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

المصدر: 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: Adaptation, Physiological, High-Intensity Interval Training/adverse effects, Humans, Male, Muscle Proteins/genetics, Muscle, Skeletal/metabolism, Physical Endurance, Soccer/physiology, Young Adult

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/8fa756af-5a12-4d59-89ce-7d0a847c5cc0Test

الإتاحة: https://doi.org/10.1007/s00421-017-3751-5Test
https://portal.findresearcher.sdu.dk/da/publications/8fa756af-5a12-4d59-89ce-7d0a847c5cc0Test

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

المصدر: 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 ....

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Child, Preschool, Dystroglycans/metabolism, Female, Genetic Predisposition to Disease, Genetic Variation, Glycosylation, Heterozygote, Homozygote, Humans, Male, Middle Aged, Muscle Proteins/genetics, Muscular Dystrophies, Limb-Girdle/genetics, Mutation, Phenotype, Whole Exome Sequencing/methods, Young Adult

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1186/s13395-018-0170-1Test
https://curis.ku.dk/portal/da/publications/detection-of-variants-in-dystroglycanopathyassociated-genes-through-the-application-of-targeted-wholeexome-sequencing-analysis-to-a-large-cohort-of-patients-with-unexplained-limbgirdleTest-muscle-weakness(0068e518-f9ce-4b5f-b7f2-313ed225bc7e).html
https://curis.ku.dk/ws/files/218088378/s13395_018_0170_1.pdfTest

المؤلفون: Elsafadi, E, Manikandan, M, Dawud, R. A., Alajez, N. M., Hamam, R., Alfayez, M., Kassem, Moustapha, Aldahmash, A., Mahmood, A.

المصدر: Elsafadi , E , Manikandan , M , Dawud , R A , Alajez , N M , Hamam , R , Alfayez , M , Kassem , M , Aldahmash , A & Mahmood , A 2016 , ' Transgelin is a TGF β -inducible gene that regulates osteoblastic and adipogenic differentiation of human skeletal stem cells through actin cytoskeleston organization ' , Cell Death & Disease , vol. 7 , no. 8 , e2321 , pp. e2321 . https://doi.org/10.1038/cddis.2016.196Test

مصطلحات موضوعية: Actin Cytoskeleton/metabolism, Adipocytes/cytology, Adipogenesis/genetics, Cell Movement/genetics, Cell Nucleus/metabolism, Cell Proliferation/genetics, Fibroblasts/cytology, Foreskin/cytology, Gene Expression Profiling, Humans, Male, Mesenchymal Stem Cells/cytology, Microfilament Proteins/genetics, Muscle Proteins/genetics, Muscle, Skeletal/cytology, Osteoblasts/cytology, RNA, Small Interfering/metabolism, Signal Transduction/genetics, Transforming Growth Factor beta/metabolism

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/5e85a946-5aff-4573-b496-df6aa93700d6Test

الإتاحة: https://doi.org/10.1038/cddis.2016.196Test
https://portal.findresearcher.sdu.dk/da/publications/5e85a946-5aff-4573-b496-df6aa93700d6Test
https://findresearcher.sdu.dk/ws/files/121940806/Transgelin_is_a_TGF_inducible_gene_that_regulates_osteoblastic_and_adipogenic_differentiation_of_human_skeletal_stem_cells_through_actin_cytoskeleston_organization.pdfTest

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

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

مصطلحات موضوعية: DOK7 congenital myasthenia, Cardiac disease, Mitral valve disease, Neuromuscular disorders, PROLAPSE, MUTATIONS, Myasthenic Syndromes, Congenital/complications, Muscle Proteins/genetics, Humans, Middle Aged, Genetic Predisposition to Disease/genetics, Male, Female, Mutation, Mitral Valve Insufficiency/complications, Siblings

الإتاحة: https://doi.org/10.1016/j.jns.2017.06.005Test
https://pure.au.dk/portal/da/publications/dok7-congenital-myasthenia-may-be-associated-with-severe-mitral-valve-insufficiencyTest(48ffb97f-f439-4471-8874-8487aebe0dd6).html
http://www.scopus.com/inward/record.url?scp=85020895129&partnerID=8YFLogxKTest

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

المصدر: 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: Cardiac disease, DOK7 congenital myasthenia, Mitral valve disease, Neuromuscular disorders, Myasthenic Syndromes, Congenital/complications, Muscle Proteins/genetics, Humans, Middle Aged, Genetic Predisposition to Disease/genetics, Male, Female, Mutation, Mitral Valve Insufficiency/complications, Siblings

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/955a56e8-636c-4366-980c-9d21d1c3a322Test

الإتاحة: https://doi.org/10.1016/j.jns.2017.06.005Test
https://portal.findresearcher.sdu.dk/da/publications/955a56e8-636c-4366-980c-9d21d1c3a322Test

المؤلفون: Abdallah, Basem M., Figeac, Florence, Larsen, Kenneth H., Ditzel, Nicholas, Keshari, Pankaj, Isa, Adiba, Jafari, Abbas, Andersen, Thomas L., Delaisse, Jean Marie, Goshima, Yoshio, Ohshima, Toshio, Kassem, Moustapha

المصدر: Abdallah , B M , Figeac , F , Larsen , K H , Ditzel , N , Keshari , P , Isa , A , Jafari , A , Andersen , T L , Delaisse , J M , Goshima , Y , Ohshima , T & Kassem , M 2017 , ' CRMP4 Inhibits Bone Formation by Negatively Regulating BMP and RhoA Signaling ' , Journal of Bone and Mineral Research , vol. 32 , no. 5 , pp. 913-926 . https://doi.org/10.1002/jbmr.3069Test

مصطلحات موضوعية: BONE REMODELING, CRMP4, DPYSL3, OSTEOBLAST, OSTEOPOROSIS, Focal Adhesion Kinase 1/genetics, Stromal Cells/cytology, Muscle Proteins/genetics, rho GTP-Binding Proteins/genetics, Mice, Knockout, Signal Transduction/physiology, Osteoblasts/cytology, Animals, Cyclin-Dependent Kinase Inhibitor p27/genetics, Cell Proliferation/genetics, Osteogenesis, Bone Morphogenetic Protein 2/genetics

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/7d99d343-4853-4a63-a7b2-9ec53e370acfTest

الإتاحة: https://doi.org/10.1002/jbmr.3069Test
https://portal.findresearcher.sdu.dk/da/publications/7d99d343-4853-4a63-a7b2-9ec53e370acfTest

المؤلفون: 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

المصدر: 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 , ....

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Aging/physiology, Animals, Autophagy-Related Protein 7, Female, Forkhead Box Protein O1, Forkhead Transcription Factors/physiology, Humans, Insulin-Like Growth Factor I/physiology, Male, Mice, Inbred C57BL, Inbred DBA, Knockout, Transgenic, Microtubule-Associated Proteins/genetics, Models, Animal, Muscle Proteins/genetics, Muscle, Skeletal/physiology, Proto-Oncogene Proteins c-akt/physiology, SKP Cullin F-Box Protein Ligases/genetics, Sarcopenia/physiopathology, Serpin E2/genetics, Signal Transduction/physiology, TOR Serine-Threonine Kinases/physiology

العلاقة: https://research.vu.nl/en/publications/c3edf814-3c90-4667-8713-c3a120aff07aTest

الإتاحة: https://doi.org/10.1007/s10522-013-9432-9Test
https://research.vu.nl/en/publications/c3edf814-3c90-4667-8713-c3a120aff07aTest
https://hdl.handle.net/1871.1/c3edf814-3c90-4667-8713-c3a120aff07aTest

المؤلفون: 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

المصدر: 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 , ....

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Aging/physiology, Animals, Autophagy-Related Protein 7, Female, Forkhead Box Protein O1, Forkhead Transcription Factors/physiology, Humans, Insulin-Like Growth Factor I/physiology, Male, Mice, Inbred C57BL, Inbred DBA, Knockout, Transgenic, Microtubule-Associated Proteins/genetics, Models, Animal, Muscle Proteins/genetics, Muscle, Skeletal/physiology, Proto-Oncogene Proteins c-akt/physiology, SKP Cullin F-Box Protein Ligases/genetics, Sarcopenia/physiopathology, Serpin E2/genetics, Signal Transduction/physiology, TOR Serine-Threonine Kinases/physiology

العلاقة: https://research.vu.nl/en/publications/c3edf814-3c90-4667-8713-c3a120aff07aTest

الإتاحة: https://doi.org/10.1007/s10522-013-9432-9Test
https://research.vu.nl/en/publications/c3edf814-3c90-4667-8713-c3a120aff07aTest
https://hdl.handle.net/1871.1/c3edf814-3c90-4667-8713-c3a120aff07aTest

المؤلفون: van Haagen, Herman H H B M, 't Hoen, Peter A C, de Morrée, Antoine, van Roon-Mom, Willeke M C, Peters, Dorien J M, Roos, Marco, Mons, Barend, van Ommen, Gert-Jan, Schuemie, Martijn J

المصدر: van Haagen , H H H B M , 't Hoen , P A C , de Morrée , A , van Roon-Mom , W M C , Peters , D J M , Roos , M , Mons , B , van Ommen , G-J & Schuemie , M J 2011 , ' In silico discovery and experimental validation of new protein-protein interactions ' , Proteomics , vol. 11 , no. 5 , pp. 843-53 . https://doi.org/10.1002/pmic.201000398Test

مصطلحات موضوعية: Algorithms, Animals, Computational Biology/methods, Databases, Protein, Drosophila, Dysferlin, Gene Expression, Humans, Huntingtin Protein, Huntington Disease/genetics, Membrane Proteins/genetics, Mice, Molecular Targeted Therapy, Muscle Proteins/genetics, Muscular Dystrophies/genetics, Nerve Tissue Proteins/genetics, Nuclear Proteins/genetics, Polycystic Kidney Diseases/genetics, Predictive Value of Tests, Probability, Protein Binding, Protein Interaction Mapping/methods, Protein Structure, Tertiary, RNA, Messenger

العلاقة: https://pure.au.dk/portal/en/publications/9fec32d3-d7f2-43e8-90ed-edc6bc211d2dTest

الإتاحة: https://doi.org/10.1002/pmic.201000398Test
https://pure.au.dk/portal/en/publications/9fec32d3-d7f2-43e8-90ed-edc6bc211d2dTest

المؤلفون: Gallardo, Eduard, de Luna, Noemi, Diaz-Manera, Jordi, Rojas-García, Ricardo, Gonzalez-Quereda, Lidia, Flix, Bàrbara, de Morrée, Antoine, van der Maarel, Silvère, Illa, Isabel

المصدر: 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: Adult, Biopsy, DNA Mutational Analysis, Dysferlin, Female, Humans, Lipopolysaccharide Receptors/metabolism, Male, Membrane Proteins/genetics, Monocytes/metabolism, Muscle Proteins/genetics, Muscle, Skeletal/metabolism, Muscular Dystrophies, Limb-Girdle/diagnosis, Mutation/genetics, Solubility

الإتاحة: https://doi.org/10.1371/journal.pone.0029061Test
https://pure.au.dk/portal/da/publications/comparison-of-dysferlin-expression-in-human-skeletalTest-muscle-with-that-in-monocytes-for-the-diagnosis-of-dysferlin-myopathy(a8908b65-83f6-4cc8-8cce-2259645f1c20).html