يعرض 1 - 10 نتائج من 15 نتيجة بحث عن '"Laura van Vliet"', وقت الاستعلام: 0.88s تنقيح النتائج
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    المساهمون: Physiology, ACS - Atherosclerosis & ischemic syndromes, Academic Medical Center

    المصدر: PLoS ONE, 13(3)
    PLoS ONE, 13(3):0194636. Public Library of Science
    Kogelman, B, Khmelinskii, A, Verhaart, I, van Vliet, L, Bink, D I, Aartsma-Rus, A, van Putten, M & van der Weerd, L 2018, ' Influence of full-length dystrophin on brain volumes in mouse models of Duchenne muscular dystrophy ', PLoS ONE, vol. 13, no. 3, 0194636 . https://doi.org/10.1371/journal.pone.0194636
    PLoS ONE, Vol 13, Iss 3, p e0194636 (2018)
    PLoS ONE
    PLoS ONE, 13(3):e0194636. Public Library of Science
    PLoS ONE, 13(3). PUBLIC LIBRARY SCIENCE

    وصف الملف: application/pdf

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    المصدر: PLoS ONE, 13(2)
    PLoS ONE, Vol 13, Iss 2, p e0193289 (2018)
    PLoS ONE

    مصطلحات موضوعية: Genome engineering, 0301 basic medicine, mdx mouse, Heredity, Morpholino, Genetic Linkage, Duchenne muscular dystrophy, Drug Evaluation, Preclinical, Artificial Gene Amplification and Extension, Engineering and technology, Duchenne Muscular Dystrophy, Synthetic genome editing, Biochemistry, Polymerase Chain Reaction, Muscular Dystrophies, Oligodeoxyribonucleotides, Antisense, Dystrophin, Mice, Exon, Medicine and Health Sciences, Synthetic bioengineering, Muscular dystrophy, Genetics (clinical), Sequence Deletion, Multidisciplinary, biology, Chemistry, Gene targeting, Exons, Animal Models, Cell biology, TALENs, Experimental Organism Systems, Neurology, X-Linked Traits, Sex Linkage, Gene Targeting, Antisense oligonucleotides, Medicine, Research Article, Biotechnology, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, Science, Mice, Transgenic, Mouse Models, Bioengineering, Research and Analysis Methods, 03 medical and health sciences, Model Organisms, Genetics, medicine, Animals, Humans, Molecular Biology Techniques, Molecular Biology, Synthetic biology, Clinical Genetics, Base Sequence, Synthetic genomics, Biology and Life Sciences, Proteins, medicine.disease, Molecular biology, Exon skipping, Muscular Dystrophy, Duchenne, Cytoskeletal Proteins, 030104 developmental biology, Artificial Genetic Recombination, Mutation, Pediatrics, Perinatology and Child Health, Mice, Inbred mdx, biology.protein, Neurology (clinical), Cloning

    وصف الملف: application/pdf

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    المساهمون: Pediatrics, Neurology, Epidemiology, Clinical Genetics

    المصدر: Journal of Inherited Metabolic Disease
    Journal of Inherited Metabolic Disease, 33, 133-139. Springer Netherlands
    Journal of Inherited Metabolic Disease; Vol 33

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