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Science, ISSN 0036-8075, 5/2007, Volume 316, Issue 5826, pp. 836 - 837
Well-intentioned regulations protecting privacy are denying important information to patient subjects. Advances in information technology mean that a better... 
Medical research | Broadcasting industry | Genomics | Medical genetics | Policy Forum | Institutional review boards | Human genetics | Public health | Research ethics | Human population genetics | Laws, regulations and rules | Ethical aspects | Disclosure of information | Privacy | Health | Laws | Insurance | Risk | Patients | Failure | Offices
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 05/2013, Volume 201, Issue 4, pp. 499 - 510
The muscular dystrophies are a group of heterogeneous genetic diseases characterized by progressive degeneration and weakness of skeletal muscle. Since the... 
SKELETAL-MUSCLE | ALPHA-DYSTROGLYCAN | ABNORMAL GLYCOSYLATION | ALPHA-7-BETA-1 INTEGRIN | 3 UNTRANSLATED REGION | WALKER-WARBURG-SYNDROME | NITRIC-OXIDE | DILATED CARDIOMYOPATHY | MYOTONIC-DYSTROPHY | MEMBRANE REPAIR | CELL BIOLOGY | Dystrophin | Utrophin | Analysis | Muscular dystrophy | Musculoskeletal system | Genotype & phenotype | Neuromuscular diseases | Genes | Reviews
Journal Article
Clinical Immunology, ISSN 1521-6616, 2016, Volume 172, pp. 21 - 22
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2014, Volume 23, Issue 12, pp. 3180 - 3188
Journal Article
Science, ISSN 0036-8075, 11/1995, Volume 270, Issue 5237, pp. 819 - 822
Journal Article
AMERICAN JOURNAL OF HUMAN GENETICS, ISSN 0002-9297, 02/2005, Volume 76, Issue 2, pp. 205 - 214
In a speech to the ASHG, Louis M. Kunkel discusses the cloning of the gene responsible for Duchenne muscular dystrophy and tells about where things are... 
MDX MOUSE | SYSTEMIC DELIVERY | SKELETAL-MUSCLE | CLONED DNA-SEQUENCES | SHORT ARM | HUMAN X-CHROMOSOME | GLYCOPROTEIN COMPLEX | GENETICS & HEREDITY | BETA-SARCOGLYCAN | DUCHENNE MUSCULAR-DYSTROPHY | MYOBLAST TRANSPLANTATION | Speeches, lectures and essays | Human genetics | Achievements and awards | Genetic research | Scientists | Nobel prizes | Cloning
Journal Article
Journal of Neuromuscular Diseases, ISSN 2214-3599, 01/2019, Volume 6, Issue 3, p. 271
The recent availability and development of mutant and transgenic zebrafish strains that model human muscular dystrophies has created new research opportunities... 
Zebrafish | Phenotypes | Dystrophy | Drug development | Bioactive compounds | Muscular dystrophy
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2007, Volume 104, Issue 43, pp. 17016 - 17021
Journal Article
Drug Discovery Today: Technologies, ISSN 1740-6749, 2013, Volume 10, Issue 1, pp. e91 - e96
Recently, a number of chemical and drug screens using zebrafish embryos have been published. Using zebrafish dystrophin mutants, we screened a chemical library... 
Index Medicus
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 2005, Volume 76, Issue 2, pp. 205 - 214
Journal Article
Journal of Neuromuscular Diseases, ISSN 2214-3599, 2015, Volume 2, Issue 1, pp. 1 - 11
MicroRNAs (miRNAs) are small 21-24 nucleotide RNAs that are capable of regulating multiple signaling pathways across multiple tissues. MicroRNAs are... 
Therapy | Biomarker | Muscle disease | MicroRNA | Dystrophy | Skeletal muscle
Journal Article
Cell, ISSN 0092-8674, 11/2015, Volume 163, Issue 5, pp. 1204 - 1213
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 3/2011, Volume 108, Issue 13, pp. 5331 - 5336
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 6, pp. 601 - 606
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2012, Volume 109, Issue 4, p. 16234
  Facioscapulohumeral muscular dystrophy (FSHD) is a progressive neuromuscular disorder caused by contractions of repetitive elements within the macrosatellite... 
Tissue | Neuromuscular diseases | Biomarkers | Gene expression | Chromosomes
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2014, Volume 124, Issue 6, pp. 2651 - 2667
Duchenne muscular dystrophy (DMD) is caused by mutations in the gene encoding dystrophin, which results in dysfunctional signaling pathways within muscle.... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | MDX MOUSE | MESSENGER-RNAS | CENTRONUCLEAR MYOPATHY | GLYCOPROTEIN COMPLEX | C2C12 MYOBLAST | TUMOR-SUPPRESSOR | CELL-PROLIFERATION | MYOBLAST FUSION | PROTEIN-KINASE B | Muscular Dystrophy, Animal - genetics | Up-Regulation | Humans | Male | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Muscle Fibers, Skeletal - metabolism | Muscular Dystrophy, Animal - pathology | Guanine Nucleotide Exchange Factors - metabolism | Base Sequence | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cell Line | Guanine Nucleotide Exchange Factors - genetics | Signal Transduction | Mice, Inbred C57BL | PTEN Phosphohydrolase - metabolism | Mice, Transgenic | Muscular Dystrophy, Duchenne - pathology | Nerve Tissue Proteins - genetics | Sequence Homology, Nucleic Acid | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Muscle Fibers, Skeletal - pathology | Mice | MicroRNAs - genetics | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | MicroRNA | Cellular signal transduction | Genetic aspects | Diagnosis | Properties | Genetic regulation | Muscular dystrophy | Muscular system | Mutation | Rodents | Index Medicus | Abridged Index Medicus
Journal Article