يعرض 1 - 20 نتائج من 28 نتيجة بحث عن '"metabolism [Protein Kinases]"', وقت الاستعلام: 1.01s تنقيح النتائج
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    المساهمون: Medicum, Research Programs Unit, Doctoral Programme in Biomedicine, Research Programme for Molecular Neurology, Neuroscience Center, University of Helsinki, Clinicum, Pentti Tienari / Principal Investigator, Genome-Scale Biology (GSB) Research Program, Department of Neurosciences, Neurologian yksikkö, University Management, Anu Wartiovaara / Principal Investigator, HUS Neurocenter

    المصدر: Open Biology
    'Open Biology ', vol: 8, pages: 180108-1-180108-18 (2018)
    Open biology 8(11), 180108 (2018). doi:10.1098/rsob.180108
    Open Biology, Vol 8, Iss 11 (2018)

    وصف الملف: application/pdf

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    المصدر: Jouy, F, Müller, S A, Wagner, J, Otto, W, von Bergen, M & Tomm, J M 2015, ' Integration of conventional quantitative and phospho-proteomics reveals new elements in activated Jurkat T-cell receptor pathway maintenance ', Proteomics, vol. 15, no. 1, pp. 25-33 . https://doi.org/10.1002/pmic.201400119
    Practical proteomics 15(1), 25-33 (2014). doi:10.1002/pmic.201400119

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    المصدر: Human molecular genetics 22(14), 2829-2841 (2013). doi:10.1093/hmg/ddt132
    Human Molecular Genetics; Vol 22
    Human Molecular Genetics

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    المساهمون: Publica

    المصدر: Brain 140(9), 2444-2459 (2017). doi:10.1093/brain/awx202
    Brain, Vol. 140, No 9 (2017) pp. 2444-2459
    Brain

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    المصدر: Neurobiology of disease 96, 115-126 (2016). doi:10.1016/j.nbd.2016.09.002
    Neurobiology of Disease, Vol 96, Iss, Pp 115-126 (2016)

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    المصدر: The EMBO journal 29(20), 3571-3589 (2010). doi:10.1038/emboj.2010.223

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    المصدر: The journal of neuroscience 30(36), 11938-11950 (2010). doi:10.1523/JNEUROSCI.2357-10.2010

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    المؤلفون: Suzanne Lesage, Valérie Drouet, Elisa Majounie, Vincent Deramecourt, Maxime Jacoupy, Aude Nicolas, Florence Cormier-Dequaire, Sidi Mohamed Hassoun, Claire Pujol, Sorana Ciura, Zoi Erpapazoglou, Tatiana Usenko, Claude-Alain Maurage, Mourad Sahbatou, Stefan Liebau, Jinhui Ding, Basar Bilgic, Murat Emre, Nihan Erginel-Unaltuna, Gamze Guven, François Tison, Christine Tranchant, Marie Vidailhet, Jean-Christophe Corvol, Paul Krack, Anne-Louise Leutenegger, Michael A. Nalls, Dena G. Hernandez, Peter Heutink, J. Raphael Gibbs, John Hardy, Nicholas W. Wood, Thomas Gasser, Alexandra Durr, Jean-François Deleuze, Meriem Tazir, Alain Destée, Ebba Lohmann, Edor Kabashi, Andrew Singleton, Olga Corti, Alexis Brice, Yves Agid, Mathieu Anheim, Anne-Marie Bonnet, Michel Borg, Emmanuel Broussolle, Philippe Damier, Alexandra Dürr, Franck Durif, Stephan Klebe, Maria Martinez, Pierre Pollak, Olivier Rascol, Marc Vérin, François Viallet, Jean Christophe Corvol, Sampath Arepalli, Roger A. Barker, Yoav Ben-Shlomo, Daniela Berg, Francesco Bettella, Kailash Bhatia, Rob M.A. de Bie, Alessandro Biffi, Bastiaan R. Bloem, Zoltan Bochdanovits, Michael Bonin, Jose M. Bras, Kathrin Brockmann, Janet Brooks, David J. Burn, Gavin Charlesworth, Honglei Chen, Patrick F. Chinnery, Sean Chong, Carl E. Clarke, Mark R. Cookson, Carl Counsell, Jean-François Dartigues, Panos Deloukas, Günther Deuschl, David T. Dexter, Karin D. van Dijk, Allissa Dillman, Jing Dong, Frank Durif, Sarah Edkins, Valentina Escott-Price, Jonathan R. Evans, Thomas Foltynie, Jianjun Gao, Michelle Gardner, Alison Goate, Emma Gray, Rita Guerreiro, Clare Harris, Jacobus J. van Hilten, Albert Hofman, Albert Hollenbeck, Peter Holmans, Janice Holton, Michèle Hu, Xuemei Huang, Heiko Huber, Gavin Hudson, Sarah E. Hunt, Johanna Huttenlocher, Thomas Illig, Pálmi V. Jónsson, Laura L. Kilarski, Iris E. Jansen, Jean-Charles Lambert, Cordelia Langford, Andrew Lees, Peter Lichtner, Patricia Limousin, Grisel Lopez, Delia Lorenz, Steven Lubbe, Codrin Lungu, María Martinez, Walter Mätzler, Alisdair McNeill, Catriona Moorby, Matthew Moore, Karen E. Morrison, Ese Mudanohwo, Sean S. O’Sullivan, Michael J. Owen, Justin Pearson, Joel S. Perlmutter, Hjörvar Pétursson, Vincent Plagnol, Bart Post, Simon Potter, Bernard Ravina, Tamas Revesz, Olaf Riess, Fernando Rivadeneira, Patrizia Rizzu, Mina Ryten, Mohamad Saad, Javier Simón-Sánchez, Stephen Sawcer, Anthony Schapira, Hans Scheffer, Claudia Schulte, Manu Sharma, Karen Shaw, Una-Marie Sheerin, Ira Shoulson, Joshua Shulman, Ellen Sidransky, Chris C.A. Spencer, Hreinn Stefánsson, Kári Stefánsson, Joanna D. Stockton, Amy Strange, Kevin Talbot, Carlie M. Tanner, Avazeh Tashakkori-Ghanbaria, Daniah Trabzuni, Bryan J. Traynor, André G. Uitterlinden, Daan Velseboer, Robert Walker, Bart van de Warrenburg, Mirdhu Wickremaratchi, Caroline H. Williams-Gray, Sophie Winder-Rhodes, Isabel Wurster, Nigel Williams, Huw R. Morris, Andrew B. Singleton

    المساهمون: Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Complex Trait Genetics, Neurology, Graduate School, ANS - Cellular & Molecular Mechanisms, Krack, Paul, Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute (ICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Department of Neurodegenerative Diseases, Eberhard Karls Universität Tübingen = Eberhard Karls University of Tuebingen, Laboratory of Neurogenetics, National Institute of Aging, Département d'histologie et de pathologie, Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Centre d'investigation clinique Neurosciences [CHU Pitié Salpêtrière] (CIC Neurosciences), CHU Pitié-Salpêtrière [AP-HP], Fondation Jean Dausset CEPH, Institute of Neuroanatomy, Department of Neurology, Behavioural Neurology and Movement Disorders Unit, Istanbul Faculty of Medicine, Istanbul University, Department of Genetics, Institut des Maladies Neurodégénératives [Bordeaux] (IMN), Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Pôle Tête-Cou-CETD, Les Hôpitaux Universitaires de Strasbourg (HUS), Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Département de neurologie, Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble, Variabilité Génétique et Maladies Humaines, Institut Universitaire d'Hématologie (IUH), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Paris Diderot - Paris 7 (UPD7), Hertie Institute for Clinical Brain Research [Tubingen], University of Tübingen, Department of Molecular Neuroscience, University College of London [London] (UCL)-Institute of Neurology, Service de génétique, cytogénétique, embryologie [Pitié-Salpétrière], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Pierre et Marie Curie - Paris 6 (UPMC), Commissariat à l'Energie Atomique Saclay, Service de Neurologie, CHU Mustapha, Movement Disorders Unit, HAL-UPMC, Gestionnaire, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Centre d'investigation clinique pluridisciplinaire [CHU Pitié Salpêtrière] (CIC-P 1421), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Service de génétique, cytogénétique, embryologie [CHU Pitié-Salpétrière], Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)

    المصدر: Lesage, S, Drouet, V, Majounie, E, Bochdanovits, Z & Brice, A 2016, ' Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. ', American Journal of Human Genetics, no. 98, 3, pp. 500-513 . https://doi.org/10.1016/j.ajhg.2016.01.014
    American Journal of Human Genetics, 98, 3, pp. 500-13
    American Journal of Human Genetics, 500-513. Cell Press
    ISSUE=98;STARTPAGE=500;ENDPAGE=513;ISSN=0002-9297;TITLE=American Journal of Human Genetics
    American Journal of Human Genetics, 98, 500-13
    American journal of human genetics, 98(3), 500-513. Cell Press
    American Journal of Human Genetics, Vol. 98, No 3 (2016) pp. 500-513
    American Journal of Human Genetics
    American Journal of Human Genetics, Elsevier (Cell Press), 2016, 98 (3), pp.500-513. ⟨10.1016/j.ajhg.2016.01.014⟩
    American Journal of Human Genetics, 2016, 98 (3), pp.500-513. ⟨10.1016/j.ajhg.2016.01.014⟩
    American Journal of Human Genetics, 98(3), 500-513
    The American journal of human genetics 98(3), 500-513 (2016). doi:10.1016/j.ajhg.2016.01.014

    وصف الملف: application/pdf; applicaton/octet-stream

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    المصدر: The journal of biological chemistry 279, 48647-48653 (2004). doi:10.1074/jbc.M402516200

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    المصدر: Biochemistry 42, 5917-5924 (2003). doi:10.1021/bi0340595

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    المصدر: Oncogene 34(11), 1363-1374 (2014). doi:10.1038/onc.2014.81

    وصف الملف: Print-Electronic

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    المصدر: Journal of cell science 127(15), 3280-3293 (2014). doi:10.1242/jcs.146035

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    المصدر: Journal of Biological Chemistry
    The journal of biological chemistry 287(11), 8174-8186 (2012). doi:10.1074/jbc.M111.262287

    وصف الملف: application/pdf

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    المصدر: PLoS ONE, Vol 6, Iss 7, p e22143 (2011)
    PLoS ONE
    PLoS one 6, e22143 (2011). doi:10.1371/journal.pone.0022143
    online available

    مصطلحات موضوعية: Histidine Kinase, Operon, Mutant, lcsh:Medicine, Corynebacterium glutamicum, genetics [Homeostasis], Molecular cell biology, Signaling in Cellular Processes, Homeostasis, Bacterial Physiology, metabolism [Protein Kinases], Phosphorylation, lcsh:Science, drug effects [Stress, Physiological], genetics [Nucleotide Motifs], Cellular Stress Responses, Multidisciplinary, drug effects [Gene Expression Regulation, Bacterial], genetics [Protein Kinases], physiology [Corynebacterium glutamicum], metabolism [DNA, Bacterial], genetics [Genes, Bacterial], Adaptation, Physiological, toxicity [Copper], Biochemistry, ddc:500, Transmembrane Signaling, genetics [Bacterial Proteins], Research Article, Signal Transduction, DNA, Bacterial, drug effects [Signal Transduction], drug effects [Adaptation, Physiological], metabolism [Bacterial Proteins], DNA transcription, genetics [Stress, Physiological], drug effects [Corynebacterium glutamicum], Biology, genetics [Signal Transduction], Multicopper oxidase, Microbiology, genetics [Adaptation, Physiological], drug effects [Phosphorylation], Bacterial Proteins, genetics [DNA, Bacterial], Stress, Physiological, Microbial Control, Nucleotide Motifs, genetics [Phosphorylation], drug effects [Homeostasis], cytology [Corynebacterium glutamicum], Binding Sites, Base Sequence, Histidine kinase, lcsh:R, Wild type, genetics [Corynebacterium glutamicum], Bacteriology, Gene Expression Regulation, Bacterial, Molecular biology, genetics [Gene Expression Regulation, Bacterial], Response regulator, Regulon, Genes, Bacterial, protein-histidine kinase, Mutation, lcsh:Q, Gene expression, Protein Kinases, Copper

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