يعرض 1 - 10 نتائج من 39 نتيجة بحث عن '"Hydroxamic Acids: pharmacology"', وقت الاستعلام: 1.15s تنقيح النتائج
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    رسالة جامعية
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    المساهمون: UMR - Interactions Plantes Microorganismes Environnement (UMR IPME), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Université de Montpellier (UM)-Institut de Recherche pour le Développement (IRD [France-Sud]), Département Systèmes Biologiques (Cirad-BIOS), Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)

    المصدر: Scientific Reports
    Scientific Reports, Nature Publishing Group, 2020, 10 (1), pp.810. ⟨10.1038/s41598-020-57800-6⟩
    Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
    Scientific Reports, 2020, 10 (1), pp.810. ⟨10.1038/s41598-020-57800-6⟩

    وصف الملف: text

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    المساهمون: Romier, Christophe, Martin-Luther-Universität Halle Wittenberg (MLU), Albert-Ludwigs-Universität Freiburg, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 (CIIL), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Centre National de la Recherche Scientifique (CNRS), This work and the authors of this article received funding from the European Union’s Seventh Framework Programme for Research, Technological Development and Demonstration under Grant Agreements 241865 (SEtTReND) and 602080 (A-ParaDDisE). Further support was received by the Deutsche Forschungsgemeinschaft (Ju-295/13-1, SI-868/13-1). MM, TBS and CR are supported by institutional funds from the Centre National de la Recherche Scientifique (CNRS), the Institut National de la Santé et de la Recherche Médicale (INSERM) and the Université de Strasbourg., The authors acknowledge the support and the use of resources of the French Infrastructure for Integrated Structural Biology FRISBI ANR-10-INBS-05 and of Instruct-ERIC. We wish to thank members of the ESRF-EMBL joint structural biology groups and the SOLEIL synchrotron for the use of their beamline facilities and for help during data collection. We are grateful to Pierre Legrand (SOLEIL) for his kind assistance for data processing, Centre National de la Recherche Scientifique (CNRS)-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille)-Université de Lille-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)

    المصدر: Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
    Molecules
    Molecules, 2018, 23 (3), pp.566. ⟨10.3390/molecules23030566⟩
    Molecules, Vol 23, Iss 3, p 566 (2018)
    Molecules; Volume 23; Issue 3; Pages: 566
    Molecules, MDPI, 2018, 23 (3), pp.566. ⟨10.3390/molecules23030566⟩

    مصطلحات موضوعية: 0301 basic medicine, Pyrrolidines, MESH: Helminth Proteins/metabolism, MESH: Histone Deacetylases/metabolism, MESH: Histone Deacetylases/genetics, Pharmaceutical Science, MESH: Protein Structure, Secondary, Gene Expression, Apoptosis, Crystallography, X-Ray, Hydroxamic Acids, Molecular Docking Simulation, MESH: Helminth Proteins/antagonists & inhibitors, MESH: Chelating Agents/chemical synthesis, Protein Structure, Secondary, Analytical Chemistry, 0302 clinical medicine, MESH: Structure-Activity Relationship, MESH: Hydroxamic Acids/chemical synthesis, Drug Discovery, MESH: Zinc/metabolism, MESH: Animals, [SDV.BBM.BC] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], MESH: Histone Deacetylase Inhibitors/pharmacology, Chelating Agents, Anthelmintics, biology, Chemistry, MESH: Anthelmintics/pharmacology, Helminth Proteins, Schistosoma mansoni, epigenetics, crystal structure, docking, histone deacetylase (HDAC) inhibitors, schistosomiasis, virtual screening, MESH: Histone Deacetylases/chemistry, 3. Good health, MESH: Schistosoma mansoni/drug effects, MESH: Pyrrolidines/pharmacology, Zinc, Biochemistry, Chemistry (miscellaneous), Molecular Medicine, Protein Binding, MESH: Apoptosis/drug effects, MESH: Gene Expression, In silico, 030231 tropical medicine, MESH: Zinc/chemistry, Article, Histone Deacetylases, lcsh:QD241-441, 03 medical and health sciences, Structure-Activity Relationship, lcsh:Organic chemistry, MESH: Molecular Docking Simulation, Structure–activity relationship, MESH: Protein Binding, Animals, MESH: Helminth Proteins/genetics, Protein Interaction Domains and Motifs, Physical and Theoretical Chemistry, MESH: Histone Deacetylase Inhibitors/chemical synthesis, [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biochemistry [q-bio.BM], Virtual screening, MESH: Protein Interaction Domains and Motifs, Binding Sites, Organic Chemistry, MESH: Hydroxamic Acids/pharmacology, HDAC8, MESH: Schistosoma mansoni/growth & development, Epigenome, biology.organism_classification, MESH: Crystallography, X-Ray, MESH: Anthelmintics/chemical synthesis, Histone Deacetylase Inhibitors, 030104 developmental biology, MESH: Binding Sites, Docking (molecular), MESH: Chelating Agents/pharmacology, MESH: Schistosoma mansoni/enzymology, MESH: Helminth Proteins/chemistry, MESH: Schistosoma mansoni/genetics, MESH: Pyrrolidines/chemical synthesis

    وصف الملف: application/pdf

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    المساهمون: School of Pharmaceutical Sciences, University of Geneva [Switzerland]-Université de Lausanne (UNIL), Environnements et Paléoenvironnements OCéaniques (EPOC), Observatoire aquitain des sciences de l'univers (OASU), Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Sciences et Technologies - Bordeaux 1-Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Centre National de la Recherche Scientifique (CNRS), Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), Institut national des sciences de l'Univers (INSU - CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Poitiers-Institut de Chimie du CNRS (INC), Université de Lausanne (UNIL)-University of Geneva [Switzerland]

    المصدر: Expert Opinion on Therapeutic Patents
    Expert Opinion on Therapeutic Patents, Informa Healthcare, 2017, 27 (3), pp.229-236. ⟨10.1080/13543776.2017.1282945⟩
    Expert Opinion on Therapeutic Patents, Vol. 27, No 3 (2017) pp. 229-236

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    المصدر: Ali, D, Hamam, R, Alfayez, M, Kassem, M, Aldahmash, A & Alajez, N M 2016, ' Epigenetic Library Screen Identifies Abexinostat as Novel Regulator of Adipocytic and Osteoblastic Differentiation of Human Skeletal (Mesenchymal) Stem Cells ', Stem Cells Translational Medicine, vol. 5, no. 8, pp. 1036-1047 . https://doi.org/10.5966/sctm.2015-0331
    Stem Cells Translational Medicine, Vol 5, Iss 8, Pp 1036-1047 (2016)

    مصطلحات موضوعية: 0301 basic medicine, Epigenetic regulation of neurogenesis, Hydroxamic Acids, Epigenesis, Genetic, Myoblasts, Skeletal/drug effects, 0302 clinical medicine, Adipogenesis/drug effects, Osteogenesis, Histone deacetylase inhibitors, Signal Transduction/drug effects, Adipocytes, Oligonucleotide Array Sequence Analysis, lcsh:R5-920, Adipocyte, Adipogenesis, lcsh:Cytology, Osteoblast, Wnt signaling pathway, Epigenetic, Gene Expression Regulation, Developmental, Cell Differentiation, General Medicine, Benzofurans/pharmacology, Cell biology, Osteogenesis/drug effects, Mesenchymal Stem Cells/drug effects, Phenotype, 030220 oncology & carcinogenesis, Stem cell, lcsh:Medicine (General), Signal Transduction, Chromatin Immunoprecipitation, Genotype, Myoblasts, Skeletal, Transcription Factors/genetics, Biology, Epigenesis, Genetic/drug effects, Cell Line, 03 medical and health sciences, Osteoblasts/drug effects, Humans, Cell Lineage, Epigenetics, lcsh:QH573-671, Transcription factor, Benzofurans, Gene Library, Osteoblasts, Gene Expression Profiling, Mesenchymal stem cell, Computational Biology, Mesenchymal Stem Cells, Cell Biology, Cell-Based Drug Development, Screening, and Toxicology, equipment and supplies, Molecular biology, Histone Deacetylase Inhibitors, 030104 developmental biology, Cell Differentiation/drug effects, Mesenchymal stem cells, Histone deacetylase, Gene Expression Profiling/methods, Chromatin immunoprecipitation, Histone Deacetylase Inhibitors/pharmacology, Developmental Biology, Adipocytes/drug effects, Hydroxamic Acids/pharmacology, Transcription Factors

    وصف الملف: application/pdf

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