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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 -
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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 -
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المؤلفون: Benjamin K.C. Ong, Raymond C.S. Seet, Roland Baur, Chew Soh Eng, Shang Huifang, Erle C.H. Lim, Walter Hunziker, Pascal Béguin, Erwin Sigel, Jean-Marc Burgunder
المصدر: Neuromuscular disorders : NMD. 18(8)
مصطلحات موضوعية: musculoskeletal diseases, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, China, DNA, Complementary, Adolescent, Xenopus, Pain, Biology, Compound heterozygosity, medicine.disease_cause, Myotonia, Variable features, Chloride Channels, Internal medicine, medicine, Animals, Humans, Muscle, Skeletal, Exercise, Genetics (clinical), Genetics, Neurologic Examination, CLCN1, Mutation, Myotonia congenita, Electromyography, Reverse Transcriptase Polymerase Chain Reaction, medicine.disease, biology.organism_classification, Electrophysiology, Endocrinology, Neurology, Pediatrics, Perinatology and Child Health, Chloride channel, biology.protein, Oocytes, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0c2fdf4dfca35d7248e8e99f8ec0c33Test
https://pubmed.ncbi.nlm.nih.gov/18579381Test -
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المؤلفون: Lie Chen, Zen H. Lu, Lilianne Kappeler, Joachim Weis, Franziska Joncourt, Doris Lang, Martin T. Schaerer, Sabina Gallati, Jean-Marc Burgunder, Juerg Fritschi, Erwin Sigel
المصدر: Musclenerve. 29(5)
مصطلحات موضوعية: musculoskeletal diseases, Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Myotonia Congenita, Physiology, DNA Mutational Analysis, Genes, Recessive, medicine.disease_cause, Cellular and Molecular Neuroscience, Exon, Xenopus laevis, Chloride Channels, Physiology (medical), medicine, Animals, Humans, Point Mutation, Aged, Genetics, Mutation, CLCN1, biology, Myotonia congenita, Point mutation, Single-strand conformation polymorphism, Exons, Myotonia, medicine.disease, Reverse transcription polymerase chain reaction, biology.protein, Female, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716323dcd8850de16e82e18f95f078cdTest
https://pubmed.ncbi.nlm.nih.gov/15116370Test -
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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 -
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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