 by stress signals and coupling with JNK signaling pathway | Q24323778 | ||
Activation of extracellular signal-regulated kinase, ERK2, by p21ras oncoprotein | Q24555703 | ||
The tumor promoter arsenite stimulates AP-1 activity by inhibiting a JNK phosphatase | Q24561826 | ||
ATF-2 is preferentially activated by stress-activated protein kinases to mediate c-jun induction in response to genotoxic agents | Q24568306 | ||
ATF-2 contains a phosphorylation-dependent transcriptional activation domain | Q24568315 | ||
Activation of stress-activated protein kinase by MEKK1 phosphorylation of its activator SEK1 | Q28114883 | ||
Specificity of receptor tyrosine kinase signaling: transient versus sustained extracellular signal-regulated kinase activation | Q28131755 | ||
Activation of ternary complex factor Elk-1 by stress-activated protein kinases | Q28272395 | ||
Pro-inflammatory cytokines and environmental stress cause p38 mitogen-activated protein kinase activation by dual phosphorylation on tyrosine and threonine | Q28287650 | ||
The jun proto-oncogene is positively autoregulated by its product, Jun/AP-1 | Q28291340 | ||
Lysophosphatidic acid, a multifunctional phospholipid messenger | Q28302384 | ||
Transcription factor ATF2 regulation by the JNK signal transduction pathway | Q28305631 | ||
Evidence for multiple activators for stress-activated protein kinase/c-Jun amino-terminal kinases. Existence of novel activators | Q28576079 | ||
ERK phosphorylation potentiates Elk-1-mediated ternary complex formation and transactivation | Q28578241 | ||
MAPKs: new JNK expands the group | Q28611010 | ||
The role of Jun, Fos and the AP-1 complex in cell-proliferation and transformation | Q29400446 | ||
Selective activation of the JNK signaling cascadeand c-Jun transcriptional activity by the small GTPases Rac and Cdc42Hs | Q29547308 | ||
An Essential Role for Rho, Rac, and Cdc42 GTPases in Cell Cycle Progression Through G 1 | Q29614256 | ||
The small GTP-binding proteins Rac1 and Cdc42 regulate the activity of the JNK/SAPK signaling pathway | Q29614258 | ||
The stress-activated protein kinase subfamily of c-Jun kinases | Q29620001 | ||
Relationship between cell killing, chromosomal aberrations, sister-chromatid exchanges and point mutations induced by monofunctional alkylating agents in Chinese hamster cells. A correlation with different ethylation products in DNA | Q70596611 | ||
Selective modification of glutathione metabolism | Q71695892 | ||
Dual effect of beta-adrenergic receptors on mitogen-activated protein kinase. Evidence for a beta gamma-dependent activation and a G alpha s-cAMP-mediated inhibition | Q71743487 | ||
Glutathione can rescue the inhibitory effects of nickel on DNA ligation and repair synthesis | Q71988369 | ||
Roles for oxidative stress and poly(ADP-ribosyl)ation in the killing of cultured hepatocytes by methyl methanesulfonate | Q72632996 | ||
69 Methods for enucleation and reconstruction of interferon-producing cells | Q72657621 | ||
Involvement of growth factor receptors in the mammalian UVC response | Q72710815 | ||
Tumor necrosis factor alpha stimulates AP-1 activity through prolonged activation of the c-Jun kinase | Q72724630 | ||
Role of SAPK/ERK kinase-1 in the stress-activated pathway regulating transcription factor c-Jun | Q29620103 | ||
Identification of an oncoprotein- and UV-responsive protein kinase that binds and potentiates the c-Jun activation domain | Q29620169 | ||
Differential activation of ERK and JNK mitogen-activated protein kinases by Raf-1 and MEKK | Q29620274 | ||
Autocrine transformation by chimeric signal peptide-basic fibroblast growth factor: reversal by suramin | Q33687824 | ||
Phosphorylation of c-jun mediated by MAP kinases. | Q34947174 | ||
Rapid and preferential activation of the c-jun gene during the mammalian UV response | Q36693305 | ||
Intracellular glutathione levels regulate Fos/Jun induction and activation of glutathione S-transferase gene expression | Q36757863 | ||
Oncoprotein-mediated signalling cascade stimulates c-Jun activity by phosphorylation of serines 63 and 73 | Q36821325 | ||
Glutathione deficiency produced by inhibition of its synthesis, and its reversal; Applications in research and therapy | Q36936660 | ||
Stimulus-transcription coupling in the nervous system: involvement of the inducible proto-oncogenes fos and jun. | Q37334431 | ||
Efficient reversion of simian sarcoma virus-transformation and inhibition of growth factor-induced mitogenesis by suramin | Q37397266 | ||
Response to adversity: molecular control of gene activation following genotoxic stress | Q37422748 | ||
Induction of c-fos expression through JNK-mediated TCF/Elk-1 phosphorylation. | Q37625844 | ||
The chemical effects of nucleic acid alkylation and their relation to mutagenesis and carcinogenesis | Q38111405 | ||
UV irradiation and heat shock mediate JNK activation via alternate pathways. | Q38289506 | ||
JunB differs from c-Jun in its DNA-binding and dimerization domains, and represses c-Jun by formation of inactive heterodimers | Q38321318 | ||
Heterodimer formation of cJun and ATF-2 is responsible for induction of c-jun by the 243 amino acid adenovirus E1A protein | Q38322155 | ||
Protein synthesis inhibitors reveal differential regulation of mitogen-activated protein kinase and stress-activated protein kinase pathways that converge on Elk-1. | Q40017118 | ||
Lysophosphatidic acid signalling | Q40444988 | ||
Rho family members: Activators of MAP kinase cascades | Q40476489 | ||
A review of the genotoxicity of 1-ethyl-1-nitrosourea | Q40487875 | ||
Growth factor-like effects of lysophosphatidic acid, a novel lipid mediator. | Q40567927 | ||
Fos is an essential component of the mammalian UV response | Q40789823 | ||
UV-induced activation of AP-1 involves obligatory extranuclear steps including Raf-1 kinase | Q40872239 | ||
Dephosphorylation of receptor tyrosine kinases as target of regulation by radiation, oxidants or alkylating agents | Q41077480 | ||
Signaling from G protein-coupled receptors to c-Jun kinase involves beta gamma subunits of heterotrimeric G proteins acting on a Ras and Rac1-dependent pathway | Q41226993 | ||
Cdc42 and PAK-mediated signaling leads to Jun kinase and p38 mitogen-activated protein kinase activation | Q41269491 | ||
Activation of the c-Abl tyrosine kinase in the stress response to DMA-damaging agents | Q41307866 | ||
Rapid turnover of the platelet-derived growth factor receptor in sis-transformed cells and reversal by suramin. Implications for the mechanism of autocrine transformation | Q41336412 | ||
Anisomycin-activated protein kinases p45 and p55 but not mitogen-activated protein kinases ERK-1 and -2 are implicated in the induction of c-fos and c-jun | Q41431597 | ||
c-Fos transcriptional activity stimulated by H-Ras-activated protein kinase distinct from JNK and ERK. | Q41442860 | ||
Phosphorylation of transcription factor p62TCF by MAP kinase stimulates ternary complex formation at c-fos promoter | Q41612990 | ||
Alkylation of protein by methyl methanesulfonate and 1-methyl-1-nitrosourea in vitro | Q42247067 | ||
Three distinct signalling responses by murine fibroblasts to genotoxic stress | Q42807014 | ||
Oncogenic and transcriptional cooperation with Ha-Ras requires phosphorylation of c-Jun on serines 63 and 73 | Q42825163 | ||
Preventive action of thioethers towards in vitro DNA binding and mutagenesis in E. coli K12 by alkylating agents | Q45085447 | ||
NF-kappa B activation by ultraviolet light not dependent on a nuclear signal. | Q45971622 | ||
Transfection and expression of human O6-methylguanine-DNA methyltransferase (MGMT) cDNA in Chinese hamster cells: the role of MGMT in protection against the genotoxic effects of alkylating agents | Q46067039 | ||
An osmosensing signal transduction pathway in mammalian cells | Q48080102 | ||
A comprehensive quantitative analysis of methylated and ethylated DNA using high pressure liquid chromatography. | Q53576351 | ||
Cellular glutathione (GSH) and glutathione S-transferase (GST) activity in human ovarian tumor biopsies following exposure to alkylating agents | Q54280548 | ||
Integration of MAP kinase signal transduction pathways at the serum response element | Q58415341 | ||
The mammalian ultraviolet response is triggered by activation of src tyrosine kinases | Q60621256 | ||
A null mutation at the c-jun locus causes embryonic lethality and retarded cell growth in culture | Q62555340 | ||
The role of glutathione and glutathione S-transferases in the metabolism of chemical carcinogens and other electrophilic agents | Q66919004 | ||
Ultraviolet-radiation induced c-jun gene transcription: two AP-1 like binding sites mediate the response | Q68093019 | ||
The antioxidant action of N-acetylcysteine: its reaction with hydrogen peroxide, hydroxyl radical, superoxide, and hypochlorous acid | Q69353201 | ||
Co-purification of mitogen-activated protein kinases with phorbol ester-induced c-Jun kinase activity in U937 leukaemic cells | Q70545093 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | glutathione | Q116907 |
P304 | page(s) | 4792-4800 | |
P577 | publication date | 1997-08-01 | |
P1433 | published in | Molecular and Cellular Biology | Q3319478 |
P1476 | title | The level of intracellular glutathione is a key regulator for the induction of stress-activated signal transduction pathways including Jun N-terminal protein kinases and p38 kinase by alkylating agents | |
P478 | volume | 17 |
Q92641670 | 1,4-Benzoquinone antimicrobial agents against Staphylococcus aureus and Mycobacterium tuberculosis derived from scorpion venom |
Q39456231 | A novel AP-1 element in the CD95 ligand promoter is required for induction of apoptosis in hepatocellular carcinoma cells upon treatment with anticancer drugs |
Q27936881 | A systems approach to delineate functions of paralogous transcription factors: role of the Yap family in the DNA damage response. |
Q41007018 | Activation of CD95 (APO-1/Fas) signaling by ceramide mediates cancer therapy-induced apoptosis |
Q33964540 | Activation of MEK kinase 1 by the c-Abl protein tyrosine kinase in response to DNA damage |
Q43615470 | Activation of a p53-independent, sphingolipid-mediated cytolytic pathway in p53-negative mouse fibroblast cells treated with N-methyl-N-nitro-N-nitrosoguanidine |
Q43625274 | Activation of c-Jun N-terminal kinase 1 (JNK-1) after amino acid deficiency in HeLa cells |
Q28609379 | Activation of c-Jun N-terminal kinase 1 by UV irradiation is inhibited by wortmannin without affecting c-iun expression |
Q38874840 | Air pollution and short-term clinical outcomes of patients with acute myocardial infarction |
Q28138890 | Amino-terminal phosphorylation of c-Jun regulates stress-induced apoptosis and cellular proliferation |
Q44203939 | Aplidin induces apoptosis in human cancer cells via glutathione depletion and sustained activation of the epidermal growth factor receptor, Src, JNK, and p38 MAPK. |
Q34800495 | Are mitogen-activated protein kinases glucose transducers for diabetic neuropathies? |
Q40775264 | Attenuation of catalase activity in the malignant phenotype plays a functional role in an in vitro model for tumor progression |
Q35196825 | Autocrine growth and anchorage independence: two complementing Jun-controlled genetic programs of cellular transformation. |
Q40966218 | Bcl-xL blocks activation of related adhesion focal tyrosine kinase/proline-rich tyrosine kinase 2 and stress-activated protein kinase/c-Jun N-terminal protein kinase in the cellular response to methylmethane sulfonate |
Q39840406 | Bilberry extract reduces UVA-induced oxidative stress in HaCaT keratinocytes: a pilot study. |
Q53630784 | Bystander effects are induced by CENU treatment and associated with altered protein secretory activity of treated tumor cells: a relay for chemotherapy? |
Q34667098 | Cell signaling in aging and apoptosis |
Q27692108 | Cellular stress response and innate immune signaling: integrating pathways in host defense and inflammation. |
Q35613557 | Comparative genomics of duplicate γ-glutamyl transferase genes in teleosts: medaka (Oryzias latipes), stickleback (Gasterosteus aculeatus), green spotted pufferfish (Tetraodon nigroviridis), fugu (Takifugu rubripes), and zebrafish (Danio rerio). |
Q51811183 | Comparative proteomic analysis to study molecular events during gonad development in mice. |
Q39863634 | Comparison of gene expression profiles in HepG2 cells exposed to arsenic, cadmium, nickel, and three model carcinogens for investigating the mechanisms of metal carcinogenesis |
Q34608929 | Connexin43 hemichannel-mediated regulation of connexin43. |
Q34997018 | Curcuminoids activate p38 MAP kinases and promote UVB-dependent signalling in keratinocytes |
Q44606796 | Differential expression of c-fos in a mouse model of fetal alcohol syndrome |
Q54710581 | Differential modulation of MAPKs in relation to increased intraocular pressure in the aqueous humor of rat eye injected with hyaluronic acid. |
Q42157176 | Differential role of glutaredoxin and thioredoxin in metabolic oxidative stress-induced activation of apoptosis signal-regulating kinase 1. |
Q23918704 | Dose-dependent thiol and immune responses to ovalbumin challenge in Brown Norway rats |
Q43583359 | Down-regulation of the c-Jun N-terminal kinase (JNK) phosphatase M3/6 and activation of JNK by hydrogen peroxide and pyrrolidine dithiocarbamate |
Q78176014 | Effects of capsaicin on induction of c-jun proto-oncogene expression in Fisher-344 rats by N-methyl-N'-nitro-N-nitrosoguanidine |
Q39528509 | Enhanced ROS production in oncogenically transformed cells potentiates c-Jun N-terminal kinase and p38 mitogen-activated protein kinase activation and sensitization to genotoxic stress |
Q33605331 | Environmental factors as regulators and effectors of multistep carcinogenesis |
Q28204361 | Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1 |
Q42732112 | Fibroblasts from long-lived bird species are resistant to multiple forms of stress. |
Q33859467 | Functional specialization of Chlamydomonas reinhardtii cytosolic thioredoxin h1 in the response to alkylation-induced DNA damage |
Q33678083 | Gamma-glutamyl transpeptidase gene organization and expression: a comparative analysis in rat, mouse, pig and human species |
Q46540672 | Genetic and epigenetic inactivation of T-cadherin in human hepatocellular carcinoma cells |
Q33948213 | Genomic expression responses to DNA-damaging agents and the regulatory role of the yeast ATR homolog Mec1p |
Q43698438 | H(2)O(2) mediates oxidative stress-induced epidermal growth factor receptor phosphorylation |
Q35745543 | Human gastric cancer kinase profile and prognostic significance of MKK4 kinase |
Q43713575 | Hyperosmotic stress activates the insulin receptor in CHO cells |
Q24298595 | Immediate-early gene induction by the stresses anisomycin and arsenite in human osteosarcoma cells involves MAPK cascade signaling to Elk-1, CREB and SRF |
Q40424750 | Immobilization stress induces c-Fos accumulation in liver. |
Q53228638 | Immunomodulatory and immunotoxic effects of bilirubin: molecular mechanisms. |
Q40920084 | Increased ROS levels contribute to elevated transcription factor and MAP kinase activities in malignantly progressed mouse keratinocyte cell lines |
Q40795912 | Induction of the SAPK activator MIG-6 by the alkylating agent methyl methanesulfonate. |
Q40629870 | Inhibition of JNK signaling diminishes early but not late cellular stress-induced apoptosis |
Q48087861 | Inhibitors of mitogen-activated protein kinases protect axotomized developing neurons |
Q31894597 | Intracellular glutathione regulates tumour necrosis factor-alpha-induced p38 MAP kinase activation and RANTES production by human bronchial epithelial cells |
Q43159491 | Involvement of ATM/ATR-p38 MAPK cascade in MNNG induced G1-S arrest |
Q31859902 | Involvement of glutathione metabolism in the cytotoxicity of the phenethyl isothiocyanate and its cysteine conjugate to human leukaemia cells in vitro |
Q41959498 | Ionizing radiation affects the expression of Toll-like receptors 2 and 4 in human monocytic cells through c-Jun N-terminal kinase activation. |
Q39770977 | Kaempferol suppresses cisplatin-induced apoptosis via inductions of heme oxygenase-1 and glutamate-cysteine ligase catalytic subunit in HEI-OC1 cell |
Q28215317 | Keratin 8 phosphorylation by p38 kinase regulates cellular keratin filament reorganization: modulation by a keratin 1-like disease causing mutation |
Q28509902 | Late activation of stress kinases (SAPK/JNK) by genotoxins requires the DNA repair proteins DNA-PKcs and CSB |
Q41876225 | Late activation of stress-activated protein kinases/c-Jun N-terminal kinases triggered by cisplatin-induced DNA damage in repair-defective cells. |
Q43928313 | Lead induced DNA strand breaks in lymphocytes of exposed workers: role of reactive oxygen species and protein kinase C. |
Q43639978 | Low concentration N-methyl-N'-nitro-N-nitrosoguanidine activates DNA polymerase-beta expression via cyclic-AMP-protein kinase A-cAMP response element binding protein pathway |
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