Suchergebnisse - "p38 Mitogen-Activated Protein Kinases genetics"
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1
Autoren: et al.
Quelle: Cell reports. Medicine, vol. 5, no. 11, pp. 101823
Schlagwörter: Hematopoietic Stem Cells/metabolism, CRISPR-Cas Systems/genetics, p38 Mitogen-Activated Protein Kinases/metabolism, p38 Mitogen-Activated Protein Kinases/genetics, Gene Editing/methods, DNA Damage/genetics, Animals, Cell Proliferation/genetics, Reactive Oxygen Species/metabolism, Mice, Humans, Inbred C57BL, Cell Differentiation/genetics, Tumor Suppressor Protein p53/metabolism, Tumor Suppressor Protein p53/genetics, CRISPR-Cas9, DNA damage, DNA damage response, cell cycle, clonal output, differentiation, gene editing, hematopoietic stem cells, p38 MAPK-ROS, proliferative stress, single-cell analyses
Dateibeschreibung: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/39536752; info:eu-repo/semantics/altIdentifier/eissn/2666-3791; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4C0238456CA75; https://serval.unil.ch/notice/serval:BIB_4C0238456CA7; https://serval.unil.ch/resource/serval:BIB_4C0238456CA7.P001/REF.pdf
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2
Autoren: et al.
Quelle: Sci Signal. 2022 Dec 13;15(764)
Schlagwörter: 0301 basic medicine, Interferons/genetics, Transcription, Genetic, p38 Mitogen-Activated Protein Kinases, name=Cell Biology, Interferon-gamma, 03 medical and health sciences, 106023 Molekularbiologie, Genetic, Macrophages/metabolism, Transcription Factors/metabolism, Phosphorylation, 106052 Cell biology, Interferon-gamma/metabolism, 0303 health sciences, Macrophages, p38 Mitogen-Activated Protein Kinases/genetics, name=Biochemistry, name=Molecular Biology, 106023 Molecular biology, Interferons, 106052 Zellbiologie, Transcription, Signal Transduction, Transcription Factors
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3
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Mol Oncol
Molecular Oncology, Vol 12, Iss 5, Pp 579-593 (2018)Schlagwörter: 0301 basic medicine, cell migration, sialyl‐Lewis X/A, Oligosaccharides, Ligands, p38 Mitogen-Activated Protein Kinases, MAP Kinase Signaling System / drug effects, E-Selectin / metabolismo, Fucose / analogs & derivatives, Carcinoma, Ductal, Breast / enzymology, RC254-282, Research Articles, Fucose / pharmacology, Carcinoma, Ductal, Breast, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Middle Aged, Fucosyltransferases, 3. Good health, Carcinoma, Ductal, Breast / pathology, Breast Neoplasms / pathology, p38 Mitogen-Activated Protein Kinases / genetics, Female, Breast Neoplasms / enzymology, E-Selectin, Fucosyltransferases / antagonists & inhibitors, Oligosaccharides / metabolismo, Adult, MAP Kinase Signaling System, proliferation, Primary Cell Culture, Breast Neoplasms, E-Selectin / metabolism, Cell Adhesion / drug effects, 03 medical and health sciences, breast cancer, p38 Mitogen-Activated Protein Kinases / metabolism, E-Selectin / genetics, Cell Line, Tumor, Cell Adhesion, Humans, HSJ ANPAT, Neoplasm Invasiveness, Sialyl Lewis X Antigen, Aged, Cell Proliferation, Fucose, fucosylation, Oligosaccharides / metabolism, Cell Proliferation / drug effects
Dateibeschreibung: application/pdf
Zugangs-URL: https://febs.onlinelibrary.wiley.com/doi/pdfdirect/10.1002/1878-0261.12163
https://pubmed.ncbi.nlm.nih.gov/29215790
https://doaj.org/article/aa487eb10376413e99bc71ac96aa6fff
https://repositorio-aberto.up.pt/bitstream/10216/127061/1/10.1002-1878-0261.12163.pdf
http://europepmc.org/articles/PMC5928367
https://www.ncbi.nlm.nih.gov/pubmed/29215790
https://novaresearch.unl.pt/en/publications/inhibition-of-fucosylation-in-human-invasive-ductal-carcinoma-red
https://febs.onlinelibrary.wiley.com/doi/pdf/10.1002/1878-0261.12163
https://core.ac.uk/display/159166726
https://hdl.handle.net/10216/127061
http://hdl.handle.net/10400.17/3949 -
4
Weitere Verfasser: et al.
Schlagwörter: Cell Proliferation, Collagen, Collagen Type I / genetics, Female, Humans, Leiomyoma* / genetics, MicroRNAs* / genetics, p38 Mitogen-Activated Protein Kinases / genetics, MiR-139-5p, extracellular matrix, fibrosis, uterine leiomyoma
Relation: YONSEI MEDICAL JOURNAL; J02813; https://ir.ymlib.yonsei.ac.kr/handle/22282913/187694; T202125130
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5
Autoren: et al.
Quelle: Basic Res Cardiol
Schlagwörter: Male, 0301 basic medicine, Time Factors, Mice, Transgenic, p38 Mitogen-Activated Protein Kinases, Ventricular Function, Left, Mice, 03 medical and health sciences, Animals, Cardiac energetics, Cardiac function, Mice, Inbred C57BL [MeSH], Glycogen Synthase Kinase 3 beta/genetics [MeSH], Original Contribution, Tamoxifen/pharmacology [MeSH], Mice, Transgenic [MeSH], Proto-Oncogene Proteins c-akt/genetics [MeSH], Gene Expression Regulation/drug effects [MeSH], Male [MeSH], Myocytes, Cardiac/metabolism [MeSH], Tamoxifen/toxicity [MeSH], Energy Metabolism/drug effects [MeSH], Cardiomyopathy, Integrases/genetics [MeSH], Myocytes, Cardiac/drug effects [MeSH], Myosin Heavy Chains/genetics [MeSH], p38 Mitogen-Activated Protein Kinases/genetics [MeSH], Tamoxifen/analogs, aMHC-MerCreMer/loxP system, Gene Editing [MeSH], Fibrosis [MeSH], Ventricular Remodeling/drug effects [MeSH], Animals [MeSH], Myocytes, Cardiac/pathology [MeSH], Time Factors [MeSH], Proto-Oncogene Proteins c-akt/metabolism [MeSH], p38 Mitogen-Activated Protein Kinases/metabolism [MeSH], Ventricular Function, Left/drug effects [MeSH], 4-hydroxytamoxifen, Glycogen Synthase Kinase 3 beta/metabolism [MeSH], Myocytes, Cardiac, Gene Editing, 2. Zero hunger, 0303 health sciences, Glycogen Synthase Kinase 3 beta, Integrases, Myosin Heavy Chains, Ventricular Remodeling, Fibrosis, 3. Good health, Mice, Inbred C57BL, Tamoxifen, Gene Expression Regulation, Energy Metabolism, Proto-Oncogene Proteins c-akt
Zugangs-URL: https://link.springer.com/content/pdf/10.1007/s00395-020-00841-9.pdf
https://pubmed.ncbi.nlm.nih.gov/33544211
https://link.springer.com/content/pdf/10.1007/s00395-020-00841-9.pdf
https://link.springer.com/article/10.1007/s00395-020-00841-9
https://pubmed.ncbi.nlm.nih.gov/33544211/
https://europepmc.org/article/MED/33544211
https://khepri-node.dev.meta-infra.org/papers/4-hydroxytamoxifen-does-not-deteriorate-cardiac/33544211
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7864833
https://repository.publisso.de/resource/frl:6450770 -
6
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Clinical Nutrition. 35:414-421
Schlagwörter: Adipose Tissue/metabolism, Blood Glucose, Male, 0301 basic medicine, Anti-Inflammatory Agents/pharmacology, Interleukin-6/metabolism, Interleukin-1beta, Anti-Inflammatory Agents, Messenger/metabolism, Proto-Oncogene Proteins c-akt/genetics, Inbred C57BL, Obese, Adipose Tissue/drug effects, Mice, Macrophages/drug effects, Chalcones, Adipocytes, Nitric Oxide Synthase Type II/genetics, Chalcones/pharmacology, Cyclooxygenase 2/metabolism, Interleukin-6/genetics, Chemokine CCL2, Tumor Necrosis Factor-alpha/metabolism, 2. Zero hunger, p38 Mitogen-Activated Protein Kinases/metabolism, 0303 health sciences, Chemokine CCL2/genetics, Inflammation/drug therapy, NF-kappa B/genetics, Anti-inflammatory effect, p38 Mitogen-Activated Protein Kinases/genetics, 3. Good health, Adipose Tissue, Nitric Oxide Synthase Type II/metabolism, Signal Transduction, Licochalcone F, Obesity/drug therapy, High-Fat/adverse effects, Down-Regulation, Diet, High-Fat, Cyclooxygenase 2/genetics, 03 medical and health sciences, Macrophages/metabolism, Glucose Intolerance, Animals, Inflammation, Blood Glucose/metabolism, Glucose Intolerance/drug therapy, Interleukin-6, Macrophages, Body Weight, Obesity-induced chronic inflammation, Diet-induced obese mice, Diet, Mice, Inbred C57BL, Adipocytes/metabolism, Chemokine CCL2/metabolism, Cyclooxygenase 2, Interleukin-1beta/metabolism, NF-kappa B/metabolism, Chronic Disease, Proto-Oncogene Proteins c-akt/metabolism, RNA, Messenger/genetics, Tumor Necrosis Factor-alpha/genetics, Adipocytes/drug effects
Dateibeschreibung: 414~421
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/25823386
https://yonsei.pure.elsevier.com/en/publications/licochalcone-f-alleviates-glucose-tolerance-and-chronic-inflammat
https://www.ncbi.nlm.nih.gov/pubmed/25823386
https://ir.ymlib.yonsei.ac.kr/handle/22282913/146500
https://pubag.nal.usda.gov/catalog/5823810
https://europepmc.org/article/MED/25823386
https://www.sciencedirect.com/science/article/abs/pii/S0261561415000801 -
7
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Immunobiology. 221:70-75
Schlagwörter: Innate immune response, Lipopolysaccharides, 0301 basic medicine, MAP Kinase Kinase 4/immunology, MAP Kinase Kinase 4, Interleukin-1beta, Nod2 Signaling Adaptor Protein, Inbred C57BL, Mitogen-Activated Protein Kinase 3/immunology, Toll-Like Receptors/genetics, Mice, Macrophages/drug effects, Nod1 Signaling Adaptor Protein, Mitogen-Activated Protein Kinase 1/genetics, Interleukin-6/genetics, Mice, Knockout, Mitogen-Activated Protein Kinase 1, Nod2 Signaling Adaptor Protein/immunology, 0303 health sciences, Mitogen-Activated Protein Kinase 3, Macrophages/immunology, NF-kappa B/genetics, Toll-Like Receptors, p38 Mitogen-Activated Protein Kinases/genetics, NF-kappa B, Nod1 Signaling Adaptor Protein/deficiency, 3. Good health, Nod2 Signaling Adaptor Protein/genetics, Nod2 Signaling Adaptor Protein/deficiency, Cytokines, Interleukin-1beta/genetics, Signal Transduction, Nod1, Interleukin-1beta/immunology, Macrophages/pathology, Knockout, Primary Cell Culture, Nod1 Signaling Adaptor Protein/genetics, MAP Kinase Kinase 4/genetics, 03 medical and health sciences, Animals, Toll-Like Receptors/immunology, NF-kappa B/immunology, p38 Mitogen-Activated Protein Kinases/immunology, Nod1 Signaling Adaptor Protein/immunology, Mitogen-Activated Protein Kinase 3/genetics, Interleukin-6, Tumor Necrosis Factor-alpha, Macrophages, Mitogen-Activated Protein Kinase 1/immunology, Mycobacterium tuberculosis, Lipopolysaccharides/pharmacology, Tumor Necrosis Factor-alpha/immunology, Mycobacterium tuberculosis/immunology, Mice, Inbred C57BL, Gene Expression Regulation, Tumor Necrosis Factor-alpha/genetics, Interleukin-6/immunology
Dateibeschreibung: 70~75
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/26255090
https://www.sciencedirect.com/science/article/pii/S0171298515300395
http://www.sciencedirect.com/science/article/pii/S0171298515300395
http://europepmc.org/abstract/MED/26255090
https://yonsei.pure.elsevier.com/en/publications/the-role-of-nucleotide-binding-oligomerization-domain-1-during-cy
https://ir.ymlib.yonsei.ac.kr/handle/22282913/145528
https://www.ncbi.nlm.nih.gov/pubmed/26255090 -
8
Autoren: et al.
Weitere Verfasser: et al.
Quelle: JCI Insight. 10
Schlagwörter: 0301 basic medicine, mice, Fatty Liver, Alcoholic/etiology, Binge Drinking/complications, Inflammation/etiology, Extracellular Vesicles/drug effects, Toxicology, MAP Kinase Kinase Kinase 5, DNA, Mitochondrial, p38 Mitogen-Activated Protein Kinases, DNA, Mitochondrial/genetics, MAP Kinase Kinase Kinase 5/genetics, Binge Drinking, Extracellular Vesicles, Mice, 03 medical and health sciences, Liver/drug effects, Fatty liver, Signal Transduction/drug effects, Matrix Metalloproteinase 14, Animals, Humans, Inflammation, Hepatology, p38 Mitogen-Activated Protein Kinases/genetics, 3. Good health, Alcoholism, Disease Models, Animal, Metallothionein/genetics, Liver, Alcohols, Alcoholism/complications, Matrix Metalloproteinase 14/genetics, Hepatocytes, Alcohols/toxicity, Metallothionein, Hepatocytes/drug effects, Fatty Liver, Alcoholic, Signal Transduction
Dateibeschreibung: application/pdf
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9
Autoren: et al.
Schlagwörter: HSJ ANPAT, Adult, Aged, Female, Humans, Breast Neoplasms / enzymology, Middle Aged, Breast Neoplasms / pathology, Carcinoma, Ductal, Breast / enzymology, Breast / pathology, Cell Adhesion / drug effects, Cell Line, Tumor, Cell Proliferation / drug effects, E-Selectin / genetics, E-Selectin / metabolism, Fucose / analogs & derivatives, Fucose / pharmacology, Fucosyltransferases / antagonists & inhibitors, Ligands, MAP Kinase Signaling System / drug effects, Neoplasm Invasiveness, Oligosaccharides / metabolism, Primary Cell Culture, Sialyl Lewis X Antigen, p38 Mitogen-Activated Protein Kinases / genetics, p38 Mitogen-Activated Protein Kinases / metabolism
Dateibeschreibung: application/pdf
Relation: https://hdl.handle.net/10400.17/3949
Verfügbarkeit: https://hdl.handle.net/10400.17/3949
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10
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Kopper, F, Bierwirth, C, Schon, M, Kunze, M, Elvers, I, Kranz, D, Saini, P, Menon, M B, Walter, D, Sorensen, C S, Gaestel, M, Helleday, T, Schon, M P & Dobbelstein, M 2013, ' Damage-induced DNA replication stalling relies on MAPK-activated protein kinase 2 activity ', Proceedings of the National Academy of Sciences of the United States of America, vol. 110, no. 42, pp. 16856-16861 . https://doi.org/10.1073/pnas.1304355110
Schlagwörter: DNA Replication, 0301 basic medicine, Antimetabolites, Antineoplastic, CYCLE CHECKPOINT KINASE VERTEBRATE S-PHASE HUMAN-CELLS H2AX PHOSPHORYLATION RNA STABILIZATION FORK PROGRESSION POLYMERASE-ETA CHK1 STRESS ORIGINS, Antimetabolites, MAP Kinase Signaling System, Ultraviolet Rays, Protein-Serine-Threonine Kinases/genetics, Knockout, DNA, Single-Stranded, Protein Kinases/genetics, Protein Serine-Threonine Kinases, Deoxycytidine, p38 Mitogen-Activated Protein Kinases, Cell Line, Histones, Mice, 03 medical and health sciences, Antimetabolites, Antineoplastic/pharmacology, Deoxycytidine/analogs & derivatives, Single-Stranded, Cell Line, Tumor, Animals, Humans, Mice, Knockout, Antineoplastic/pharmacology, Histones/genetics, Tumor, DNA, Single-Stranded/genetics, p38 Mitogen-Activated Protein Kinases/genetics, Intracellular Signaling Peptides and Proteins, Single-Stranded/genetics, DNA, Protein-Serine-Threonine Kinases, Antineoplastic, G2 Phase Cell Cycle Checkpoints, Gene Knockdown Techniques, Checkpoint Kinase 1, Intracellular Signaling Peptides and Proteins/genetics, Protein Kinases, DNA Damage
Zugangs-URL: https://www.pnas.org/content/pnas/110/42/16856.full.pdf
https://pubmed.ncbi.nlm.nih.gov/24082115
http://www.diva-portal.org/smash/record.jsf?pid=diva2:664200
https://pubmed.ncbi.nlm.nih.gov/24082115/
https://core.ac.uk/display/50697802
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3801042
https://www.pnas.org/content/pnas/110/42/16856.full.pdf
https://europepmc.org/abstract/MED/24082115
https://resolver.sub.uni-goettingen.de/purl?gro-2/28446
https://portal.findresearcher.sdu.dk/da/publications/50103075-0ecf-4e12-a8b6-53d5e2ff50a9 -
11
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Journal of Biological Chemistry. 288:11378-11383
Schlagwörter: 0301 basic medicine, Inflammasomes, MAP Kinase Signaling System, Signal Transducing/genetics, Microtubules/genetics, p38, Cytoskeletal Proteins/genetics, Ribotoxic Stress, Stress, Tubulin Modulators/pharmacology, Microtubules, p38 Mitogen-Activated Protein Kinases, Colchicine/pharmacology, Inflammasome, Cell Line, Caspase 1/metabolism, 03 medical and health sciences, Stress, Physiological, Humans, Inflammasomes/metabolism, Adaptor Proteins, Signal Transducing, Inflammation, p38 Mitogen-Activated Protein Kinases/metabolism, 0303 health sciences, MAP Kinase Signaling System/drug effects, Signal Transducing/metabolism, Caspase 1, Cytoskeletal Proteins/metabolism, p38 Mitogen-Activated Protein Kinases/genetics, Adaptor Proteins, Pyrin, Caspase 1/genetics, Tubulin Modulators, Familial Mediterranean Fever, Physiological/drug effects, Cytoskeletal Proteins, Inflammasomes/genetics, Microtubules/metabolism, Caspase-1, Mutation, Physiological/physiology, MAP Kinases (MAPKs), Colchicine, Ribosomes, MAP Kinase Signaling System/physiology
Zugangs-URL: http://www.jbc.org/content/288/16/11378.full.pdf
https://pubmed.ncbi.nlm.nih.gov/23479736
https://pubmed.ncbi.nlm.nih.gov/23479736/
http://europepmc.org/articles/PMC3630843
https://www.jbc.org/article/S0021-9258(20)67214-3/fulltext
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630843/
http://www.jbc.org/content/288/16/11378.full
https://www.sciencedirect.com/science/article/pii/S0021925820672143 -
12
Autoren: et al.
Quelle: Ann Rheum Dis
De Launay, D, Van De Sande, M G H, De Hair, M J H, Grabiec, A M, Van De Sande, G P M, Lehmann, K A, Wijbrandts, C A, Van Baarsen, L G M, Gerlag, D M, Tak, P P & Reedquist, K A 2012, 'Selective involvement of ERK and JNK mitogen-activated protein kinases in early rheumatoid arthritis (1987 ACR criteria compared to 2010 ACR/EULAR criteria): A prospective study aimed at identification of diagnostic and prognostic biomarkers as well as therapeutic targets', Annals of the rheumatic diseases, vol. 71, no. 3, pp. 415-423. https://doi.org/10.1136/ard.2010.143529Schlagwörter: Enzymologic, Male, Rheumatoid: diagnosis, Messenger, Severity of Illness Index, p38 Mitogen-Activated Protein Kinases, Arthritis, Rheumatoid, 0302 clinical medicine, Rheumatoid, 80 and over, Molecular Targeted Therapy, Prospective Studies, Phosphorylation, Extracellular Signal-Regulated MAP Kinases, Basic and Translational Research, Aged, 80 and over, Synovial Membrane: enzymology, Synovial Membrane, p38 Mitogen-Activated Protein Kinases: genetics, Middle Aged, Prognosis, Rheumatoid: genetics, 3. Good health, Disease Progression, Biological Markers, Female, Adult, Extracellular Signal-Regulated MAP Kinases: geneti, Messenger: genetics, Extracellular Signal-Regulated MAP Kinases: metabo, Gene Expression Regulation, Enzymologic, JNK Mitogen-Activated Protein Kinases: genetics, Young Adult, 03 medical and health sciences, Biological Markers: metabolism, Rheumatoid: enzymology, p38 Mitogen-Activated Protein Kinases: metabolism, Humans, JNK Mitogen-Activated Protein Kinases: metabolism, Aged, Arthritis, Gene Expression Profiling, JNK Mitogen-Activated Protein Kinases, Gene Expression Profiling: methods, Molecular Targeted Therapy: methods, Enzyme Activation, Early Diagnosis, Gene Expression Regulation, RNA, Biomarkers
Zugangs-URL: https://ard.bmj.com/content/71/3/415.full.pdf
https://pubmed.ncbi.nlm.nih.gov/21953337
https://pubmed.ncbi.nlm.nih.gov/21953337/
http://dare.uva.nl/document/2/101214
https://www.narcis.nl/publication/RecordID/oai%3Apure.amc.nl%3Apublications%2F8c9025ca-6a8e-4502-8d55-627aea6b67c2
https://ard.bmj.com/content/71/3/415.full.pdf
https://ard.bmj.com/content/71/3/415
https://www.research.manchester.ac.uk/portal/en/publications/selective-involvement-of-erk-and-jnk-mitogenactivated-protein -kinases -in-early-rheumatoid-arthritis-1987-acr-criteria-compared-to-2010-acreular-criteria-a-prospective-study-aimed-at-identification-of-diagnostic-and-prognostic-biomarkers-as-well-as-therapeutic-targets(759352b6-09bf-4fba-847f-cd50eb5c2ec7).html -
13
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Toxicology in Vitro. 25:1359-1365
Schlagwörter: 0301 basic medicine, Carmustine/pharmacology, p38 Mitogen-Activated Protein Kinases/metabolism, MAP Kinase Kinase 4, Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors, Glutathione Reductase/antagonists & inhibitors, Antineoplastic Agents, Acetylcysteine/pharmacology, Reactive Oxygen Species/metabolism, PC12 Cells, p38 Mitogen-Activated Protein Kinases, MAP Kinase Kinase 4/genetics, Neurons/cytology, 03 medical and health sciences, MAP Kinase Kinase 4/metabolism, Cell Death/drug effects, MAP Kinase Kinase 4/antagonists & inhibitors, Animals, Phosphorylation, Extracellular Signal-Regulated MAP Kinases, Antineoplastic Agents, Alkylating, Neurons, 0303 health sciences, Cell Death, Caspase 3, Neurons/drug effects, p38 Mitogen-Activated Protein Kinases/genetics, Extracellular Signal-Regulated MAP Kinases/metabolism, Alkylating/pharmacology, Extracellular Signal-Regulated MAP Kinases/genetics, Carmustine, Acetylcysteine, Rats, 3. Good health, Enzyme Activation, ERK, Glutathione Reductase, JNK, Reactive oxygen species, Reactive Oxygen Species, Caspase 3/metabolism
Dateibeschreibung: 1359~1365
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/21600974
https://yonsei.pure.elsevier.com/en/publications/carmustine-induces-erk-and-jnk-dependent-cell-death-of-neuronally
https://www.ncbi.nlm.nih.gov/pubmed/21600974
https://www.sciencedirect.com/science/article/pii/S0887233311001317
https://pubmed.ncbi.nlm.nih.gov/21600974/ -
14
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Cancer Science. 102:784-791
Schlagwörter: 0301 basic medicine, Nuclear Proteins/physiology, p38 Mitogen-Activated Protein Kinases/metabolism, Mutation/genetics, Knockout, Blotting, Western, Inbred C57BL, Proto-Oncogene Proteins c-myc/metabolism, Proto-Oncogene Proteins c-myc, Mice, 03 medical and health sciences, Hematopoietic Stem Cells/physiology, Animals, Myeloproliferative Disorders/metabolism, RNA, Messenger, Tumor Suppressor Protein p53/metabolism, Myeloproliferative Disorders/pathology, Mice, Knockout, 0303 health sciences, Myeloproliferative Disorders, Blotting, Reverse Transcriptase Polymerase Chain Reaction, Blast Crisis/etiology, GTPase-Activating Proteins/physiology, rap1 GTP-Binding Proteins/genetics, rap1 GTP-Binding Proteins/metabolism, GTPase-Activating Proteins, p38 Mitogen-Activated Protein Kinases/genetics, Nuclear Proteins, Flow Cytometry, Hematopoietic Stem Cells, Hematopoiesis, Mice, Inbred C57BL, Survival Rate, Blast Crisis/metabolism, Gamma Rays, Blast Crisis/pathology, Mutation, RNA, Messenger/genetics, Tumor Suppressor Protein p53/genetics, Myeloproliferative Disorders/etiology, Proto-Oncogene Proteins c-myc/genetics, Blast Crisis, Western, Whole-Body Irradiation, DNA Damage, Signal Transduction
Dateibeschreibung: application/pdf
Zugangs-URL: https://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/142075/1/yigak03551.pdf
https://pubmed.ncbi.nlm.nih.gov/21205094
http://ci.nii.ac.jp/naid/10029292347
https://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/142075/1/yigak03551.pdf
http://onlinelibrary.wiley.com/doi/10.1111/j.1349-7006.2011.01850.x/abstract
http://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/142075
https://www.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1349-7006.2011.01850.x
https://www.ncbi.nlm.nih.gov/pubmed/21205094 -
15
Autoren: et al.
Quelle: J Biol Chem
The Journal of biological chemistry, 285 (51Schlagwörter: 0301 basic medicine, Signal Transduction -- drug effects -- physiology, Enzymologic -- drug effects -- genetics, Mice, Enzyme Activation -- drug effects -- genetics, Phosphorylation, Cells, Cultured, Mice, Knockout, 0303 health sciences, Cultured, Membrane Glycoproteins, Mitogen-Activated Protein Kinase 3, Pyrimidines -- pharmacology, Angiotensin II, Membrane Glycoproteins -- genetics -- metabolism, Mitogen-Activated Protein Kinase 3 -- genetics -- metabolism, Adenosine A2 Receptor Antagonists, 3. Good health, p38 Mitogen-Activated Protein Kinases -- genetics -- metabolism, Phosphorylation -- drug effects -- genetics, NADPH Oxidase 2, Receptor, Signal Transduction, Receptor, Adenosine A2A, Cells, Knockout, Adenosine A2A -- genetics -- metabolism, Angiotensin II -- metabolism -- pharmacology, Adenosine A2 Receptor Antagonists -- pharmacology, Reactive Oxygen Species -- metabolism, Gene Expression Regulation, Enzymologic, 03 medical and health sciences, Animals, Gene Expression Regulation, Enzymologic -- drug effects -- genetics, Proto-Oncogene Proteins c-akt -- genetics -- metabolism, Endothelial Cells, NADPH Oxidases, Cell Biology, Triazoles, Receptor, Adenosine A2A -- genetics -- metabolism, Sciences biomédicales, Enzyme Activation, Pyrimidines, Gene Expression Regulation, Triazoles -- pharmacology, Reactive Oxygen Species, NADPH Oxidase -- biosynthesis -- genetics -- metabolism, Proto-Oncogene Proteins c-akt, Endothelial Cells -- metabolism
Dateibeschreibung: 1 full-text file(s): application/pdf; text
Zugangs-URL: http://www.jbc.org/content/285/51/40104.full.pdf
https://pubmed.ncbi.nlm.nih.gov/20940302
http://www.jbc.org/content/early/2010/10/12/jbc.M110.184606?M110.184606v1
http://europepmc.org/articles/PMC3000993
https://www.jbc.org/content/285/51/40104.full
https://www.sciencedirect.com/science/article/pii/S0021925820605427
https://pubmed.ncbi.nlm.nih.gov/20940302/
https://epubs.surrey.ac.uk/205737/1/40104.full.pdf
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/124818
https://surrey.eprints-hosting.org/205737/ -
16
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Cellular Immunology. 253:81-91
Schlagwörter: T-Lymphocytes/physiology, 0301 basic medicine, Vibrio vulnificus/pathogenicity, T-Lymphocytes, Nitric Oxide Synthase Type II, Reactive Oxygen Species/metabolism, Nitric Oxide, p38 Mitogen-Activated Protein Kinases, Jurkat Cells, 03 medical and health sciences, Onium Compounds, Mitogen-Activated Protein Kinase 1/metabolism, Mitogen-Activated Protein Kinase 1/genetics, Animals, Humans, Enzyme Inhibitors, Mitogen-activated protein kinases, Vibrio vulnificus, Mitogen-Activated Protein Kinase 1, p38 Mitogen-Activated Protein Kinases/metabolism, 0303 health sciences, Mitogen-Activated Protein Kinase 3, Cell Death, Mitogen-Activated Protein Kinase 3/genetics, NADPH Oxidases/metabolism, T-Lymphocytes/microbiology, p38 Mitogen-Activated Protein Kinases/genetics, NADPH Oxidases, Enzyme Inhibitors/metabolism, Mitogen-Activated Protein Kinase 3/metabolism, Onium Compounds/metabolism, Jurkat T-cells, Enzyme Activation, Nitric Oxide/metabolism, RNA Interference, T-Lymphocytes/enzymology, Reactive oxygen species, Reactive Oxygen Species, Nitric Oxide Synthase Type II/metabolism
Dateibeschreibung: 81~91
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/18571150
https://ir.ymlib.yonsei.ac.kr/handle/22282913/108280
https://pubmed.ncbi.nlm.nih.gov/18571150/
https://www.sciencedirect.com/science/article/pii/S0008874908000877
https://www.ncbi.nlm.nih.gov/pubmed/18571150
http://www.sciencedirect.com/science/article/pii/S0008874908000877
https://europepmc.org/abstract/MED/18571150 -
17
Autoren: et al.
Quelle: Journal of Biological Chemistry. 280:6923-6932
Schlagwörter: 0301 basic medicine, Protein Structure, Biochimie, GTPase-Activating Proteins -- metabolism, Transfection, p38 Mitogen-Activated Protein Kinases, Cell Line, Mice, 03 medical and health sciences, NF-kappa B -- metabolism, Site-Directed, Animals, Humans, TNF Receptor-Associated Factor 2 -- metabolism, TNF Receptor-Associated Factor 1 -- metabolism, 0303 health sciences, Caspases -- genetics -- metabolism -- physiology, GTPase-Activating Proteins, Caspase 2, NF-kappa B, Biologie moléculaire, TNF Receptor-Associated Factor 2, TNF Receptor-Associated Factor 1, Protein Structure, Tertiary, p38 Mitogen-Activated Protein Kinases -- genetics -- metabolism, Mutagenesis, Caspases, Multiprotein Complexes, Mutagenesis, Site-Directed, Biologie cellulaire, Tertiary
Dateibeschreibung: 2 full-text file(s): application/pdf; application/pdf
Zugangs-URL: http://www.jbc.org/content/280/8/6923.full.pdf
https://pubmed.ncbi.nlm.nih.gov/15590671
http://www.jbc.org/content/280/8/6923.full
https://europepmc.org/abstract/MED/15590671
https://biblio.ugent.be/publication/300573
https://www.sciencedirect.com/science/article/pii/S0021925819628097
https://difusion.ulb.ac.be/vufind/Record/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/230671/Details
https://www.ncbi.nlm.nih.gov/pubmed/15590671 -
18
Autoren: et al.
Quelle: Int J Oncol
Schlagwörter: Lung Neoplasms, Heme oxygenase-1 - biosynthesis, Protoporphyrins, p38 Mitogen-Activated Protein Kinases, Mice, Cell Movement, Follicle stimulating hormone - administration & dosage, Luteinizing hormone - administration & dosage, Animals, Humans, Pituitary gland - metabolism, Heme oxygenase-1 - antagonists & inhibitors, Heme oxygenase-1 - genetics, Cell Proliferation, Gene expression regulation, Lung neoplasms - drug therapy, Protoporphyrins - administration & dosage, Chemotaxis, Prolactin - metabolism, neoplastic - drug effects, Cell movement - drug effects, Lung neoplasms - genetics, Articles, Luteinizing Hormone, Luteinizing hormone - metabolism, p38 mitogen-activated protein kinases - genetics, Prolactin, 3. Good health, Gene Expression Regulation, Neoplastic, Chemotaxis - drug effects, Cell proliferation - drug effects, Pituitary Gland, Lung neoplasms - pathology, Follicle stimulating hormone - metabolism, Prolactin - administration & dosage, Follicle Stimulating Hormone, Corrigendum, Heme Oxygenase-1
Zugangs-URL: https://www.spandidos-publications.com/10.3892/ijo.2019.4670/download
https://www.spandidos-publications.com/10.3892/ijo.2016.3787/download
https://pubmed.ncbi.nlm.nih.gov/30628648
https://pubmed.ncbi.nlm.nih.gov/27922667
https://www.spandidos-publications.com/10.3892/ijo.2016.3787/download
https://www.spandidos-publications.com/10.3892/ijo.2016.3787
https://europepmc.org/article/PMC/PMC6365021
https://www.spandidospublications.org/ijo/54/3/1134
http://www.ncbi.nlm.nih.gov/pubmed/27922667
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5182010
https://www.spandidospublications.info/ijo/54/3/1134/abstract
https://www.spandidos-publications.com/10.3892/ijo.2019.4670/download -
19
Weitere Verfasser: et al.
Quelle: T201304061.pdf
Schlagwörter: Animals, Cell Death, Infarction, Middle Cerebral Artery/metabolism, Lipopolysaccharides/pharmacology, MAP Kinase Kinase Kinase 5/genetics, MAP Kinase Kinase Kinase 5/metabolism, Male, Mice, Inbred C57BL, Microtubule-Associated Proteins/genetics, Microtubule-Associated Proteins/metabolism, Neural Stem Cells/cytology, Neural Stem Cells/drug effects, Neural Stem Cells/metabolism, Neurogenesis, Neuropeptides/genetics, Neuropeptides/metabolism, p38 Mitogen-Activated Protein Kinases/genetics, p38 Mitogen-Activated Protein Kinases/metabolism
Relation: EXPERIMENTAL AND MOLECULAR MEDICINE; J00860; https://ir.ymlib.yonsei.ac.kr/handle/22282913/88489; T201304061; EXPERIMENTAL AND MOLECULAR MEDICINE, Vol.45(12) : 69, 2013; 34060
-
20
Weitere Verfasser: et al.
Schlagwörter: Animals, Colon/cytology, Colon/immunology, Colon/parasitology, Enzyme Activation, Giardia lamblia/genetics, Giardia lamblia/growth & development, Giardia lamblia/metabolism, Giardia lamblia/pathogenicity, HT29 Cells, Humans, Interleukin-8/biosynthesis, Mitogen-Activated Protein Kinase 1/genetics, Mitogen-Activated Protein Kinase 1/metabolism, Mitogen-Activated Protein Kinase 3/genetics, Mitogen-Activated Protein Kinase 3/metabolism, NF-kappa B/genetics, NF-kappa B/metabolism, Protozoan Proteins/genetics, Protozoan Proteins/immunology, Protozoan Proteins/metabolism, Signal Transduction, Transcription Factor AP-1/genetics, Transcription Factor AP-1/metabolism, p38 Mitogen-Activated Protein Kinases/genetics, p38 Mitogen-Activated Protein Kinases/metabolism, excretory–secretory product, Giardia lamblia, HT-29 cells, mitogen-activated protein kinase
Dateibeschreibung: 183~198
Relation: PARASITE IMMUNOLOGY; J02466; https://ir.ymlib.yonsei.ac.kr/handle/22282913/91637; T201205323; 29525
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