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

المصدر: Annals of neurology, 87 (2

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Adult, Amino Acid Transport System y+ -- metabolism -- physiology, Cell Cycle -- physiology, Cells, Cultured, Child, Preschool, Female, Fibroblasts -- physiology, Humans, Infant, Male, Middle Aged, Muscle Proteins -- genetics, Muscle, Skeletal -- pathology -- physiopathology, Muscular Diseases -- genetics -- physiopathology, Mutation, Pedigree, Phenotype, Transcription Factors -- genetics

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

العلاقة: uri/info:doi/10.1002/ana.25660; uri/info:pmid/31794073; uri/info:scp/85077147655; uri/info:pmcid/PMC6980348; https://dipot.ulb.ac.be/dspace/bitstream/2013/307754/3/ASC1myopathy-Villar-Quiles.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307754Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/307754Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/307754/3/ASC1myopathy-Villar-Quiles.pdfTest

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

المساهمون: College of Medicine, Dept. of Pathology, Hye Min Kim, Ja Seung Koo, Koo, Ja Seung, Kim, Hye Min

مصطلحات موضوعية: Adenoma/genetics, Adenoma/metabolism, Adenoma, Oxyphilic/genetics, Oxyphilic/metabolism, Carbonic Anhydrase IX/genetics, Carbonic Anhydrase IX/metabolism, Carcinoma/genetics, Carcinoma/metabolism, Female, Glucose Transporter Type 1/genetics, Glucose Transporter Type 1/metabolism, Glycolysis, Hexokinase/genetics, Hexokinase/metabolism, Humans, Male, Middle Aged, Monocarboxylic Acid Transporters/genetics, onocarboxylic Acid Transporters/metabolism, Muscle Proteins/genetics, Muscle Proteins/metabolism, Thyroid Neoplasms/genetics, Thyroid Neoplasms/metabolism

العلاقة: DISEASE MARKERS; J00743; OAK-2017-03317; https://ir.ymlib.yonsei.ac.kr/handle/22282913/160356Test; T201702172; DISEASE MARKERS, Vol.2017 : 6230294, 2017

الإتاحة: https://doi.org/10.1155/2017/6230294Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/160356Test

المساهمون: College of Medicine, Dept. of Pathology, Ji Hae Nahm, Hye Min Kim, Ja Seung Koo, Koo, Ja Seung, Kim, Hye Min, Nahm, Ji Hae

مصطلحات موضوعية: Adenocarcinoma, Follicular/genetics, Follicular/pathology, Adenoma/genetics, Adenoma/pathology, Carbonic Anhydrase IX/biosynthesis, Carbonic Anhydrase IX/genetics, Carcinoma/genetics, Carcinoma/pathology, Carcinoma, Medullary/genetics, Medullary/pathology, Papillary, Disease-Free Survival, Female, Gene Expression Regulation, Neoplastic, Glucose/metabolism, Glucose Transporter Type 1/biosynthesis, Glucose Transporter Type 1/genetics, Glycolysis/genetics, Hexokinase/biosynthesis, Hexokinase/genetics, Humans, Male, Monocarboxylic Acid Transporters/biosynthesis, Monocarboxylic Acid Transporters/genetics, Muscle Proteins/biosynthesis, Muscle Proteins/genetics, Thyroid Neoplasms/classification

العلاقة: TUMOR BIOLOGY; J02763; OAK-2017-01499; https://ir.ymlib.yonsei.ac.kr/handle/22282913/154522Test; T201700928; TUMOR BIOLOGY, Vol.39(3) : 1-10, 2017

الإتاحة: https://doi.org/10.1177/1010428317695922Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/154522Test

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: 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

المساهمون: Ha Young Shin, Hoon Jang, Joo Hyung Han, Hyung Jun Park, Jung Hwan Lee, So Won Kim, Seung Min Kim, Young-Eun Park, Dae-Seong Kim, Duhee Bang, Min Goo Lee, Ji Hyun Lee, Young-Chul Choi, Kim, Seung Min, Shin, Ha Young, Lee, Min Goo, Lee, Jung Hwan, Lee, Ji Hyun, Choi, Young Chul

مصطلحات موضوعية: Adolescent, Adult, Child, DNA Mutational Analysis, Dysferlin, Female, High-Throughput Nucleotide Sequencing, Humans, Male, Membrane Proteins/genetics, Muscle Proteins/genetics, Muscular Dystrophies, Limb-Girdle/diagnosis, Limb-Girdle/genetics, Young Adult, DYSF, Dysferlinopathy, Hybridization capture, Mutation, Next-generation sequencing

وصف الملف: 502~510

العلاقة: NEUROMUSCULAR DISORDERS; J02344; OAK-2015-00991; https://ir.ymlib.yonsei.ac.kr/handle/22282913/140151Test; http://www.sciencedirect.com/science/article/pii/S0960896615001005Test; T201501491; NEUROMUSCULAR DISORDERS, Vol.25(6) : 502-510, 2015

الإتاحة: https://doi.org/10.1016/j.nmd.2015.03.006Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/140151Test
http://www.sciencedirect.com/science/article/pii/S0960896615001005Test

المؤلفون: Petersen, J.A., Kuntzer, T., Fischer, D., von der Hagen, M., Huebner, A., Kana, V., Lobrinus, J.A., Kress, W., Rushing, E.J., Sinnreich, M., Jung, H.H.

المصدر: Bmc Neurology, vol. 15, no. 1, pp. 182

مصطلحات موضوعية: Adolescent, Adult, Female, Founder Effect, Heterozygote, Homozygote, Humans, Male, Membrane Proteins/genetics, Middle Aged, Muscle Proteins/genetics, Muscular Dystrophies, Limb-Girdle/genetics, Mutation, Phenotype, Switzerland, Young Adult

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26444858; info:eu-repo/semantics/altIdentifier/eissn/1471-2377; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_5DFF23E46ADD9; https://serval.unil.ch/notice/serval:BIB_5DFF23E46ADDTest; urn:issn:1471-2377; https://serval.unil.ch/resource/serval:BIB_5DFF23E46ADD.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_5DFF23E46ADD9Test

الإتاحة: https://doi.org/10.1186/s12883-015-0449-3Test
https://serval.unil.ch/notice/serval:BIB_5DFF23E46ADDTest
https://serval.unil.ch/resource/serval:BIB_5DFF23E46ADD.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_5DFF23E46ADD9Test