-
1
المؤلفون: Lie Chen, Jean-Marc Burgunder
المصدر: Cell Biology International. 29:506-513
مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Utrophin, Sarcoplasm, Cell Culture Techniques, Fluorescent Antibody Technique, Dystrophin, Dystrophin-associated protein complex, Dystroglycan, medicine, Humans, Protein Isoforms, Dystroglycans, Muscle, Skeletal, Sarcolemma, biology, Skeletal muscle, Cell Differentiation, Cell Biology, General Medicine, musculoskeletal system, Clone Cells, medicine.anatomical_structure, Biochemistry, biology.protein, Pikachurin, Laminin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5115e085c6a4c0d704f143e45f9e9837Test
https://doi.org/10.1016/j.cellbi.2005.01.009Test -
2
المؤلفون: A. Von Fellenberg, Jean-Marc Burgunder, S. Lin
المصدر: Neuropathology and Applied Neurobiology. 30:255-266
مصطلحات موضوعية: Denervation, Muscle Denervation, Pathology, medicine.medical_specialty, Histology, Sarcolemma, biology, Colocalization, Pathology and Forensic Medicine, Cell biology, Neurology, Physiology (medical), Gene expression, Myosin, biology.protein, medicine, Desmin, Neurology (clinical), Dystrophin
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::99fb42758e434c8554582a0bef523a4eTest
https://doi.org/10.1046/j.0305-1846.2004.00529.xTest -
3
المؤلفون: Jean-Marc Burgunder, How-Lung Eng, Wei Cheng, Jing Tian, Walter Hunziker
المصدر: PLoS ONE, Vol 9, Iss 8, p e103445 (2014)
PLoS ONEمصطلحات موضوعية: Movement disorders, Gene Expression, lcsh:Medicine, medicine.disease_cause, Biochemistry, Ion Channels, Animals, Genetically Modified, Gene Order, Medicine and Health Sciences, lcsh:Science, Zebrafish, Musculoskeletal System, Genetics, Mutation, Multidisciplinary, Movement Disorders, biology, Muscles, Fishes, Neurodegenerative Diseases, Animal Models, Phenotype, Cell biology, Biomechanical Phenomena, Neurology, Osteichthyes, Vertebrates, medicine.symptom, Anatomy, Locomotion, Research Article, musculoskeletal diseases, Myotonia Congenita, Recombinant Fusion Proteins, Genetic Vectors, Muscle disorder, Research and Analysis Methods, Muscle Fibers, Model Organisms, Chloride Channels, medicine, Animals, Humans, Actin, Swimming, CLCN1, Myotonia congenita, lcsh:R, Organisms, Biology and Life Sciences, Proteins, biology.organism_classification, medicine.disease, Actins, Disease Models, Animal, biology.protein, lcsh:Q
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9e0505057d2bc6319fc228eb055a6c7Test
http://europepmc.org/articles/PMC4118878?pdf=renderTest -
4
المؤلفون: Kai M. Rösler, Séverine Petitprez, Lie Chen, Liliane Kappeler, D Schorderet, Hugues Abriel, Jean-Marc Burgunder, L Tiab
المصدر: Neurology. 71(21)
مصطلحات موضوعية: medicine.medical_specialty, Nav1.4, DNA Mutational Analysis, Transfection, Sodium Channels, Cell Line, Membrane Potentials, Myotonia, Internal medicine, medicine, Humans, Hyperkalemic periodic paralysis, Patch clamp, Isoleucine, NAV1.4 Voltage-Gated Sodium Channel, Membrane potential, Family Health, biology, Sodium channel, Valine, medicine.disease, Cell biology, Transmembrane domain, Protein Subunits, Endocrinology, Paramyotonia congenita, Mutation, biology.protein, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::677b1aeb0f489949f8a9ef705e45ab19Test
https://pubmed.ncbi.nlm.nih.gov/19015483Test -
5
المؤلفون: Vesna Radojevic, F. Gaschen, C. Oppliger, Jean-Marc Burgunder
المصدر: Neuropathology and applied neurobiology. 28(5)
مصطلحات موضوعية: musculoskeletal diseases, Male, congenital, hereditary, and neonatal diseases and abnormalities, Histology, Duchenne muscular dystrophy, Muscle Fibers, Skeletal, Hybrid Cells, Pathology and Forensic Medicine, Cell therapy, Dystrophin, Reference Values, Physiology (medical), Utrophin, medicine, Myocyte, Animals, Humans, Muscular dystrophy, Genetics, biology, Myogenesis, Skeletal muscle, Fibroblasts, Muscular Dystrophy, Animal, musculoskeletal system, medicine.disease, Coculture Techniques, Cell biology, Muscular Dystrophy, Duchenne, medicine.anatomical_structure, Neurology, biology.protein, Cats, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::568e4bb4cb51766b901c9f58255c19e1Test
https://pubmed.ncbi.nlm.nih.gov/12366821Test -
6
المؤلفون: Jean-Marc Burgunder, Shuo Lin
المصدر: Brain research. Developmental brain research. 119(2)
مصطلحات موضوعية: musculoskeletal diseases, Gene isoform, Utrophin, animal diseases, Desmin, Dystrophin, Fetus, Sarcolemma, Developmental Neuroscience, Pregnancy, Sarcoglycans, medicine, Animals, Dystrophin glycoprotein complex, Rats, Wistar, Dystroglycans, Muscle, Skeletal, reproductive and urinary physiology, Membrane Glycoproteins, biology, Skeletal muscle, Membrane Proteins, Embryo, Anatomy, musculoskeletal system, Cell biology, Rats, Cytoskeletal Proteins, medicine.anatomical_structure, embryonic structures, biology.protein, Immunohistochemistry, Female, Developmental Biology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0df5d306124fbe7831edb32a6205c99Test
https://pubmed.ncbi.nlm.nih.gov/10675780Test