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1دورية أكاديمية
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2Improved antisense oligonucleotide induced exon skipping in themdx mouse model of muscular dystrophy
المصدر: The Journal of Gene Medicine. 4:644-654
مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, mdx mouse, Duchenne muscular dystrophy, Blotting, Western, Nonsense mutation, Muscular Dystrophies, Dystrophin, Mice, Exon, Drug Discovery, Genetics, medicine, Animals, Muscular dystrophy, Molecular Biology, Cells, Cultured, Genetics (clinical), DNA Primers, Messenger RNA, Base Sequence, biology, Reverse Transcriptase Polymerase Chain Reaction, Exons, Oligonucleotides, Antisense, medicine.disease, Molecular biology, Exon skipping, Disease Models, Animal, Mice, Inbred mdx, biology.protein, Molecular Medicine
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المؤلفون: K. Honeyman
المصدر: Business History. 43:119-126
مصطلحات موضوعية: History, Political science, Business, Management and Accounting (miscellaneous), Women in business, Business and International Management, Review article, Management
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المؤلفون: Nigel G. Laing, K. Honeyman, Sue Fletcher, Steve D. Wilton
المصدر: Human Mutation. 11:252-258
مصطلحات موضوعية: Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Oligonucleotide, Single-strand conformation polymorphism, Biology, DNA sequencing, Restriction enzyme, chemistry.chemical_compound, chemistry, Genotype, Typing, Genotyping, Genetics (clinical), DNA
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4bf9ec3cbd7d656741fdf05efec007c
https://doi.org/10.1002/(sici)1098-1004(1998)11:3<252::aid-humu11>3.0.co;2-y -
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المؤلفون: P. K. Thomas, Veneta Georgieva, Julia Petrova, Alexey Savov, Rosalind H. H. King, Dora Angelicheva, Lefkos T. Middleton, Stella Stancheva, Luba Kalaydjieva, Amelia Nikolova, Iva Petkova, Ivailo Turnev, K. Honeyman, David Chandler, Boryana Ishpekova, Alan H. Bittles, Alexander Shmarov, Anna Hristova, Momchil Moskov, Joachim Hallmayer, Francesc Calafell
المصدر: Nature Genetics. 14:214-217
مصطلحات موضوعية: Male, Linkage disequilibrium, Roma, Adolescent, Genetic Linkage, Population, Disease, Biology, Nerve Fibers, Myelinated, Chromosome (genetic algorithm), Gene mapping, Genetics, Humans, Bulgaria, Child, education, education.field_of_study, Chromosome Mapping, Founder Effect, Pedigree, Evolutionary biology, Genetic marker, Endogamy, Female, Hereditary Sensory and Motor Neuropathy, Chromosomes, Human, Pair 8, Founder effect
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfe38239162f395bf45bc6d8f6b46b68
https://doi.org/10.1038/ng1096-214 -
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المؤلفون: K. McGuire, K. Honeyman, B. E. Fisher
المصدر: Canadian Journal of Behavioural Science / Revue canadienne des sciences du comportement. 26:476-483
مصطلحات موضوعية: Daytime, Scale (ratio), Sleep behaviour, Nocturnal, Psychology, Parental ratings, General Psychology, Developmental psychology
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7Morpholino oligomer-mediated exon skipping averts the onset of dystrophic pathology in the mdx mouse
المؤلفون: Sue Fletcher, Hong M. Moulton, K. Honeyman, Russell D. Johnsen, Patrick L. Iversen, Penny L Harding, Stephen D. Wilton, Abbie M Fall, Joshua P Steinhaus
المصدر: Molecular therapy : the journal of the American Society of Gene Therapy. 15(9)
مصطلحات موضوعية: musculoskeletal diseases, mdx mouse, congenital, hereditary, and neonatal diseases and abnormalities, Morpholino, Duchenne muscular dystrophy, Morpholines, Gene Expression, Morpholinos, Dystrophin, 03 medical and health sciences, Exon, Mice, 0302 clinical medicine, Utrophin, Drug Discovery, medicine, Genetics, Animals, Muscular dystrophy, Molecular Biology, 030304 developmental biology, Pharmacology, 0303 health sciences, biology, Reverse Transcriptase Polymerase Chain Reaction, Muscles, Exons, Genetic Therapy, Oligonucleotides, Antisense, medicine.disease, musculoskeletal system, Molecular biology, Exon skipping, Muscular Dystrophy, Duchenne, Mutation, biology.protein, Mice, Inbred mdx, Molecular Medicine, 030217 neurology & neurosurgery, Injections, Intraperitoneal
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المؤلفون: Sue Fletcher, Abbie M Fall, Steve D. Wilton, K. Honeyman, Penny L Harding
المصدر: Molecular therapy : the journal of the American Society of Gene Therapy. 15(1)
مصطلحات موضوعية: Transcription, Genetic, Nonsense mutation, Molecular Sequence Data, Biology, Cell Line, Dystrophin, 03 medical and health sciences, Exon, Mice, 0302 clinical medicine, Drug Discovery, Genetics, Animals, Humans, splice, RNA, Messenger, Enhancer, Molecular Biology, 030304 developmental biology, Pharmacology, 0303 health sciences, Messenger RNA, Base Sequence, Exons, Oligonucleotides, Antisense, Molecular biology, Exon skipping, Cell biology, RNA splicing, biology.protein, Molecular Medicine, 030217 neurology & neurosurgery
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المؤلفون: Russell D. Johnsen, Penny L Harding, K. Honeyman, Steve D. Wilton, Abbie M Fall, Sue Fletcher
المصدر: The journal of gene medicine. 8(2)
مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, mdx mouse, Morpholino, Duchenne muscular dystrophy, Nonsense mutation, Fluorescent Antibody Technique, Injections, Intramuscular, Dystrophin, Mice, Drug Discovery, Utrophin, Genetics, medicine, Animals, Muscular dystrophy, Molecular Biology, Genetics (clinical), biology, Exons, Genetic Therapy, Oligonucleotides, Antisense, medicine.disease, Molecular biology, Exon skipping, Muscular Dystrophy, Duchenne, Animals, Newborn, Codon, Nonsense, biology.protein, Mice, Inbred mdx, Molecular Medicine, RNA Splice Sites, Injections, Intraperitoneal
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