المؤلفون: Teresa Gidaro, Julien Durigneux, Emma Pierce-Hoffman, Fabio Catervi, Johann Böhm, Alan H. Beggs, Adnan Yuksel, Montse Olivé, Casie A. Genetti, Raul Juntas-Morales, Isabelle Duband-Goulet, Nicolas Deconinck, Norma B. Romero, Eva Cabet, Rocío-Nur Villar-Quiles, Asuman Koparir, Ana Ferreiro, Jocelyn Laporte, Xavière Lornage, Mireille Cossée, John Rendu, Sandra Coppens, Lara Servais

المساهمون: Unité de Biologie Fonctionnelle et Adaptative (BFA (UMR_8251 / U1133)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), Département de neurologie [Montpellier], Hôpital Gui de Chauliac [Montpellier]-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Université Montpellier 1 (UM1)-Université de Montpellier (UM), Boston Children's Hospital, Harvard Medical School [Boston] (HMS), Institut de Myologie, Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU), Biruni University, Children's University Hospital Queen Fabiola [Bruxelles, Belgium], Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02142, USA, Partenaires INRAE, 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 de référence des Maladies Neuromusculaires AOC, Groupe d'imagerie neurofonctionnelle (GIN), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut des Maladies Neurodégénératives [Bordeaux] (IMN), Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS)-Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS), Children's Hospital and Harvard Medical School, Institut d'Investigació Biomèdica de Bellvitge [Barcelone] (IDIBELL), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Université Montpellier 1 (UM1)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Gui de Chauliac [CHU Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Université de Montpellier (UM), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Institut des Maladies Neurodégénératives [Bordeaux] (IMN), Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS)-Université de Bordeaux (UB)-Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Mühendislik ve Doğa Bilimleri Fakültesi

المصدر: Annals of Neurology
Annals of Neurology, Wiley, 2020, 87 (2), pp.217-232. ⟨10.1002/ana.25660⟩
Annals of neurology, 87 (2
Annals of Neurology, 2020, 87 (2), pp.217-232. ⟨10.1002/ana.25660⟩
Ann Neurol

مصطلحات موضوعية: Male, TRANSCRIPTION COACTIVATOR, 0301 basic medicine, Pathology, animal diseases, [SDV]Life Sciences [q-bio], Cardiomyopathy, Muscle Proteins, medicine.disease_cause, SIGNAL COINTEGRATOR 1, 0302 clinical medicine, Fibroblasts -- physiology, Amyotrophic lateral sclerosis, Child, Cells, Cultured, Mutation, ABNORMALITIES, Cell Cycle -- physiology, Cell Cycle, PROLIFERATION, hemic and immune systems, Sciences bio-médicales et agricoles, Middle Aged, MUSCLE, Pedigree, 3. Good health, Phenotype, Neurology, Child, Preschool, Female, Transcription Factors -- genetics, medicine.symptom, tissues, D3, G1 phase, Adult, endocrine system, medicine.medical_specialty, Amino Acid Transport System y+, DISORDERS, Muscle Proteins -- genetics, Muscle, Skeletal -- pathology -- physiopathology, Article, 03 medical and health sciences, Muscular Diseases, Neurologie, medicine, Humans, Amino Acid Transport System y+ -- metabolism -- physiology, Muscle, Skeletal, Cell Cycle Protein, Myopathy, business.industry, Infant, Spinal muscular atrophy, Fibroblasts, medicine.disease, GENE, Congenital myopathy, eye diseases, MUSCULAR-DYSTROPHY, ADIPOGENESIS, 030104 developmental biology, Muscular Diseases -- genetics -- physiopathology, Neurology (clinical), business, 030217 neurology & neurosurgery, Transcription Factors

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::881c9cf3fea17bc40c4af016cc68a5c5Test
https://doi.org/10.1002/ana.25660Test

المؤلفون: Cas J. Fuchs, Tyler A. Churchward-Venne, Joey S J Smeets, Kevin J M Paulussen, Lex B. Verdijk, Joan M. G. Senden, Luc J. C. van Loon, Wesley J H Hermans, Joop J. A. van Loon

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

مصطلحات موضوعية: Male, Mealworm, Protein metabolism, Gene Expression Regulation/drug effects, Muscle Proteins, Medicine (miscellaneous), Phenylalanine, chemistry.chemical_compound, SYNTHESIS RATES, FSR, AMINO-ACIDS, Laboratory of Entomology, Tenebrio, RESISTANCE EXERCISE, Muscle Proteins/genetics, Nutrition and Dietetics, intrinsically labeled protein, biology, DIETARY-PROTEIN, Milk Proteins, Postprandial Period, Milk Proteins/administration & dosage, medicine.anatomical_structure, Postprandial, protein metabolism, WHEY, Milk protein concentrate, SKELETAL-MUSCLE, NUTRITION, Dietary Proteins, INTRINSICALLY LABELED MILK, Adult, Muscle tissue, medicine.medical_specialty, Protein digestion, stable isotopes, Dietary Proteins/administration & dosage, Young Adult, Double-Blind Method, milk protein, Internal medicine, medicine, Animals, Humans, Exercise, Skeletal muscle, Laboratorium voor Entomologie, biology.organism_classification, Endocrinology, Gene Expression Regulation, chemistry, YOUNG, EPS, Tenebrio/chemistry, INGESTION

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::452ac9136b62c4c7cc7da9dbb91f22beTest
https://cris.maastrichtuniversity.nl/en/publications/0637ee11-f2e4-4766-8536-510b422d6078Test

المؤلفون: Davide Susta, Ricardo Segurado, Kathleen A. J. Mitchelson, Joan M. G. Senden, Caoileann H. Murphy, Giuseppe De Vito, Ellen M Flanagan, Sinead McCarthy, Brendan Egan, Joy P B Goessens, Adrian Chabowski, Luc J. C. van Loon, Clare A. Corish, Helen M. Roche, Elena de Marco Castro, Agnieszka Mikłosz

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

المصدر: Murphy, C H, Flanagan, E M, De Vito, G, Susta, D, Mitchelson, K A J, de Marco Castro, E, Senden, J M G, Goessens, J P B, Mikłosz, A, Chabowski, A, Segurado, R, Corish, C A, McCarthy, S N, Egan, B, van Loon, L J C & Roche, H M 2021, ' Does supplementation with leucine-enriched protein alone and in combination with fish-oil-derived n-3 PUFA affect muscle mass, strength, physical performance, and muscle protein synthesis in well-nourished older adults? A randomized, double-blind, placebo-controlled trial ', The American journal of clinical nutrition, vol. 113, no. 6, pp. 1411–1427 . https://doi.org/10.1093/ajcn/nqaa449Test
American Journal of Clinical Nutrition, 113(6), 1411-1427. Oxford University Press
The American Journal of Clinical Nutrition

مصطلحات موضوعية: Male, Muscle Proteins, Medicine (miscellaneous), Gene Expression Regulation/drug effects, Isometric exercise, Muscle Strength/drug effects, AMINO-ACID SUPPLEMENTATION, AcademicSubjects/MED00160, DIETARY-FAT MODIFICATION, VITAMIN-D, chemistry.chemical_classification, Muscle Proteins/genetics, Nutrition and Dietetics, biology, LC n-3 PUFA, Physical Functional Performance, Fish oil, HEALTHY OLDER, Fatty Acids, Omega-3/administration & dosage, Original Research Communications, muscle mass, Body Composition, Female, Muscle, Skeletal/drug effects, aging, LC n–3 PUFA, leucine, protein, muscle mass, strength, sarcopenia, leucine, strength, Polyunsaturated fatty acid, medicine.medical_specialty, BODY-COMPOSITION, LC n–3 PUFA, Renal function, Nutritional Status, EXERCISE, ELDERLY-PEOPLE, sarcopenia, AcademicSubjects/MED00060, AGE, Double-Blind Method, Internal medicine, Fatty Acids, Omega-3, medicine, Humans, Muscle Strength, Muscle, Skeletal, Aged, Adiponectin, business.industry, SERUM CYSTATIN-C, aging, biomarkers, medicine.disease, Endocrinology, Gene Expression Regulation, chemistry, Cystatin C, Sarcopenia, biology.protein, Lean body mass, RISK-FACTORS, business, aged, 80 and over, protein

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6972176484f30c57816edd1eba28f8d4Test
https://pure.qub.ac.uk/en/publications/does-supplementation-with-leucineenriched-protein-alone-and-in-combination-with-fishoilderived-n3-pufa-affectTest-muscle-mass-strength-physical-performance-and-muscle-protein-synthesis-in-wellnourished-older-adults-a-randomized-doubleblind-placebocontrolled-trial(420da3a1-f13f-44cd-a354-accb2c34e334).html

المؤلفون: Tobias Schmidt Nielsen, Nikolai Baastrup Nordsborg, Magni Mohr, Paul S. Bradley, Peter Krustrup, Karl Olsson, Ioannis G. Fatouros, Tobias Christensson, Dan Fransson

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

مصطلحات موضوعية: Male, medicine.medical_specialty, Sports medicine, Physiology, Football, Muscle Proteins, High-Intensity Interval Training, SOD2 protein, Na+-K+ ATPase activity, RC1200, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Endurance training, Physiology (medical), Internal medicine, Soccer, Exercise performance, Humans, Medicine, Orthopedics and Sports Medicine, Muscle, Skeletal, Muscle fatigue, Muscle Proteins/genetics, High-Intensity Interval Training/adverse effects, Muscle, Skeletal/metabolism, business.industry, Soccer/physiology, High intensity, Public Health, Environmental and Occupational Health, Skeletal muscle, 030229 sport sciences, General Medicine, QP, Adaptation, Physiological, Antioxidant capacity, Intermittent exercise, medicine.anatomical_structure, Metabolic enzymes, Physical Endurance, Physical therapy, Cardiology, Original Article, Na+–K+ ATPase activity, business, Muscle oxidative capacity, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2fd6d620ead8651c3b9de9f27a5122fTest
https://doi.org/10.1007/s00421-017-3751-5Test

المؤلفون: Shirin Jamal-Omidi, L. Phillips, Anna Kostera-Pruszczyk, Nanna Witting, Miren Zulaica Ijurco, Maja von der Hagen, Ana Töpf, Kristl G. Claeys, Jaume Colomer, Monkol Lek, Shahriar Nafissi, L. Xu, Daniel G. MacArthur, Elise Valkanas, Jonathan Baets, Anna Potulska-Chromik, Volker Straub, Anna Łusakowska, Peter Van den Bergh, Sonja Strang-Karlsson, Thomas E. Mullen, John Vissing, Marta Bertoli, Juan Bautista Espinal Valencia, Carina Wallgren-Pettersson, Willem De Ridder, Hacer Durmus, Tracey Willis, Katherine Johnson, Andreas Hahn, Roberto Fernández-Torrón, Nicolas Deconinck

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed866fead030563b4d9ea59130e00061Test
https://hdl.handle.net/2078.1/220057Test

المؤلفون: Joshua D. Brown-Clay, Flora Moreau, Fernando Schmitt, Clément Thomas, Bárbara Sousa, Antoun Al Absi, Céline Hoffmann, Bassam Janji, Guy Berchem, Xianqing Mao, Hannah Wurzer

المساهمون: Instituto de Investigação e Inovação em Saúde

المصدر: Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP

مصطلحات موضوعية: 0301 basic medicine, Muscle Proteins / genetics, Invadopodium, LIM Domain Proteins / genetics, Muscle Proteins, Hypoxia-Inducible Factor 1, alpha Subunit / metabolism, Kaplan-Meier Estimate, Extracellular matrix, Transactivation, Mice, Neoplasm Invasiveness / pathology, Cell Movement, Breast, RNA, Small Interfering, Cytoskeleton, Promoter Regions, Genetic, Hypoxia-Responsive Elements, Regulation of gene expression, Multidisciplinary, Chemistry, Breast Neoplasms / mortality, Nuclear Proteins, LIM Domain Proteins, Middle Aged, Cell Hypoxia, Cell biology, Extracellular Matrix, Up-Regulation, Gene Expression Regulation, Neoplastic, Gene Knockdown Techniques, RNA, Small Interfering / metabolismo, Invadopodia, Medicine, Breast Neoplasms / pathology, Female, Adult, Hypoxia-Inducible Factor 1, alpha Subunit / genetics, Science, Breast Neoplasms, Nuclear Proteins / genetics, Article, 03 medical and health sciences, Downregulation and upregulation, Cell Line, Tumor, Animals, Humans, Neoplasm Invasiveness, Aged, Hypoxia-Inducible Factor 1, alpha Subunit, Breast / pathology, Extracellular Matrix / pathology, LIM Domain Proteins / metabolism, Xenograft Model Antitumor Assays, 030104 developmental biology, Breast Neoplasms / genetics, Nuclear Proteins / metabolismo, Muscle Proteins / metabolismo

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57cf1f2a0de1d1ddc5a8f435179b22b5Test
https://hdl.handle.net/10216/127417Test

المؤلفون: Henning Andersen, David Gaist, Henrik Daa Schrøder, Jens Mogensen, Jens Michael Hertz, John Vissing, Emil Greve Pedersen

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

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, PROLAPSE, DOK7 congenital myasthenia, Congenital myasthenia, Cardiac disease, 03 medical and health sciences, Mitral Valve Insufficiency/complications, 0302 clinical medicine, Mitral valve, Internal medicine, Myasthenic Syndromes, Congenital/complications, medicine, Humans, Muscle Proteins/genetics, MUTATIONS, business.industry, Genetic Predisposition to Disease/genetics, Siblings, Middle Aged, 030104 developmental biology, medicine.anatomical_structure, Mitral valve disease, Neurology, Mutation, Mutation (genetic algorithm), Cardiology, Female, Neurology (clinical), business, Neuromuscular disorders, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c89644139cf3a987757e97a6efda17cTest
https://doi.org/10.1016/j.jns.2017.06.005Test

المؤلفون: Luana Toniolo, L. Barberi, Astrid Y. Bijlsma, Antonio L. Serrano, Carel G. M. Meskers, Lars Larsson, Mario Pende, Rosario Rizzuto, Marco Sandri, Kenneth A. Dyar, Cristina Mammucari, Andrea B. Maier, Giorgia Pallafacchina, M. Roceri, Pura Muñoz-Cánoves, Stefano Schiaffino, Antonio Paoli, D. Pion, Giulia Milan, Bert Blaauw, Antonio Musarò, Carlo Reggiani, Vanina Romanello

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14f4a5d65f36ee74ba4de2ecd531c858Test
https://hdl.handle.net/1871.1/c3edf814-3c90-4667-8713-c3a120aff07aTest

المؤلفون: Hans H. Jung, Michael Sinnreich, Jens A. Petersen, Wolfram Kress, Thierry Kuntzer, Angela Huebner, Elisabeth J. Rushing, Maja von der Hagen, Johannes Alexander Lobrinus, Veronika Kana, Dirk Fischer

المساهمون: University of Zurich, Petersen, Jens A

المصدر: BMC Neurology, Vol. 15 (2015) P. 182
BMC neurology
BMC Neurology
Bmc Neurology, vol. 15, no. 1, pp. 182

مصطلحات موضوعية: Adult, Male, Heterozygote, Dysferlinopathy, Adolescent, Clinical Neurology, 10208 Institute of Neuropathology, Muscle Proteins, 610 Medicine & health, ddc:616.07, medicine.disease_cause, Dysferlin, Young Adult, medicine, Humans, Myopathy, ddc:611, Genetics, Mutation, biology, Genetic heterogeneity, business.industry, Homozygote, Haplotype, Membrane Proteins, General Medicine, Anatomy, Middle Aged, medicine.disease, Founder Effect, 10040 Clinic for Neurology, 3. Good health, 2728 Neurology (clinical), Phenotype, Muscular Dystrophies, Limb-Girdle, Female, Membrane Proteins/genetics, Muscle Proteins/genetics, Muscular Dystrophies, Limb-Girdle/genetics, Switzerland, biology.protein, Neurology (clinical), medicine.symptom, business, Research Article, Limb-girdle muscular dystrophy, Founder effect

وصف الملف: s12883-015-0449-3.pdf - application/pdf; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b5d47ec334c3e9a41a950925d0c5859Test
https://doi.org/10.1186/s12883-015-0449-3Test

المؤلفون: Jacques S. Beckmann, Melissa J. Spencer

المصدر: Neuromuscular Disorders, vol. 18, no. 12, pp. 913-921

مصطلحات موضوعية: Sarcomeres, Gene isoform, Muscle Proteins, Models, Biological, Sarcomere, Article, medicine, Animals, Humans, Calpain/genetics, Calpain/metabolism, Muscle Proteins/genetics, Muscle Proteins/metabolism, Muscular Dystrophies, Limb-Girdle/genetics, Muscular Dystrophies, Limb-Girdle/metabolism, Mutation, Sarcomeres/metabolism, Muscular dystrophy, Genetics (clinical), Loss function, Genetics, biology, Calpain, Dystrophy, medicine.disease, Cell biology, Muscular Dystrophies, Limb-Girdle, Neurology, Pediatrics, Perinatology and Child Health, biology.protein, Titin, Neurology (clinical), Limb-girdle muscular dystrophy

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d38571d4127b7b2f9c161021bded730Test
https://doi.org/10.1016/j.nmd.2008.08.005Test