يعرض 1 - 10 نتائج من 25 نتيجة بحث عن '"Mutant Proteins genetics"', وقت الاستعلام: 1.93s تنقيح النتائج
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    المصدر: International Journal of Molecular Sciences, Vol 21, Iss 8021, p 8021 (2020)
    International Journal of Molecular Sciences
    International journal of molecular sciences, vol. 21, no. 21, pp. E8021
    Volume 21
    Issue 21

    مصطلحات موضوعية: Models, Molecular, Uveal Neoplasms, Protein Conformation, Sequence Homology, medicine.disease_cause, lcsh:Chemistry, Melanoma, lcsh:QH301-705.5, Spectroscopy, Trametinib, Mutation, biology, Chemistry, Protein Stability, MEK inhibitor, General Medicine, Middle Aged, Computer Science Applications, molecular modelling, Gq alpha subunit, precision oncology, Female, Amino Acid Sequence, Antineoplastic Agents/therapeutic use, GTP-Binding Protein alpha Subunits, Gq-G11/chemistry, GTP-Binding Protein alpha Subunits, Gq-G11/genetics, GTP-Binding Protein alpha Subunits, Gq-G11/metabolism, Humans, Melanoma/drug therapy, Melanoma/genetics, Melanoma/metabolism, Melanoma/pathology, Mutant Proteins/chemistry, Mutant Proteins/genetics, Mutant Proteins/metabolism, Pyridones/therapeutic use, Pyrimidinones/therapeutic use, Receptor, Fibroblast Growth Factor, Type 4/chemistry, Receptor, Fibroblast Growth Factor, Type 4/genetics, Receptor, Fibroblast Growth Factor, Type 4/metabolism, Signal Transduction, Uveal Neoplasms/drug therapy, Uveal Neoplasms/genetics, Uveal Neoplasms/metabolism, Uveal Neoplasms/pathology, FGFR4, GNAQ, mutation, Pyridones, Antineoplastic Agents, Pyrimidinones, Catalysis, Article, Inorganic Chemistry, medicine, Receptor, Fibroblast Growth Factor, Type 4, Physical and Theoretical Chemistry, Molecular Biology, Organic Chemistry, Fibroblast growth factor receptor 4, medicine.disease, lcsh:Biology (General), lcsh:QD1-999, Personalized oncology, Cancer research, biology.protein, GTP-Binding Protein alpha Subunits, Gq-G11, Mutant Proteins

    وصف الملف: application/pdf

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    المساهمون: Laboratoire Physico-Chimie Curie [Institut Curie] (PCC), Institut Curie [Paris]-Institut de Chimie du CNRS (INC)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Compartimentation et dynamique cellulaires (CDC), Institut Curie [Paris]-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Helsingin yliopisto = Helsingfors universitet = University of Helsinki, Toxines bactériennes - Bacterial Toxins, Institut Pasteur [Paris] (IP), Institut de pharmacologie moléculaire et cellulaire (IPMC), Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA), Université Paris Descartes - Paris 5 (UPD5), Institut de Recherche en Infectiologie de Montpellier (IRIM), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), This work was supported by Institut Curie, Centre National de la Recherche Scientifique (CNRS), the Agence Nationale pour la Recherche (grant ANR-15-CE18-0016 to F-CT, M-CT, EL and PB), the Investments for the Future’ LABEX SIGNALIFE (grant ANR-11-LABX-0028–01 for M-CT and EL), the European Research Council (EC and PB partners of the advanced grant, project 339847) and the Human Frontier Science Program Organization (RGP0005/2016 to YS, PL, F-CT, EC and PB). EC and PB groups belong to the CNRS consortium CellTiss, to the Labex CelTisPhyBio (ANR-11-LABX0038) and to Paris Sciences et Lettres (ANR-10-IDEX-0001–02). F-C Tsai was funded by the EMBO Long-Term fellowship (ALTF 1527–2014) and Marie Curie actions (H2020-MSCA-IF-2014, project membrane-ezrin-actin)., ANR-15-CE18-0016,TransEndotheliaTunnel,Vers la prévention de dysfonctions vasculaires et la délivrance de médicaments au travers des endothelia(2015), ANR-11-LABX-0028,SIGNALIFE,Réseau d'Innovation sur les Voies de Signalisation en Sciences de la Vie(2011), ANR-10-IDEX-0001,PSL,Paris Sciences et Lettres(2010), European Project: 339847,EC:FP7:ERC,ERC-2013-ADG,MYODYN(2014), European Project: 656442,H2020,H2020-MSCA-IF-2014,membrane-ezrin-actin(2016), Institute of Biotechnology, Doctoral Programme in Integrative Life Science, Pekka Lappalainen / Principal Investigator, University Management, University of Helsinki, Institut Pasteur [Paris], Centre National de la Recherche Scientifique (CNRS)-Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Université Côte d'Azur (UCA), Picas, Laura, Vers la prévention de dysfonctions vasculaires et la délivrance de médicaments au travers des endothelia - - TransEndotheliaTunnel2015 - ANR-15-CE18-0016 - AAPG2015 - VALID, Centres d'excellences - Réseau d'Innovation sur les Voies de Signalisation en Sciences de la Vie - - SIGNALIFE2011 - ANR-11-LABX-0028 - LABX - VALID, Initiative d'excellence - Paris Sciences et Lettres - - PSL2010 - ANR-10-IDEX-0001 - IDEX - VALID, Myosins and the dynamics of intracellular membranes - MYODYN - - EC:FP7:ERC2014-02-01 - 2019-01-31 - 339847 - VALID, Membrane-ezrin-actin interactions mediated by ezrin binding proteins in reconstituted systems - membrane-ezrin-actin - - H20202016-01-01 - 2018-01-01 - 656442 - VALID

    المصدر: eLife, Vol 7 (2018)
    eLife
    eLife, 2018, 7, pp.e37262. ⟨10.7554/eLife.37262⟩
    eLife, eLife Sciences Publication, 2018, 7, pp.e37262. ⟨10.7554/eLife.37262⟩

    مصطلحات موضوعية: 0301 basic medicine, Protein Conformation, Lipid Bilayers, Mutant, [SDV.BC.IC] Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], Ezrin, MESH: Protein Conformation, physics of living systems, [SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB], ezrin-membrane interaction, cellular protrusions, Biology (General), phosphorylation, General Neuroscience, CYTOSKELETAL LINKER, EPITHELIAL-CELLS, General Medicine, QUANTITATIVE-ANALYSIS, I-BAR domain proteins, [SDV.BBM.BP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biophysics, Membrane, Membrane curvature, C. elegans, Phosphorylation, Medicine, MESH: Actins/chemistrys, MESH: Lipid Bilayers/chemistry, Protein Binding, Research Article, MESH: Cell Membrane/genetics, GIANT UNILAMELLAR VESICLES, MESH: Mutant Proteins/chemistry, QH301-705.5, MESH: Cytoskeletal Proteins/chemistry, Science, PHYSIOLOGICAL CONDITIONS, MESH: Cytoskeletal Proteins/metabolism, [SDV.BBM.BP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Biophysics, NATIVE MEMBRANES, macromolecular substances, PARIETAL-CELLS, Curvature, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Protein Domains, MESH: Cell Membrane/chemistry, MESH: Mutant Proteins/metabolism, Actin, MESH: Actins/geneticss, General Immunology and Microbiology, MESH: Phosphorylation, APICAL MEMBRANE, MESH: Mutant Proteins/genetics, Cell Membrane, MESH: Protein Binding/genetics, Apical membrane, Actins, F-ACTIN BINDING, In vitro, Protein enrichment, ezrin, Cytoskeletal Proteins, 030104 developmental biology, MESH: Lipid Bilayers/metabolisms, MESH: Protein Domains/genetics, membrane curvature, Biophysics, 1182 Biochemistry, cell and molecular biology, Mutant Proteins, ERM PROTEINS

    وصف الملف: application/pdf

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    المساهمون: Pharmaceutical and Pharmacological Sciences

    المصدر: RUC. Repositorio da Universidade da Coruña
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    المصدر: Athanasiou, D, Aguila, M, Opefi, C A, South, K, Bellingham, J, Bevilacqua, D, Munro, P M, Kanuga, N, Mackenzie, F E, Dubis, A M, Georgiadis, A, Graca, A B, Pearson, R A, Ali, R R, Sakami, S, Palczewski, K, Sherman, M Y, Reeves, P J & Cheetham, M E 2017, ' Rescue of mutant rhodopsin traffic by metformin-induced AMPK activation accelerates photoreceptor degeneration ', Human Molecular Genetics, vol. 26, no. 2, pp. 305-319 . https://doi.org/10.1093/hmg/ddw387

    وصف الملف: application/pdf

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    المصدر: Journal of Clinical Investigation. 123:4627-4640

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    المصدر: Cardiovascular Research, vol. 93, no. 1, pp. 130-140
    Kronstein, Romy; Seebach, Jochen; Grossklaus, Sylvia; Minten, Carsten; Engelhardt, Britta; Drab, Marek; Liebner, Stefan; Arsenijevic, Yvan; Taha, Abdallah Abu; Afanasieva, Tatiana; Schnittler, Hans-Joachim (2012). Caveolin-1 opens endothelial cell junctions by targeting catenins. Cardiovascular research, 93(1), pp. 130-40. Oxford: Oxford University Press 10.1093/cvr/cvr256 <http://dx.doi.org/10.1093/cvr/cvr256>

    وصف الملف: application/pdf

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    المساهمون: UCL - MD/FARM - Ecole de pharmacie

    المصدر: BMC Structural Biology
    BMC Structural Biology, Vol. 9, no. 3, p. [1-18] (2009)
    BMC structural biology, 9
    BMC Structural Biology, Vol 9, Iss 1, p 3 (2009)

    وصف الملف: 1 full-text file(s): application/pdf