يعرض 1 - 20 نتائج من 28 نتيجة بحث عن '"metabolism [Muscle Proteins]"', وقت الاستعلام: 0.56s تنقيح النتائج
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    المساهمون: Abrams, A.J., Hufnagel, R.B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M.A., Campeanu, I.J., Griffin, L.B., Groenewald, S., Strickland, A.V., Tao, F., Speziani, F., Abreu, L., Schule, R., Caporali, L., La Morgia, C., Maresca, A., Liguori, R., Lodi, R., Ahmed, Z.M., Sund, K.L., Wang, X., Krueger, L.A., Peng, Y., Prada, C.E., Prows, C.A., Schorry, E.K., Antonellis, A., Zimmerman, H.H., Abdul-Rahman, O.A., Yang, Y., Downes, S.M., Prince, J., Fontanesi, F., Barrientos, A., Nemeth, A.H., Carelli, V., Huang, T., Zuchner, S., Dallman, J.E.

    المصدر: Europe PubMed Central
    Nature genetics 47(8), 926-932 (2015). doi:10.1038/ng.3354
    Nature genetics

    مصطلحات موضوعية: Male, Embryo, Nonmammalian, MFN2, Muscle Proteins, IMMT protein, human, DOA, genetics [Muscle Proteins], medicine.disease_cause, Animals, Genetically Modified, pathology [Optic Atrophy, Autosomal Dominant], metabolism [Optic Atrophy, Autosomal Dominant], 0302 clinical medicine, Charcot-Marie-Tooth Disease, Chlorocebus aethiops, genetics [Phosphate Transport Proteins], genetics [Exome], Phosphate Transport Proteins, Exome, metabolism [Zebrafish], genetics [Genetic Predisposition to Disease], embryology [Embryo, Nonmammalian], Zebrafish, Genetics, 0303 health sciences, Mutation, Microscopy, Confocal, biology, Pedigree, genetics [Membrane Proteins], xonal peripheral neuropathy, mitochondrial fusion, Mitochondrial Membranes, COS Cells, Female, genetics [Mitochondrial Proteins], RNA Interference, genetics [Charcot-Marie-Tooth Disease], Protein Binding, UGO1 protein, S cerevisiae, metabolism [Embryo, Nonmammalian], Saccharomyces cerevisiae Proteins, Dominant optic atrophy, Charcot-Marie-Tooth type 2, CMT2, metabolism [Muscle Proteins], genetics [Optic Atrophy, Autosomal Dominant], metabolism [Phosphate Transport Proteins], Article, ultrastructure [Embryo, Nonmammalian], metabolism [Mitochondrial Proteins], Mitochondrial Proteins, 03 medical and health sciences, Atrophy, Microscopy, Electron, Transmission, ddc:570, Optic Atrophy, Autosomal Dominant, metabolism [Mitochondrial Membranes], medicine, Animals, Humans, Inner membrane, Genetic Predisposition to Disease, Hereditary Neurodegenerative Disorder, genetics [Saccharomyces cerevisiae Proteins], 030304 developmental biology, Membrane Proteins, Sequence Analysis, DNA, metabolism [Saccharomyces cerevisiae Proteins], biology.organism_classification, medicine.disease, eye diseases, HEK293 Cells, metabolism [Charcot-Marie-Tooth Disease], Membrane protein, embryology [Zebrafish], hereditary neurodegenerative disorder, metabolism [Membrane Proteins], 030217 neurology & neurosurgery, SLC25A46 protein, human

    وصف الملف: STAMPA

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    المصدر: Proceedings of the National Academy of Sciences of the United States of America 109(8), 3125-3130 (2012). doi:10.1073/pnas.1113793109

    مصطلحات موضوعية: metabolism [DNA (Cytosine-5-)-Methyltransferases], Bipolar Disorder, drug therapy [Schizophrenia], Muscle Proteins, pharmacology [Antipsychotic Agents], drug effects [Gene Expression Regulation], physiopathology [Brain], Polymerase Chain Reaction, drug effects [Cerebral Cortex], physiopathology [Cerebral Cortex], DNA Methyltransferase 3A, Mice, metabolism [MicroRNAs], Databases, Genetic, genetics [Schizophrenia], genetics [MicroRNAs], DNA (Cytosine-5-)-Methyltransferases, Prefrontal cortex, metabolism [GATA2 Transcription Factor], DPYSL3 protein, human, Oligonucleotide Array Sequence Analysis, Cerebral Cortex, Regulation of gene expression, Multidisciplinary, DNA methyltransferase 3A, growth & development [Brain], GATA2, Brain, Biological Sciences, metabolism [N-Methylaspartate], GATA2 Transcription Factor, medicine.anatomical_structure, therapeutic use [Antipsychotic Agents], Cerebral cortex, Schizophrenia, drug effects [Brain], ddc:500, Antipsychotic Agents, Signal Transduction, Adult, drug therapy [Bipolar Disorder], drug effects [Signal Transduction], N-Methylaspartate, physiopathology [Bipolar Disorder], metabolism [Muscle Proteins], GATA2 protein, human, Biology, Receptors, N-Methyl-D-Aspartate, Open Reading Frames, MIRN132 microRNA, human, microRNA, medicine, Animals, Humans, Epigenetics, Bipolar disorder, metabolism [Receptors, N-Methyl-D-Aspartate], Demography, metabolism [Cerebral Cortex], Reproducibility of Results, medicine.disease, Rats, Disease Models, Animal, MicroRNAs, HEK293 Cells, Gene Expression Regulation, pathology [Cerebral Cortex], physiopathology [Schizophrenia], genetics [Open Reading Frames], Neuroscience, genetics [Bipolar Disorder]

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    المصدر: The journal of clinical investigation
    The Journal of clinical investigation 122 (2012): 538–544. doi:10.1172/JCI60560
    info:cnr-pdr/source/autori:Montenegro G.; Rebelo A.P., Connell J.; Allison R.; Babalini C.; D'Aloia M.; Montieri P.; Schüle R.; Ishiura H.; Price J.; Strickland A.; Gonzalez M.A.; Baumbach-Reardon L.; Deconinck T.; Huang J.; Bernardi G.; Vance J.M.; Rogers M.T.; Tsuji S.; De Jonghe P.; Pericak-Vance M.A.; Schöls L.; Orlacchio A.; Reid E.; Züchner S./titolo:Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12/doi:10.1172%2FJCI60560/rivista:The Journal of clinical investigation/anno:2012/pagina_da:538/pagina_a:544/intervallo_pagine:538–544/volume:122
    The journal of clinical investigation 122(2), 538-544 (2012). doi:10.1172/JCI60560

    وصف الملف: pdf

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    المصدر: Cell Reports, Vol 17, Iss 4, Pp 1071-1086 (2016)
    Cell reports 17(4), 1071-1086 (2016). doi:10.1016/j.celrep.2016.09.058
    Cell Reports

    مصطلحات موضوعية: Male, Aging, genetics [SKP Cullin F-Box Protein Ligases], Transcription, Genetic, Muscle Proteins, Apoptosis, metabolism [Hippocampus], genetics [Muscle Proteins], Hippocampus, pathology [Ataxia], metabolism [Forkhead Box Protein O3], genetics [Homeostasis], Mice, pathology [Aging], genetics [Parkinson Disease], metabolism [Ubiquitin], complications [Movement Disorders], Fbxo32 protein, mouse, Homeostasis, lcsh:QH301-705.5, Mice, Knockout, protein homeostasis, Movement Disorders, Forkhead Box Protein O3, neurodegeneration, Brain, pathology [Nerve Degeneration], Parkinson Disease, genetics [Ataxia], metabolism [Autophagosomes], Up-Regulation, metabolism [Acyltransferases], Protein Binding, Proteasome Endopeptidase Complex, autophagy, metabolism [Muscle Proteins], FBXO32 protein, human, genetics [Mutation], Article, FBXO32, endophilin, Autophagy, deficiency [Acyltransferases], Animals, Humans, endocytosis, FoxO3 protein, mouse, ddc:610, metabolism [Proteasome Endopeptidase Complex], SKP Cullin F-Box Protein Ligases, Endophilin-A, Ubiquitin-Proteasome System, Ubiquitin, ataxia, Autophagosomes, metabolism [SKP Cullin F-Box Protein Ligases], pathology [Movement Disorders], pathology [Parkinson Disease], complications [Nerve Degeneration], pathology [Hippocampus], lcsh:Biology (General), metabolism [Brain], Mutation, Nerve Degeneration, Parkinson’s disease, genetics [Forkhead Box Protein O3], 2-acylglycerophosphate acyltransferase, next-generation sequencing, ubiquitin-proteasome system, Acyltransferases, HeLa Cells

    وصف الملف: Print-Electronic; application/pdf

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    المساهمون: Institut de Génomique Fonctionnelle (IGF), Université de Montpellier (UM)-Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Montpellier 2 - Sciences et Techniques (UM2)-Centre National de la Recherche Scientifique (CNRS), Experimental Neuropediatrics, Universitaetsklinikum Hamburg-Eppendorf = University Medical Center Hamburg-Eppendorf [Hamburg] (UKE), Department of Cellular and Integrative Physiology, Institut de génétique humaine (IGH), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Center for Experimental Medicine, Department of Experimental Pharmacology and Toxicology, Institut de Biologie du Développement de Marseille (IBDM), Aix Marseille Université (AMU)-Centre National de la Recherche Scientifique (CNRS), Cardiovascular Research Center Hamburg (CVRC), University Hamburg, Department of Pharmacology, University of Minnesota [Twin Cities] (UMN), University of Minnesota System-University of Minnesota System, Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Nature Communications 5(1), 4664 (2014). doi:10.1038/ncomms5664
    Nature Communications
    Nature Communications, Nature Publishing Group, 2014, 5, pp.4664. ⟨10.1038/ncomms5664⟩
    Nature communications
    Nature Communications, 2014, 5, pp.4664. ⟨10.1038/ncomms5664⟩

    مصطلحات موضوعية: Male, Patch-Clamp Techniques, Potassium Channels, sinoatrial node, Xenopus, General Physics and Astronomy, Muscle Proteins, 030204 cardiovascular system & hematology, genetics [Muscle Proteins], physiology [Oocytes], Mice, 0302 clinical medicine, Kcnj5 protein, mouse, Heart Rate, Pregnancy, Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels, Myocytes, Cardiac, Ivabradine, ComputingMilieux_MISCELLANEOUS, Calcium signaling, pathology [Myocytes, Cardiac], 0303 health sciences, Multidisciplinary, genetics [Potassium Channels], ion channels, pharmacology [Benzazepines], drug therapy [Arrhythmias, Cardiac], genetics [G Protein-Coupled Inwardly-Rectifying Potassium Channels], metabolism [Potassium Channels], Potassium channel, 3. Good health, HCN4 protein, human, medicine.anatomical_structure, Female, ddc:500, drug effects [Heart Rate], medicine.drug, medicine.medical_specialty, pacemaker activity, metabolism [Muscle Proteins], Mice, Transgenic, Biology, arrhythmia, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, genetics [Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels], Internal medicine, Heart rate, medicine, metabolism [G Protein-Coupled Inwardly-Rectifying Potassium Channels], Gene silencing, Animals, Humans, Calcium Signaling, 030304 developmental biology, [SDV.GEN]Life Sciences [q-bio]/Genetics, physiopathology [Arrhythmias, Cardiac], Sinoatrial node, Cardiac arrhythmia, Arrhythmias, Cardiac, General Chemistry, Benzazepines, electrophysiology, Mice, Inbred C57BL, Autonomic nervous system, Disease Models, Animal, Endocrinology, genetics [Arrhythmias, Cardiac], metabolism [Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels], G Protein-Coupled Inwardly-Rectifying Potassium Channels, Oocytes, metabolism [Myocytes, Cardiac], genetics [Calcium Signaling], Neuroscience

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    Academic Journal
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    المصدر: Journal of proteomics 75(8), 2384-2395 (2012). doi:10.1016/j.jprot.2012.02.019
    Journal of Proteomics

    وصف الملف: application/pdf

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    المساهمون: Cusimano, Vincenza, Pampinella, Francesca, Giacomello, Emiliana, Sorrentino, Vincenzo

    وصف الملف: STAMPA

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    Academic Journal
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    المصدر: Nature 439, 233 (2006). doi:10.1038/nature04343

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    المساهمون: Bagnato, Paola, Barone, Virigina, Giacomello, Emiliana, Rossi, Daniela, Sorrentino, Vincenzo

    المصدر: The Journal of Cell Biology

    مصطلحات موضوعية: Ryanodine receptors, Muscle Fibers, Skeletal, genetics/metabolism, Muscle Proteins, Endoplasmic Reticulum, Mice, Skeletal Muscle Proteins, Myofibrils, Myocyte, Guanine Nucleotide Exchange Factors, Protein Isoforms, genetics, biology, Ryanodine receptor, Cell Differentiation, Skeletal, 3T3 Cells, musculoskeletal system, Cell biology, Sarcoplasmic Reticulum, medicine.anatomical_structure, Biochemistry, obscurin, sarcoplasmic reticulum, calcium release, ryanodine receptors, InsP3 receptors, endoplasmic reticulum, Muscle, Titin, Protein Binding, Muscle Contraction, Ankyrins, Protein Structure, Recombinant Fusion Proteins, Sarcoplasmic reticulum, Obscurin, Protein Serine-Threonine Kinases, Muscle Fibers, Article, ANK1, Microsomes, Two-Hybrid System Techniques, medicine, 3T3 Cells, Amino Acid Sequence, genetics, Animals, Ankyrins, genetics/metabolism, Binding Sites, physiology, Cell Differentiation, physiology, Endoplasmic Reticulum, metabolism, Guanine Nucleotide Exchange Factors, genetics/metabolism, Humans, Mice, Microsomes, metabolism, Muscle Contraction, physiology, Muscle Fibers, metabolism, Muscle Proteins, genetics/metabolism, Muscle, metabolism/ultrastructure, Myofibrils, metabolism/ultrastructure, Protein Binding, physiology, Protein Isoforms, genetics/metabolism, Protein Structure, Tertiary, genetics, Recombinant Fusion Proteins, metabolism, Sarcoplasmic Reticulum, metabolism/ultrastructure, Two-Hybrid System Techniques, Muscle Fibers, Skeletal Muscle Protein, Animals, Humans, Calcium release, Muscle Fibers, Skeletal Muscle Proteins, Amino Acid Sequence, Muscle, Skeletal, metabolism/ultrastructure, Binding Sites, Endoplasmic reticulum, Skeletal muscle, Cell Biology, Sarcoplasmic reticulum membrane, Protein Structure, Tertiary, physiology, biology.protein, metabolism, Rho Guanine Nucleotide Exchange Factors

    وصف الملف: STAMPA

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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal

    المؤلفون: Eisner, David, Trafford, A. W.

    المصدر: Eisner , D & Trafford , A W 1996 , ' A sideways look at sparks, quarks, puffs and blips ' , Journal of Physiology , vol. 497 , no. 1 , pp. 2 .

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    Academic Journal