المؤلفون: Frank Bradke, Andrea Tedeschi

المصدر: EMBO reports 14(7), 605-614 (2013). doi:10.1038/embor.2013.64

مصطلحات موضوعية: Central Nervous System, Nervous system, metabolism [Apoptosis Regulatory Proteins], Neurogenesis, metabolism [Calcium-Calmodulin-Dependent Protein Kinases], genetics [Mitogen-Activated Protein Kinase Kinases], Apoptosis, Review Article, metabolism [Axons], metabolism [Neurodegenerative Diseases], Biology, Mitogen-activated protein kinase kinase, Biochemistry, physiology [Regeneration], ddc:570, physiology [Signal Transduction], Genetics, medicine, Animals, Humans, Regeneration, Axon, Protein kinase A, Molecular Biology, genetics [Calcium-Calmodulin-Dependent Protein Kinases], Mitogen-Activated Protein Kinase Kinases, pathology [Axons], Regeneration (biology), pathology [Neurodegenerative Diseases], Gene Expression Regulation, Developmental, Neurodegenerative Diseases, physiology [Neurogenesis], physiology [Central Nervous System], Axons, Cell biology, genetics [Apoptosis Regulatory Proteins], Isoenzymes, Death-Associated Protein Kinases, medicine.anatomical_structure, metabolism [Isoenzymes], genetics [Neurodegenerative Diseases], Calcium-Calmodulin-Dependent Protein Kinases, Neuron, metabolism [Mitogen-Activated Protein Kinase Kinases], genetics [Isoenzymes], Apoptosis Regulatory Proteins, Neural development, Signal Transduction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::992e41bf4a6b594ef3bd0c4e995eacbb
https://doi.org/10.1038/embor.2013.64

المؤلفون: Karsten Boldt, David Romano, Mohamed Ali Jarboui, Walter Kolch, Yves Texier, Nicola Horn, Alex von Kriegsheim, Armin Zebisch, Christian Johannes Gloeckner, Marius Ueffing, Nora Rauch, Layal Dernayka

المساهمون: Interactions cellulaires neuroendocriniennes (ICN), Université de la Méditerranée - Aix-Marseille 2-Centre National de la Recherche Scientifique (CNRS), Centre de recherche en neurobiologie - neurophysiologie de Marseille (CRN2M), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Department of Protein Science, Helmholtz Zentrum München = German Research Center for Environmental Health, Division of Experimental Ophthalmology, Eberhard Karls Universität Tübingen = Eberhard Karls University of Tuebingen-Center of Ophthalmology-Medical Proteome Center, Conway Institute of Biomolecular and Biomedical Research [Dublin, Irlande], University College Dublin [Dublin] (UCD), Systems Biology Ireland, School of Medicine and Medical Science [Dublin, Irlande], German Research Center for Environmental Health-Helmholtz-Zentrum München (HZM)

المصدر: Cellular Signalling
Cellular Signalling, 2016, 28 (9), pp.1432--1439. ⟨10.1016/j.cellsig.2016.06.016⟩
Dernayka, L, Rauch, N, Jarboui, M-A, Zebisch, A, Texier, Y, Horn, N, Romano, D, Gloeckner, C J, Kriegsheim, A V, Ueffing, M, Kolch, W & Boldt, K 2016, ' Autophosphorylation on S614 inhibits the activity and the transforming potential of BRAF ', Cellular Signalling, vol. 28, no. 9, pp. 1432-9 . https://doi.org/10.1016/j.cellsig.2016.06.016
Cellular signalling 28(9), 1432-1439 (2016). doi:10.1016/j.cellsig.2016.06.016

مصطلحات موضوعية: 0301 basic medicine, MAPK/ERK pathway, Proto-Oncogene Proteins B-raf, endocrine system diseases, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology, genetics [Mutation], medicine.disease_cause, Proto-Oncogene Mas, Cell Line, BRAF, 03 medical and health sciences, Mice, Phosphoserine, Inhibition of kinase activity and transformation, metabolism [Proto-Oncogene Proteins B-raf], medicine, metabolism [Phosphoserine], Animals, Humans, ddc:610, Amino Acid Sequence, Kinase activity, Phosphorylation, Protein kinase A, skin and connective tissue diseases, neoplasms, Mitogen-Activated Protein Kinase Kinases, Mutation, S614 autophosphorylation, biology, Chemistry, metabolism [Cell Transformation, Neoplastic], Autophosphorylation, Cell Biology, digestive system diseases, Rats, enzymes and coenzymes (carbohydrates), 030104 developmental biology, Cell Transformation, Neoplastic, Mitogen-activated protein kinase, chemistry [Proto-Oncogene Proteins B-raf], Cancer research, biology.protein, metabolism [Mitogen-Activated Protein Kinase Kinases], pathology [Cell Transformation, Neoplastic], V600E, Protein Binding

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b926b99ebb81ba42e737a96a699f67
https://hal.science/hal-01474295

المؤلفون: Ralf Kühn, Caroline Nothdurfter, Theo Rein, Rainer Rupprecht, Wolfgang Wurst, Barbara Di Benedetto

المصدر: Neuropharmacology 62(1), 209-216 (2012). doi:10.1016/j.neuropharm.2011.07.001

مصطلحات موضوعية: MAPK/ERK pathway, CM 40534, Pyridines, drug effects [Gene Expression Regulation, Neoplastic], Mitogen-activated protein kinase kinase, Pharmacology, metabolism [Lactate Dehydrogenases], pharmacology [Propylamines], metabolism [Mitogen-Activated Protein Kinase 3], Glial cell line-derived neurotrophic factor, pharmacology [Dibenzothiazepines], RNA, Small Interfering, Mitogen-Activated Protein Kinase 3, biology, Propylamines, Chemistry, Reboxetine, metabolism [Glial Cell Line-Derived Neurotrophic Factor], Glioma, Antidepressive Agents, Gene Expression Regulation, Neoplastic, Antidepressant, pharmacology [Antidepressive Agents], metabolism [Mitogen-Activated Protein Kinase Kinases], medicine.drug, endocrine system, Dibenzothiazepines, medicine.drug_class, MAP Kinase Signaling System, Atypical antipsychotic, Enzyme-Linked Immunosorbent Assay, Transfection, metabolism [RNA, Messenger], Cellular and Molecular Neuroscience, Enzyme activator, drug effects [MAP Kinase Signaling System], Quetiapine Fumarate, Downregulation and upregulation, Cell Line, Tumor, medicine, Animals, ddc:610, metabolism [RNA, Small Interfering], Glial Cell Line-Derived Neurotrophic Factor, RNA, Messenger, Lactate Dehydrogenases, Mitogen-Activated Protein Kinase Kinases, Dose-Response Relationship, Drug, urogenital system, pharmacology [Pyridines], Rats, Enzyme Activation, nervous system, biology.protein, drug effects [Enzyme Activation], pathology [Glioma]

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::738610c504eef86fb805c720c2bcf3b2
https://pub.dzne.de/record/136346

المؤلفون: Kleemann, R., Hausser, A., Geiger, G., Mischke, R., Burger-Kentischer, A., Flieger, O., Johannes, F. J., Roger, T., Calandra, T., Kapurniotu, A., Grell, M., Finkelmeier, D., Brunner, H., Bernhagen, J.

المصدر: Nature, vol. 408, no. 6809, pp. 211-6

مصطلحات موضوعية: Cell Cycle/*physiology *Cell Cycle Proteins Cell Line Cyclin-Dependent Kinase Inhibitor p27 DNA-Binding Proteins/*physiology Gene Expression Regulation Hela Cells Humans Intracellular Signaling Peptides and Proteins *JNK Mitogen-Activated Protein Kinases Luciferases/genetics MAP Kinase Kinase 4 Macrophage Migration-Inhibitory Factors/*physiology Microtubule-Associated Proteins/metabolism Mitogen-Activated Protein Kinase Kinases/metabolism NF-kappa B/metabolism Peptide Hydrolases Precipitin Tests Protein Binding Proto-Oncogene Proteins c-jun/metabolism Recombinant Fusion Proteins/genetics/metabolism Transcription Factor AP-1/antagonists & inhibitors/*physiology Transcription Factors/*physiology *Tumor Suppressor Proteins

Relation: info:eu-repo/semantics/altIdentifier/pmid/11089976; info:eu-repo/semantics/altIdentifier/pissn/0028-0836; https://serval.unil.ch/notice/serval:BIB_7A0C6CAC86B2

الاتاحة: https://serval.unil.ch/notice/serval:BIB_7A0C6CAC86B2
https://doi.org/10.1038/35041591