The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
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Citations
Cites
Dystrophin: the protein product of the Duchenne muscular dystrophy locus
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Self-citationRapid similarity searches of nucleic acid and protein data banks.
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Cited by
Dystrophin protects the sarcolemma from stresses developed during muscle contraction
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The Molecular Basis of Muscular Dystrophy in the mdx Mouse: a Point Mutation
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Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
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The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
Cooper, B. J., Winand, N. J., Stedman, H., Valentine, B. A., Hoffman, E. P., Kunkel, L. M., Scott, M.-O., Fischbeck, K. H., Kornegay, J. N., Avery, R. J., et al. (1988) · Nature · doi:10.1038/334154a0 · Cited by 428
Self-citationOxidative Stress, Chronic Disease, and Muscle Wasting
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Distributions of Exons and Introns in the Human Genome
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Structure and Evolution of Neurexin Genes: Insight into the Mechanism of Alternative Splicing
Tabuchi, K., & Südhof, T. C. (2002) · Genomics · doi:10.1006/geno.2002.6780 · Cited by 305
Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
Gehrig, S. M., van der Poel, C., Sayer, T. A., Schertzer, J. D., Henstridge, D. C., Church, J. E., Lamon, S., Russell, A. P., Davies, K. E., Febbraio, M. A., et al. (2012) · Nature · doi:10.1038/nature10980 · Cited by 250
Pharmacological strategies for muscular dystrophy
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Creatine monohydrate enhances strength and body composition in Duchenne muscular dystrophy
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Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
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Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia
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Treatment of human disease by adeno-associated viral gene transfer
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Human artificial chromosomes for gene delivery and the development of animal models
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Duchenne's cardiomyopathy in a canine model: electrocardiographic and echocardiographic studies
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A Novel Brain-Specific Isoform of β Spectrin: Isolation and Its Interaction with Munc13
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Metadata
- Authors
- Koenig, M., Monaco, A. P., & Kunkel, L. M.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1988-04
- Volume
- 53
- Issue
- 2
- Pages
- 219-228
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2093377166
- Cited by
- 1,538
- References
- 2
- FWCI
- 36.85
- Type
- journal article
- Language
- en
- Open access
- closed
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.