يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"Muscle Proteins/genetics"', وقت الاستعلام: 1.75s تنقيح النتائج
  1. 1

    المساهمون: Humane Biologie, RS: NUTRIM - R3 - Respiratory & Age-related Health, Physiotherapy, Human Physiology and Anatomy, Human Physiology and Sports Physiotherapy Research Group

    المصدر: American Journal of Clinical Nutrition, 114(3), 934-944. Oxford University Press
    The American journal of clinical nutrition 114 (2021) 3
    The American journal of clinical nutrition, 114(3), 934-944

    وصف الملف: application/pdf

  2. 2

    المصدر: European Journal of Applied Physiology
    Fransson, D, Nielsen, T S, Olsson, K, Christensson, T, Bradley, P S, Fatouros, I G, Krustrup, P, Nordsborg, N B & Mohr, M 2018, ' Skeletal muscle and performance adaptations to high-intensity training in elite male soccer players : speed endurance runs versus small-sided game training ', European Journal of Applied Physiology, vol. 118, no. 1, pp. 111-121 . https://doi.org/10.1007/s00421-017-3751-5Test

    وصف الملف: application/pdf

  3. 3

    المساهمون: UCL - (SLuc) Service de neurologie, UCL - SSS/IONS/NEUR - Clinical Neuroscience, Medicum, Department of Medical and Clinical Genetics, University of Helsinki, Clinicum, Children's Hospital, HUS Children and Adolescents

    المصدر: Skeletal Muscle, Vol. 8, no. 1, p. 23 [1-12] (2018)
    Skeletal muscle 8(1), 23 (2018). doi:10.1186/s13395-018-0170-1
    Skeletal Muscle
    Johnson, K, Bertoli, M, Phillips, L, Töpf, A, Van den Bergh, P, Vissing, J, Witting, N, Nafissi, S, Jamal-Omidi, S, Łusakowska, A, Kostera-Pruszczyk, A, Potulska-Chromik, A, Deconinck, N, Wallgren-Pettersson, C, Strang-Karlsson, S, Colomer, J, Claeys, K G, De Ridder, W, Baets, J, von der Hagen, M, Fernández-Torrón, R, Zulaica Ijurco, M, Espinal Valencia, J B, Hahn, A, Durmus, H, Willis, T, Xu, L, Valkanas, E, Mullen, T E, Lek, M, MacArthur, D G & Straub, V 2018, ' Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness ', Skeletal Muscle, vol. 8, 23 . https://doi.org/10.1186/s13395-018-0170-1Test
    SKELET MUSCLE
    r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
    instname
    Skeletal Muscle, 8 (1
    r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
    Fundació Sant Joan de Déu
    Skeletal Muscle, Vol 8, Iss 1, Pp 1-12 (2018)
    Skeletal muscle

    مصطلحات موضوعية: 0301 basic medicine, Male, lcsh:Diseases of the musculoskeletal system, Glycosylation, Whole Exome Sequencing/methods, Muscle Proteins, Hygiène et médecine sportives, Bioinformatics, WALKER-WARBURG-SYNDROME, 0302 clinical medicine, Orthopedics and Sports Medicine, Limb-girdle muscle weakness, Child, Dystroglycans, Exome sequencing, Muscle Proteins/genetics, Aged, 80 and over, Homozygote, Middle Aged, Dystroglycanopathies, 3. Good health, Whole-exome sequencing, medicine.anatomical_structure, Phenotype, Dystroglycans/metabolism, Child, Preschool, Orthopédie, Congenital muscular dystrophy, SKELETAL-MUSCLE, Female, medicine.symptom, GLYCOPROTEIN COMPLEX, Life Sciences & Biomedicine, ALPHA-DYSTROGLYCAN, Adult, Heterozygote, Proximal muscle weakness, Adolescent, EYE-BRAIN DISEASE, 03 medical and health sciences, Young Adult, Glycoprotein complex, Exome Sequencing, medicine, Humans, ABNORMAL GLYCOSYLATION, Genetic Predisposition to Disease, Walker–Warburg syndrome, Biology, Molecular Biology, POMT2 MUTATIONS, Aged, Science & Technology, Genetic heterogeneity, business.industry, Research, Muscular Dystrophies, Limb-Girdle/genetics, Muscle weakness, Skeletal muscle, Genetic Variation, Cell Biology, medicine.disease, Cancérologie, 030104 developmental biology, Muscular Dystrophies, Limb-Girdle, Mutation, CONGENITAL MUSCULAR-DYSTROPHY, 1182 Biochemistry, cell and molecular biology, Biologie cellulaire, Human medicine, DEFECTIVE GLYCOSYLATION, 3111 Biomedicine, lcsh:RC925-935, business, 030217 neurology & neurosurgery, MENTAL-RETARDATION

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

  4. 4

    المصدر: Gaist, D, Mogensen, J, Pedersen, E G, Schroder, H D, Vissing, J, Andersen, H & Hertz, J M 2017, ' DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency ', Journal of the Neurological Sciences, vol. 379, pp. 217-218 . https://doi.org/10.1016/j.jns.2017.06.005Test
    Gaist, D, Mogensen, J, Pedersen, E G, Schrøder, H D, Vissing, J, Andersen, H & Hertz, J M 2017, ' DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency ', Journal of the Neurological Sciences, vol. 379, pp. 217-218 . https://doi.org/10.1016/j.jns.2017.06.005Test

  5. 5

    المساهمون: Faculty of Behavioural and Movement Sciences, Neuromechanics, AMS - Ageing and Morbidity, Dulbecco Telethon Institute, Venetian Institute Molecular Medicine (VIMM), CNR Institute of Neuroscience, National Research Council [Italy] (CNR), Department of Biomedical Sciences, Universita degli Studi di Padova, Department of Anatomy, Histology, Forensic Medicine and Orthopedic [Roma] (DAHFMO), Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Department of internal Medicine, University of Amsterdam [Amsterdam] (UvA), Department of Gerontology and Geriatrics, Leiden University Medical Center (LUMC), Department of Rehabilitation, Centre de recherche Croissance et signalisation (UMR_S 845), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Descartes - Paris 5 (UPD5), ICREA Infection Biology Laboratory (Department of Experimental and Health Sciences), Universitat Pompeu Fabra [Barcelona] (UPF), Department of Biobehavioral Health, Pennsylvania State University (Penn State), Penn State System-Penn State System, Department of Neuroscience, Clinical Neurophysiology, Uppsala University, Supported by the EC FP7 Project MYOAGE (to LL, ABM, PM-C, AM, MP, CR, MS, and SS), Fondation Thierry Latran, MIUR and AFM (to AM), the Swedish Research Council (8651 to LL), MDA, Ministerio de Ciencia e Innovacion of Spain SAF2012-38547, FIS-PS09/01267, PLE2009-0124, Marató/TV3 and AFM (to PM-C and ALS), EU interregio project PANGEA (to CR), King Gustaf V and Queen Victoria’s Foundation, and the National Institute of Health Grants (AG-14731, AR-45627 and AR-47318 to LL)., European Project: 223576,EC:FP7:HEALTH,FP7-HEALTH-2007-B,MYOAGE(2009), Università degli Studi di Padova = University of Padua (Unipd), Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome] (UNIROMA), Universiteit Leiden-Universiteit Leiden, Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), MOVE Research Institute, Internal medicine, Venetian Institute of Molecular Medicine, Padua, Department of Anatomy, Histology, Forensic Medicine and Orthopedic, Università degli Studi di Roma 'La Sapienza' [Rome]-Réseau International des Instituts Pasteur (RIIP)-Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP), Venetian Institute of Molecular Medicine, Padova, Italy, Universitat Pompeu Fabra [Barcelona]

    المصدر: Biogerontology, 14(3), 303-23. Springer Netherlands
    Biogerontology
    Biogerontology, Springer Verlag, 2013, 14 (3), pp.303-23. ⟨10.1007/s10522-013-9432-9⟩
    Biogerontology; Vol 14
    Sandri, M, Barberi, L, Bijlsma, A Y, Blaauw, B, Dyar, K A, Milan, G, Mammucari, C, Meskers, C G M, Pallafacchina, G, Paoli, A, Pion, D, Roceri, M, Romanello, V, Serrano, A L, Toniolo, L, Larsson, L, Maier, A B, Munoz-Canoves, P, Musaro, A, Pende, M, Reggiani, C, Rizzuto, R & Schiaffino, S 2013, ' Signalling pathways regulating muscle mass in ageing skeletal muscle. The role of the IGF1-Akt-mTOR-FoxO pathway ', Biogerontology, vol. 14, no. 3, pp. 303-323 . https://doi.org/10.1007/s10522-013-9432-9Test
    Biogerontology, 2013, 14 (3), pp.303-23. ⟨10.1007/s10522-013-9432-9⟩
    Biogerontology, 14(3), 303-323. Springer Netherlands
    Biogerontology, 14(3), 303-323
    Sandri, M, Barberi, L, Bijlsma, A Y, Blaauw, B, Dyar, K A, Milan, G, Mammucari, C, Meskers, C G M, Pallafacchina, G, Paoli, A, Pion, D, Roceri, M, Romanello, V, Serrano, A L, Toniolo, L, Larsson, L, Maier, A B, Muñoz-Cánoves, P, Musarò, A, Pende, M, Reggiani, C, Rizzuto, R & Schiaffino, S 2013, ' Signalling pathways regulating muscle mass in ageing skeletal muscle : the role of the IGF1-Akt-mTOR-FoxO pathway ', Biogerontology, vol. 14, no. 3, pp. 303-23 . https://doi.org/10.1007/s10522-013-9432-9Test

    مصطلحات موضوعية: Male, Sarcopenia, FOXO1, mTORC1, Transgenic, Muscle hypertrophy, Sarcopenia/physiopathology, MESH: Serpin E2, Mice, SKP Cullin F-Box Protein Ligases/genetics, 0302 clinical medicine, Models, Serpin E2, 80 and over, MESH: Aging, MESH: Animals, MESH: Sarcopenia, Aged, 80 and over, Muscle Proteins/genetics, 0303 health sciences, Insulin-Like Growth Factor I/physiology, TOR Serine-Threonine Kinases, IGF1, Forkhead Transcription Factors/physiology, MESH: Young Adult, Mice, Inbred DBA, MESH: SKP Cullin F-Box Protein Ligases, medicine.medical_specialty, Knockout, muscle atrophy, signaling, aging, IGF-1, 03 medical and health sciences, MESH: Muscle Proteins, SDG 3 - Good Health and Well-being, MESH: Forkhead Transcription Factors, Skeletal/physiology, Serpin E2/genetics, Humans, Inbred DBA, Ubiquitin-Protein Ligases/genetics, Protein kinase B, Aged, MESH: Adolescent, MESH: Humans, MESH: Mice, Inbred DBA, MESH: Proto-Oncogene Proteins c-akt, Animal, MESH: Adult, medicine.disease, MESH: Ubiquitin-Protein Ligases, Mice, Inbred C57BL, Muscle, Skeletal/physiology, Ageing, MESH: Microtubule-Associated Proteins, Endocrinology, TOR Serine-Threonine Kinases/physiology, FoxO, Geriatrics and Gerontology, Gerontology, MESH: Female, 030217 neurology & neurosurgery, MESH: Signal Transduction, MESH: Insulin-Like Growth Factor I, Muscle Proteins, Inbred C57BL, MESH: Mice, Knockout, Autophagy-Related Protein 7, Tripartite Motif Proteins, MESH: Aged, 80 and over, Insulin-Like Growth Factor I, MESH: Aged, Mice, Knockout, MESH: Muscle, Skeletal, Forkhead Box Protein O1, Forkhead Transcription Factors, medicine.anatomical_structure, MESH: Models, Animal, Models, Animal, mTOR, Muscle, Female, Microtubule-Associated Proteins, Signal Transduction, Adult, Adolescent, MESH: Mice, Transgenic, Ubiquitin-Protein Ligases, Mice, Transgenic, Protein degradation, Biology, Young Adult, MESH: Mice, Inbred C57BL, Internal medicine, medicine, Animals, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, Muscle, Skeletal, MESH: Mice, PI3K/AKT/mTOR pathway, MESH: TOR Serine-Threonine Kinases, 030304 developmental biology, SKP Cullin F-Box Protein Ligases, Signal Transduction/physiology, Akt, Skeletal muscle, Proto-Oncogene Proteins c-akt/physiology, Microtubule-Associated Proteins/genetics, MESH: Male, Aging/physiology, Proto-Oncogene Proteins c-akt

  6. 6

    المصدر: JOURNAL OF BIOLOGICAL CHEMISTRY
    r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
    instname
    Journal of Biological Chemistry, 288(20), 14147-14157
    de Morrée, A, Flix, B, Bagaric, I, Wang, J, van den Boogaard, M, Grand Moursel, L, Frants, R R, Illa, I, Gallardo, E, Toes, R & van der Maarel, S M 2013, ' Dysferlin regulates cell adhesion in human monocytes ', The Journal of Biological Chemistry, vol. 288, no. 20, pp. 14147-14157 . https://doi.org/10.1074/jbc.M112.448589Test

  7. 7

    المساهمون: University of Zurich, Dotto, G P

    المصدر: CELL
    Cell, vol. 149, no. 6, pp. 1207-1220

    وصف الملف: 513_Hu_B_et_al._-_Cell_2012.pdf - application/pdf; application/pdf

  8. 8

    المصدر: PLoS ONE
    Dipòsit Digital de Documents de la UAB
    Universitat Autònoma de Barcelona
    PLoS ONE, 6(12)
    PLoS One
    r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
    instname
    PLoS ONE, Vol 6, Iss 12, p e29061 (2011)
    Gallardo, E, de Luna, N, Diaz-Manera, J, Rojas-García, R, Gonzalez-Quereda, L, Flix, B, de Morrée, A, van der Maarel, S & Illa, I 2011, ' Comparison of dysferlin expression in human skeletal muscle with that in monocytes for the diagnosis of dysferlin myopathy ', PLOS ONE, vol. 6, no. 12, pp. e29061 . https://doi.org/10.1371/journal.pone.0029061Test

    مصطلحات موضوعية: Male, Pathology, Anatomy and Physiology, dysferlin myopathy, Biopsy, DNA Mutational Analysis, Lipopolysaccharide Receptors, Muscle Proteins, DYSF protein, human, Protein Synthesis, medicine.disease_cause, preschool child, Biochemistry, Muscular Dystrophies, Monocytes, Western blotting, Dysferlin, Monocytes/metabolism, membrane protein, genetics, gene mutation, Musculoskeletal System, comparative study, limb girdle muscular dystrophy, Muscle Proteins/genetics, Mutation, child, clinical article, Multidisciplinary, biology, medicine.diagnostic_test, adult, article, Neuromuscular Diseases, dysferlinopathy, aged, medicine.anatomical_structure, female, Neurology, immunohistochemistry, monocyte, Blood Chemistry, Lipopolysaccharide Receptors/metabolism, Immunohistochemistry, Muscle, Medicine, Female, dysferlin gene, medicine.symptom, muscle biopsy, myopathy, Research Article, mutational analysis, Adult, Dysferlinopathy, medicine.medical_specialty, Mutation/genetics, Science, Muscular Dystrophies, Limb-Girdle/diagnosis, muscle protein, Antigens, CD14, medicine, Humans, controlled study, human, Membrane Proteins/genetics, skeletal muscle, Myopathy, gene, Muscle, Skeletal, protein expression, Biology, Muscle, Skeletal/metabolism, Muscle biopsy, Plasma Proteins, human cell, solubility, Skeletal muscle, Proteins, Membrane Proteins, nucleotide sequence, CD14 antigen, medicine.disease, human tissue, dysferlin, Muscular Dystrophies, Limb-Girdle, Solubility, adolescent, biology.protein, gene expression, pathology, metabolism

    وصف الملف: application/pdf

  9. 9

    المصدر: FASEB Journal, Vol. 22, No 11 (2008) pp. 3919-3924