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1. Full Text C-Jun N-terminal phosphorylation antagonises recruitment of the Mbd3/NuRD repressor complex
by Aguilera, Cristina and Nakagawa, Kentaro and Sancho, Rocio and Chakraborty, Atanu and Hendrich, Brian and Behrens, Axel
Nature, ISSN 0028-0836, 01/2011, Volume 469, Issue 7329, pp. 231 - 236
AP-1 (activator protein 1) activity is strongly induced in response to numerous signals, including growth factors, cytokines and extracellular stresses(1). The... 
MBD3 | STEM-CELLS | ACTIVATION | MULTIDISCIPLINARY SCIENCES | MI-2/NURD | BINDING DOMAIN | MAP KINASES | COMPONENT | COLON | NURD | TUMORIGENESIS | Phosphorylation | Cell Proliferation | Transcription Factors - deficiency | Gene Expression Regulation, Neoplastic | JNK Mitogen-Activated Protein Kinases - metabolism | Mi-2 Nucleosome Remodeling and Deacetylase Complex - metabolism | Stem Cells - cytology | Promoter Regions, Genetic - genetics | Colonic Neoplasms - metabolism | DNA-Binding Proteins - deficiency | DNA-Binding Proteins - metabolism | Mi-2 Nucleosome Remodeling and Deacetylase Complex - antagonists & inhibitors | Proto-Oncogene Proteins c-jun - chemistry | Acetylation | DNA-Binding Proteins - antagonists & inhibitors | Transcription Factors - antagonists & inhibitors | Transcription Factors - metabolism | Animals | Proto-Oncogene Proteins c-jun - metabolism | Colonic Neoplasms - pathology | Mi-2 Nucleosome Remodeling and Deacetylase Complex - chemistry | Cell Line, Tumor | Protein Binding | Mice | Receptors, G-Protein-Coupled - genetics | Histones - metabolism | Intestines - cytology | Physiological aspects | Models | Chemical properties | Repressor proteins | Proteins | Colon | Peptides | Binding sites | Recruitment
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2. Full Text The same pocket in menin binds both MLL and JUND but has opposite effects on transcription
by Huang, Jing and Gurung, Buddha and Wan, Bingbing and Matkar, Smita and Veniaminova, Natalia A and Wan, Ke and Merchant, Juanita L and Hua, Xianxin and Lei, Ming
Nature, ISSN 0028-0836, 02/2012, Volume 482, Issue 7386, pp. 542 - 546
Menin is a tumour suppressor protein whose loss or inactivation causes multiple endocrine neoplasia 1 (MEN1), a hereditary autosomal dominant tumour syndrome... 
PROTEIN | GENE | HISTONE METHYLTRANSFERASE COMPLEX | INTERACTS | MULTIDISCIPLINARY SCIENCES | ENDOCRINE NEOPLASIA TYPE-1 | FAMILY | Chromatin - metabolism | Myeloid-Lymphoid Leukemia Protein - metabolism | Phosphorylation | Humans | Protein Multimerization | Molecular Sequence Data | Crystallography, X-Ray | JNK Mitogen-Activated Protein Kinases - metabolism | Proto-Oncogene Proteins - chemistry | Structure-Activity Relationship | Myeloid-Lymphoid Leukemia Protein - chemistry | Intercellular Signaling Peptides and Proteins - metabolism | HEK293 Cells | Fibroblasts | Proto-Oncogene Proteins c-jun - chemistry | Transcription, Genetic | Binding Sites | Proto-Oncogene Proteins - metabolism | Amino Acid Sequence | Histone-Lysine N-Methyltransferase | Models, Molecular | Amino Acid Motifs | Animals | Proto-Oncogene Proteins c-jun - metabolism | Protein Binding | Mice | Leukemia | Physiological aspects | Genetic aspects | Genetic transcription | Research | Tumor proteins | Risk factors | Proteins | Genetics | Mutation | Kinases
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3. Full Text Down-Regulation of c-Fos/c-Jun AP-1 Dimer Activity by Sumoylation
by Guillaume Bossis and Cécile E. Malnou and Rosa Farras and Elisabetta Andermarcher and Robert Hipskind and Manuel Rodriguez and Darja Schmidt and Stefan Muller and Isabelle Jariel-Encontre and Marc Piechaczyk
Molecular and Cellular Biology, ISSN 0270-7306, 08/2005, Volume 25, Issue 16, pp. 6964 - 6979
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
TRANSCRIPTIONAL ACTIVATION | ACTIVATED PROTEIN-KINASE | CBP-INDUCED STIMULATION | EARLY GENE-PRODUCTS | PROTEASOMAL DEGRADATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | TRANSFORMING ACTIVITY | TERMINAL TRANSACTIVATION DOMAIN | SUMO-1 MODIFICATION | BINDING PROTEIN | CELL BIOLOGY | Phosphorylation | Threonine - chemistry | Immunoprecipitation | Luciferases - metabolism | Humans | Transcriptional Activation | Gene Expression Regulation, Neoplastic | Immunoblotting | Transcription Factor AP-1 - metabolism | Transfection | Time Factors | Proto-Oncogene Proteins c-jun - chemistry | Transcription, Genetic | Binding Sites | Dimerization | Proto-Oncogene Proteins p21(ras) - metabolism | Protein Structure, Tertiary | Mutagenesis, Site-Directed | Small Ubiquitin-Related Modifier Proteins - metabolism | Down-Regulation | Proto-Oncogene Proteins c-fos - metabolism | Glutathione Transferase - metabolism | Recombinant Fusion Proteins - chemistry | Transcription Factor AP-1 - chemistry | Mitogen-Activated Protein Kinase 3 - metabolism | Proto-Oncogene Proteins c-jun - metabolism | Protein Binding | SUMO-1 Protein - metabolism | HeLa Cells | Kinetics | Lysine - chemistry | Subcellular Fractions | Microscopy, Fluorescence | Mitogen-Activated Protein Kinase 1 - metabolism | Gene Expression
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4. Full Text miR200c attenuates P-gp-mediated MDR and metastasis by targeting JNK2/c-Jun signaling pathway in colorectal cancer
by Sui, Hua and Cai, Guo-Xiang and Pan, Shu-Fang and Deng, Wan-Li and Wang, Yu-Wei and Chen, Zhe-Sheng and Cai, San-Jun and Zhu, Hui-Rong and Li, Qi
Molecular Cancer Therapeutics, ISSN 1535-7163, 12/2014, Volume 13, Issue 12, pp. 3137 - 3151
MicroRNA-200c (miR200c) recently emerged as an important regulator of tumorigenicity and cancer metastasis; however, its role in regulating multidrug... 
MICRORNA-200C OVEREXPRESSION | CELLS | ONCOLOGY | N-TERMINAL KINASE | JNK2 | PROLIFERATION | MULTIDRUG-RESISTANCE | C-JUN | SUPPRESSION | EXPRESSION | CONTRIBUTES | Colorectal Neoplasms - genetics | Humans | ATP-Binding Cassette, Sub-Family B, Member 1 - metabolism | Male | Antineoplastic Agents - therapeutic use | Mitogen-Activated Protein Kinase 9 - genetics | Cell Movement - genetics | Matrix Metalloproteinase 9 - metabolism | Neoplasm Metastasis | RNA Interference | Base Sequence | Colorectal Neoplasms - drug therapy | Proto-Oncogene Proteins c-jun - chemistry | Antineoplastic Agents - pharmacology | 3' Untranslated Regions | Binding Sites | Colorectal Neoplasms - metabolism | Disease Models, Animal | Mitogen-Activated Protein Kinase 9 - chemistry | Gene Expression | Signal Transduction | Matrix Metalloproteinase 2 - metabolism | Mitogen-Activated Protein Kinase 9 - metabolism | Proto-Oncogene Proteins c-jun - genetics | RNA, Messenger - genetics | Xenograft Model Antitumor Assays | Drug Resistance, Neoplasm - genetics | Animals | ATP-Binding Cassette, Sub-Family B, Member 1 - genetics | Proto-Oncogene Proteins c-jun - metabolism | Cell Line, Tumor | Mice | MicroRNAs - genetics | Colorectal Neoplasms - pathology | MicroRNAs - chemistry
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5. Full Text Visualization of Interactions among bZIP and Rel Family Proteins in Living Cells Using Bimolecular Fluorescence Complementation
by Hu, Chang-Deng and Chinenov, Yurii and Kerppola, Tom K
Molecular Cell, ISSN 1097-2765, 2002, Volume 9, Issue 4, pp. 789 - 798
Networks of protein interactions coordinate cellular functions. We describe a bimolecular fluorescence complementation (BiFC) assay for determination of the... 
TRANSCRIPTION FACTORS | DNA-BINDING | ACTIVATION | GENE | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | DIMERIZATION | FOS | INDUCTION | NF-KAPPA-B | DOMAINS | CELL BIOLOGY | Sequence Deletion | Alternative Splicing | Humans | Leucine Zippers | Bacterial Proteins - chemistry | Cercopithecus aethiops | Fluorescence | NF-kappa B - chemistry | Ligases - chemistry | Cell Compartmentation | Transfection | Luminescent Proteins - chemistry | Proto-Oncogene Proteins c-jun - chemistry | Transcription, Genetic | Dimerization | Protein Structure, Tertiary | Proto-Oncogene Proteins c-fos - chemistry | NF-KappaB Inhibitor alpha | I-kappa B Proteins | Recombinant Fusion Proteins - chemistry | DNA-Binding Proteins - chemistry | Macromolecular Substances | Protein Transport | Protein Interaction Mapping - methods | Peptide Fragments - chemistry | Animals | Mice | HeLa Cells | COS Cells | 3T3 Cells | Microscopy, Fluorescence | Subcellular Fractions - chemistry
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6. Full Text A reinvestigation of the multisite phosphorylation of the transcription factor c-Jun
by Cohen, Philip and Davis, Roger J and Morton, Simon and McLaren, Ann
The EMBO Journal, ISSN 0261-4189, 08/2003, Volume 22, Issue 15, pp. 3876 - 3886
We have used phospho‐specific antibodies to re‐examine the multisite phosphorylation of c‐Jun in murine RAW macrophages and embryonic fibroblasts. Our results... 
c‐Jun | GSK3 | JNK | LPS | ERK | C-Jun | ONCOPROTEIN | DNA-BINDING | ACTIVATION | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GLYCOGEN-SYNTHASE KINASE-3 | CELL-PROLIFERATION | AP-1 | CELL BIOLOGY | c-Jun | INHIBITION | TYROSINE | LITHIUM | Amino Acid Sequence | Cell Line | Phosphorylation | Molecular Sequence Data | Proto-Oncogene Proteins c-jun - immunology | Threonine - metabolism | Serine - metabolism | Animals | Proto-Oncogene Proteins c-jun - metabolism | Antibodies - immunology | Proto-Oncogene Proteins c-jun - chemistry | Anisomycin - pharmacology | Mice | Mitogen-Activated Protein Kinases - metabolism
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7. Full Text Peptide-DNA conjugates as tailored bivalent binders of the oncoprotein c-Jun
by Pazos, Elena and Portela, Cecilia and Penas, Cristina and Vázquez, M. Eugenio and Mascareñas, José L
Organic and Biomolecular Chemistry, ISSN 1477-0520, 05/2015, Volume 13, Issue 19, pp. 5385 - 5390
We describe a ds-oligonucleotide-peptide conjugate that is able to efficiently dismount preformed DNA complexes of the bZIP regions of oncoproteins c-Fos and... 
TRANSCRIPTION FACTORS | CHEMISTRY, ORGANIC | DIMERIZATION | FOS | BINDING | EXPRESSION | REGION | Protein Structure, Tertiary | Amino Acid Sequence | Peptides - chemistry | Oligonucleotides | Molecular Sequence Data | DNA - metabolism | DNA - chemistry | Peptides - metabolism | Proto-Oncogene Proteins c-jun - metabolism | Base Sequence | Proto-Oncogene Proteins c-jun - chemistry | Electrophoretic Mobility Shift Assay | Fluorescence Polarization
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8. Full Text Characterization of c-Jun from orange-spotted grouper, Epinephelus coioides involved in SGIV infection
by Wei, Shina and Huang, Xiaohong and Huang, Youhua and Qin, Qiwei
Fish and Shellfish Immunology, ISSN 1050-4648, 03/2015, Volume 43, Issue 1, pp. 230 - 240
The nuclear phosphoprotein c-Jun is a member of the AP1 family of transcription activating complex, can be induced by various extracellular stimuli such as... 
Epinephelus coioides | c-Jun | DN-Ec-c-Jun | Virus replication | Singapore grouper iridovirus (SGIV) | C-Jun | CELLS | SIGNALING PATHWAYS | DELETION MUTANT | N-TERMINAL KINASE | SINGAPORE | IMMUNOLOGY | AP-1 | FISHERIES | VIRUS-REPLICATION | MARINE & FRESHWATER BIOLOGY | GENE-EXPRESSION | VETERINARY SCIENCES | ACTIVATED PROTEIN-KINASES | TRANSCRIPTION FACTOR | Bass | Amino Acid Sequence | DNA Virus Infections - veterinary | Fish Proteins - chemistry | Proto-Oncogene Proteins c-jun - genetics | Fish Proteins - metabolism | Molecular Sequence Data | Iridovirus - physiology | Phylogeny | DNA Virus Infections - genetics | Fish Diseases - genetics | Fish Proteins - genetics | Animals | Fish Diseases - virology | Proto-Oncogene Proteins c-jun - metabolism | Base Sequence | Proto-Oncogene Proteins c-jun - chemistry | DNA Virus Infections - virology | Fluorescence | Amino acids | Chemical properties | Health aspects | Analysis | Fishes
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9. Full Text Methyl-dependent and spatial-specific DNA recognition by the orthologous transcription factors human AP-1 and Epstein-Barr virus Zta
by Hong, Samuel and Wang, Dongxue and Horton, John R and Zhang, Xing and Speck, Samuel H and Blumenthal, Robert M and Cheng, Xiaodong and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Nucleic Acids Research, ISSN 0305-1048, 03/2017, Volume 45, Issue 5, pp. 2503 - 2515
Activator protein 1 (AP-1) is a transcription factor that recognizes two versions of a 7-base pair response element, either 5'-TGAGTCA-3'or 5'-MGAGTCA-3'... 
ACTIVATION | LYTIC SWITCH | MAMMALIAN DNA | STRUCTURAL BASIS | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | EMBRYONIC STEM-CELLS | CPG METHYLATION | BINDING-SITES | ZEBRA PROTEIN | CYTOSINE METHYLATION | Thymine - chemistry | Response Elements | Humans | Protein Multimerization | DNA - metabolism | Trans-Activators - chemistry | Transcription Factor AP-1 - metabolism | 5-Methylcytosine - chemistry | Transcription Factor AP-1 - chemistry | DNA - chemistry | DNA Methylation | Base Pairing | Proto-Oncogene Proteins c-jun - metabolism | Protein Binding | Proto-Oncogene Proteins c-jun - chemistry | Trans-Activators - metabolism | Binding Sites | Gene regulation, Chromatin and Epigenetics
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10. Full Text SIRT1 Suppresses Activator Protein-1 Transcriptional Activity and Cyclooxygenase-2 Expression in Macrophages
by Ran Zhang and Hou-Zao Chen and Jin-Jing Liu and Yu-Yan Jia and Zhu-Qin Zhang and Rui-Feng Yang and Yuan Zhang and Jing Xu and Yu-Sheng Wei and De-Pei Liu and Chih-Chuan Liang
Journal of Biological Chemistry, ISSN 0021-9258, 03/2010, Volume 285, Issue 10, pp. 7097 - 7110
SIRT1 (Sirtuin type 1), a mammalian orthologue of yeast SIR2 (silent information regulator 2), has been shown to mediate a variety of calorie restriction... 
IN-VITRO | DNA-BINDING | EPITHELIAL-CELLS | MOLECULE | DEACETYLASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MICE | KAPPA-B | C-JUN | CHRONIC INFLAMMATION | CALORIE RESTRICTION | Sirtuin 1 - metabolism | Caloric Restriction | Transcription Factor AP-1 - genetics | Humans | Leucine Zippers | Male | Sirtuin 1 - genetics | Transcription Factor AP-1 - metabolism | Cyclooxygenase 2 - genetics | Proto-Oncogene Proteins c-jun - chemistry | Transcription, Genetic | Macrophages - physiology | Proto-Oncogene Proteins c-fos - chemistry | Cell Line | Proto-Oncogene Proteins c-jun - genetics | Mice, Inbred C57BL | Gene Expression Regulation | Proto-Oncogene Proteins c-fos - metabolism | Macrophages - cytology | Random Allocation | Animals | Proto-Oncogene Proteins c-jun - metabolism | Cyclooxygenase 2 - metabolism | Proto-Oncogene Proteins c-fos - genetics | Mice | Gene Regulation | Calorie Restriction | Immunology | Transcription | Cellular Response | Post-translational Modification | Sirtuin Type 1 (SIRT1) | AP-1 | Protein | Protein-Protein Interactions | Cyclooxygenase-2 (COX-2) | Macrophage
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11. Full Text Opposing Roles for ATF2 and c-Fos in c-Jun-Mediated Neuronal Apoptosis
by Zhongmin Yuan and Shoufang Gong and Jingyan Luo and Zhihao Zheng and Bin Song and Shanshan Ma and Jiaoli Guo and Ce Hu and Gerald Thiel and Charles Vinson and Chang-Deng Hu and Yizheng Wang and Mingtao Li
Molecular and Cellular Biology, ISSN 0270-7306, 05/2009, Volume 29, Issue 9, pp. 2431 - 2442
Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley... 
CEREBELLAR GRANULE NEURONS | PROGRAMMED CELL-DEATH | RESPONSE ELEMENT | FAS LIGAND | BIOCHEMISTRY & MOLECULAR BIOLOGY | N-TERMINAL KINASE | GENE-EXPRESSION | POTASSIUM DEPRIVATION | SYMPATHETIC NEURONS | ACTIVATED PROTEIN-KINASES | TRANSCRIPTION FACTOR | CELL BIOLOGY | Potassium - metabolism | Proto-Oncogene Proteins c-jun - genetics | Cells, Cultured | Proto-Oncogene Proteins c-fos - metabolism | Rats | Neurons - cytology | Rats, Sprague-Dawley | Activating Transcription Factor 2 - genetics | Activating Transcription Factor 2 - metabolism | Animals | RNA Interference | Activating Transcription Factor 2 - chemistry | Proto-Oncogene Proteins c-jun - metabolism | Neurons - physiology | Protein Structure, Quaternary | Proto-Oncogene Proteins c-jun - chemistry | Proto-Oncogene Proteins c-fos - genetics | Signal Transduction - physiology | Apoptosis - physiology | Dimerization
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12. Full Text Activator protein-1: Redox switch controlling structure and DNA-binding
by Yin, Zhou and Machius, Mischa and Nestler, Eric J and Rudenko, Gabby and Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)
Nucleic Acids Research, ISSN 0305-1048, 2017, Volume 45, Issue 19, pp. 11425 - 11436
The transcription factor, activator protein-1 (AP-1), binds to cognate DNA under redox control; yet, the underlying mechanism has remained enigmatic. A series... 
TRANSITION | LEUCINE-ZIPPER | JUN | BIOCHEMISTRY & MOLECULAR BIOLOGY | EQUILIBRIUM | VALIDATION | MECHANISMS | FOS | AP-1 | ASSOCIATION | DOMAINS | Proto-Oncogene Proteins c-fos - chemistry | Amino Acid Sequence | Oxidation-Reduction | Proto-Oncogene Proteins c-jun - genetics | Transcription Factor AP-1 - genetics | Humans | Proto-Oncogene Proteins c-fos - metabolism | Models, Molecular | Crystallography, X-Ray | DNA - metabolism | DNA-Binding Proteins - genetics | DNA-Binding Proteins - chemistry | Transcription Factor AP-1 - metabolism | DNA - genetics | DNA-Binding Proteins - metabolism | Sequence Homology, Amino Acid | Transcription Factor AP-1 - chemistry | DNA - chemistry | Animals | Proto-Oncogene Proteins c-jun - metabolism | Protein Binding | Protein Domains | Proto-Oncogene Proteins c-jun - chemistry | Proto-Oncogene Proteins c-fos - genetics | BASIC BIOLOGICAL SCIENCES | Structural Biology
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13. Full Text Truncation, randomization, and selection: Generation of a reduced length c-jun antagonist that retains high interaction stability
by Crooks, Richard O and Rao, Tara and Mason, Jody M
Journal of Biological Chemistry, ISSN 0021-9258, 08/2011, Volume 286, Issue 34, pp. 29470 - 29479
The DNA binding activity of the transcriptional regulator activator protein-1 shows considerable promise as a target in cancer therapy. A number of different... 
OLIGOMERIZATION DOMAIN | EMPIRICAL PARAMETERS | DNA-BINDING | PEPTIDES | HELICAL COILED-COILS | FOLDING PROBLEM | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | CHAIN-LENGTH | ALPHA-HELICES | PROTEIN-INTERACTION | Protein Structure, Tertiary | Proto-Oncogene Proteins c-fos - antagonists & inhibitors | Proto-Oncogene Proteins c-fos - chemistry | Peptides - chemistry | Humans | Leucine Zippers | Proto-Oncogene Proteins c-fos - metabolism | Structure-Activity Relationship | Proto-Oncogene Proteins c-jun - antagonists & inhibitors | Peptides - metabolism | Proto-Oncogene Proteins c-jun - metabolism | Protein Binding | Proto-Oncogene Proteins c-jun - chemistry | Protein Structure and Folding | Coiled Coil | Library Design | Circular Dichroism (CD) | Protein Design | Protein Stability | AP-1 Transcription Factor | Peptide Interactions | Protein-Protein Interactions
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14. Full Text Dynamic acetylation of all lysine 4-methylated histone H3 in the mouse nucleus: Analysis at c-fos and c-jun
by Hazzalin, Catherine A and Mahadevan, Louis C
PLoS Biology, ISSN 1545-7885, 12/2005, Volume 3, Issue 12, pp. 1 - 16
A major focus of current research into gene induction relates to chromatin and nucleosomal regulation, especially the significance of multiple histone... 
METHYLATION | ACTIVATION | CHROMATIN-STRUCTURE | PHOSPHORYLATION | MAP KINASE | DEACETYLASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | BIOLOGY | CYCLIC TETRAPEPTIDE | EARLY GENE INDUCTION | ACTIVE GENES | Proto-Oncogene Proteins c-fos - chemistry | Tetradecanoylphorbol Acetate - pharmacology | Histones - chemistry | Proto-Oncogene Proteins c-jun - genetics | Cells, Cultured | Proto-Oncogene Proteins c-fos - metabolism | Enzyme Activation - drug effects | Acetylation - drug effects | Animals | Cell Nucleus - metabolism | Methylation - drug effects | Proto-Oncogene Proteins c-jun - metabolism | Proto-Oncogene Proteins c-jun - chemistry | Proto-Oncogene Proteins c-fos - genetics | Cell Nucleus - chemistry | Lysine - metabolism | Mice | Histones - metabolism | Phosphorylation - drug effects | Cell Nucleus - drug effects | Lysine - chemistry | Hydroxamic Acids - pharmacology | Mitogen-Activated Protein Kinases - metabolism | Molecular Biology | Gene Therapy | Genomics | Structural Biology | Mus (Mouse) | Genetics | Cancer Biology | Biochemistry | Mammals | Cell Biology | Proteins | Chromatin | Phosphorylation | Acids | Genes
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